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

机译:带有多发性淋巴瘤性息肉和肠套叠的套细胞淋巴瘤:一例报告

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摘要

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.
机译:套细胞淋巴瘤(MCL)是胃肠道(GI)罕见的恶性淋巴瘤,可能表现为多发性淋巴瘤性息肉病(MLP);但是,在MCL中很少报道有肠套叠的MLP。在本研究中,一名54岁的男性患者被诊断为MCL,伴有完整胃肠道的多息肉样病变,并伴有回盲肠套叠。进行右半结肠切除术是为了防止复杂的肠套叠并减轻肿瘤。此外,利妥昔单抗加高CVAD方案进行了6个化疗周期。在计划的化疗周期之后,随访检查显示反应完全,并且缓解持续了3年直至目前。

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