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[嗜酸性粒细胞增多性血管淋巴样增生。组织学研究及氩激光治疗成功案例]

[Angiolymphoid hyperplasia with eosinophilia. Histologic study and successful therapy with the argon laser].

作者信息

Metze D, Neumann R, Chott A

机构信息

II. Universitäts-Hautklinik Wien.

出版信息

Hautarzt. 1991 Feb;42(2):101-6.

PMID:2037484
Abstract

We report a case of angiolymphoid hyperplasia with eosinophilia (AHE) with regional lymphadenopathy. The multiple papules were composed of both a lymphoid infiltrate of predominant T-cell type with eosinophils and anomalous vascular proliferation lined by "histiocytoid" endothelial cells, which were in close association with a ruined artery at the subcutaneous level in the largest nodule. Immunoelectron microscopy revealed factor-VIII-related antigen to be concentrated within the Weibel-Palade bodies of the endothelial cells. Their cytoplasmic filaments consisted of vimentin. In the pericytes large amounts of actin were demonstrable. Since AHE has a benign progressive course and only local recurrence is noted, the lesions were treated with argon laser. Subsequently, lymphadenopathy resolved spontaneously and the blood parameters normalized. There is no evidence of recurrence 1 year after treatment.

摘要

我们报告一例伴有局部淋巴结病的嗜酸性粒细胞性血管淋巴样增生症(AHE)。多个丘疹由主要为T细胞型的淋巴细胞浸润伴嗜酸性粒细胞以及由“组织细胞样”内皮细胞衬里的异常血管增生组成,在最大结节的皮下水平与一条破损动脉密切相关。免疫电子显微镜显示因子VIII相关抗原集中在内皮细胞的魏尔-帕拉德小体中。其细胞质细丝由波形蛋白组成。在周细胞中可证实有大量肌动蛋白。由于AHE病程呈良性进展且仅见局部复发,故对病变采用氩激光治疗。随后,淋巴结病自发消退,血液参数恢复正常。治疗1年后无复发迹象。

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