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
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.
Oncol Lett. 2016 Jan;11(1):654-656. doi: 10.3892/ol.2015.3954. Epub 2015 Nov 23.
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.
套细胞淋巴瘤(MCL)是一种罕见的胃肠道恶性淋巴瘤,可表现为多发性淋巴瘤性息肉病(MLP);然而,MCL中伴有肠套叠的MLP鲜有报道。在本研究中,一名54岁男性患者被诊断为MCL,表现为全胃肠道多发息肉样病变并伴有回盲部肠套叠。为预防复杂肠套叠及肿瘤减瘤,行右半结肠切除术。此外,采用利妥昔单抗加hyper-CVAD方案进行了6个周期的化疗。在计划的化疗周期之后,随访检查显示完全缓解,缓解持续至今已3年。