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尼日利亚男性运动诱发胸壁 Mondor 病 1 例报告。

Exercise-Induced Mondor's Disease of the Chest Wall in a Nigerian Man: A Case Report.

机构信息

Department of Family Medicine, Niger Foundation Hospital, 5, Presidential Close, Independence Layout, Enugu State, Nigeria.

Department of Surgery, University of Nigeria Teaching Hospital, Ituku-Ozalla, Enugu State, Nigeria.

出版信息

West Afr J Med. 2022 Apr 29;39(4):425-428.

Abstract

BACKGROUND

Mondor's disease (MD) is a rare cause of chest pain, characterized by thrombophlebitis of the subcutaneous veins of the anterolateral thoracoabdominal wall. It is a benign, self-limiting condition that is often underdiagnosed due to lack of knowledge of the condition. Although the exact aetiology is unclear, several predisposing factors, including excessive physical activity have been postulated. To the best of our knowledge, there is no previous published report of MD of the chest wall in an adult Nigerian man.

OBJECTIVE

To describe the association between muscular strain and the development of MD.

CASE PRESENTATION

A 40-year-old Nigerian man presented with a one-month history of dull, aching right-sided chest pain. He gave a history of engaging in intense thoracoabdominal exercises for 6 weeks prior to onset of symptoms. Physical examination revealed a tender, subcutaneous cord-like swelling extending from below the right anterior axillary fold to the right hypochondrium and accentuated by overhead abduction of the right arm. Ultrasonography revealed a hypoechoic, noncompressible right thoracoepigastric vein with no flow on Doppler interrogation, in keeping with superficial venous thrombosis. He was treated with nonsteroidal anti-inflammatory agents and paracetamol. The pain and lesion resolved completely within two weeks after presentation and there was no recurrence over the subsequent four months of follow-up.

CONCLUSION

MD is an uncommon cause of chest pain that is often underdiagnosed and underreported due to lack of awareness. It can suddenly appear in persons performing extreme thoracoabdominal exercises. Treatment is essentially symptomatic. Prompt diagnosis of this self-limiting condition is essential in distinguishing it from malignant diseases.

摘要

背景

芒多氏病(MD)是一种罕见的胸痛原因,其特征为前外侧胸腹壁皮下静脉血栓性静脉炎。这是一种良性、自限性疾病,由于对该病缺乏认识,往往诊断不足。尽管确切的病因尚不清楚,但已经提出了几种易患因素,包括过度的体力活动。据我们所知,以前没有关于尼日利亚成年男性胸壁 MD 的报道。

目的

描述肌肉劳损与 MD 发病之间的关联。

病例介绍

一名 40 岁的尼日利亚男子因右侧胸痛一个月来就诊。他在出现症状前 6 周开始进行强烈的胸腹壁运动,有此病史。体格检查发现,右腋前褶皱下方至右季肋区有一条触痛、条索状皮下肿胀,上肢过头外展时加重。超声检查显示右胸上腹静脉呈低回声、不可压缩,多普勒检查无血流,符合浅表静脉血栓形成。给予非甾体抗炎药和对乙酰氨基酚治疗。疼痛和病变在就诊后两周内完全缓解,随后的 4 个月随访中没有复发。

结论

MD 是胸痛的一种罕见原因,由于缺乏认识,往往诊断不足且报道较少。它可能突然出现在进行极端胸腹壁运动的人中。治疗主要是对症治疗。及时诊断这种自限性疾病对于将其与恶性疾病区分开来至关重要。

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