Colonic primary mantel cell lymphoma

2019 ◽  
Vol 48 (6) ◽  
pp. 728-729
Author(s):  
Dorra Trad ◽  
Sabbah Meriam ◽  
Fatma Khanchel ◽  
Asma Ouakaa ◽  
Dalila Gargouri
2016 ◽  
Vol 2016 ◽  
pp. 1-4 ◽  
Author(s):  
Fady Daniel ◽  
Hazem I. Assi ◽  
Walid Karaoui ◽  
Jean El Cheikh ◽  
Sami Bannoura ◽  
...  

Mantle cell lymphoma (MCL) is a subtype of non-Hodgkin’s lymphoma (NHL) comprising around 7% of adult NHL. It is characterized by a chromosomal translocation t(11:14) and overexpression of Cyclin D1. The incidence of secondary gastrointestinal tract involvement in MCL ranges from 10 to 28% in various series. However primary gastrointestinal MCL is very rare, accounting for only 1 to 4% of primary gastrointestinal lymphomas. The most common endoscopic feature of primary intestinal MCL is multiple lymphomatous polyposis. In rare cases it presents as protruded lesions or superficial lesions. Single colonic mass presentation is an extremely infrequent presentation. MCL has an aggressive course with quick progression, and most cases are discovered in the advanced stages. Colonic biopsies with histologic examination and specific immunohistochemical staining are the gold standard for a proper diagnosis. We report a case of a single mass forming mantle cell lymphoma of the ascending colon in a 57-year-old female patient with unusual colonoscopic and radiologic features and describe the therapy the patient received, thereby adding to the spectrum of clinical presentations of this aggressive lymphoproliferative disorder.


2010 ◽  
Vol 52 (3) ◽  
pp. 169-170 ◽  
Author(s):  
Renzo Nino Incani ◽  
Marcos Hernández ◽  
Jackeline Cortez ◽  
María Elena González ◽  
Yaimir Dorel Salazar

A case of meningitis due to Staphylococcus warneri in a patient with a hyperinfection with Strongyloides stercoralis possibly associated with rituximab treatment for mantel cell lymphoma is reported for the first time in the literature. The patient was a 59-year-old woman, with a 3-year history of an apparently well controlled lymphoma after treatment with chemotherapy-immunotherapy and then immunotherapy alone, and diagnosis of strongyloidiasis. Meningitis was diagnosed by cerebrospinal fluid culture and tested with an automated plate system. The patient was successfully treated with vancomycin; although fever and productive cough persisted. Severe gastrointestinal symptoms and pneumonia developed three weeks later. Hyperinfection syndrome by S. stercoralis was diagnosed, with abundant larvae in feces and expectoration.


2016 ◽  
Vol 111 ◽  
pp. S629-S630
Author(s):  
Fady Daniel ◽  
Hazem Assi ◽  
Walid R. Karaoui ◽  
Jean El Cheikh ◽  
Sami Bannoura ◽  
...  

2015 ◽  
Vol 33 (15_suppl) ◽  
pp. 8542-8542
Author(s):  
Yucai Wang ◽  
Maria Lourdes Dela Rosa ◽  
Shouhao Zhou ◽  
Maria Badillo ◽  
Alicia Addison ◽  
...  

2013 ◽  
Vol 31 (7) ◽  
pp. 494-499 ◽  
Author(s):  
Charles F. Streckfus ◽  
Jorge Romaguera ◽  
Cynthia Guajardo-Streckfus

Endoscopy ◽  
2007 ◽  
Vol 39 (S 1) ◽  
pp. E60-E60 ◽  
Author(s):  
J. Penyige ◽  
E. Farczadi ◽  
K. Boer ◽  
I. Kaszas ◽  
J. Csomor ◽  
...  

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