Multiple endocrine neoplasia type 1 differential diagnosis: Difference between revisions
No edit summary |
|||
| Line 3: | Line 3: | ||
{{CMG}}; {{AE}} {{Ammu}} | {{CMG}}; {{AE}} {{Ammu}} | ||
==Overview== | ==Overview== | ||
Multiple endocrine neoplasia type 1 must be differentiated from other | Multiple endocrine neoplasia type 1 must be differentiated from other diseases that cause [[hyperparathyroiodism]], [[gastric ulcer]]s, and neurological symptoms such as [[von Hippel-Lindau syndrome]], [[tuberous sclerosis]], [[carney complex]], [[neurofibromatosis type 1]], [[Li-Fraumeni syndrome]], [[multiple endocrine neoplasia type 2]], [[familial hyperparathyroidism]], [[pheochromocytoma]] and [[acromegaly]]. | ||
==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>== | ||
Revision as of 21:57, 4 September 2015
|
Multiple endocrine neoplasia type 1 Microchapters |
|
Differentiating Multiple endocrine neoplasia type 1 from other Diseases |
|---|
|
Diagnosis |
|
Treatment |
|
Case Studies |
|
Multiple endocrine neoplasia type 1 differential diagnosis On the Web |
|
American Roentgen Ray Society Images of Multiple endocrine neoplasia type 1 differential diagnosis |
|
FDA on Multiple endocrine neoplasia type 1 differential diagnosis |
|
CDC on Multiple endocrine neoplasia type 1 differential diagnosis |
|
Multiple endocrine neoplasia type 1 differential diagnosis in the news |
|
Blogs on Multiple endocrine neoplasia type 1 differential diagnosis |
|
Directions to Hospitals Treating Multiple endocrine neoplasia type 1 |
|
Risk calculators and risk factors for Multiple endocrine neoplasia type 1 differential diagnosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]
Overview
Multiple endocrine neoplasia type 1 must be differentiated from other diseases that cause hyperparathyroiodism, gastric ulcers, and neurological symptoms such as von Hippel-Lindau syndrome, tuberous sclerosis, carney complex, neurofibromatosis type 1, Li-Fraumeni syndrome, multiple endocrine neoplasia type 2, familial hyperparathyroidism, pheochromocytoma and acromegaly.
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.