Al Smady Moaath, Zahari Nurul Nadia Binti, Mohd Sahid Noor Syahirah Binti, Saparudin Nurul Syuhada Binti
Department of Cardiothoracic Surgery, Jordan University Hospital, Aljubeiha, Amman, Jordan.
J Surg Case Rep. 2019 May 9;2019(5):rjz136. doi: 10.1093/jscr/rjz136. eCollection 2019 May.
Mediastinal teratoma is an uncommon finding in the pediatric age group, accounting for only 7-11% of extragonadal teratomas. Rarely, the tumor can rupture and erode into the pericardium or pleural space. However, pericardial effusion due to rupture is infrequent. We report a case of such a rare presentation in a 10-year-old young female. The patient underwent a mediastinal tumor excision. Histopathology revealed that there was ruptured mature cystic teratoma with inflammatory reaction. Numerous cases of mediastinal teratoma with pericardial effusion have been reported but only few have been presented in the pediatric age group.
纵隔畸胎瘤在儿童年龄组中并不常见,仅占性腺外畸胎瘤的7 - 11%。该肿瘤很少会破裂并侵蚀进入心包或胸膜腔。然而,因破裂导致的心包积液并不常见。我们报告一例10岁年轻女性的这种罕见病例。患者接受了纵隔肿瘤切除术。组织病理学显示为破裂的成熟囊性畸胎瘤伴炎症反应。已有许多纵隔畸胎瘤合并心包积液的病例报道,但儿科年龄组的病例仅少数。