Multiple endocrine neoplasia type 1 differential diagnosis
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]
Overview
Differential Diagnosis[1]
- von Hippel-Lindau syndrome
- Tuberous sclerosis
- Carney complex
- Neurofibromatosis type 1
- Li-Fraumeni syndrome
- Inherited pancreatic endocrine tumor syndromes
- Familial adenomatous polyposis/Gardner syndrome
- Multiple endocrine neoplasia type 2
- Cowden syndrome
- Familial Cushing's syndrome
- Multiple endocrine neoplasia type 4
- Isolated familial acromegaly/gigantism
- Familial primary aldosteronoma
- Familial isolated pituitary adenoma
- Familial isolated hyperparathyroidism
- Familial papillary thyroid carcinoma
- Familial isolated pheochromocytoma/paraganglioma
- Inherited adrenocortical carcinoma
Reference
- ↑ Toledo SP, Lourenço DM, Toledo RA (2013). "A differential diagnosis of inherited endocrine tumors and their tumor counterparts". Clinics (Sao Paulo). 68 (7): 1039–56. doi:10.6061/clinics/2013(07)24. PMC 3715026. PMID 23917672.