Multiple endocrine neoplasia type 1 differential diagnosis: Difference between revisions
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(/* Differential Diagnosis{{cite journal| author=Toledo SP, Lourenço DM, Toledo RA| title=A differential diagnosis of inherited endocrine tumors and their tumor counterparts. | journal=Clinics (Sao Paulo) | year= 2013 | volume= 68 | issue= 7 | pages= 1...) |
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==Overview== | ==Overview== | ||
==Differential Diagnosis<ref name="pmid23917672">{{cite journal| author=Toledo SP, Lourenço DM, Toledo RA| title=A differential diagnosis of inherited endocrine tumors and their tumor counterparts. | journal=Clinics (Sao Paulo) | year= 2013 | volume= 68 | issue= 7 | pages= 1039-56 | pmid=23917672 | doi=10.6061/clinics/2013(07)24 | pmc=PMC3715026 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23917672 }} </ref>== | ==Differential Diagnosis<ref name="pmid23917672">{{cite journal| author=Toledo SP, Lourenço DM, Toledo RA| title=A differential diagnosis of inherited endocrine tumors and their tumor counterparts. | journal=Clinics (Sao Paulo) | year= 2013 | volume= 68 | issue= 7 | pages= 1039-56 | pmid=23917672 | doi=10.6061/clinics/2013(07)24 | pmc=PMC3715026 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23917672 }} </ref>== | ||
* von Hippel-Lindau syndrome | * [[von Hippel-Lindau syndrome]] | ||
* Tuberous sclerosis | * [[Tuberous sclerosis]] | ||
* Carney complex | * [[Carney complex]] | ||
* Neurofibromatosis type 1 | * [[Neurofibromatosis type 1]] | ||
* Li-Fraumeni syndrome | * [[Li-Fraumeni syndrome]] | ||
* Inherited pancreatic endocrine tumor syndromes | * Inherited pancreatic endocrine tumor syndromes | ||
* Familial adenomatous polyposis/Gardner syndrome | * [[Familial adenomatous polyposis]]/[[Gardner syndrome]] | ||
* Multiple endocrine neoplasia type 2 | * [[Multiple endocrine neoplasia type 2]] | ||
* Cowden syndrome | * [[Cowden syndrome]] | ||
* Familial Cushing's syndrome | * Familial [[Cushing's syndrome]] | ||
* Multiple endocrine neoplasia type 4 | * [[Multiple endocrine neoplasia type 4 | ||
* Isolated familial acromegaly/gigantism | * Isolated familial [[acromegaly]]/[[gigantism]] | ||
* Familial primary aldosteronoma | * Familial primary [[aldosteronoma]] | ||
* Familial isolated pituitary adenoma | * Familial isolated pituitary adenoma | ||
* Familial isolated hyperparathyroidism | * Familial isolated [[hyperparathyroidism]] | ||
* Familial papillary thyroid carcinoma | * Familial papillary [[thyroid carcinoma]] | ||
* Familial isolated pheochromocytoma/paraganglioma | * Familial isolated [[pheochromocytoma]]/[[paraganglioma]] | ||
* Inherited adrenocortical carcinoma | * Inherited [[adrenocortical carcinoma]] | ||
==Reference== | ==Reference== | ||
{{Reflist}} | {{Reflist}} | ||
Revision as of 21:24, 4 September 2015
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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.