Multiple endocrine neoplasia type 2 differential diagnosis: Difference between revisions

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==Differential Diagnosis==
==Differential Diagnosis==
Multiple endocrine neoplasia type 2 must be differentiated from the following hereditary diseases.
Multiple endocrine neoplasia type 2 must be differentiated from the following hereditary diseases.<ref name ="Men type 2" {{Cite journal| author = [[Jessica Marquard]] & [[Charis Eng]]
| title = Multiple Endocrine Neoplasia Type 2
| year = 1993
| month =
| pmid = 020301434
}}</ref>
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| style="padding: 5px 5px; background: #F5F5F5;" |An [[autosomal dominant]] genetic disorder causing [[tumor]]s of [[parathyroid]], [[pancreas]], and [[pituitary gland]].
| style="padding: 5px 5px; background: #F5F5F5;" |An [[autosomal dominant]] genetic disorder causing [[tumor]]s of [[parathyroid]], [[pancreas]], and [[pituitary gland]].
|-
|-
| style="padding: 5px 5px; background: #F5F5F5;" colspan="2"|<small>Adapted from Marquard J, Eng C. Multiple Endocrine Neoplasia Type 2. 1999 Sep 27 [Updated 2015 Jun 25]. In: Pagon RA, Adam MP, Ardinger HH, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2015. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1257/<ref>{{Cite journal| author = [[Jessica Marquard]] & [[Charis Eng]]
| style="padding: 5px 5px; background: #F5F5F5;" colspan="2"|<small>Adapted from Marquard J, Eng C. Multiple Endocrine Neoplasia Type 2. 1999 Sep 27 [Updated 2015 Jun 25]. In: Pagon RA, Adam MP, Ardinger HH, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2015. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1257/<ref name ="Men type 2" {{Cite journal| author = [[Jessica Marquard]] & [[Charis Eng]]
  | title = Multiple Endocrine Neoplasia Type 2
  | title = Multiple Endocrine Neoplasia Type 2
  | year = 1993
  | year = 1993

Revision as of 16:05, 5 October 2017

Multiple endocrine neoplasia type 2 Microchapters

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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

Multiple endocrine neoplasia type 2 must be differentiated from other hereditary tumors such as medullary thyroid carcinoma, C-cell hyperplasia, pheochromocytoma, von Hippel Lindau syndrome, hereditary paraganglioma-pheochromocytoma, polycythemia and paraganglioma/pheochromocytoma syndrome, neurofibromatosis type 1, and multiple endocrine neoplasia type 1 (MEN 1).

Differential Diagnosis

Multiple endocrine neoplasia type 2 must be differentiated from the following hereditary diseases. |}

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