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首页> 外文期刊>Leukemia and lymphoma >Extranodal non-Hodgkin's lymphoma presenting as an abdominal wall mass. A case report and review of the literature.
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Extranodal non-Hodgkin's lymphoma presenting as an abdominal wall mass. A case report and review of the literature.

机译:结外非霍奇金淋巴瘤表现为腹壁肿块。病例报告和文献复习。

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摘要

Soft tissue lymphoma is a very rare clinical entity with varying presentation characteristics and atypical clinical and imaging features. The present report describes a patient who presented with a painless soft tissue mass on the posterolateral surface of the abdominal wall, simulating a neoplasm of mesenchymal origin. After complete surgical excision, the tumor was diagnosed as a diffuse large B-cell lymphoma. No B-symptoms were present and clinical staging did not reveal other sites of disease (stage I EA). The International Prognostic Index score was equal to 1 and classified the patient to the good risk group. Post-operatively the patient was treated with immuno-chemotherapy consisting of rituximab plus cyclophosphamide, epirubicin, vincristine and prednisolone and is currently free of disease for 10 months. The case is discussed with a brief review of the literature on the diagnosis, treatment and outcome of soft tissue lymphomas.
机译:软组织淋巴瘤是一种非常罕见的临床实体,具有不同的表现特征以及非典型的临床和影像学特征。本报告描述了一名患者,其在腹壁后外侧表面表现出无痛的软组织肿块,模拟了间充质来源的肿瘤。完全手术切除后,该肿瘤被诊断为弥漫性大B细胞淋巴瘤。没有B症状出现,临床分期未显示其他疾病部位(I EA期)。国际预后指数评分等于1,并将患者分类为高风险组。术后患者接受了由利妥昔单抗加环磷酰胺,表柔比星,长春新碱和泼尼松龙组成的免疫化学疗法,目前无病持续10个月。对该病例进行了简要回顾,讨论了软组织淋巴瘤的诊断,治疗和结局。

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