Takamatsu H, Noguchi H, Tahara H, Kajiya H, Akiyama H
Department of Pediatric Surgery, Kagoshima University, Faculty of Medicine, Japan.
Surg Today. 1996;26(7):527-31. doi: 10.1007/BF00311561.
We report herein the case of a male neonate with a giant cystic lymphangioma confined to the bilateral anterior mediastinum. He developed very severe respiratory distress on the 8th day of life due to the mediastinal mass, and almost total excision of the bilateral mass was performed on the 12th day of life through a right axillar thoracotomy. The pathological diagnosis was cystic lymphangioma. Postoperatively, right phrenic nerve dysfunction was evident, for which diaphragmatic plication could only be performed 5 weeks after the initial surgery due to the prolonged respiratory support. In the 4 years since undergoing surgery the child has shown no sign of recurrence and has not experienced any further respiratory problems.
我们在此报告一例男性新生儿,其患有局限于双侧前纵隔的巨大囊性淋巴管瘤。出生第8天,由于纵隔肿物,他出现了非常严重的呼吸窘迫,出生第12天通过右腋下开胸术对双侧肿物进行了几乎完全切除。病理诊断为囊性淋巴管瘤。术后,右侧膈神经功能障碍明显,由于呼吸支持时间延长,只能在初次手术后5周进行膈肌折叠术。自手术以来的4年里,该患儿没有复发迹象,也没有出现任何进一步的呼吸问题。