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Extensive extramedullary disease involving the colon in multiple myeloma: A case report and review of literature

机译:多发性骨髓瘤涉及结肠的广泛髓外疾病:一例报道并文献复习

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Introduction: Organ involvement in multiple myeloma (MM) is characterized by infiltrative disease or by a myelomatous mass known as a plasmacytoma. We present a patient with MM who had extensive extramedullary involvement of the colon and a review of the literature on colon plasmacytomas. Case report: A 57-year-old male with MM presented with disease relapse in 2007, workup showing biopsy confirmed left perinephric extra-medullary disease involving the adjacent colon. Positron emission-tomography (PET) exhibited intense pan-colonic fluoro-deoxyglucose (FDG) uptake and computed-tomography confirmed extensive infiltrating soft tissue thickening in the ascending, transverse, and descending colon representing plasmacytomas. The patient underwent an autologous hematopoietic stem cell transplantation after conditioning with high-dose melphalan. Restaging PET-scan showed complete resolution of colonic extra-medullary plasmacytomas. Extramedullary plasmacytomas (EMP) are rare and constitute 4% of all plasma cell tumors. Discussion and Conclusion: Colonic plasmacytoma is an extremely rare site, with fewer than 25 cases reported in the literature. Colonic plasmacytomas have different presentations depending on the size and location. Treatment options for primary EMPs include surgical resection, radiotherapy, and chemotherapy. The primary treatment option for secondary EMP is systemic chemotherapy. This rare pan-colonic plasmacytoma, as a part of extramedullary myeloma, showed an impressive response to chemotherapy.
机译:简介:累及多发性骨髓瘤(MM)的器官的特征是浸润性疾病或称为浆细胞瘤的骨髓瘤。我们介绍了一位MM,他的结肠广泛侵犯了髓外,并回顾了结肠浆细胞瘤的文献。病例报告:一名57岁的MM男性患者于2007年出现疾病复发,检查结果显示活检证实左肾周围性髓外疾病累及相邻结肠。正电子发射断层扫描(PET)表现出强烈的泛结肠氟脱氧葡萄糖(FDG)摄取,计算机断层扫描证实在代表浆细胞瘤的升结肠,横结肠和降结肠中广泛浸润的软组织增厚。用高剂量美法仑调理后,患者进行了自体造血干细胞移植。重新进行PET扫描显示结肠结肠髓质浆细胞瘤完全消退。髓外浆细胞瘤(EMP)很少见,占所有浆细胞肿瘤的4%。讨论与结论:结肠浆细胞瘤是一个极为罕见的部位,文献报道少于25例。结肠浆细胞瘤有不同的表现,具体取决于大小和位置。主要EMP的治疗选择包括手术切除,放疗和化疗。继发性EMP的主要治疗选择是全身化疗。这种罕见的泛结肠浆细胞瘤,作为髓外骨髓瘤的一部分,对化学疗法表现出令人印象深刻的反应。

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