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[特发性腋网综合征]

[Idiopathic axillary web syndrome].

作者信息

Puentes Gutiérrez A B, García Bascones M, Puentes Gutiérrez R, Díaz Jiménez M

机构信息

Servicio de Rehabilitación, Hospital Virgen de la Salud, Toledo, España.

Servicio de Rehabilitación, Hospital Virgen de la Salud, Toledo, España.

出版信息

Rehabilitacion (Madr). 2020 Jan-Mar;54(1):68-72. doi: 10.1016/j.rh.2019.10.002. Epub 2019 Dec 5.

Abstract

We report the case of a 67-year-old woman who developed a cord of subcutaneous tissue extending from the axilla into the medial arm, accompanied by axillary neuropathic pain, with no history of surgery or infection. The patient was instructed in home exercises, and the condition progressively improved. Four months later, a small cord was visible on abduction with mild axillary dysesthesia, which was less severe than at onset. Diagnosis of exclusion was idiopathic axillary web syndrome (AWS). This syndrome is widely recognized after surgical axillary lymph node removal to treat breast cancer, but the etiopathogenesis is still unknown. Published reports of AWS with no history of surgery are rare, but a few reports have described this entity after infection or intense exercise. There are currently no previous reports of idiopathic AWS. The anatomical and clinical presentation, and clinical course of AWS without prior surgery, are similar to those of postoperative AWS.

摘要

我们报告了一例67岁女性病例,该患者出现一条从腋窝延伸至上臂内侧的皮下组织条索,并伴有腋窝神经性疼痛,既往无手术或感染史。指导患者进行家庭锻炼,病情逐渐改善。四个月后,外展时可见一条小条索,伴有轻度腋窝感觉异常,较发病时症状减轻。排除其他疾病后诊断为特发性腋窝网状综合征(AWS)。该综合征在因治疗乳腺癌而进行腋窝淋巴结清扫术后被广泛认识,但其发病机制仍不清楚。既往无手术史的AWS报道很少,但有少数报道描述了感染或剧烈运动后出现的该疾病。目前尚无特发性AWS的既往报道。无既往手术史的AWS的解剖学和临床表现以及临床病程与术后AWS相似。

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