先天性门体分流关闭后肺动脉高压和高锰水平的进展
Progress of pulmonary hypertension and high manganese levels through congenital portosystemic shunt closure.
作者信息
Kakiuchi Toshihiko, Baba Yuta, Minematsu Nobuya, Doi Hirohito, Kumamoto Takashi
机构信息
Department of Pediatrics, Faculty of Medicine Saga University Saga Japan.
出版信息
Clin Case Rep. 2022 Sep 12;10(9):e6318. doi: 10.1002/ccr3.6318. eCollection 2022 Sep.
Abstract
A 6-year-old girl with congenital portosystemic shunt presented with abnormal manganese levels and improving pulmonary hypertension even 1 year after shunt vascular ligation. As the progress after portal vein blood flow recovery varies among individuals, long-term follow-up of patients with congenital portosystemic shunt is needed.
摘要
一名患有先天性门体分流的6岁女孩，在分流血管结扎术后1年出现锰水平异常且肺动脉高压有所改善。由于门静脉血流恢复后的进展因人而异，因此需要对先天性门体分流患者进行长期随访。
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