[Primary pulmonary mucosa-associated lymphoid tissue lymphoma: a case report].

Bartosz Kubisa, Anna Bocheńska, Maria Piotrowska, Paweł Dec, Anna Lesińska, Anna Kubisa, Janusz Wójcik, Jarosław Pieróg, Tomasz Grodzki
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引用次数: 6

Abstract

Primary pulmonary lymphoma accounts only 0,5% of all primary lung neoplasms. Mucosa-associated lymphoid tissue (MALT) lymphoma is a low grade B-cell extranodal lymphoma. It is a quite infrequent entity, however it constitutes from 72% to 90% of all pulmonary lung lymphomas. Long-term stimulation of bronchus-associated lymphoid tissue by antigens, smoking, inflammatory disorders or autoimmune diseases are thought to be leading to the development of MALT lymphoma. We present the case of primary pulmonary mucosa-associated lymphoid tissue lymphoma. A 76-year-old man with a history of heavy smoking (22.5 pack years) was admitted to the hospital for a further diagnostics of an abnormal finding in the right lung visualized on the chest X-ray. The diagnostic process, including imagining studies did not reveal the etiology of a lesion in the right lung. The patient was qualified for surgical diagnostics. The histological finding confirmed extranodal marginal low-grade B-cell lymphoma of mucosa -associated lymphoid tissue.

[原发性肺粘膜相关淋巴组织淋巴瘤1例]。
原发性肺淋巴瘤仅占所有原发性肺肿瘤的0.5%。粘膜相关淋巴组织(MALT)淋巴瘤是一种低级别b细胞结外淋巴瘤。这是一个非常罕见的实体,但它占所有肺淋巴瘤的72%至90%。抗原、吸烟、炎症性疾病或自身免疫性疾病对支气管相关淋巴组织的长期刺激被认为是导致MALT淋巴瘤发展的原因。我们报告一例原发性肺粘膜相关淋巴组织淋巴瘤。76岁男性,有重度吸烟史(22.5包年),因胸部x线检查右肺异常而入院。诊断过程,包括影像学检查并没有揭示右肺病变的病因。该患者符合外科诊断的条件。组织学检查证实结外边缘低级别b细胞淋巴瘤粘膜相关淋巴组织。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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