腹腔内浆细胞瘤演变为多发性骨髓瘤的大剂量化疗和同种异体外周血干细胞移植。

Kun-Ming Chung, Shih-Sung Chuang, Wei-Shou Hwang, Po-Shing Lee, Chin-Yang Li
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引用次数: 0

摘要

孤立性浆细胞瘤包括髓外浆细胞瘤和骨内浆细胞瘤。70%的患者为男性,中位年龄为50-55岁,比浆细胞骨髓瘤年轻。大多数孤立的骨浆细胞瘤最终在2-10年内演变为浆细胞骨髓瘤,而髓外的浆细胞瘤很少发生这种情况。我们报告一个不寻常的病例腹腔内浆细胞瘤在一个年轻的妇女,这是误诊和治疗最初的T细胞淋巴瘤。一年后出现浆细胞骨髓瘤的典型表现。给予大剂量化疗后异基因外周血干细胞移植(alloo - pbsct)。异体pbsct术后1年皮肤复发,采用大面积切除和局部照射治疗。在胸壁孤立性浆细胞瘤广泛切除及局部放疗4年后,患者健康生存,无疾病迹象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High dose chemotherapy and allogenic peripheral blood stem cell transplantation for multiple myeloma evolving from intra-abdominal plasmacytoma.

Solitary plasmacytomas include extramedullary plasmacytomas and those found in the bone. Seventy percent of patients are male and the median age is 50-55 years, younger than that for plasma cell myeloma. Most solitary plasmacytomas of bone eventually evolve to plasma cell myeloma within 2-10 years, while the extramedullary ones do so infrequently. We present an unusual case of intra-abdominal plasmacytoma in a young woman which was misdiagnosed and treated as T cell lymphoma initially. Typical manifestations of plasma cell myeloma appeared one year later. High dose chemotherapy followed by allogeneic peripheral stem cell blood transplantation (allo-PBSCT) was given. Relapse in skin occurred one year after allo-PBSCT, and was treated with wide excision and local irradiation. The patient was well and alive without evidence of disease 4 years after wide excision of the recurrence of chest wall solitary plasmacytoma and local radiotherapy.

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