CC BY-NC-ND 4.0 · Laryngorhinootologie 2021; 100(S 01): S1-S28
DOI: 10.1055/a-1337-6994
Referat

Seltene Erkrankungen der Speicheldrüsen und des Nervus Facialis

Article in several languages: deutsch | English
Claudia Scherl
1   Klinik für Hals-Nasen-Ohrenheilkunde, Kopf- und Halschirurgie, Universitätsklinikum Mannheim
› Author Affiliations

Zusammenfassung

Speicheldrüsenerkrankungen sind, insgesamt gesehen eher selten. In der Europäischen Union (EU) gilt eine Erkrankung als selten, wenn nicht mehr als 5 von 10,000 Menschen in der EU von ihr betroffen sind. Allein in Deutschland leben Schätzungen zufolge etwa 4 Millionen Menschen mit einer seltenen Erkrankung, in der gesamten EU geht man von 30 Millionen aus [1]. Die meisten in der vorliegenden Arbeit beschriebenen Krankheitsbilder der Speicheldrüsen und des N. facialis fallen unter diese Kategorie. Sie bilden eine sehr heterogene Gruppe, deren Behandlung sich auf spezialisierte Zentren konzentriert. Dennoch ist es für den HNO-Arzt unerlässlich, auch diese seltenen Erkrankungen zu erkennen und zu diagnostizieren, um dann die richtigen therapeutischen Schritte einzuleiten. Die Arbeit ist eine Zusammenstellung des gesamten Spektrums angeborener und erworbener seltener Speicheldrüsen- und N. facialis-Erkrankungen. Dabei werden die Ätiologien entzündlicher Erkrankungen, Autoimmunerkrankungen und Tumoren berücksichtigt. Für die einzelnen Themenkomplexe wurde, soweit vorhanden, die aktuelle Literatur ausgewertet und für den Leser in Fakten zusammengefasst. Dazu wird auf die Entwicklung neuer Verfahren in Diagnostik, Bildgebung und Therapie eingegangen. Auch genetische Hintergründe von Tumorerkrankungen bei Speicheldrüsentumoren und die Trends in der Behandlung tumoröser Läsionen des N. facialis werden aufgegriffen. Des Weiteren werden auch seltene Erkrankungen der Speicheldrüsen im Kindesalter betrachtet. Diese können zwar teilweise auch bei Erwachsenen vorkommen, unterscheiden sich aber doch in Häufigkeit und Symptomatik. Auf Grund der Seltenheit der hier abgehandelten Erkrankungen ist es zu empfehlen, diese in spezialisierten Zentren mit entsprechender Erfahrung zu behandeln. Abschließend werden die Schwierigkeiten der Studiendurchführung und die Problematik der Erstellung von Krankheitsregistern beim Thema Speicheldrüsenerkrankungen besprochen, da diese auf Grund der allgemeinen Seltenheit dieser Pathologien besonders relevant sind.



Publication History

Article published online:
30 April 2021

© 2021. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • Literatur

  • 1 Bundesgesundheitsministerium Im Internet https://www.bundesgesundheitsministerium.de/themen/praevention/gesundheitsgefahren/seltene-erkrankungen.html Stand: 28.06.2020. In
  • 2 Thompson RC. Assyrian Medical Texts. Proc R Soc Med 1924; 17: 1-34
  • 3 Melo GM, Cervantes O, Abrahao M. et al. A brief history of salivary gland surgery. Rev Col Bras Cir 2017; 44: 403-412
  • 4 Adams F. The genuine work of Hippocrates. Translated from the Greek with a preliminary discourse and annotations Sydenham Society. 1849
  • 5 Coxe JR. The writings of Hippocrates and Galen Lindsay and Blakiston. 1846
  • 6 Kaadan AN, Dababo MH. Ranula in the Arab Medical Heritage JISHIM. 2006; 5: 57-59
  • 7 Vesalius A. De humani corporis fabrica libre septem. Basileae: Ex officina Ioannis Oporini; 1543
  • 8 Cook HJ. Thomas Wharton’s Adenographia. Med Hist 1998; 42: 411-412
  • 9 Stenonis N. Disputatio Anatomica De glandulis oris, et nuper observatis inde prodeuntibus vasis prima Apud Johannem Elsevirium. 1661
  • 10 Heister L. A general system of surgery in three parts. London: W. Innys, C Davis; 1750
  • 11 Pattison GS. Lecture delivered in Jefferson Medical College. Has the parotid gland ever been extirpated Philadelphia: Jefferson Medical College. 1833
  • 12 Heyfelder JF. Die Versuche mit dem Schwefeläther. Erlangen: Verlag von Carl Heyder; 1847
  • 13 Bradley PatrickJ., Guntinas-Lichius O. Salivary Gland Disorders and Diseases: Diagnosis and Management. 1. Auflg. Stuttgart: Thieme; 2011
  • 14 Bailey H. Parotidectomy: indications and results. Br Med J 1947; 1: 404-407
  • 15 Shucksmith HS, Boyle TM, Walls WK. The surgery of parotid tumours; exposure of main trunk of facial nerve. Br Med J 1951; 2: 830-831
  • 16 Iro H, Uttenweiler V, Zenk J. Kopf-Hals-Sonographie. 1. Aufl . Berlin Heidelberg: Springer; 2000. DOI: 10.1007/978-3-642-57012-4
  • 17 Vogl TJ, Albrecht MH, Nour-Eldin NA. et al. Assessment of salivary gland tumors using MRI and CT: impact of experience on diagnostic accuracy. Radiol Med 2018; 123: 105-116
  • 18 Vogl TJ, Harth M, Siebenhandl P. Different imaging techniques in the head and neck: Assets and drawbacks. World J Radiol 2010; 2: 224-229
  • 19 Lell M, Mantsopoulos K, Uder M. et al. Imaging of the head and neck region. Radiologe 2016; 56: 181-201 quiz 202
  • 20 Iro H, Zenk J. Salivary gland diseases in childhood. Laryngorhinootologie 2014; 93: S103-S125
  • 21 Miyamoto RT, Hamaker RC, Lingeman RE. Goldenhar syndrome. Associated with submandibular gland hyperplasia and hemihypoplasia of the mobile tongue. Arch Otolaryngol 1976; 102: 313-314
  • 22 Sun Z, Sun L, Zhang Z. et al. Congenital salivary fistula of an accessory parotid gland in Goldenhar syndrome. J Laryngol Otol 2012; 126: 103-107
  • 23 Østerhus IN, Skogedal N, Akre H. et al. Salivary gland pathology as a new finding in Treacher Collins syndrome. Am J Med Genet A 2012; 158a: 1320-1325
  • 24 Wiedemann HR. Salivary gland disorders and heredity. Am J Med Genet 1997; 68: 222-224
  • 25 Morton RP, Ahmad Z, Jain P. Plunging ranula: congenital or acquired?. Otolaryngol Head Neck Surg 2010; 142: 104-107
  • 26 Taylor GP. Congenital epithelial tumor of the parotid-sialoblastoma. Pediatr Pathol 1988; 8: 447-452
  • 27 Krolls SO, Trodahl JN, Boyers RC. Salivary gland lesions in children. A survey of 430 cases. Cancer 1972; 30: 459-469
  • 28 Muenscher A, Diegel T, Jaehne M. et al. Benign and malignant salivary gland diseases in children A retrospective study of 549 cases from the Salivary Gland Registry, Hamburg. Auris Nasus Larynx 2009; 36: 326-331
  • 29 Seifert G, Okabe H, Caselitz J. Epithelial salivary gland tumors in children and adolescents. Analysis of 80 cases (Salivary Gland Register 1965–1984). ORL J Otorhinolaryngol Relat Spec 1986; 48: 137-149
  • 30 Callender DL, Frankenthaler RA, Luna MA. et al. Salivary gland neoplasms in children. Arch Otolaryngol Head Neck Surg 1992; 118: 472-476
  • 31 Thariat J, Vedrine PO, Temam S. et al. The role of radiation therapy in pediatric mucoepidermoid carcinomas of the salivary glands. J Pediatr 2013; 162: 839-843
  • 32 Kupferman ME, de la Garza GO, Santillan AA. et al. Outcomes of pediatric patients with malignancies of the major salivary glands. Ann Surg Oncol 2010; 17: 3301-3307
  • 33 Mehta D, Willging JP. Pediatric salivary gland lesions. Semin Pediatr Surg 2006; 15: 76-84
  • 34 Agaimy A, Iro H, Zenk J. Pediatric salivary gland tumors and tumor-like lesions. Pathologe 2017; 38: 294-302
  • 35 Megged O, Baskin E. Neonatal Parotitis. J Pediatr 2018; 196: 319
  • 36 Markowitz-Spence L, Brodsky L, Seidell G. et al. Self-induced pneumoparotitis in an adolescent. Report of a case and review of the literature. Int J Pediatr Otorhinolaryngol 1987; 14: 113-121
  • 37 Han S, Isaacson G. Recurrent pneumoparotid: cause and treatment. Otolaryngol Head Neck Surg 2004; 131: 758-761
  • 38 Tremblay V, Ayad T, Lapointe A. et al. Nontuberculous mycobacterial cervicofacial adenitis in children: epidemiologic study. J Otolaryngol Head Neck Surg 2008; 37: 616-622
  • 39 Mahadevan M, Neeff M, Van Der Meer G. et al. Non-tuberculous mycobacterial head and neck infections in children: Analysis of results and complications for various treatment modalities. Int J Pediatr Otorhinolaryngol 2016; 82: 102-106
  • 40 Lindeboom JA, Kuijper EJ, Bruijnesteijn van Coppenraet ES. et al. Surgical excision versus antibiotic treatment for nontuberculous mycobacterial cervicofacial lymphadenitis in children: a multicenter, randomized, controlled trial. Clin Infect Dis 2007; 44: 1057-1064
  • 41 Zeharia A, Eidlitz-Markus T, Haimi-Cohen Y. et al. Management of nontuberculous mycobacteria-induced cervical lymphadenitis with observation alone. Pediatr Infect Dis J 2008; 27: 920-922
  • 42 Vitali C, Bombardieri S, Jonsson R. et al. Classification criteria for Sjögren’s syndrome: a revised version of the European criteria proposed by the American-European Consensus Group. Ann Rheum Dis 2002; 61: 554-558
  • 43 Nikitakis NG, Rivera H, Lariccia C. et al. Primary Sjögren syndrome in childhood: report of a case and review of the literature. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2003; 96: 42-47
  • 44 Shiboski SC, Shiboski CH, Criswell L. et al. American College of Rheumatology classification criteria for Sjögren’s syndrome: a data-driven, expert consensus approach in the Sjögren’s International Collaborative Clinical Alliance cohort. Arthritis Care Res (Hoboken) 2012; 64: 475-487
  • 45 Pijpe J, Kalk WW, van der Wal JE. et al. Parotid gland biopsy compared with labial biopsy in the diagnosis of patients with primary Sjogren’s syndrome. Rheumatology (Oxford) 2007; 46: 335-341
  • 46 Rice DH. Chronic inflammatory disorders of the salivary glands. Otolaryngol Clin North Am 1999; 32: 813-818
  • 47 Norman JE. M MM Color Atlas and Text of the Salivary Glands London. Mosby; Wolfe: 1997: 337-339
  • 48 Iserì M, Aydìner O, Celìk L. et al. Tuberculosis of the parotid gland. J Laryngol Otol 2005; 119: 311-313
  • 49 Ugga L, Ravanelli M, Pallottino AA. et al. Diagnostic work-up in obstructive and inflammatory salivary gland disorders. Acta Otorhinolaryngol Ital 2017; 37: 83-93
  • 50 Zenk J, Iro H, Klintworth N. et al. Diagnostic imaging in sialadenitis. Oral Maxillofac Surg Clin North Am 2009; 21: 275-292
  • 51 Mourad WF, Young R, Kabarriti R. et al. 25-year follow-up of HIV-positive patients with benign lymphoepithelial cysts of the parotid glands: a retrospective review. Anticancer Res 2013; 33: 4927-4932
  • 52 Lawn SD, Checkley A, Wansbrough-Jones MH. Acute bilateral parotitis caused by Mycobacterium scrofulaceum: immune reconstitution disease in a patient with AIDS. Sex Transm Infect 2005; 81: 517-518
  • 53 Schiødt M, Dodd CL, Greenspan D. et al. Natural history of HIV-associated salivary gland disease. Oral Surg Oral Med Oral Pathol 1992; 74: 326-331
  • 54 Mastroianni A. Emergence of Sjögren’s syndrome in AIDS patients during highly active antiretroviral therapy. Aids 2004; 18: 1349-1352
  • 55 Greaves WO, Wang SA. Selected topics on lymphoid lesions in the head and neck regions. Head and neck pathology 2011; 5: 41-50
  • 56 Naidoo M, Singh B, Ramdial PK. et al. Lymphoepithelial lesions of the parotid gland in the HIV era--a South African experience. South African journal of surgery Suid-Afrikaanse tydskrif vir chirurgie 2007; 45: 136-138 140
  • 57 McArthur CP, Africa CW, Castellani WJ. et al. Salivary gland disease in HIV/AIDS and primary Sjögren’s syndrome: analysis of collagen I distribution and histopathology in American and African patients. J Oral Pathol Med 2003; 32: 544-551
  • 58 Mandel L, Surattanont F. Bilateral parotid swelling: a review. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2002; 93: 221-237
  • 59 Carrozzo M. Oral diseases associated with hepatitis C virus infection. Part 1. sialadenitis and salivary glands lymphoma. Oral Dis 2008; 14: 123-130
  • 60 Haddad J, Deny P, Munz-Gotheil C. et al. Lymphocytic sialadenitis of Sjögren’s syndrome associated with chronic hepatitis C virus liver disease. Lancet 1992; 339: 321-323
  • 61 Jorgensen C, Legouffe MC, Perney P. et al. Sicca syndrome associated with hepatitis C virus infection. Arthritis Rheum 1996; 39: 1166-1171
  • 62 Doffoël-Hantz V, Loustaud-Ratti V, Ramos-Casals M. et al. Evolution of Sjögren syndrome associated with hepatitis C virus when chronic hepatitis C is treated by interferon or the association of interferon and ribavirin. Rev Med Interne 2005; 26: 88-94
  • 63 Ascoli V, Lo Coco F, Artini M. et al. Extranodal lymphomas associated with hepatitis C virus infection. Am J Clin Pathol 1998; 109: 600-609
  • 64 Ambrosetti A, Zanotti R, Pattaro C. et al. Most cases of primary salivary mucosa-associated lymphoid tissue lymphoma are associated either with Sjoegren syndrome or hepatitis C virus infection. Br J Haematol 2004; 126: 43-49
  • 65 Bartels LJ, Vrabec DP. Cervicofacial actinomycosis. Arch Otolaryngol 1978; 104: 705-708
  • 66 Mullins JE, Ogle O, Cottrell DA. Painless mass in the parotid region. J Oral Maxillofac Surg 2000; 58: 316-319
  • 67 Lang-Roth R, Schippers C, Eckel HE. Cervical actinomycosis. A rare differential diagnosis of parotid tumor. Hno 1998; 46: 354-358
  • 68 Ermis I, Topalan M, Aydin A. et al. Actinomycosis of the frontal and parotid regions. Ann Plast Surg 2001; 46: 55-58
  • 69 Barabás J, Suba Z, Szabó G. et al. False diagnosis caused by Warthin tumor of the parotid gland combined with actinomycosis. J Craniofac Surg 2003; 14: 46-50
  • 70 Jackson LA, Perkins BA, Wenger JD. Cat scratch disease in the United States: an analysis of three national databases. Am J Public Health 1993; 83: 1707-1711
  • 71 Hadley S, Albrecht MA, Tarsy D. Cat-scratch encephalopathy: a cause of status epilepticus and coma in a healthy young adult. Neurology 1995; 45: 196
  • 72 Xu DL, Wang Z, Song YJ. Cat-scratch disease encephalopathy. Chin Med J (Engl) 1994; 107: 104-106
  • 73 Dolan MJ, Wong MT, Regnery RL. et al. Syndrome of Rochalimaea henselae adenitis suggesting cat scratch disease. Ann Intern Med 1993; 118: 331-336
  • 74 Demers DM, Bass JW, Vincent JM. et al. Cat-scratch disease in Hawaii: etiology and seroepidemiology. J Pediatr 1995; 127: 23-26
  • 75 Dalton MJ, Robinson LE, Cooper J. et al. Use of Bartonella antigens for serologic diagnosis of cat-scratch disease at a national referral center. Arch Intern Med 1995; 155: 1670-1676
  • 76 Finkensieper M, Volk GF, Guntinas-Lichius O. Inflammatory salivary gland diseases. Laryngorhinootologie 2013; 92: 119-136 quiz 137
  • 77 Qin B, Wang J, Yang Z. et al. Epidemiology of primary Sjögren’s syndrome: a systematic review and meta-analysis. Ann Rheum Dis 2015; 74: 1983-1989
  • 78 Meijer JM, Meiners PM, Huddleston Slater JJ. et al. Health-related quality of life, employment and disability in patients with Sjogren’s syndrome. Rheumatology (Oxford) 2009; 48: 1077-1082
  • 79 Mariette X, Criswell LA. Primary Sjögren’s Syndrome. N Engl J Med 2018; 378: 931-939
  • 80 Shiboski CH, Shiboski SC, Seror R. et al. 2016 American College of Rheumatology/European League Against Rheumatism Classification Criteria for Primary Sjögren’s Syndrome: A Consensus and Data-Driven Methodology Involving Three International Patient Cohorts. Arthritis Rheumatol 2017; 69: 35-45
  • 81 Gallo A, Benazzo M, Capaccio P. et al. Sialoendoscopy: state of the art, challenges and further perspectives. Round Table, 101(st) SIO National Congress, Catania 2014. Acta Otorhinolaryngol Ital 2015; 35: 217-233
  • 82 Rusakiewicz S, Nocturne G, Lazure T. et al. NCR3/NKp30 contributes to pathogenesis in primary Sjogren’s syndrome. Sci Transl Med 2013; 5: 195ra196
  • 83 Hall JC, Casciola-Rosen L, Berger AE. et al. Precise probes of type II interferon activity define the origin of interferon signatures in target tissues in rheumatic diseases. Proc Natl Acad Sci U S A 2012; 109: 17609-17614
  • 84 Ramos-Casals M, Tzioufas AG, Stone JH. et al. Treatment of primary Sjögren syndrome: a systematic review. Jama 2010; 304: 452-460
  • 85 Nocturne G, Mariette X. B cells in the pathogenesis of primary Sjögren syndrome. Nat Rev Rheumatol 2018; 14: 133-145
  • 86 Himi T, Takano K, Yamamoto M. et al. A novel concept of Mikulicz’s disease as IgG4-related disease. Auris Nasus Larynx 2012; 39: 9-17
  • 87 Li W, Chen Y, Sun ZP. et al. Clinicopathological characteristics of immunoglobulin G4-related sialadenitis. Arthritis Res Ther 2015; 17: 186
  • 88 Küttner H. Über entzündiche Tumoren der submaxillären Speicheldrüse. Beitr Klin Chir, bruns beitrag klin chir 1896; 15: 815-828
  • 89 Billroth T, Mikulicz J. Über eine eigenartige symmetrishe Erkrankung der Thränen-und Mundspeicheldrüsen. Stuttgart: Beitr z Chir Festschr f Theodor Billroth; 1892: 610-630
  • 90 Yamamoto M, Takahashi H, Ohara M. et al. A new conceptualization for Mikulicz’s disease as an IgG4-related plasmacytic disease. Mod Rheumatol 2006; 16: 335-340
  • 91 Mulholland GB, Jeffery CC, Satija P. et al. Immunoglobulin G4-related diseases in the head and neck: a systematic review. J Otolaryngol Head Neck Surg 2015; 44: 24
  • 92 Moriyama M, Tanaka A, Maehara T. et al. T helper subsets in Sjögren’s syndrome and IgG4-related dacryoadenitis and sialoadenitis: a critical review. J Autoimmun 2014; 51: 81-88
  • 93 Yamamoto M, Yajima H, Takahashi H. et al. Everyday clinical practice in IgG4-related dacryoadenitis and/or sialadenitis: results from the SMART database. Mod Rheumatol 2015; 25: 199-204
  • 94 Wu JJ, Schiff KR. Sarcoidosis. Am Fam Physician 2004; 70: 312-322
  • 95 Rosen Y. Pathology of sarcoidosis. Semin Respir Crit Care Med 2007; 28: 36-52
  • 96 Mrówka-Kata K, Kata D, Lange D. et al. Sarcoidosis and its otolaryngological implications. Eur Arch Otorhinolaryngol 2010; 267: 1507-1514
  • 97 Sinha R, Gaur SN. Sarcoidosis presenting as acute bilateral parotid swelling. Asian Pac J Allergy Immunol 2004; 22: 171-174
  • 98 Teymoortash A, Werner JA. Parotid gland involvement in sarcoidosis: sonographic features. J Clin Ultrasound 2009; 37: 507-510
  • 99 Walter C, Schwarting A, Hansen T. et al. Heerfordt’s syndrome – a rare initial manifestation of sarcoidosis. Mund Kiefer Gesichtschir 2005; 9: 43-47
  • 100 Fischer T, Filimonow S, Petersein J. et al. Diagnosis of Heerfordt’s syndrome by state-of-the-art ultrasound in combination with parotid biopsy: a case report. Eur Radiol 2002; 12: 134-137
  • 101 Cakmak SK, Gönül M, Gül U. et al. Sarcoidosis involving the lacrimal, submandibular, and parotid glands with panda sign. Dermatol Online J 2009; 15: 8
  • 102 Aladesanmi OA. Sarcoidosis: an update for the primary care physician. MedGenMed 2004; 6: 7
  • 103 Ussmüller J, Donath K, Shimizu M. et al. Differential diagnosis of tumorous space-occupying lesions of the parotid gland: angiolymphoid hyperplasia with eosinophilia and Kimura disease. Laryngorhinootologie 1997; 76: 110-115
  • 104 Kumar V, Salini Haridas S. Kimura’s disease: An uncommon cause of lymphadenopathy. Indian J Med Paediatr Oncol 2010; 31: 89-90
  • 105 Rosai J, Dorfman RF. Sinus histiocytosis with massive lymphadenopathy. A newly recognized benign clinicopathological entity. Arch Pathol 1969; 87: 63-70
  • 106 Goodnight JW, Wang MB, Sercarz JA. et al. Extranodal Rosai-Dorfman disease of the head and neck. Laryngoscope 1996; 106: 253-256
  • 107 Eisen RN, Buckley PJ, Rosai J. Immunophenotypic characterization of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease). Semin Diagn Pathol 1990; 7: 74-82
  • 108 Foucar E, Rosai J, Dorfman RF. Sinus histiocytosis with massive lymphadenopathy. Current status and future directions. Arch Dermatol 1988; 124: 1211-1214
  • 109 Reiß M. Facharztwissen HNO-Heilkunde: Differenzierte Diagnostik und Therapie. 1. Auflg. Heidelberg: Springer; 2009
  • 110 López-Pintor RM, Casañas E, González-Serrano J. et al. Xerostomia, Hyposalivation, and Salivary Flow in Diabetes Patients. J Diabetes Res 2016; 2016: 4372852
  • 111 Alavi AA, Amirhakimi E, Karami B. The prevalence of dental caries in 5 – 18-year-old insulin-dependent diabetics of Fars Province, southern Iran. Arch Iran Med 2006; 9: 254-260
  • 112 Syrjälä AM, Raatikainen L, Komulainen K. et al. Salivary flow rate and periodontal infection - a study among subjects aged 75 years or older. Oral Dis 2011; 17: 387-392
  • 113 de la Rosa García E, Mondragón Padilla A, Aranda Romo S. et al. Oral mucosa symptoms, signs and lesions, in end stage renal disease and non-end stage renal disease diabetic patients. Med Oral Patol Oral Cir Bucal 2006; 11: E467-E473
  • 114 von Bültzingslöwen I, Sollecito TP, Fox PC. et al. Salivary dysfunction associated with systemic diseases: systematic review and clinical management recommendations. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2007; 103: S57.e51-15
  • 115 Carbone DF, Sweeney EA, Shaw JH. The comparative influence of thyroid imbalance and limited body weight gain on submandibular gland weight, the protein components of saliva and dental caries in the rat. Arch Oral Biol 1966; 11: 781-792
  • 116 Muralidharan D, Fareed N, Pradeep PV. et al. Qualitative and quantitative changes in saliva among patients with thyroid dysfunction prior to and following the treatment of the dysfunction. Oral Surg Oral Med Oral Pathol Oral Radiol 2013; 115: 617-623
  • 117 Psoter WJ, Spielman AL, Gebrian B. et al. Effect of childhood malnutrition on salivary flow and pH. Arch Oral Biol 2008; 53: 231-237
  • 118 Brown S, Bonifazi DZ. An overview of anorexia and bulimia nervosa, and the impact of eating disorders on the oral cavity. Compendium. 1993 14. 1594, 1596–1602, 1604-1598; quiz 1608
  • 119 Dreiling DA, Noronha M, Nacchiero M. et al. The parotid and the pancreas. VI. Clinical and physiologic associations between the pancreas and parotid glands. Am J Gastroenterol 1978; 70: 627-634
  • 120 Riad M, Barton JR, Wilson JA. et al. Parotid salivary secretory pattern in bulimia nervosa. Acta Otolaryngol 1991; 111: 392-395
  • 121 Herrlinger P, Gundlach P. Hypertrophy of the salivary glands in bulimia. Hno 2001; 49: 557-559
  • 122 Abdollahi M, Radfar M. A review of drug-induced oral reactions. J Contemp Dent Pract 2003; 4: 10-31
  • 123 Strychowsky JE, Sommer DD, Gupta MK. et al. Sialendoscopy for the management of obstructive salivary gland disease: a systematic review and meta-analysis. Arch Otolaryngol Head Neck Surg 2012; 138: 541-547
  • 124 Ngu RK, Brown JE, Whaites EJ. et al. Salivary duct strictures: nature and incidence in benign salivary obstruction. Dentomaxillofac Radiol 2007; 36: 63-67
  • 125 Koch M, Zenk J, Bozzato A. et al. Sialoscopy in cases of unclear swelling of the major salivary glands. Otolaryngol Head Neck Surg 2005; 133: 863-868
  • 126 Nahlieli O, Shacham R, Yoffe B. et al. Diagnosis and treatment of strictures and kinks in salivary gland ducts. J Oral Maxillofac Surg 2001; 59: 484-490 discussion, 490–482
  • 127 Roberts DN, Juman S, Hall JR. et al. Parotid duct stenosis: interventional radiology to the rescue. Ann R Coll Surg Engl 1995; 77: 444-446
  • 128 Buckenham T, Guest P. Interventional sialography using digital imaging. Australas Radiol 1993; 37: 76-79
  • 129 Koch M, Iro H. Salivary duct stenosis: diagnosis and treatment. Acta Otorhinolaryngol Ital 2017; 37: 132-141
  • 130 Gadodia A, Seith A, Sharma R. et al. Magnetic resonance sialography using CISS and HASTE sequences in inflammatory salivary gland diseases: comparison with digital sialography. Acta radiologica (Stockholm, Sweden: 1987) 2010; 51: 156-163
  • 131 Koch M, Iro H, Zenk J. Role of sialoscopy in the treatment of Stensen’s duct strictures. Ann Otol Rhinol Laryngol 2008; 117: 271-278
  • 132 Katz P. Endoscopy of the salivary glands. Ann Radiol (Paris) 1991; 34: 110-113
  • 133 Marchal F, Dulguerov P, Becker M. et al. Specificity of parotid sialendoscopy. Laryngoscope 2001; 111: 264-271
  • 134 Nahlieli O, Baruchin AM. Long-term experience with endoscopic diagnosis and treatment of salivary gland inflammatory diseases. Laryngoscope 2000; 110: 988-993
  • 135 Zenk J, Koch M, Bozzato A. et al. Sialoscopy – initial experiences with a new endoscope. Br J Oral Maxillofac Surg 2004; 42: 293-298
  • 136 Motamed M, Laugharne D, Bradley PJ. Management of chronic parotitis: a review. J Laryngol Otol 2003; 117: 521-526
  • 137 McGurk M, Escudier MP, Thomas BL. et al. A revolution in the management of obstructive salivary gland disease. Dent Update 2006; 33: 28-30, 33–26
  • 138 Koch M, Iro H, Künzel J. et al. Diagnosis and gland-preserving minimally invasive therapy for Wharton’s duct stenoses. Laryngoscope 2012; 122: 552-558
  • 139 Koch M, Zenk J, Iro H. Diagnostic and interventional sialoscopy in obstructive diseases of the salivary glands. Hno 2008; 56: 139-144
  • 140 Salerno S, Lo Casto A, Comparetto A. et al. Sialodochoplasty in the treatment of salivary-duct stricture in chronic sialoadenitis: technique and results. Radiol Med 2007; 112: 138-144
  • 141 Qi S, Liu X, Wang S. Sialoendoscopic and irrigation findings in chronic obstructive parotitis. Laryngoscope 2005; 115: 541-545
  • 142 Yu C, Zheng L, Yang C. et al. Causes of chronic obstructive parotitis and management by sialoendoscopy. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2008; 105: 365-370
  • 143 Koch M, Iro H, Zenk J. Stenosis and other non-sialolithiasis-related obstructions of the major salivary gland ducts. Modern treatment concepts. Hno 2010; 58: 218-224
  • 144 Luers JC, Guntinas-Lichius O, Klussmann JP. et al. The incidence of Warthin tumours and pleomorphic adenomas in the parotid gland over a 25-year period. Clin Otolaryngol 2016; 41: 793-797
  • 145 Geiger A, Storck C. ORL 15. Basal cell adenoma of the right parotid gland. Praxis (Bern 1994; 104: 480-481
  • 146 González-García R, Nam-Cha SH, Muñoz-Guerra MF. et al. Basal cell adenoma of the parotid gland. Case report and review of the literature. Med Oral Patol Oral Cir Bucal 2006; 11: E206-E209
  • 147 Wilson TC, Robinson RA. Basal cell adenocarcinoma and Basal cell adenoma of the salivary glands: a clinicopathological review of seventy tumors with comparison of morphologic features and growth control indices. Head and neck pathology 2015; 9: 205-213
  • 148 Agaimy A, Ihrler S, Märkl B. et al. Lipomatous salivary gland tumors: a series of 31 cases spanning their morphologic spectrum with emphasis on sialolipoma and oncocytic lipoadenoma. Am J Surg Pathol 2013; 37: 128-137
  • 149 Ihrler S, Guntinas-Lichius O, Haas C. et al. Updates on tumours of the salivary glands : 2017 WHO classification. Pathologe 2018; 39: 11-17
  • 150 Sharma V, Kumar S, Sethi A. Oncocytoma Parotid Gland. Ann Maxillofac Surg 2018; 8: 330-332
  • 151 Alós L, Cardesa A, Bombí JA. et al. Myoepithelial tumors of salivary glands: a clinicopathologic, immunohistochemical, ultrastructural, and flow-cytometric study. Semin Diagn Pathol 1996; 13: 138-147
  • 152 Lehmann S, Tzamalis G, Reichelt U. et al. Leiomyoma. A rare neoplasia of the parotid gland. Hno 2012; 60: 659-661
  • 153 Kido T, Sekitani T. Vascular leiomyoma of the parotid gland. ORL J Otorhinolaryngol Relat Spec 1989; 51: 187-191
  • 154 Geissler M, Just T, Prall F. et al. Space-occupying lesion of the hard palate. Hno 2007; 55: 48-50
  • 155 Hansen T, Katenkamp D. Rhabdomyoma of the head and neck: morphology and differential diagnosis. Virchows Archiv: an international journal of pathology 2005; 447: 849-854
  • 156 Amelia Souza A, de Araújo VC, Passador Santos F. et al. Intraoral adult rhabdomyoma: a case report. Case reports in dentistry 2013; 2013: 741548
  • 157 McGregor DK, Krishnan B, Green L. Fine-needle aspiration of adult rhabdomyoma: a case report with review of the literature. Diagnostic cytopathology 2003; 28: 92-95
  • 158 Favia G, Lo Muzio L, Serpico R. et al. Rhabdomyoma of the head and neck: clinicopathologic features of two cases. Head & neck 2003; 25: 700-704
  • 159 Bellis D, Torre V, Nunziata R. et al. Submandibular rhabdomyoma: a case report. Acta cytologica 2006; 50: 557-559
  • 160 Welzel C, Gajda M, Jamali Y. et al. Adult multilocular rhabdomyoma as etiology of a space-occupying lesion in the area of the neck. Hno 2001; 49: 553-556
  • 161 Testa D, Galera F, Insabato L. et al. Submandibular gland myoepithelioma. Acta Otolaryngol 2005; 125: 664-666
  • 162 Podzimek J, Jecker P, Daliri A. A rare cause of swelling in the parotid region. Hno 2018; 66: 702-704
  • 163 Woodhouse NR, Gok G, Saha S. et al. A rare cause of a parotid mass: spontaneous pseudoaneurysm of the superficial temporal artery. International journal of oral and maxillofacial surgery 2010; 39: 1234-1236
  • 164 Pennell DJ, Asimakopoulos P, Vallamkondu V. et al. Idiopathic pseudoaneurysm: a rare cause of parotid mass. BMJ case reports 2015; 2015; 1-3
  • 165 Wong KT, Ahuja AT, King AD. et al. Vascular lesions of parotid gland in adult patients: diagnosis with high-resolution ultrasound and MRI. The British journal of radiology 2004; 77: 600-606
  • 166 Ganc DT, Prestigiacomo C, Baredes S. Intraparotid arterial aneurysm treated with embolization followed by surgical resection. Ear, nose, & throat journal 2012; 91: E4-E6
  • 167 Bernstein JM, Bury RW, Nigam A. Superficial temporal artery pseudoaneurysm: first reported case after parotid surgery. J Laryngol Otol 2010; 124: 441-442
  • 168 Brandt A, Schaefer IM, Rustenbeck HH. et al. Aneurysm of the superficial temporal artery following parotid gland surgery – case report and review of the literature. Oral and maxillofacial surgery 2013; 17: 307-309
  • 169 Trainotti S, Schick M, Scheithauer M. et al. Pulsatile tumor in the parotideal area. Laryngorhinootologie 2014; 93: 256-257
  • 170 Bradley PJ. ’Metastasizing pleomorphic salivary adenoma’ should now be considered a low-grade malignancy with a lethal potential. Curr Opin Otolaryngol Head Neck Surg 2005; 13: 123-126
  • 171 Seethala RR, Stenman G. Update from the 4th Edition of the World Health Organization Classification of Head and Neck Tumours: Tumors of the Salivary Gland. Head and neck pathology 2017; 11: 55-67
  • 172 Watson M, McAllister P, Conn B. et al. Metastasising Pleomorphic Salivary Adenoma: A Rare Case Report of a Massive Untreated Minor Salivary Gland Pleomorphic Adenoma with Concurrent Ipsilateral Cervical Node Metastases. Head and neck pathology 2019; 13: 500-506
  • 173 Howlader N NA Krapcho M, Miller D, Brest A, Yu M, Ruhl J, Tatalovich Z, Mariotto A, Lewis DR, Chen HS, Feuer EJ, Cronin KA. SEER Cancer Statistics Review, 1975-2016, National Cancer Institute. Bethesda, MD: Im Internet: https://seer.cancer.gov/csr/1975_2016/ Stand: April 2019
  • 174 Jones AV, Craig GT, Speight PM. et al. The range and demographics of salivary gland tumours diagnosed in a UK population. Oral Oncol 2008; 44: 407-417
  • 175 Bastian T, D’Heygere V, Deuß E. et al. Results of surgical and radiotherapeutic treatment of adenoid cystic carcinoma of the salivary glands. Hno 2020; 68: 678-687
  • 176 Vázquez A, Patel TD, D’Aguillo CM. et al. Epithelial-Myoepithelial Carcinoma of the Salivary Glands: An Analysis of 246 Cases. Otolaryngol Head Neck Surg 2015; 153: 569-574
  • 177 Bishop JA, Westra WH. MYB Translocation Status in Salivary Gland Epithelial-Myoepithelial Carcinoma: Evaluation of Classic, Variant, and Hybrid Forms. Am J Surg Pathol 2018; 42: 319-325
  • 178 Savera AT, Sloman A, Huvos AG. et al. Myoepithelial carcinoma of the salivary glands: a clinicopathologic study of 25 patients. Am J Surg Pathol 2000; 24: 761-774
  • 179 Takahashi H, Fujita S, Tsuda N. et al. Intraoral minor salivary gland tumors: a demographic and histologic study of 200 cases. Tohoku J Exp Med 1990; 161: 111-128
  • 180 Chaudhari P, Kaur J, Nalwa A. et al. Epithelial Myoepithelial Carcinoma of Parotid Gland. Indian J Otolaryngol Head Neck Surg 2019; 71: 62-65
  • 181 Hosal AS, Fan C, Barnes L. et al. Salivary duct carcinoma. Otolaryngol Head Neck Surg 2003; 129: 720-725
  • 182 Scherl C, Haderlein M, Agaimy A. et al. Outcome and management of rare high-grade “salivary” adenocarcinoma: the important role of adjuvant (chemo)radiotherapy. Strahlenther Onkol 2019; 195: 1050-1059
  • 183 Johnston ML, Huang SH, Waldron JN. et al. Salivary duct carcinoma: Treatment, outcomes, and patterns of failure. Head & neck 2016; 38: E820-E826
  • 184 Kleinsasser O, Klein HJ, Hübner G. Salivary duct carcinoma. A group of salivary gland tumors analogous to mammary duct carcinoma. Arch Klin Exp Ohren Nasen Kehlkopfheilkd 1968; 192: 100-105
  • 185 Jayaprakash V, Merzianu M, Warren GW. et al. Survival rates and prognostic factors for infiltrating salivary duct carcinoma: Analysis of 228 cases from the Surveillance, Epidemiology, and End Results database. Head & neck 2014; 36: 694-701
  • 186 Huang X, Hao J, Chen S. et al. Salivary duct carcinoma: A clinopathological report of 11 cases. Oncol Lett 2015; 10: 337-341
  • 187 Udager AM, Chiosea SI. Salivary Duct Carcinoma: An Update on Morphologic Mimics and Diagnostic Use of Androgen Receptor Immunohistochemistry. Head and neck pathology 2017; 11: 288-294
  • 188 Gilbert MR, Sharma A, Schmitt NC. et al. A 20-Year Review of 75 Cases of Salivary Duct Carcinoma. JAMA Otolaryngol Head Neck Surg 2016; 142: 489-495
  • 189 Xiao CC, Zhan KY, White-Gilbertson SJ. et al. Predictors of Nodal Metastasis in Parotid Malignancies: A National Cancer Data Base Study of 22,653 Patients. Otolaryngol Head Neck Surg 2016; 154: 121-130
  • 190 Haderlein M, Scherl C, Semrau S. et al. Impact of postoperative radiotherapy and HER2/new overexpression in salivary duct carcinoma: A monocentric clinicopathologic analysis. Strahlenther Onkol 2017; 193: 961-970
  • 191 Skálová A, Gnepp DR, Simpson RH. et al. Clonal nature of sclerosing polycystic adenosis of salivary glands demonstrated by using the polymorphism of the human androgen receptor (HUMARA) locus as a marker. Am J Surg Pathol 2006; 30: 939-944
  • 192 Agaimy A, Hartmann A. Head and neck neoplasms : News from the WHO classification of 2017. Pathologe 2018; 39: 1-2
  • 193 Chiosea SI, Griffith C, Assaad A. et al. Clinicopathological characterization of mammary analogue secretory carcinoma of salivary glands. Histopathology 2012; 61: 387-394
  • 194 Drilon A, Li G, Dogan S. et al. What hides behind the MASC: clinical response and acquired resistance to entrectinib after ETV6-NTRK3 identification in a mammary analogue secretory carcinoma (MASC). Ann Oncol 2016; 27: 920-926
  • 195 Costa AF, Altemani A, Hermsen M. Current concepts on dedifferentiation/high-grade transformation in salivary gland tumors. Patholog Res Int 2011; 2011: 325965
  • 196 Williams L, Thompson LD, Seethala RR. et al. Salivary duct carcinoma: the predominance of apocrine morphology, prevalence of histologic variants, and androgen receptor expression. Am J Surg Pathol 2015; 39: 705-713
  • 197 Seethala RR, Dacic S, Cieply K. et al. A reappraisal of the MECT1/MAML2 translocation in salivary mucoepidermoid carcinomas. Am J Surg Pathol 2010; 34: 1106-1121
  • 198 Skálová A, Vanecek T, Sima R. et al. Mammary analogue secretory carcinoma of salivary glands, containing the ETV6-NTRK3 fusion gene: a hitherto undescribed salivary gland tumor entity. Am J Surg Pathol 2010; 34: 599-608
  • 199 Antonescu CR, Katabi N, Zhang L. et al. EWSR1-ATF1 fusion is a novel and consistent finding in hyalinizing clear-cell carcinoma of salivary gland. Genes Chromosomes Cancer 2011; 50: 559-570
  • 200 Persson M, Andrén Y, Mark J. et al. Recurrent fusion of MYB and NFIB transcription factor genes in carcinomas of the breast and head and neck. Proc Natl Acad Sci U S A 2009; 106: 18740-18744
  • 201 Carlson J, Licitra L, Locati L. et al. Salivary gland cancer: an update on present and emerging therapies. Am Soc Clin Oncol Educ Book 2013; 257-263 DOI: 10.14694/EdBook_AM.2013.33.257.
  • 202 Takahashi H, Tada Y, Saotome T. et al. Phase II Trial of Trastuzumab and Docetaxel in Patients With Human Epidermal Growth Factor Receptor 2-Positive Salivary Duct Carcinoma. J Clin Oncol 2019; 37: 125-134
  • 203 Limaye SA, Posner MR, Krane JF. et al. Trastuzumab for the treatment of salivary duct carcinoma. The oncologist 2013; 18: 294-300
  • 204 Fushimi C, Tada Y, Takahashi H. et al. A prospective phase II study of combined androgen blockade in patients with androgen receptor-positive metastatic or locally advanced unresectable salivary gland carcinoma. Ann Oncol 2018; 29: 979-984
  • 205 Skálová A, Stenman G, Simpson RHW. et al. The Role of Molecular Testing in the Differential Diagnosis of Salivary Gland Carcinomas. Am J Surg Pathol 2018; 42: e11-e27
  • 206 Doescher J, Schuler PJ, Greve J. et al. Salivary gland malignancies-highlights of the 2019 ASCO Annual Meeting. Hno 2019; 67: 931-934
  • 207 U.S. National Library of Medicine. Im Internet https://clinicaltrials.gov/ct2/show/NCT02749903 Stand: 01.07.2020
  • 208 U.S. National Library of Medicine. https://clinicaltrials.gov/ct2/show/NCT01969578
  • 209 Rack SLY, McKay C. A study to determine the utility of focused genomic profiling to guide selection of drug therapy in salivary gland cancer. J Clin Oncol. 2019 37. 6086. https://doi-orgezproxymedmauni-heidelbergde/101200/JCO2019
  • 210 U.S. National Library of Medicine. Im Internet https://clinicaltrials.gov/ct2/show/NCT03132038; Stand: 01.07.2020
  • 211 U.S. National Library of Medicine. Im Internet https://clinicaltrials.gov/ct2/show/NCT03087019; Stand: 01.07.2020
  • 212 U.S. National Library of Medicine. Im Internet: https://clinicaltrials.gov/ct2/show/NCT03172624; Stand: 01.07.2020
  • 213 Guntinas-Lichius O. Quality of Care for Salivary Gland Diseases. Laryngorhinootologie 2020; 99: S301-S335
  • 214 Berufsverband Medizinischer Informatiker e.V. Im Internet: https://www.bvmi.de/index.php?option=com_content&view=article&id=96:krankheitsregister&catid=18 Stand: 01.07.2020
  • 215 Scherl C, Kato MG, Erkul E. et al. Outcomes and prognostic factors for parotid acinic cell Carcinoma: A National Cancer Database study of 2362 cases. Oral Oncol 2018; 82: 53-60
  • 216 knw Kindernetzwerk e.V. Im Internet https://www.kindernetzwerk.de/downloads/aktiv/2019/chronisch.pdf;Stand: 01.07.2020
  • 217 Tawfik EA, Walker FO, Cartwright MS. A Pilot Study of Diagnostic Neuromuscular Ultrasound in Bell’s Palsy. Journal of neuroimaging : official journal of the American Society of Neuroimaging 2015; 25: 564-570
  • 218 Lo YL, Fook-Chong S, Leoh TH. et al. High-resolution ultrasound in the evaluation and prognosis of Bell’s palsy. European journal of neurology 2010; 17: 885-889
  • 219 Wegscheider H, Volk GF, Guntinas-Lichius O. et al. High-resolution ultrasonography of the normal extratemporal facial nerve. Eur Arch Otorhinolaryngol 2018; 275: 293-299
  • 220 Rabinov JD, Barker FG, McKenna MJ. et al. Virtual cisternoscopy: 3D MRI models of the cerebellopontine angle for lesions related to the cranial nerves. Skull base: official journal of North American Skull Base Society [et al] 2004; 14: 93-99 discussion 99
  • 221 Guenette JP, Seethamraju RT, Jayender J. et al. MR Imaging of the Facial Nerve through the Temporal Bone at 3T with a Noncontrast Ultrashort Echo Time Sequence. AJNR American journal of neuroradiology 2018; 39: 1903-1906
  • 222 Chu J, Zhou Z, Hong G. et al. High-resolution MRI of the intraparotid facial nerve based on a microsurface coil and a 3D reversed fast imaging with steady-state precession DWI sequence at 3T. AJNR American journal of neuroradiology 2013; 34: 1643-1648
  • 223 Guenette JP, Ben-Shlomo N, Jayender J. et al. MR Imaging of the Extracranial Facial Nerve with the CISS Sequence. AJNR American journal of neuroradiology 2019; 40: 1954-1959
  • 224 Takahashi N, Okamoto K, Ohkubo M. et al. High-resolution magnetic resonance of the extracranial facial nerve and parotid duct: demonstration of the branches of the intraparotid facial nerve and its relation to parotid tumours by MRI with a surface coil. Clinical radiology 2005; 60: 349-354
  • 225 Wen J, Desai NS, Jeffery D. et al. High-Resolution Isotropic Three-Dimensional MR Imaging of the Extraforaminal Segments of the Cranial Nerves. Magnetic resonance imaging clinics of North America 2018; 26: 101-119
  • 226 Takahara T, Hendrikse J, Yamashita T. et al. Diffusion-weighted MR neurography of the brachial plexus: feasibility study. Radiology 2008; 249: 653-660
  • 227 Lee MK, Choi Y, Jang J. et al. Identification of the intraparotid facial nerve on MRI: a systematic review and meta-analysis. Eur Radiol. 2020 DOI: 10.1007/s00330-020-07222-9
  • 228 Harvey SA, Fox MC. Relevant issues in revision canal-wall-down mastoidectomy. Otolaryngol Head Neck Surg 1999; 121: 18-22
  • 229 Selesnick SH, Lynn-Macrae AG. The incidence of facial nerve dehiscence at surgery for cholesteatoma. Otol Neurotol 2001; 22: 129-132
  • 230 Di Martino E, Sellhaus B, Haensel J. et al. Fallopian canal dehiscences: a survey of clinical and anatomical findings. Eur Arch Otorhinolaryngol 2005; 262: 120-126
  • 231 Welling DB, Glasscock ME, Gantz BJ. Avulsion of the anomalous facial nerve at stapedectomy. Laryngoscope 1992; 102: 729-733
  • 232 Djerić D, Savić D. Otogenic facial paralysis. A histopathological study. Eur Arch Otorhinolaryngol 1990; 247: 143-146
  • 233 Shinnabe A, Yamamoto H, Hara M. et al. Fallopian canal dehiscence at pediatric cholesteatoma surgery. Eur Arch Otorhinolaryngol 2014; 271: 2927-2930
  • 234 De la Cruz A, Teufert K. Congenital malformation of the external auditory canal and middle ear. In: Brackmann, D, Shelton, C, Arriaga, M eds. Otologic Surgery. 3. Aufl. Philadelphia: Saunders; 2010: 55–72
  • 235 Jahrsdoerfer RA, Lambert PR. Facial nerve injury in congenital aural atresia surgery. Am J Otol 1998; 19: 283-287
  • 236 Hohman MH, Hadlock TA. Etiology, diagnosis, and management of facial palsy: 2000 patients at a facial nerve center. Laryngoscope 2014; 124: E283-E293
  • 237 Teasdall RD, Frayha RA, Shulman LE. Cranial nerve involvement in systemic sclerosis (scleroderma): a report of 10 cases. Medicine (Baltimore) 1980; 59: 149-159
  • 238 Lin TY, Chiang CH, Cheng PS. Melkersson-Rosenthal syndrome. J Formos Med Assoc 2016; 115: 583-584
  • 239 Fraga RC, Kakizaki P, Valente NYS. et al. Do you know this syndrome? Heerfordt-Waldenström syndrome. An Bras Dermatol 2017; 92: 571-572
  • 240 Traynor AE, Gertz MA, Kyle RA. Cranial neuropathy associated with primary amyloidosis. Ann Neurol 1991; 29: 451-454
  • 241 Martins AM, Ferreira FS, Leite IM. et al. Facial Paralysis as Initial Manifestation of Light-chain Amyloidosis. Cureus 2019; 11: e5521
  • 242 May M, Klein SR. Differential diagnosis of facial nerve palsy. Otolaryngol Clin North Am 1991; 24: 613-645
  • 243 Papan C, Kremp L, Weiß C. et al. Infectious causes of peripheral facial nerve palsy in children-a retrospective cohort study with long-term follow-up. Eur J Clin Microbiol Infect Dis 2019; 38: 2177-2184
  • 244 Sathirapanya P, Fujitnirun C, Setthawatcharawanich S. et al. Peripheral facial paralysis associated with HIV infection: A case series and literature review. Clin Neurol Neurosurg 2018; 172: 124-129
  • 245 Álvarez-Argüelles ME, Rojo-Alba S, Rodríguez Pérez M. et al. Infant Facial Paralysis Associated with Epstein-Barr Virus Infection. Am J Case Rep 2019; 20: 1216-1219
  • 246 Vogelnik K, Matos A. Facial nerve palsy secondary to Epstein-Barr virus infection of the middle ear in pediatric population may be more common than we think. Wien Klin Wochenschr 2017; 129: 844-847
  • 247 Kanerva M, Jääskeläinen AJ, Suvela M. et al. Human herpesvirus-6 and -7 DNA in cerebrospinal fluid of facial palsy patients. Acta Otolaryngol 2008; 128: 460-464
  • 248 Pitkäranta A, Lahdenne P, Piiparinen H. Facial nerve palsy after human herpesvirus 6 infection. Pediatr Infect Dis J 2004; 23: 688-689
  • 249 Vrabec JT, Isaacson B, Van Hook JW. Bell’s palsy and pregnancy. Otolaryngol Head Neck Surg 2007; 137: 858-861
  • 250 Kunze M, Arndt S, Zimmer A. et al. Idiopathic facial palsy during pregnancy. Hno 2012; 60: 98-101
  • 251 Hussain A, Nduka C, Moth P. et al. Bell’s facial nerve palsy in pregnancy: a clinical review. J Obstet Gynaecol 2017; 37: 409-415
  • 252 AWMF 2017; S2k-Leitlinie Therapie der idiopathischen Fazialisparese (Bell’s palsy), Stand: 31.03.2017. In: Leitlinienkommission Der Deutschen Gesellschaft für Neurologie e.V. (DGN). 22–24. https:// www.awmf.org/leitlinien/detail/ll/030-013.html
  • 253 Lockhart P, Daly F, Pitkethly M. et al. Antiviral treatment for Bell’s palsy (idiopathic facial paralysis). Cochrane Database Syst Rev 2009; 4: 1-35 DOI: 10.1002/14651858.CD001869.pub4. Cd001869
  • 254 Butler DP, Henry FP, Leckenby JI. et al. The incidence of facial vessel agenesis in patients with syndromic congenital facial palsy. Plast Reconstr Surg 2014; 134: 955e-958e
  • 255 Cardenas-Mejia A, Palafox D. Facial reanimation surgery in Möbius syndrome: Experience from 76 cases from a tertiary referral hospital in Latin America. Ann Chir Plast Esthet 2018; 63: 338-342
  • 256 Bogusiak K, Puch A, Arkuszewski P. Goldenhar syndrome: current perspectives. World J Pediatr 2017; 13: 405-415
  • 257 Hall BD. Choanal atresia and associated multiple anomalies. J Pediatr 1979; 95: 395-398
  • 258 Blake KD, Prasad C. CHARGE syndrome. Orphanet J Rare Dis 2006; 1: 34
  • 259 Chaudhry N, Srivastava A, Joshi L. Hemifacial spasm: The past, present and future. J Neurol Sci 2015; 356: 27-31
  • 260 Schultze F. Linksseitiger facialiskrampf in folge eines aneurysma der arteriavertebralis sinistra. Arch Pathol Anat 1875; 65: 385-391
  • 261 Yaltho TC, Jankovic J. The many faces of hemifacial spasm: differential diagnosis of unilateral facial spasms. Mov Disord 2011; 26: 1582-1592
  • 262 Jost WH, Laskawi R, Palmowski-Wolfe A. et al. Therapy of Hemifacial Spasm with Botulinum Toxin. Laryngorhinootologie 2019; 98: 247-251
  • 263 Jannetta PJ, Abbasy M, Maroon JC. et al. Etiology and definitive microsurgical treatment of hemifacial spasm. Operative techniques and results in 47 patients. J Neurosurg 1977; 47: 321-328
  • 264 Saito H, Baxter A. Undiagnosed intratemporal facial nerve neurilemomas. Arch Otolaryngol 1972; 95: 415-419
  • 265 Nam SI, Linthicum FH, Merchant SN. Temporal bone histopathology in neurofibromatosis type 2. Laryngoscope 2011; 121: 1548-1554
  • 266 Thompson AL, Aviv RI, Chen JM. et al. Magnetic resonance imaging of facial nerve schwannoma. Laryngoscope 2009; 119: 2428-2436
  • 267 Abdullah A, Mahmud MR, Sabir HA. et al. The different faces of facial nerve schwannomas. Med J Malaysia 2003; 58: 450-453
  • 268 Li Y, Liu H, Cheng Y. Subtotal resection of facial nerve schwannoma is not safe in the long run. Acta Otolaryngol 2014; 134: 433-436
  • 269 Beckmann S, Caversaccio M, Anschuetz L. Conductive hearing loss and peripheral facial nerve palsy. Hno 2019; 67: 710-711
  • 270 McRackan TR, Wilkinson EP, Rivas A. Primary tumors of the facial nerve. Otolaryngol Clin North Am 2015; 48: 491-500
  • 271 Wilkinson EP, Hoa M, Slattery WH. et al. Evolution in the management of facial nerve schwannoma. Laryngoscope 2011; 121: 2065-2074
  • 272 Park SH, Kim J, Moon IS. et al. The best candidates for nerve-sparing stripping surgery for facial nerve schwannoma. Laryngoscope 2014; 124: 2610-2615
  • 273 Angeli SI, Brackmann DE. Is surgical excision of facial nerve schwannomas always indicated?. Otolaryngol Head Neck Surg 1997; 117: S144-S147
  • 274 Mowry S, Hansen M, Gantz B. Surgical management of internal auditory canal and cerebellopontine angle facial nerve schwannoma. Otol Neurotol 2012; 33: 1071-1076
  • 275 Sheehan JP, Kano H, Xu Z. et al. Gamma Knife radiosurgery for facial nerve schwannomas: a multicenter study. J Neurosurg 2015; 123: 387-394
  • 276 Kida Y, Yoshimoto M, Hasegawa T. Radiosurgery for facial schwannoma. J Neurosurg 2007; 106: 24-29
  • 277 Hillman TA, Chen DA, Fuhrer R. An alternative treatment for facial nerve tumors: short-term results of radiotherapy. Ear, nose, & throat journal 2008; 87: 574-577
  • 278 Woodruff JM. Pathology of tumors of the peripheral nerve sheath in type 1 neurofibromatosis. Am J Med Genet 1999; 89: 23-30
  • 279 Marocchio LS, Oliveira DT, Pereira MC. et al. Sporadic and multiple neurofibromas in the head and neck region: a retrospective study of 33 years. Clin Oral Investig 2007; 11: 165-169
  • 280 McGuirt WF, Johnson PE, McGuirt WT. Intraparotid facial nerve neurofibromas. Laryngoscope 2003; 113: 82-84
  • 281 Mangham CA, Carberry JN, Brackmann DE. Management of intratemporal vascular tumors. Laryngoscope 1981; 91: 867-876
  • 282 Balkany T, Fradis M, Jafek BW. et al. Hemangioma of the facial nerve: role of the geniculate capillary plexus. Skull Base Surg 1991; 1: 59-63
  • 283 Friedman O, Neff BA, Willcox TO. et al. Temporal bone hemangiomas involving the facial nerve. Otol Neurotol 2002; 23: 760-766
  • 284 Semaan MT, Slattery WH, Brackmann DE. Geniculate ganglion hemangiomas: clinical results and long-term follow-up. Otol Neurotol 2010; 31: 665-670
  • 285 Dutcher PO, Brackmann DE. Glomus tumor of the facial canal. A case report. Arch Otolaryngol Head Neck Surg 1986; 112: 986-987
  • 286 Petrus LV, Lo WM. Primary paraganglioma of the facial nerve canal. AJNR American journal of neuroradiology 1996; 17: 171-174
  • 287 Sanchez-Cuadrado I, Lassaletta L, González-Otero T. et al. Radiology quiz case 1: glomus facialis paraganglioma. JAMA Otolaryngol Head Neck Surg 2013; 139: 93-94
  • 288 Bartels LJ, Pennington J, Kamerer DB. et al. Primary fallopian canal glomus tumors. Otolaryngol Head Neck Surg 1990; 102: 101-105
  • 289 Kania RE, Bouccara D, Colombani JM. et al. Primary facial canal paraganglioma. Am J Otolaryngol 1999; 20: 318-322
  • 290 Mafee MF, Raofi B, Kumar A. et al. Glomus faciale, glomus jugulare, glomus tympanicum, glomus vagale, carotid body tumors, and simulating lesions. Role of MR imaging. Radiol Clin North Am 2000; 38: 1059-1076
  • 291 Connor SE, Gleeson MJ, Odell E. Extracranial glomus faciale tumour. J Laryngol Otol 2008; 122: 986-989
  • 292 Künzel J, Zenk J, Koch M. et al. Paraganglioma of the facial nerve, a rare differential diagnosis for facial nerve paralysis: case report and review of the literature. Eur Arch Otorhinolaryngol 2012; 269: 693-698
  • 293 Parker NP, Huang TC. Progressive facial paralysis secondary to a rare temporal bone tumor: glomus faciale. Arch Otolaryngol Head Neck Surg 2011; 137: 712-715
  • 294 Takahashi K, Yamamoto Y, Ohshima S. et al. Primary paraganglioma in the facial nerve canal. Auris Nasus Larynx 2014; 41: 93-96
  • 295 Nadimi S, Leonetti JP, Marzo SJ. et al. Glomus faciale tumors: A report of 3 cases and literature review. Ear, nose, & throat journal 2017; 96: E7-e12
  • 296 Frisch CD, Driscoll CL, Neff BA. Paraganglioma of the facial canal: a report of 2 cases and literature review. Am J Otolaryngol 2014; 35: 800-805
  • 297 Gunn S, Cosetti M, Roland JT. Processed allograft: novel use in facial nerve repair after resection of a rare racial nerve paraganglioma. Laryngoscope 2010; 120: S206
  • 298 Magliulo G, Parnasi E, Savastano V. et al. Multiple familial facial glomus: case report and review of the literature. Ann Otol Rhinol Laryngol 2003; 112: 287-292
  • 299 Waldron MN, Flood LM, Clifford K. A primary glomus tumour of the facial nerve canal. J Laryngol Otol 2002; 116: 156-158
  • 300 Wippold FJ, Neely JG, Haughey BH. Primary paraganglioma of the facial nerve canal. Otol Neurotol 2004; 25: 79-80
  • 301 Boedeker CC, Ridder GJ, Schipper J. Paragangliomas of the head and neck: diagnosis and treatment. Fam Cancer 2005; 4: 55-59