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胸廓出口的硬纤维瘤:胸廓出口综合征的一种罕见病因。

Desmoid tumour of the thoracic outlet: an unusual cause of thoracic outlet syndrome.

作者信息

Gehman K E, Currie I, Ahmad D, Parrent A, Rizkalla K, Novick R J

机构信息

Department of Surgery, University of Western Ontario, London Health Sciences Centre.

出版信息

Can J Surg. 1998 Oct;41(5):404-6.

Abstract

Desmoid tumour is an unusual and aggressive tumour associated with a high recurrence rate. A 35-year-old man presented with recurrent debilitating left arm pain 2 years after undergoing bilateral transaxillary first rib resection for thoracic outlet syndrome. Nerve conduction studies demonstrated impairment of nerve conduction in the left arm. Magnetic resonance imaging of the brachial plexus demonstrated a mass at the apex of the left hemithorax involving the lower cord of the brachial plexus. Subsequent percutaneous needle biopsies failed to provided a definitive diagnosis. A cervicothoracic approach as described by Dartevelle was used to resect the lesion. Histologic and ultrastructural studies confirmed the diagnosis of a desmoid tumour. This report describes the atypical presentation of this unusual tumour and the application of the novel Dartevelle approach to secure its complete excision.

摘要

硬纤维瘤是一种罕见且侵袭性强的肿瘤,复发率很高。一名35岁男性在因胸廓出口综合征接受双侧经腋窝第一肋切除术后2年,出现复发性左臂剧痛。神经传导研究显示左臂神经传导受损。臂丛神经磁共振成像显示左半胸顶部有一肿块,累及臂丛神经下干。随后的经皮针吸活检未能提供明确诊断。采用Dartevelle描述的颈胸入路切除病变。组织学和超微结构研究证实为硬纤维瘤。本报告描述了这种罕见肿瘤的非典型表现以及采用新型Dartevelle入路确保其完整切除的情况。

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