Rare primary B‐cell lymphoma of small intestine presenting as giant jejunal diverticulum and complicated by phytobezoar and intestinal obstruction

2020 ◽  
Author(s):  
Geraldine Yanlei Lei ◽  
Kon Voi Tay ◽  
Li Tserng Teo
2018 ◽  
Vol 33 (2) ◽  
pp. 438-441 ◽  
Author(s):  
Ji Hyun Yang ◽  
Jain Lee ◽  
Shin Bum Kim ◽  
Seon Hoo Kim ◽  
Guk Jin Lee

2013 ◽  
Vol 31 (15_suppl) ◽  
pp. e19523-e19523
Author(s):  
Wei-Hsun Hsu ◽  
Kun-Huei Yeh ◽  
Chung-Wu Lin ◽  
Chih-Hung Hsu ◽  
Ann-Lii Cheng ◽  
...  

e19523 Background: Primary intestinal non-Hodgkin lymphoma (NHL) is a rare but heterogeneous disease in East Asia. However, the benefit of multidisciplinary treatment is still in debate. We characterized the clinicopathologic features, and treatment outcome in a single institute database. Methods: Patients with NHL primarily involving the intestine and treated during 1992 to 2008 were selected from the Cancer Registry of National Taiwan University Hospital. The medical charts and pathology records were carefully reviewed. Results: There were 64 men and 17 women with a median age of 51.5 years. Sites involved were colon/rectum (53.2%), small intestine (30.9%), and duodenum (13%). Histopathology subclassification included diffuse large B-cell lymphoma (DLBCL) (61.7%), mucosa-associated lymphoid tissue lymphoma (11.1%), Burkitt’s lymphoma (8.6%), T cell lymphoma (6.2%), follicular lymphoma (2.5%), mantle cell lymphoma (1.2 %) and others (8.6%). Ann Arbor stage IE to IIE accounted for 61.7%, whereas lower IPI score (1-2) were 54.8%. Among them, 27 patients received surgery plus chemotherapy, 60 received chemotherapy, and 4 had radiotherapy. At average follow-up of 48.7 months, 5 year survival rate were 59%, 43% and 51% for colon/rectum, small intestine, and duodenal NHL, respectively (p=0.45). Surgery plus chemotherapy versus chemotherapy alone showed no survival benefit in lower IPI group (p=0.682) nor in higher IPI (3-5) group (p=0.939). A trend of better median overall survival (mOS) was seen in rituximab group than in non-rituximab group in DLBCL subtypes (not reach vs. 39.8mo, p=0.075). In univariate analysis, stage III/IV (p=0.008), IPI score greater than 2 (p=0.011), and T cell histology (p<0.001) were significant prognostic factors for poor OS. In multivariate analysis, T cell histology remained the independent prognostic factor for inferior OS (p<0.001, HR: 20.3, 95% CI: 5.1-80.4). Conclusions: Although B cell NHL was the majority of primary intestinal NHL in our institute, T cell histology has significant inferior survival. Chemotherapy is still the backbone of treatment for primary intestinal NHL. The benefit of rituximab to intestinal DLBCL needs further confirmation.


2011 ◽  
Vol 31 (1) ◽  
pp. 18-21 ◽  
Author(s):  
Do Yeun Kim ◽  
Yong-Seok Kim ◽  
Hee Jin Huh ◽  
Jong Sun Choi ◽  
Jeong Seok Yeo ◽  
...  

2003 ◽  
Vol 27 (6) ◽  
pp. 790-798 ◽  
Author(s):  
Mi Seon Kwon ◽  
Jai Hyang Go ◽  
Jong Sun Choi ◽  
Seung-Sook Lee ◽  
Young H. Ko ◽  
...  

2004 ◽  
Vol 54 (9) ◽  
pp. 712-718 ◽  
Author(s):  
Tadashi Saito ◽  
Jun-ichi Tamaru ◽  
Hirohisa Kishi ◽  
Junko Kayao ◽  
Yoshihiko Kuzuu ◽  
...  

2009 ◽  
Vol 104 ◽  
pp. S110-S111
Author(s):  
Crystal Chin ◽  
Michael Schafer ◽  
Laith Jamil ◽  
Simon Lo

2011 ◽  
Vol 26 (5) ◽  
pp. 686 ◽  
Author(s):  
Sanghui Park ◽  
Hyun Yee Cho ◽  
Seung Yeon Ha ◽  
Dong Hae Chung ◽  
Na Rae Kim ◽  
...  

2019 ◽  
Vol 101 (2) ◽  
pp. e43-e44
Author(s):  
S Kumar ◽  
K Raja ◽  
S Gnanasekaran ◽  
B Pottakkat

Intussusception in adolescents is usually idiopathic in nature. A 17-year-old woman with diffuse large B cell lymphoma presented with signs of intestinal obstruction after initiation of induction chemotherapy. On evaluation, the patient was diagnosed to have ileoileal intussusception with intestinal lymphangiectasia as the lead point. Intestinal lymphangiectasia as a rare cause for intussusception and its relationship with lymphoma is discussed in this case report.


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