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[多发性外生骨疣的一种罕见并发症:血胸]

[A rare complication of multiple exostoses: hemothorax].

作者信息

Dendale J, Amram S, Dermakar S, Guillaud R, Lesbros D

机构信息

Service de pédiatrie, hôpital Gaston-Doumergue, Nîmes, France.

出版信息

Arch Pediatr. 1995 Jun;2(6):548-50. doi: 10.1016/0929-693x(96)81199-7.

Abstract

BACKGROUND

Hemothorax is a rare complication of hereditary multiple exostosis.

CASE REPORT

A 12 year-old boy suffered from abrupt thoracic pain, firstly attributed to pleural effusion. He had hereditary multiple exostosis known since the age of 9 years. The patients was given anti-inflammatory drugs and erythromycin but the pleural effusion became more abundant 6 days later requiring thoracentesis which showed hemothorax. All bacteriological and cytologic investigations were negative. X rays, ultra-sonography and CT scan showed several costal exostoses developing into the thoracic cavity. The hemothorax disappeared within 12 days and the patient was well 4 months later, without pleural sequelae.

CONCLUSIONS

Hemothorax may be due to internal costal exostosis. It may be cured with thoracentesis; more aggressive therapy should be performed in exceptional cases with severe and/or recurrent bleeding.

摘要

背景

血胸是遗传性多发性骨软骨瘤的一种罕见并发症。

病例报告

一名12岁男孩突发胸痛,最初归因于胸腔积液。他自9岁起就患有遗传性多发性骨软骨瘤。患者接受了抗炎药物和红霉素治疗,但6天后胸腔积液增多,需要进行胸腔穿刺术,结果显示为血胸。所有细菌学和细胞学检查均为阴性。X线、超声和CT扫描显示数根肋骨骨软骨瘤向胸腔内生长。血胸在12天内消失,4个月后患者情况良好,无胸膜后遗症。

结论

血胸可能是由于肋骨内骨软骨瘤引起的。胸腔穿刺术可能治愈;在严重和/或反复出血的特殊情况下应采取更积极的治疗措施。

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