Neuroradiologie Scan 2016; 06(02): 133-155
DOI: 10.1055/s-0042-105531
Fortbildung
© Georg Thieme Verlag KG Stuttgart · New York

Ultraschallgesteuerte Biopsie von Kopf-Hals-Pathologien aus der Sicht des Neuroradiologen[1]

US-guided biopsy of neck lesions: the head and neck neuroradiologist’s perspective
Kim O. Learned
,
Anna S. Lev-Toaff (†)
,
Bonnie J. Brake
,
Roseann I. Wu
,
Jill E. Langer
,
Laurie A. Loevner
Further Information

Publication History

Publication Date:
21 April 2016 (online)

Zusammenfassung

Die ultraschallgesteuerte perkutane Biopsie einer Läsion am Hals ist eine kosteneffiziente, sichere und zielführende diagnostische Maßnahme ohne Strahlenbelastung. Sie ermöglicht eine Sichtkontrolle der Nadelposition in Echtzeit. Das hat den Vorteil, dass die Vorschubrichtung der Nadel sofort korrigiert und die Gewebeentnahme infolgedessen ohne größere Risiken an der richtigen Stelle und in kurzer Zeit durchgeführt werden kann. Eine effektive ultraschallgesteuerte Biopsie erfordert Erfahrung mit der Technik, Gründlichkeit bei der klinischen Beurteilung und Geschicklichkeit bei der Durchführung der Biopsie. Gute Kenntnisse der Anatomie und Pathologie von Kopf und Hals erlauben dem Neuroradiologen die Korrelierung der Ultraschallbildgebung mit transversalen Schnittbildern und erleichtern deren Interpretation. Vertrautheit mit den gängigen Halsoperationen und -rekonstruktionen und die Fähigkeit zur Beurteilung von Aufnahmen des behandelten Halses in verschiedenen Bildgebungsmodalitäten sind von unschätzbarem Wert bei der Bestimmung des Zieles einer ultraschallgesteuerten Biopsie bei Patienten mit behandlungsbedingten Veränderungen der anatomischen Gegebenheiten. Nach Knoten in der Schilddrüse kommen die folgenden Raumforderungen am Hals von Erwachsenen häufig vor: Lymphadenopathien, Kopf-Hals-Malignome, Speicheldrüsenneoplasien, Nervenscheidentumoren sowie entzündliche und infektiöse Herde. Auch die diagnostische Expertise mit Blick auf die Bildgebungsmerkmale der genannten Erkrankungen und auf ihre Differenzialdiagnose spielt eine wichtige Rolle bei der Wahl der Biopsietechnik und der Gewinnung einer geeigneten Gewebeprobe für die Diagnose einschließlich Materials für zusätzliche Laboruntersuchungen. Einer Einteilung in anatomische Zonen folgend skizziert dieser Artikel die praktischen Überlegungen bei der Auswahl der Patienten, bei der methodischen Analyse der präprozeduralen Querschnittsbildgebung und deren Korrelierung mit der Beurteilung der Echtzeit-Ultraschallbildgebung sowie bei den allgemeinen Prinzipien zur Optimierung der Ultraschallinstrumentierung und der Biopsietechnik. In geübten Händen ist die Sonografie aufgrund ihrer Vielseitigkeit und ihrer Portabilität eine wertvolle Modalität für die Gewinnung von Gewebeproben von oberflächlichen Kopf- und Halsläsionen.

Abstract

Ultrasonographically (US) guided percutaneous biopsy of a neck lesion is a cost-effective, safe, and diagnostically effective procedure without radiation exposure. The benefit of real-time visualization of the needle location allows for instantaneous maneuvering of the needle trajectory for safe and accurate tissue sampling with short procedural time. Effective US-guided biopsy requires technical experience, strong clinical acumen, and skillful biopsy technique. A neuroradiologist’s knowledge of head and neck anatomy and pathology allows correlation with cross-sectional imaging and enhances the understanding of US imaging evaluation. Familiarity with a spectrum of neck surgeries and reconstructions and expertise in imaging evaluation of the treated neck are invaluable in accurate identification of the target for biopsy in patients with treatment-related altered anatomy using US guidance. After thyroid nodules, the common adult neck masses are lymphadenopathy, head and neck cancer, salivary neoplasms, nerve sheath tumors, and inflammatory and infectious pseudomasses. Diagnostic expertise in the imaging characteristics of these individual pathologic conditions and their differential diagnoses also play an important role in choosing the biopsy technique and in procuring an adequate sample for diagnosis, including material for ancillary laboratory testing. Using an anatomic zone approach, this article illustrates the practical considerations in patient selection, the methodical analysis of preprocedure cross-sectional imaging and its correlation with real-time US evaluation, general principles for optimizing US instrumentation, and biopsy technique. In skillful hands, the versatility and portability of US make it the valuable modality for histologic sampling of superficial head and neck lesions.

1 © 2016 The Radiological Society of North America. All rights reserved. Originally puplished in English in RadioGraphics 2016; 36: 226 – 243. Online published in 10.1148 /rg.2016150087. Translated and reprinted with permission of RSNA. RSNA is not responsible for any inaccuracy or error arising from the translation from English to German.


 
  • Literatur

  • 1 Matt BH, Woodward-Hagg HK, Wade CL et al. Lean Six Sigma applied to ultrasound guided needle biopsy in the head and neck. Otolaryngol Head Neck Surg 2014; 151: 65-72
  • 2 Learned KO, Malloy KM, Langer JE et al. Adults with palpable neck mass: evidence-based neuroimaging. In: Medina LS, Sanelli PC, Jarvik JG, , eds. Evidence-based neuroimaging diagnosis and treatment improving the quality of neuroimaging in patient care: evidence-based imaging. New York, NY: Springer; 2013: 641-667
  • 3 Robitschek J, Straub M, Wirtz E et al. Diagnostic efficacy of surgeon-performed ultrasound-guided fine needle aspiration: a randomized controlled trial. Otolaryngol Head Neck Surg 2010; 142: 306-309
  • 4 Haldar S, Mandalia U, Skelton E et al. Diagnostic investigation of parotid neoplasms: a 16-year experience of freehand fine needle aspiration cytology and ultrasound-guided core needle biopsy. Int J Oral Maxillofac Surg 2015; 44: 151-157
  • 5 Badran K, Jani P, Berman L. Otolaryngologist-performed head and neck ultrasound: outcomes and challenges in learning the technique. J Laryngol Otol 2014; 128: 447-453
  • 6 Lorenzo G, Saindane AM. Pitfalls in image guided tissue sampling in the head and neck. Neuroimaging Clin N Am 2013; 23: 167-178
  • 7 Ganguly A, Burnside G, Nixon P. A systematic review of ultrasound-guided FNA of lesions in the head and neck: focusing on operator, sample inadequacy and presence of on-spot cytology service. Br J Radiol 2014; 87: 20130571
  • 8 Novoa E, Gürtler N, Arnoux A et al. Role of ultrasound-guided core-needle biopsy in the assessment of head and neck lesions: a meta-analysis and systematic review of the literature. Head Neck 2012; 34: 1497-1503
  • 9 Schmidt RL, Hall BJ, Wilson AR et al. A systematic review and meta-analysis of the diagnostic accuracy of fine-needle aspiration cytology for parotid gland lesions. Am J Clin Pathol 2011; 136: 45-59
  • 10 Fakhry N, Antonini F, Michel J et al. Fine-needle aspiration cytology in the management of parotid masses: evaluation of 249 patients. Eur Ann Otorhinolaryngol Head Neck Dis 2012; 129: 131-135
  • 11 Huang YC, Wu CT, Lin G et al. Comparison of ultrasonographically guided fine-needle aspiration and core needle biopsy in the diagnosis of parotid masses. J Clin Ultrasound 2012; 40: 189-194
  • 12 Burke C, Thomas R, Inglis C et al. Ultrasound-guided core biopsy in the diagnosis of lymphoma of the head and neck: a 9 year experience. Br J Radiol 2011; 84: 727-732
  • 13 Abu-Yousef MM, Larson JH, Kuehn DM et al. Safety of ultrasound-guided fine needle aspiration biopsy of neck lesions in patients taking antithrombotic/anticoagulant medications. Ultrasound Q 2011; 27: 157-159
  • 14 Lo WC, Cheng PW, Wang CT et al. Pain levels associated with ultrasound-guided fine-needle aspiration biopsy for neck masses. Head Neck 2014; 36: 252-256
  • 15 Iro H, Bozzato A, Zenk J. Atlas of head and neck ultrasound. Stuttgart: Thieme; 2013: 1-230
  • 16 Ahuja AT, Evans RM , eds. Practical head and neck ultrasound. London, England: Greenwich Medical Media; 2000
  • 17 Royer MC, Davidson DD, Dimitrov RK et al. Ultrasound gel causes fine needle aspiration artifact? A clear choice. Acta Cytol 2012; 56: 146-154
  • 18 Lee EW, Chen C, Sauk S et al. How diagnostic is ultrasound-guided neck mass biopsy (fine-needle capillary sampling biopsy technique)? Evaluation of 132 nonthyroid neck mass biopsies with pathologic analysis over 7 years at a single institution. J Ultrasound Med 2009; 28: 1679-1684
  • 19 Kraft M, Laeng H, Schmuziger N et al. Comparison of ultrasound-guided core-needle biopsy and fine-needle aspiration in the assessment of head and neck lesions. Head Neck 2008; 30: 1457-1463
  • 20 Pfeiffer J, Ridder GJ. How safe is the use of ultrasound-guided cutting needle biopsy in the head and neck?. Eur Radiol 2010; 20: 2933-2938
  • 21 Huang SH, Xu W, Waldron J et al. Refining American Joint Committee on Cancer/Union for International Cancer Control TNM stage and prognostic groups for human papillomavirus-related oropharyngeal carcinomas. J Clin Oncol 2015; 33: 836-845
  • 22 Brizel DM. Different strokes for different folks: new paradigms for staging oropharynx cancer. J Clin Oncol 2015; 33: 817-818
  • 23 Giovanella L, Bongiovanni M, Trimboli P. Diagnostic value of thyroglobulin assay in cervical lymph node fine-needle aspirations for metastatic differentiated thyroid cancer. Curr Opin Oncol 2013; 25: 6-13
  • 24 Lee YH, Seo HS, Suh SI et al. Cut-off value for needle washout thyroglobulin in athyrotropic patients. Laryngoscope 2010; 120: 1120-1124
  • 25 Trimboli P, Cremonini N, Ceriani L et al. Calcitonin measurement in aspiration needle washout fluids has higher sensitivity than cytology in detecting medullary thyroid cancer: a retrospective multicentre study. Clin Endocrinol (Oxf) 2014; 80: 135-140
  • 26 Lastra RR, Pramick MR, Nakashima MO et al. Adequacy of fine-needle aspiration specimens for human papillomavirus infection molecular testing in head and neck squamous cell carcinoma. Cytojournal 2013; 10: 21
  • 27 Langer JE, Mandel SJ. Sonographic imaging of cervical lymph nodes in patients with thyroid cancer. Neuroimaging Clin N Am 2008; 18: 479-489, vii-viii
  • 28 Klem C. Head and neck anatomy and ultrasound correlation. Otolaryngol Clin North Am 2010; 43: 1161-1169, v
  • 29 Sofferman RA. Interpretation of ultrasound. Otolaryngol Clin North Am 2010; 43: 1171-1202, v-vi
  • 30 Fernandes T, Lobo JC, Castro R et al. Anatomy and pathology of the masticator space. Insights Imaging 2013; 4: 605-616
  • 31 Bialek EJ, Jakubowski W, Zajkowski P et al. US of the major salivary glands: anatomy and spatial relationships, pathologic conditions, and pitfalls. RadioGraphics 2006; 26: 745-763
  • 32 Gervasio A, D’Orta G, Mujahed I et al. Sonographic anatomy of the neck: the suprahyoid region. J Ultrasound 2011; 14: 130-135
  • 33 Kanekar SG, Mannion K, Zacharia T et al. Parotid space: anatomic imaging. Otolaryngol Clin North Am 2012; 45: 1253-1272
  • 34 Som PM, Brandwein-Gensler MS. Lymph nodes of the neck. In: Som PM, Curtin HD, eds. Head and neck imaging. St Louis, Mo: Mosby; 2011: 2287-2383
  • 35 Wan YL, Chan SC, Chen YL et al. Ultrasonography-guided core-needle biopsy of parotid gland masses. AJNR Am J Neuroradiol 2004; 25: 1608-1612
  • 36 Howlett DC, Menezes LJ, Lewis K et al. Sonographically guided core biopsy of a parotid mass. AJR Am J Roentgenol 2007; 188: 223-227
  • 37 Meltzer DE, Shatzkes DR. Masticator space: imaging anatomy for diagnosis. Otolaryngol Clin North Am 2012; 45: 1233-1251
  • 38 Erickson D, Kudva YC, Ebersold MJ et al. Benign paragangliomas: clinical presentation and treatment outcomes in 236 patients. J Clin Endocrinol Metab 2001; 86: 5210-5216
  • 39 Lenders JW, Duh QY, Eisenhofer G et al. Pheochromocytoma and paraganglioma: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab 2014; 99: 1915-1942
  • 40 Colen TY, Mihm FG, Mason TP et al. Catecholamine-secreting paragangliomas: recent progress in diagnosis and perioperative management. Skull Base 2009; 19: 377-385
  • 41 Meacham RK, Boughter Jr JD, Sebelik ME. Ultrasound-guided fine-needle aspiration of the tongue base: a cadaver feasibility study. Otolaryngol Head Neck Surg 2012; 147: 864-869
  • 42 Wang CP, Chen TC, Yang TL et al. Transcutaneous ultrasound for evaluation of vocal fold movement in patients with thyroid disease. Eur J Radiol 2012; 81: e288-e291
  • 43 Chen CN, Hsiao TY, Ko JY et al. Ultrasound-guided core biopsy for hypopharyngeal cancer with difficult endoscopic approaches: our experience in eleven patients. Clin Otolaryngol 2014; 39: 45-49
  • 44 Lopchinsky RA, Amog-Jones GF, Pathi R. Ultrasound-guided fine needle aspiration diagnosis of supraglottic laryngeal cancer. Head Neck 2013; 35: E31-E35
  • 45 Yom SS, Garden AS, Staerkel GA et al. Sonographic examination of the neck after definitive radiotherapy for node-positive oropharyngeal cancer. AJNR Am J Neuroradiol 2011; 32: 1532-1538
  • 46 Zini C, Thomas S, Raad R et al. Fine-needle aspiration biopsy of thyroid bed lesions in post-thyroidectomy patients: What is the importance of nondiagnostic biopsy results?. J Ultrasound Med 2012; 31: 1973-1976
  • 47 Bumpous JM, Randolph GW. The expanding utility of office-based ultrasound for the head and neck surgeon. Otolaryngol Clin North Am 2010; 43: 1203-1208, vi
  • 48 Perera P, Mailhot T, Riley D et al. The RUSH exam: Rapid Ultrasound in SHock in the evaluation of the critically lll. Emerg Med Clin North Am 2010; 28: 29-56, vii
  • 49 Green JS, Tsui BC. Applications of ultrasonography in ENT: airway assessment and nerve blockade. Anesthesiol Clin 2010; 28: 541-553