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累及骨骼肌的嗜酸性粒细胞增多性血管淋巴样增生。

Angiolymphoid hyperplasia with eosinophilia involving skeletal muscle.

作者信息

Buchanan R, Sworn M J, Mousley J M

出版信息

Histopathology. 1980 Mar;4(2):197-204. doi: 10.1111/j.1365-2559.1980.tb02912.x.

DOI:10.1111/j.1365-2559.1980.tb02912.x
PMID:7358348
Abstract

A vascular tumour involving the trapezius muscle is described. In addition to proliferating blood vessels with perithelial cuffing, there was a distinctive stroma of lymphoid aggregates, plasmacytoid cells, some mast cells and large numbers of eosinophils, many with a perivascular distribution. This solely intramuscular lesion was considered to be an example of angiolymphoid hyperplasia with eosinophilia. The aetiology and pathogenesis are discussed.

摘要

本文描述了一例累及斜方肌的血管肿瘤。除了有伴周皮套叠的增生血管外,还有独特的淋巴样聚集、浆细胞样细胞、一些肥大细胞和大量嗜酸性粒细胞组成的基质,许多嗜酸性粒细胞呈血管周围分布。这个仅位于肌肉内的病变被认为是嗜酸性粒细胞增多性血管淋巴样增生的一个例子。本文还讨论了其病因和发病机制。

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Angiolymphoid hyperplasia with eosinophilia involving skeletal muscle.累及骨骼肌的嗜酸性粒细胞增多性血管淋巴样增生。
Histopathology. 1980 Mar;4(2):197-204. doi: 10.1111/j.1365-2559.1980.tb02912.x.
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Angiolymphoid hyperplasia with eosinophils in oral mucosa.口腔黏膜嗜酸性粒细胞性血管淋巴样增生
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[Angiolymphoid hyperplasia with eosinophilia].[嗜酸性粒细胞增多性血管淋巴样增生]
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Angiolymphoid hyperplasia with eosinophilia in association with a vascular malformation.伴嗜酸性粒细胞增多的血管淋巴样增生与血管畸形相关
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[Angiolymphoid hyperplasia with eosinophils. Case report and differentiation from Kimura disease].[伴有嗜酸性粒细胞的血管淋巴样增生。病例报告及与木村病的鉴别]
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Angiolymphoid hyperplasia with eosinophilia.伴嗜酸性粒细胞增多的血管淋巴样增生
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Cellular Cutaneous Epithelioid Hemangioma Harboring the Rare GATA6::FOXO1 Gene Fusion.细胞皮肤上皮样血管内皮瘤中存在罕见的 GATA6::FOXO1 基因融合。
Am J Dermatopathol. 2024 Apr 1;46(4):223-227. doi: 10.1097/DAD.0000000000002647.
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Angiolymphoid hyperplasia with eosinophilia involving the common digital artery of the hand: A case report and classification of upper limb lesions.手部指总动脉嗜酸性粒细胞增多性血管淋巴样增生症:一例报告及上肢病变分类
Int J Surg Case Rep. 2017;39:84-87. doi: 10.1016/j.ijscr.2017.08.007. Epub 2017 Aug 10.
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Orbital Kimura's disease.
J R Soc Med. 1993 Apr;86(4):234-5. doi: 10.1177/014107689308600421.