Familial Papillary Thyroid Carcinoma: Genetics, Criteria for Diagnosis, Clinical Features, and Surgical Treatment

2000 ◽  
Vol 24 (11) ◽  
pp. 1409-1417 ◽  
Author(s):  
Thomas J. Musholt ◽  
Petra B. Musholt ◽  
Thorsten Petrich ◽  
Gundula Oetting ◽  
Wolfram H. Knapp ◽  
...  
2004 ◽  
Vol 28 (12) ◽  
pp. 1275-1281 ◽  
Author(s):  
Apostolos Goropoulos ◽  
Konstantinos Karamoshos ◽  
Andreas Christodoulou ◽  
Theodoros Ntitsias ◽  
Konstantinos Paulou ◽  
...  

2011 ◽  
Vol 2011 ◽  
pp. 1-4 ◽  
Author(s):  
David F. Schaeffer ◽  
Eric M. Yoshida ◽  
David A. Owen ◽  
Kenneth W. Berean

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.


2016 ◽  
Vol 32 (2) ◽  
pp. 1-4
Author(s):  
Nam Young Kim ◽  
◽  
Kyoung Hun Kim ◽  
Sung Ho Park ◽  
Guk Haeng Lee ◽  
...  

2003 ◽  
Vol 29 (5) ◽  
pp. 446-449 ◽  
Author(s):  
S.-M. Chow ◽  
J.K.C. Chan ◽  
S.C.K. Law ◽  
D.L.C. Tang ◽  
C.-M. Ho ◽  
...  

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