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嗜酸性粒细胞增多性血管淋巴样增生:一种病理上类似于皮肤木村病的骨病变。两例报告。

Angiolymphoid hyperplasia with eosinophilia: a bone lesion pathologically resembling Kimura's disease of skin. A report of two cases.

作者信息

Fornasier V L, Finkelstein S, Gardiner G W, Wong D

出版信息

Clin Orthop Relat Res. 1982 Jun(166):243-8.

PMID:7083679
Abstract

Primary osseous lesions morphologically identical to the soft tissue entity known as angiolymphoid hyperplasia with eosinophilia were diagnosed by means of light and electron microscopy in two men, ages 20 and 27 years, respectively. The characteristics of the lesions were reactive rather than neoplastic. The soft tissue counterpart of this lesion has shown no indication of aggressive behavior nor of a potential to metastasize. Further investigations are necessary to determine whether a similar benign behavior can be established for angiolymphoid hyperplasia with eosinophilia arising primarily in bone.

摘要

通过光镜和电镜诊断,两名分别为20岁和27岁的男性患有形态上与软组织中称为嗜酸性粒细胞增多性血管淋巴样增生相同的原发性骨病变。这些病变的特征是反应性而非肿瘤性。该病变的软组织对应物未显示侵袭性行为迹象,也没有转移潜能。有必要进一步研究以确定原发性骨嗜酸性粒细胞增多性血管淋巴样增生是否也具有类似的良性行为。

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