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胸膜黏膜相关淋巴组织结外边缘区淋巴瘤表现:病例报告及文献复习。

Pleuric presentation of extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue: a case report and a review of the literature.

机构信息

Department of Experimental Oncology, Mediterranean Institute of Oncology, Viagrande, Catania, Italy.

出版信息

Int J Hematol. 2010 Sep;92(2):369-73. doi: 10.1007/s12185-010-0645-2. Epub 2010 Aug 20.

Abstract

A primary pleural marginal zone B cell lymphoma of mucosa-associated lymphoid tissue (MALT) is a very rare eventuality. Here, we report a rare case of MALT lymphoma arising in the pleura and update the literature on this topic. A 74-year-old female was hospitalized for persistent cough and weakness. A chest radiograph and total-body CT scan showed only large right-sided pleural effusion, and the coexistence of pleural thickening. Video-assisted thoracoscopic exploration and a talc pleurodesis were performed and microscopic and immunohistochemical findings showed that the tumor was a pleural MALT lymphoma. The patient received immunotherapy with Rituximab and obtained a good response that lasted 2 years. To the best of our knowledge, only seven cases of primary pleural MALT lymphoma have been documented until recently, mostly from Japan with a mean age for all patients of 60.5 years. The pathogenesis of MALT lymphomas remains unclear, although a possible chronic antigenic stimulation by microbial pathogens and/or autoantigens has been hypothesized. Surgical resection was performed in most cases, and some patients received postoperative chemotherapy or immunotherapy. The clinicopathologic characteristics and management of this extremely rare disease are also discussed.

摘要

黏膜相关淋巴组织(MALT)的原发性胸膜边缘区 B 细胞淋巴瘤非常罕见。在此,我们报告一例罕见的胸膜 MALT 淋巴瘤,并对该主题的文献进行更新。一名 74 岁女性因持续性咳嗽和乏力住院。胸部 X 线和全身 CT 扫描仅显示右侧大量胸腔积液和胸膜增厚并存。进行了电视辅助胸腔镜检查和滑石粉胸膜固定术,显微镜和免疫组织化学检查结果显示肿瘤为胸膜 MALT 淋巴瘤。患者接受了利妥昔单抗免疫治疗,取得了持续 2 年的良好反应。据我们所知,直到最近,只有 7 例原发性胸膜 MALT 淋巴瘤被记录在案,主要来自日本,所有患者的平均年龄为 60.5 岁。MALT 淋巴瘤的发病机制尚不清楚,尽管假设可能存在微生物病原体和/或自身抗原的慢性抗原刺激。大多数情况下进行了手术切除,一些患者接受了术后化疗或免疫治疗。还讨论了这种极其罕见疾病的临床病理特征和治疗方法。

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