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DOI: 10.1055/s-0042-101732
Infantile Hämangiome
Infantile HemangiomasPublikationsverlauf
Publikationsdatum:
21. März 2016 (online)

Zusammenfassung
Infantile Hämangiome (IH) sind die häufigsten Tumoren des Säuglings- und Kleinkindesalters. Im Gegensatz zu vielen anderen Tumoren haben sie nach einer anfänglichen Proliferationsphase die Eigenschaft einer spontanen Remission durch Involution. Ein Großteil der IH kann diese Abfolge spontan durchlaufen, ohne dass therapeutisch interveniert werden muss. Bei einem kleinen Teil der ansonsten gutartigen Tumoren kommt es jedoch schon frühzeitig zu Komplikationen, welche selten lebensbedrohlich sein können und oft bleibende funktionelle Schäden, Schmerzen oder dauerhaft entstellende Befunde hinterlassen. Die Herausforderung für den Dermatologen ist eine frühzeitige Diagnosestellung und im Falle drohender Komplikation die rasche Einleitung einer angepassten Therapie zu bahnen. Dabei stehen je nach Lage und Art des IH sowie der Größe, welche auch vom Zeitpunkt der Erstpräsentation abhängt, unterschiedliche therapeutische Optionen zur Verfügung. Gerade in der sehr frühen Phase lassen sich manchmal sowohl Folgeschäden als auch Therapieintensität und -dauer positiv beeinflussen.
In diesem Artikel sollen Eigenschaften infantiler Hämangiome, Entwicklungsverlauf und therapeutische Modalitäten daher aktualisiert besprochen werden.
Abstract
Infantile hemangiomas are the most common tumors of infancy. Following an initial period of proliferation they have the capability of spontaneous remission by involution. The majority of infantile hemangiomas will pass through this sequence without the need for intervention. Within a small percentage of these per se benign tumors, however, complications can occur. These complications are rarely life threatening but often leave permanent functional damage, pain or disfigurement. The challenge for the dermatologist lies in the need for an early diagnosis and the prompt initiation of a clinical finding based therapy in case of impending complications.
Different therapeutic options are available depending on the localization, subtype and size of infantile hemangioma, the latter again depending on the time of the patient’s first presentation. Especially in the very early stages possible distortion, tissue damage as well as treatment intensity and duration can be influenced positively.
This article will summarize and update the current knowledge on characteristics, development, diagnosis and therapy of infantile hemangiomas.
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Literatur
- 1 Wassef M, Blei F, Adams D et al. Vascular Anomalies Classification: Recommendations from the International Society for the Study of Vascular Anomalies. Pediatrics 2015; 136: e203-214
- 2 Mulliken JB, Enjolras O. Congenital hemangiomas and infantile hemangioma: missing links. J Am Acad Dermatol 2004; 50: 875-882
- 3 North PE, Waner M, Mizeracki A et al. GLUT1: a newly discovered immunohistochemical marker for juvenile hemangiomas. Hum Pathol 2000; 31: 11-22
- 4 North PE, Waner M, James CA et al. Congenital nonprogressive hemangioma: a distinct clinicopathologic entity unlike infantile hemangioma. Arch Dermatol 2001; 137: 1607-1620
- 5 Darrow DH, Greene AK, Mancini AJ et al. Diagnosis and Management of Infantile Hemangioma. Pediatrics 2015; 136: e1060-104
- 6 Hoeger PH, Harper JI, Baselga E et al. Treatment of infantile haemangiomas: recommendations of a European expert group. Eur J Pediatr 2015; 174: 855-865
- 7 Schmittenbecher PP, Grantzow R, Rößler JH et al. S2k Leitlinie der DGKCh, DGKJ, DDG, DGMKG: Infantile Hämangiome im Säuglings- und Kleinkindesalter. AWMF Leitlinien 2015; AWMF Register Nr. 006/100: 1-13
- 8 Theiler M, Walchli R, Weibel L. Vascular anomalies – a practical approach. J Dtsch Dermatol Ges 2013; 11: 397-405
- 9 Dickison P, Christou E, Wargon O. A prospective study of infantile hemangiomas with a focus on incidence and risk factors. Pediatr Dermatol 2011; 28: 663-669
- 10 Kilcline C, Frieden IJ. Infantile hemangiomas: how common are they? A systematic review of the medical literature. Pediatr Dermatol 2008; 25: 168-173
- 11 Munden A, Butschek R, Tom WL et al. Prospective study of infantile haemangiomas: incidence, clinical characteristics and association with placental anomalies. Br J Dermatol 2014; 170: 907-913
- 12 Goelz R, Poets CF. Incidence and treatment of infantile haemangioma in preterm infants. Arch Dis Child Fetal Neonatal Ed 2015; 100: F85-91
- 13 Janmohamed SR, Madern GC, de Laat PC et al. Educational paper: Pathogenesis of infantile haemangioma, an update 2014 (part I). Eur J Pediatr 2015; 174: 97-103
- 14 Tollefson MM, Frieden IJ. Early growth of infantile hemangiomas: what parents’ photographs tell us. Pediatrics 2012; 130: e314-e320
- 15 Chang LC, Haggstrom AN, Drolet BA et al. Growth characteristics of infantile hemangiomas: implications for management. Pediatrics 2008; 122: 360-367
- 16 Haggstrom AN, Drolet BA, Baselga E et al. Prospective study of infantile hemangiomas: clinical characteristics predicting complications and treatment. Pediatrics 2006; 118: 882-887
- 17 Mulliken JB, Burrows PE, Fishman SJ. Mulliken and Young’s vascular anomalies: hemangiomas and malformations. Oxford: Oxford University Press; 2013
- 18 Dickie B, Dasgupta R, Nair R et al. Spectrum of hepatic hemangiomas: management and outcome. J Pediatr Surg 2009; 44: 125-133
- 19 Shin HT, Orlow SJ, Chang MW. Ulcerated haemangioma of infancy: a retrospective review of 47 patients. Br J Dermatol 2007; 156: 1050-1052
- 20 Bauland CG, Luning TH, Smit JM et al. Untreated hemangiomas: growth pattern and residual lesions. Plast Reconstr Surg 2011; 127: 1643-1648
- 21 Orlow SJ, Isakoff MS, Blei F. Increased risk of symptomatic hemangiomas of the airway in association with cutaneous hemangiomas in a “beard” distribution. J Pediatr 1997; 131: 643-646
- 22 Huang SA, Tu HM, Harney JW et al. Severe hypothyroidism caused by type 3 iodothyronine deiodinase in infantile hemangiomas. N Engl J Med 2000; 343: 185-189
- 23 Hoeger PH. An update on infantile haemangiomas. Br J Dermatol 2013; 169: 11
- 24 Leaute-Labreze C, Hoeger P, Mazereeuw-Hautier J et al. A randomized, controlled trial of oral propranolol in infantile hemangioma. N Engl J Med 2015; 372: 735-746
- 25 Léauté-Labrèze C, Dumas de la Roque E, Hubiche T et al. Propranolol for severe hemangiomas of infancy. N Engl J Med 2008; 358: 2649-2651
- 26 Dermo-Kosmetiks PF. Fachinfo: HEMANGIOL® 3,75 mg/ml Lösung zum Einnehmen. Rote Liste Fachinfo Service 2014; 1-6
- 27 Drolet BA, Frommelt PC, Chamlin SL et al. Initiation and use of propranolol for infantile hemangioma: report of a consensus conference. Pediatrics 2013; 131: 128-140
- 28 Bernabeu-Wittel J, Narváez-Moreno B, de la Torre-García JM et al. Oral Nadolol for Children with Infantile Hemangiomas and Sleep Disturbances with Oral Propranolol. Pediatr Dermatol 2015; 32: 853-857
- 29 Pope E, Chakkittakandiyil A, Lara-Corrales I et al. Expanding the therapeutic repertoire of infantile haemangiomas: cohort-blinded study of oral nadolol compared with propranolol. Br J Dermatol 2013; 168: 222-224
- 30 Chan H, McKay C, Adams S et al. RCT of timolol maleate gel for superficial infantile hemangiomas in 5- to 24-week-olds. Pediatrics 2013; 131: e1739-e1747
- 31 Ovadia SA, Landy DC, Cohen ER et al. Local administration of β-blockers for infantile hemangiomas: a systematic review and meta-analysis. Ann Plast Surg 2015; 74: 256-262
- 32 Qiu Y, Yang J, Chen M et al. A prospective self-controlled study of topical timolol 0.5 % cream for large superficial infantile hemangiomas. J Dermatol 2015; 42: 363-366
- 33 Schneider M, Reimer A, Cremer H et al. Topical treatment with propranolol gel as a supplement to the existing treatment of hemangiomas. World J Pediatr 2014; 10: 313-317
- 34 Boon LM, Enjolras O, Mulliken JB. Congenital hemangioma: evidence of accelerated involution. J Pediatr 1996; 128: 329-335
- 35 Enjolras O, Picard A, Soupre V. Congenital haemangiomas and other rare infantile vascular tumours. Ann Chir Plast Esthet 2006; 51: 339-346
- 36 Frieden IJ, Reese V, Cohen D. PHACE syndrome. The association of posterior fossa brain malformations, hemangiomas, arterial anomalies, coarctation of the aorta and cardiac defects, and eye abnormalities. Arch Dermatol 1996; 132: 307-311
- 37 Girard C, Bigorre M, Guillot B et al. PELVIS Syndrome. Arch Dermatol 2006; 142: 884-888
- 38 Iacobas I, Burrows PE, Frieden IJ et al. LUMBAR: association between cutaneous infantile hemangiomas of the lower body and regional congenital anomalies. J Pediatr 2010; 157: 795-801.e1
- 39 Metry DW, Haggstrom AN, Drolet BA et al. A prospective study of PHACE syndrome in infantile hemangiomas: demographic features, clinical findings, and complications. Am J Med Genet A 2006; 140: 975-986
- 40 Metry DW, Siegel DH, Cordisco MR et al. A comparison of disease severity among affected male versus female patients with PHACE syndrome. J Am Acad Dermatol 2008; 58: 81-87
- 41 Stockman A, Boralevi F, Taieb A et al. SACRAL syndrome: spinal dysraphism, anogenital, cutaneous, renal and urologic anomalies, associated with an angioma of lumbosacral localization. Dermatology 2007; 214: 40-45