Thoracic outlet syndrome caused by superior mediastinal mass: A case report.

IF 0.7 Q3 Medicine ASIAN CARDIOVASCULAR & THORACIC ANNALS Pub Date : 2024-06-01 Epub Date: 2024-02-07 DOI:10.1177/02184923241230706
Fahmi H Kakamad, Saywan Kakarash Asaad, Soran H Tahir, Nasren Sharef Sabr, Adullah K Ghafour, Choman Sabah Omer, Rezheen J Rashid, Bnar J Hama Amin, Pavel Mustafa Kareem, Mohammed Subhan Mohammed
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Abstract

Introduction: Thoracic outlet syndrome (TOS) caused by superior mediastinal soft tissue mass has never been reported in the literature, the aim of this study is to discuss a case of TOS caused by a superior mediastinal mass in which the histopathological examinations of the mass showed vascular malformation.

Case report: A 45-year-old female presented with left upper limb pain and numbness for three months, associated with swelling and attacks of shortness of breath. Imaging studies showed soft tissue mass involving the superior mediastinum. The condition of the patient deteriorated and the signs and symptoms of TOS became clearer, all provocative tests and nerve conduction studies were positive. The patient underwent thoracic outlet decompression. The patient did not respond and the symptoms deteriorated further. After a multidisciplinary board discussion, the patient was prepared for median sternotomy under general anesthesia. A total resection of the mass was done. The patient was totally relieved a few hours after the operation.

Discussion: The etiology of TOS can be multifaceted. Several factors contribute to its onset, and these can be categorized as congenital or acquired. Congenital causes include anatomical anomalies such as a cervical rib, or an elongated transverse process of the cervical vertebrae. These anatomical deviations can reduce the size of the thoracic outlet and make it prone to compression.

Conclusion: Although it is rare, TOS could be due to superior mediastinal mass and the treatment of choice is total resection either through median sternotomy or thoracoscopic procedure.

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上纵隔肿块引起的胸廓出口综合征:病例报告
导言:由上纵隔软组织肿块引起的胸廓出口综合征(TOS)在文献中从未有过报道,本研究旨在讨论一例由上纵隔肿块引起的胸廓出口综合征,肿块的组织病理学检查显示为血管畸形:一名 45 岁女性因左上肢疼痛和麻木 3 个月,伴有肿胀和气短发作就诊。影像学检查显示软组织肿块累及上纵隔。患者病情恶化,TOS 的症状和体征变得更加明显,所有诱导试验和神经传导检查均呈阳性。患者接受了胸廓出口减压术。患者没有任何反应,症状进一步恶化。经过多学科委员会讨论后,患者准备在全身麻醉下进行胸骨正中切开术。手术对肿块进行了全切除。术后数小时,患者症状完全缓解:讨论:TOS 的病因可能是多方面的。讨论:TOS 的病因是多方面的,可分为先天性和后天性。先天性原因包括解剖异常,如颈部肋骨或颈椎横突过长。这些解剖上的偏差会缩小胸廓出口的尺寸,使其容易受到挤压:尽管 TOS 很罕见,但它可能是由上纵隔肿块引起的,治疗方法是通过胸骨正中切开术或胸腔镜手术进行全切除。
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来源期刊
CiteScore
1.30
自引率
0.00%
发文量
78
期刊介绍: The Asian Cardiovascular and Thoracic Annals is an international peer-reviewed journal pertaining to cardiovascular and thoracic medicine. Besides original clinical manuscripts, we welcome research reports, product reviews, reports of new techniques, and findings of special significance to Asia and the Pacific Rim. Case studies that have significant novel original observations, are instructive, include adequate methodological details and provide conclusions. Workshop proceedings, meetings and book reviews, letters to the editor, and meeting announcements are encouraged along with relevant articles from authors.
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