A Rare Case of Hamartoma Chest Wall Following Trauma in a 42-year-old Man

M. Ahmadinejad, A. A. Pour, P. Hosseini, A. Hashemian, K. Ahmadi
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引用次数: 3

Abstract

Background: Chest wall mesenchymal hamartoma (CWH) is a distinct and extremely rare tumor-like lesion of the thorax. It usually presents in the neonatal period or in infancy. The common presentation is in the form of a visible chest wall mass with or without respiratory distress. Case presentation: A 42-year-old man with a history of chest wall trauma since 5 years ago was admitted with a swelling of the anterior of the chest wall and during this period has grown slowly. Physical examination showed a left anterior chest wall deformity. Chest radiographs and chest CT showed a left anterolateral chest wall mass involving the fourth and fifth ribs. Thoracotomy was performed. The tumor and involved ribs were resected with a 5cm safe margin. The histopathologic examination showed hamartoma. The patient has been fallowed up since 60 month ago, and has not had any complaints in this time. Result: Despite the rarity of chest wall hematoma, this side effect must always be taken into consideration while studying the chest wall injuries especially in the case of trauma history due to other differential diagnosis and her side effects such as respiratory problems. Conclusion: Although rare, this condition ought to be kept in mind while dealing with hamartoma Chest wall following trauma in order to avoid its complications such as respiratory problems. Surgical excision is usually curative in combination with conservative therapy if possible.
一例42岁男性外伤后胸壁错构瘤的罕见病例
背景:胸壁间充质错构瘤(胸壁间充质错构瘤)是一种罕见的胸腔肿瘤样病变。它通常出现在新生儿期或婴儿期。常见表现为胸壁可见肿块,伴或不伴呼吸窘迫。病例介绍:一名42岁男性,5年前有胸壁外伤史,因胸壁前部肿胀而入院,在此期间肿胀缓慢。体格检查显示左前胸壁畸形。胸片和胸部CT显示左侧胸壁前外侧肿块,累及第四和第五根肋骨。进行开胸手术。肿瘤及受累肋骨以5cm的安全边缘切除。组织病理学检查为错构瘤。患者自60个月前开始随访,在此期间没有任何抱怨。结果:尽管胸壁血肿是罕见的,但在研究胸壁损伤时必须考虑到这一副作用,特别是在有创伤史的情况下,由于其他鉴别诊断及其副作用,如呼吸问题。结论:胸壁错构瘤虽罕见,但在治疗外伤后胸壁错构瘤时应注意避免其并发症,如呼吸系统疾病。如果可能的话,手术切除和保守治疗通常是可以治愈的。
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