Familial Adenomatous Polyposis—Rendering a Diagnosis Based on Recognition of an Unusual Primary Thyroid Neoplasm
It has been well established in the literature that the cribriform-morular variant of papillary thyroid carcinoma (CMVPTC) has been observed with higher frequency in familial adenomatous polyposis (FAP) patients. In the usual setting, patients with FAP are identified based on their germline mutation...
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2011-01-01
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Online Access: | http://dx.doi.org/10.1155/2011/767610 |
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doaj-6a800c9d38fc416488052205dc271b5f2020-11-25T00:48:56ZengHindawi LimitedCase Reports in Medicine1687-96271687-96352011-01-01201110.1155/2011/767610767610Familial Adenomatous Polyposis—Rendering a Diagnosis Based on Recognition of an Unusual Primary Thyroid NeoplasmDavid F. Schaeffer0Eric M. Yoshida1David A. Owen2Kenneth W. Berean3Department of Pathology and Laboratory Medicine, The University of British Columbia, Vancouver, BC, V6T 1Z4, CanadaDepartment of Medicine, The University of British Columbia, Vancouver, BC, V6T 1Z4, CanadaDepartment of Pathology and Laboratory Medicine, The University of British Columbia, Vancouver, BC, V6T 1Z4, CanadaDepartment of Pathology and Laboratory Medicine, The University of British Columbia, Vancouver, BC, V6T 1Z4, CanadaIt has been well established in the literature that the cribriform-morular variant of papillary thyroid carcinoma (CMVPTC) has been observed with higher frequency in familial adenomatous polyposis (FAP) patients. In the usual setting, patients with FAP are identified based on their germline mutations and the diagnosis of thyroid neoplasm is made after the FAP diagnosis. We herein report a case in which the recognition of a CMVPTC led to the initial diagnosis of FAP. The histological and clinical features of CMVPTC are reviewed with emphasis on its relationship to FAP.http://dx.doi.org/10.1155/2011/767610 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
David F. Schaeffer Eric M. Yoshida David A. Owen Kenneth W. Berean |
spellingShingle |
David F. Schaeffer Eric M. Yoshida David A. Owen Kenneth W. Berean Familial Adenomatous Polyposis—Rendering a Diagnosis Based on Recognition of an Unusual Primary Thyroid Neoplasm Case Reports in Medicine |
author_facet |
David F. Schaeffer Eric M. Yoshida David A. Owen Kenneth W. Berean |
author_sort |
David F. Schaeffer |
title |
Familial Adenomatous Polyposis—Rendering a Diagnosis Based on Recognition of an Unusual Primary Thyroid Neoplasm |
title_short |
Familial Adenomatous Polyposis—Rendering a Diagnosis Based on Recognition of an Unusual Primary Thyroid Neoplasm |
title_full |
Familial Adenomatous Polyposis—Rendering a Diagnosis Based on Recognition of an Unusual Primary Thyroid Neoplasm |
title_fullStr |
Familial Adenomatous Polyposis—Rendering a Diagnosis Based on Recognition of an Unusual Primary Thyroid Neoplasm |
title_full_unstemmed |
Familial Adenomatous Polyposis—Rendering a Diagnosis Based on Recognition of an Unusual Primary Thyroid Neoplasm |
title_sort |
familial adenomatous polyposis—rendering a diagnosis based on recognition of an unusual primary thyroid neoplasm |
publisher |
Hindawi Limited |
series |
Case Reports in Medicine |
issn |
1687-9627 1687-9635 |
publishDate |
2011-01-01 |
description |
It has been well established in the literature that the cribriform-morular variant of papillary thyroid carcinoma (CMVPTC) has been observed with higher frequency in familial adenomatous polyposis (FAP) patients. In the usual setting, patients with FAP are identified based on their germline mutations and the diagnosis of thyroid neoplasm is made after the FAP diagnosis. We herein report a case in which the recognition of a CMVPTC led to the initial diagnosis of FAP. The histological and clinical features of CMVPTC are reviewed with emphasis on its relationship to FAP. |
url |
http://dx.doi.org/10.1155/2011/767610 |
work_keys_str_mv |
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