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具有不寻常特征的原发性肺淋巴肉瘤

Primary lymphosarcoma of the lung with unusual features.

作者信息

Veliath A J, Khanna K K, Subhas B S, Ramakrishnan M R, Aurora A L

出版信息

Thorax. 1977 Oct;32(5):632-6. doi: 10.1136/thx.32.5.632.

Abstract

Two unusual cases of primary lymphocytic lymphosarcoma of the lung are presented. The first patient is a 5-year-old girl who showed a massive involvement of the entire right lung by tumour. She was treated by radiotherapy followed by cyclophosphamide and was alive and well one year later. The second patient was an adult man who presented clinically with a tumour of the chest wall. Necropsy revealed an extensive direct spread of pulmonary lymphosarcoma with infiltration of the chest wall but without metastatic dissemination or lymph node involvement. Neither primary lymphocytic lymphosarcoma of the lung in a girl of 5 years nor presentation of such a tumour as a chest wall mass in an adult seems to have been described previously.

摘要

本文报告了两例不寻常的原发性肺淋巴细胞性淋巴肉瘤病例。首例患者为一名5岁女孩,肿瘤广泛累及整个右肺。她接受了放射治疗,随后使用环磷酰胺治疗,一年后存活且状况良好。第二例患者是一名成年男性,临床上表现为胸壁肿瘤。尸检显示肺淋巴肉瘤广泛直接蔓延至胸壁并伴有浸润,但无转移扩散或淋巴结受累。5岁女孩的原发性肺淋巴细胞性淋巴肉瘤以及成年患者以胸壁肿块形式出现的此类肿瘤,此前似乎均未见报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a420/470804/12ae430112ad/thorax00155-0116-a.jpg

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本文引用的文献

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Primary lymphosarcoma of the lung.原发性肺淋巴肉瘤
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Primary lymphosarcoma of the lung.原发性肺淋巴肉瘤
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