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血管免疫母细胞性淋巴结病中的细支气管肺泡癌

Bronchiolo-alveolar carcinoma in angio-immunoblastic lymphadenopathy.

作者信息

Cremers S, Dutrieux-Fauchet M C, Dutrieux C

出版信息

Eur J Respir Dis. 1983 Apr;64(3):222-8.

PMID:6301870
Abstract

A 78-year-old woman presented progressive weakness of three months' duration and generalized lymphadenopathy. Lymph-node biopsy histopathology was diagnosed as immunoblastic lymphadenopathy. As the patient's condition was deteriorating rapidly, she was given corticosteroid with clinical improvement. Initially no distinct radiographic abnormalities of the lungs were seen however, a subsequent solitary nodule in the left lung base was detected. Histology showed a bronchiolo-alveolar carcinoma. Pulmonary parenchymal involvement in angioimmunoblastic lymphadenopathy (A.I.L.) has been previously well documented and radiographic abnormalities usually consist of well-circumscribed parenchymal infiltrates. The possibility of a development of bronchiolo-alveolar carcinoma in A.I.L. may be the consequence of a deficiency of the cellular immunity aggravated in part by an immunosuppressive treatment. The hypothesis of the paraneoplastic nature of A.I.L. has also been raised. There are, therefore, always compulsory reasons to check the nature of the pulmonary involvement.

摘要

一名78岁女性,出现进行性肌无力3个月,伴有全身淋巴结肿大。淋巴结活检组织病理学诊断为免疫母细胞性淋巴结病。由于患者病情迅速恶化,给予皮质类固醇治疗后临床症状改善。最初未发现肺部有明显的影像学异常,但随后在左肺底部发现了一个孤立结节。组织学检查显示为细支气管肺泡癌。血管免疫母细胞性淋巴结病(A.I.L.)累及肺实质此前已有充分记录,影像学异常通常表现为边界清晰的实质浸润。A.I.L.中发生细支气管肺泡癌的可能性可能是细胞免疫缺陷的结果,部分原因是免疫抑制治疗加重了这种缺陷。也有人提出A.I.L.具有副肿瘤性质的假说。因此,始终有必要检查肺部受累的性质。

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