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Head and neck paragangliomas: clinical and molecular genetic classification
Offergeld, Christian; Brase, Christoph; Yaremchuk, Svetlana; Mader, Irina; Rischke, Hans Christian; Gläsker, Sven; Schmid, Kurt W; Wiech, Thorsten; Preuss, Simon F; Suárez, Carlos; Kopć, Tomasz; Patocs, Attila; Wohllk, Nelson; Malekpour, Mahdi; Boedeker, Carsten C; Neumann, Hartmut PH.
  • Offergeld, Christian; Albert-Ludwigs-University. University Medical Center. Department of Otorhinolaryngology. Freiburg. DE
  • Brase, Christoph; , Friedrich-Alexander-University of Erlangen-Nürnberg. Department of Otorhinolarnygology. Erlangen. DE
  • Yaremchuk, Svetlana; Academy of Medical Science. Institute of Otolaryngology. Kiev. UA
  • Mader, Irina; Albert-Ludwigs-University. University Medical Center. Department of Neuroradiology. Freiburg. DE
  • Rischke, Hans Christian; Albert-Ludwigs-University. University Medical Center. Department of Nuclear Medicine. Freiburg. DE
  • Gläsker, Sven; AlbertLudwigs-University. University Medical Center. Department of Neurosurgery. Freiburg. DE
  • Schmid, Kurt W; University of Duisburg-Essen. University Hospital of Essen. Institute of Pathology and Neuropathology. Essen. DE
  • Wiech, Thorsten; Albert-Ludwigs-University. University Hospital Freiburg. Institute of Pathology. Freiburg. DE
  • Preuss, Simon F; University of Cologne. Department of Otorhinolarnygology. Cologne. DE
  • Suárez, Carlos; Hospital Universitario Central de Asturias. Department of Otolaryngology. Oviedo. ES
  • Kopć, Tomasz; Poznan University of Mediacal Sciences. Department of Otolaryngology. Poznan. PL
  • Patocs, Attila; Semmelweis-University. 2nd Department of Medicine. Budapest. HU
  • Wohllk, Nelson; University of Chile. Hospital del Salvador. Department of Endocrinology. Santiago de Chile. CL
  • Malekpour, Mahdi; Tehran University of Medical Sciences. Department of Otorhinolaryngology. Tehran. IR
  • Boedeker, Carsten C; Albert-Ludwigs-University. University Medical Center. Department of Otorhinolaryngology. Freiburg. DE
  • Neumann, Hartmut PH; Albert-Ludwigs-Albert-Ludwigs-University. University Medical Center. Department of Nephrology and General Medicine. Freiburg. DE
Clinics ; 67(supl.1): 19-28, 2012. ilus, tab
Article in English | LILACS | ID: lil-623126
ABSTRACT
Head and neck paragangliomas are tumors arising from specialized neural crest cells. Prominent locations are the carotid body along with the vagal, jugular, and tympanic glomus. Head and neck paragangliomas are slowly growing tumors, with some carotid body tumors being reported to exist for many years as a painless lateral mass on the neck. Symptoms depend on the specific locations. In contrast to paraganglial tumors of the adrenals, abdomen and thorax, head and neck paragangliomas seldom release catecholamines and are hence rarely vasoactive. Petrous bone, jugular, and tympanic head and neck paragangliomas may cause hearing loss. The internationally accepted clinical classifications for carotid body tumors are based on the Shamblin Class I-III stages, which correspond to postoperative permanent side effects. For petrous-bone paragangliomas in the head and neck, the Fisch classification is used. Regarding the molecular genetics, head and neck paragangliomas have been associated with nine susceptibility genes NF1, RET, VHL, SDHA, SDHB, SDHC, SDHD, SDHAF2 (SDH5), and TMEM127. Hereditary HNPs are mostly caused by mutations of the SDHD gene, but SDHB and SDHC mutations are not uncommon in such patients. Head and neck paragangliomas are rarely associated with mutations of VHL, RET, or NF1. The research on SDHA, SDHAF2 and TMEM127 is ongoing. Multiple head and neck paragangliomas are common in patients with SDHD mutations, while malignant head and neck paraganglioma is mostly seen in patients with SDHB mutations. The treatment of choice is surgical resection. Good postoperative results can be expected in carotid body tumors of Shamblin Class I and II, whereas operations on other carotid body tumors and other head and neck paragangliomas frequently result in deficits of the cranial nerves adjacent to the tumors. Slow growth and the tendency of hereditary head and neck paragangliomas to be multifocal may justify less aggressive treatment strategies.
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Full text: Available Index: LILACS (Americas) Main subject: Paraganglioma / Head and Neck Neoplasms Limits: Humans Language: English Journal: Clinics Journal subject: Medicine Year: 2012 Type: Article / Project document Affiliation country: Chile / Germany / Hungary / Iran / Poland / Spain / Ukraine Institution/Affiliation country: , Friedrich-Alexander-University of Erlangen-Nürnberg/DE / Academy of Medical Science/UA / Albert-Ludwigs-Albert-Ludwigs-University/DE / Albert-Ludwigs-University/DE / AlbertLudwigs-University/DE / Hospital Universitario Central de Asturias/ES / Poznan University of Mediacal Sciences/PL / Semmelweis-University/HU / Tehran University of Medical Sciences/IR / University of Chile/CL

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Full text: Available Index: LILACS (Americas) Main subject: Paraganglioma / Head and Neck Neoplasms Limits: Humans Language: English Journal: Clinics Journal subject: Medicine Year: 2012 Type: Article / Project document Affiliation country: Chile / Germany / Hungary / Iran / Poland / Spain / Ukraine Institution/Affiliation country: , Friedrich-Alexander-University of Erlangen-Nürnberg/DE / Academy of Medical Science/UA / Albert-Ludwigs-Albert-Ludwigs-University/DE / Albert-Ludwigs-University/DE / AlbertLudwigs-University/DE / Hospital Universitario Central de Asturias/ES / Poznan University of Mediacal Sciences/PL / Semmelweis-University/HU / Tehran University of Medical Sciences/IR / University of Chile/CL