Mantle cell lymphoma with multiple lymphomatous polyposis 
and intussusception: A case report

Lee,Jae  Min; Kim,Eun  Sun; Choi,Hyuk  Soon; Keum,Bora; Jeen,Yoon  Tae; Lee,Hong  Sik; Chun,Hoon  Jai; Kim,Chang  Duck; Ryu,Ho  Sang; Kim,Insun

doi:10.3892/ol.2015.3954

January-2016 Volume 11 Issue 1

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January-2016 Volume 11 Issue 1

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Case Report

Mantle cell lymphoma with multiple lymphomatous polyposis and intussusception: A case report

Authors:
- Jae Min Lee
- Eun Sun Kim
- Hyuk Soon Choi
- Bora Keum
- Yoon Tae Jeen
- Hong Sik Lee
- Hoon Jai Chun
- Chang Duck Kim
- Ho Sang Ryu
- Insun Kim
View Affiliations / Copyright

Affiliations: Department of Internal Medicine, Division of Gastroenterology and Hepatology, Korea University College of Medicine, Seoul 136‑705, Republic of Korea, Department of Pathology, Korea University Anam Hospital, Seoul 136‑705, Republic of Korea
Pages: 654-656
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Published online on: November 23, 2015

https://doi.org/10.3892/ol.2015.3954
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Abstract

Mantle cell lymphoma (MCL) is a rare malignant lymphoma of the gastrointestinal (GI) tract that may present as multiple lymphomatous polyposis (MLP); however, MLP with intussusception is rarely reported in MCL. In the present study, a 54‑year‑old male patient was diagnosed with MCL, presenting with numerous polypoid lesions of the complete GI tract combined with ileocecal intussusception. Right hemicolectomy was performed in order to prevent complicated intussusception and for tumor debulking. In addition, 6 cycles of chemotherapy were performed with the rituximab plus hyper‑CVAD regimen. Subsequent to the planned chemotherapy cycles, follow‑up examination demonstrated a complete response and the remission lasted for 3 years until the present time.

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