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嗜酸性肉芽肿作为恶性淋巴瘤中的偶然发现。

Eosinophilic granuloma as an incidental finding in malignant lymphoma.

作者信息

Kjeldsberg C R, Kim H

出版信息

Arch Pathol Lab Med. 1980 Mar;104(3):137-40.

PMID:6892595
Abstract

A histiocytic lesion that is histologically indistinguishable from eosinophilic granuloma was discovered as an incidental finding in lymph nodes from six patients with malignant lymphoma. Three patients had Hodgkin's disease and three had non-Hodgkin's lymphoma. The occurrence of epitheloid histocytes or granulomatous reactions, or both, in lymphoid tissue is well known in malignant lymphomas, but the combination of eosinophillic granuloma and malignant lymphoma in the same lymph node has not been described previously. In all of our cases, the malignant lymphoma was more conspicuous than the histiocytic lesion, and the latter was limited to the sinuses. Both lesions were well delineated; features suggesting transition of one into the other were absent, even in sites where the two were juxtaposed. No extranodal eosinophilic granuloma was observed.

摘要

在6例恶性淋巴瘤患者的淋巴结中,偶然发现了一种组织学上与嗜酸性肉芽肿无法区分的组织细胞病变。3例患者患有霍奇金病,3例患有非霍奇金淋巴瘤。在恶性淋巴瘤中,淋巴组织中出现上皮样组织细胞或肉芽肿反应,或两者皆有,这是众所周知的,但同一淋巴结中嗜酸性肉芽肿与恶性淋巴瘤并存的情况此前尚未见报道。在我们所有的病例中,恶性淋巴瘤比组织细胞病变更明显,后者局限于窦内。两种病变界限清晰;即使在两者相邻的部位,也没有提示一种病变向另一种病变转变的特征。未观察到结外嗜酸性肉芽肿。

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