Multiplex endokrin adenomatosis IIB.

O. Dohán, W. Höppner, F. Salamon, M. Góth, L. Kovács, G. Szilágyi, I. Szabolcs

Research output: Review article


The first Hungarian MEN IIB (multiplex endocrine neoplasia) syndrome is reported with the short summary of the literature about the pathogenesis and diagnosis of medullary thyroid carcinoma, presenting 80% in sporadic, 20% in hereditary form. The appearance of the patients alone (marfanoid stature, bulky lips, and ganglioneuromatosis of the tongue) may be almost enough for the presumption for the diagnosis of MEN IIB: For screening and preventing the clinical manifestation of the very aggressive medullary carcinoma in the relatives of the patient, the genetic screening is indispensable. The costs of the genetic screening and early treatment of the patients are much lower than the expenses of the traditional annual biochemical screening and the--delayed, often only supportive--treatment of the clinically manifested illness.

Translated title of the contributionMultiple endocrine adenomatosis IIB
Original languageHungarian
Pages (from-to)3117-3120
Number of pages4
JournalOrvosi hetilap
Issue number52
Publication statusPublished - dec. 27 1998

ASJC Scopus subject areas

  • Medicine(all)

Fingerprint Dive into the research topics of 'Multiplex endokrin adenomatosis IIB.'. Together they form a unique fingerprint.

  • Cite this

    Dohán, O., Höppner, W., Salamon, F., Góth, M., Kovács, L., Szilágyi, G., & Szabolcs, I. (1998). Multiplex endokrin adenomatosis IIB. Orvosi hetilap, 139(52), 3117-3120.