儿童巨大胸膜心包囊肿继发心包填塞:撒哈拉以南非洲一例外科病例报告。

IF 0.7 Q4 SURGERY
European Journal of Pediatric Surgery Reports Pub Date : 2025-07-28 eCollection Date: 2025-01-01 DOI:10.1055/a-2655-3348
Abdel Kémal Bori Bata, Yacoubou Imorou-Souaibou, Ahmad Ibrahim, Désiré Nékoua, Joseph Adoco, Arnaud Sonou
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引用次数: 0

摘要

胸膜心包囊肿是一种罕见的纵隔肿瘤,临床表现多变,常为严重的儿童,偶尔需要紧急干预。我们报告的情况下,以前健康的14岁男性谁是入院严重充血性心力衰竭的迹象和心脏填塞的临床证据。经胸超声心动图和胸部CT扫描证实存在压缩纵隔囊性肿块。患者经胸骨正中切开术行紧急手术切除。组织病理学检查证实为良性心包囊肿。术后恢复平稳,随访2年无复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cardiac Tamponade Secondary to a Giant Pleuropericardial Cyst in a Child: A Surgical Case Report from Sub-Saharan Africa.

Cardiac Tamponade Secondary to a Giant Pleuropericardial Cyst in a Child: A Surgical Case Report from Sub-Saharan Africa.

Cardiac Tamponade Secondary to a Giant Pleuropericardial Cyst in a Child: A Surgical Case Report from Sub-Saharan Africa.

Cardiac Tamponade Secondary to a Giant Pleuropericardial Cyst in a Child: A Surgical Case Report from Sub-Saharan Africa.

Pleuropericardial cysts are rare mediastinal tumors with variable, often severe, clinical presentations in children, occasionally requiring urgent intervention. We report the case of a previously healthy 14-year-old male who was admitted with signs of severe congestive heart failure and clinical evidence of cardiac tamponade. Transthoracic echocardiography and thoracic CT scan confirmed the presence of a compressive mediastinal cystic mass. The patient underwent emergency surgical resection via median sternotomy. Histopathological examination confirmed a benign pericardial cyst. Postoperative recovery was uneventful, and no recurrence was observed after 2 years of follow-up.

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来源期刊
自引率
33.30%
发文量
39
审稿时长
12 weeks
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