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neoplázia endokrinná mnohopočetná, typ 2b
Č. záznamu d018814 Dátum 06.06.2025 Typ M Tematický termín neoplázia endokrinná mnohopočetná, typ 2b Iný termín Angličtina (Pseudonym) MEN 2b
Angličtina (Pseudonym) MEN 3
Angličtina (Pseudonym) Neoplasia, Multiple Endocrine Type 2b
Angličtina (Pseudonym) Neoplasms, Multiple Endocrine Type 2b
Slovenčina (Pseudonym) nádory endokrinné mnohopočetné, typ 2b
Slovenčina (Pseudonym) MEN2b
Slovenčina (Pseudonym) MEN 2b
Slovenčina (Pseudonym) MEN 3
Pozri tiež (Novšie záhlavie) feochromocytóm
(Novšie záhlavie) karcinóm medulárny
MDT C04.588.322.400.510C04.651.600.510C04.700.630.510C16.320.700.630.510C19.344.400.510 Poznámka Similar to MEN2A, it is also caused by mutations of the MEN2 gene, also known as the RET proto-oncogene. Its clinical symptoms include medullary carcinoma (CARCINOMA, MEDULLARY) of THYROID GLAND and PHEOCHROMOCYTOMA of ADRENAL MEDULLA (50%). Unlike MEN2a, MEN2b does not involve PARATHYROID NEOPLASMS. It can be distinguished from MEN2A by its neural abnormalities such as mucosal NEUROMAS on EYELIDS; LIP; and TONGUE, and ganglioneuromatosis of GASTROINTESTINAL TRACT leading to MEGACOLON. It is an autosomal dominant inherited disease. 
predmetové heslo
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