scholarly journals Differential diagnosis of small bowel occlusions

2009 ◽  
Vol 3 (2) ◽  
pp. 81-87
Author(s):  
Paolo Ghiringhelli

Hereditary nonpolyposis colorectal cancer (HNPCC), also known as Lynch syndrome, is a common autosomal dominant syndrome characterized by early age at onset, and microsatellite instability (MSI). Patients with Lynch syndrome have a markedly increased risk of colorectal cancer. We report a case of a 28-year-old male with Lynch syndrome; the case allows to describe clinical manifestations and diagnostic criteria of this syndrome, and to underline the importance of genetics in the diagnosis of this disease.

2003 ◽  
Vol 46 (3) ◽  
pp. 305-312 ◽  
Author(s):  
Salvatore Pucciarelli ◽  
Marco Agostini ◽  
Alessandra Viel ◽  
Roberta Bertorelle ◽  
Valentina Russo ◽  
...  

1988 ◽  
Vol 31 (5) ◽  
pp. 372-377 ◽  
Author(s):  
Henry T. Lynch ◽  
Patrice Watson ◽  
Mary Kriegler ◽  
Jane F. Lynch ◽  
Stephen J. Lanspa ◽  
...  

Author(s):  
Verena Steinke ◽  
Christoph Engel ◽  
Reinhard Büttner ◽  
Hans Konrad Schackert ◽  
Wolff H. Schmiegel ◽  
...  

2008 ◽  
Vol 1 (6) ◽  
pp. 470-475 ◽  
Author(s):  
Elena M. Stoffel ◽  
D. Kim Turgeon ◽  
David H. Stockwell ◽  
Lili Zhao ◽  
Daniel P. Normolle ◽  
...  

2019 ◽  
Vol 10 (2) ◽  
pp. 180-185
Author(s):  
Christopher K.H. Burris ◽  
Maria E. Rodriguez ◽  
Meisha L. Raven ◽  
Devasis N. Reddy ◽  
Yaohui G. Xu ◽  
...  

Muir-Torre syndrome, a variant of Lynch syndrome or hereditary nonpolyposis colorectal cancer, is an autosomal dominant disease characterized by skin neoplasms (sebaceous or keratoacanthomas) and visceral malignancies. Due to the rarity of the syndrome there are no firm guidelines on how and when to test patients with its typical skin lesions. We describe a case that highlights the importance of a detailed family history.


2007 ◽  
Vol 67 (19) ◽  
pp. 9603-9603 ◽  
Author(s):  
Heather Hampel ◽  
Jenny Panescu ◽  
Janet Lockman ◽  
Kaisa Sotamaa ◽  
Daniel Fix ◽  
...  

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