[线粒体呼吸链紊乱伴膀胱输尿管反流:一例儿科病例报告]。

Shinta Suenaga, Satoko Matsuyama, Futoshi Matsui, Koji Yazawa, Fumi Matsumoto
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引用次数: 0

摘要

线粒体呼吸链疾病(MRCD)在临床表现和潜在的遗传/生化缺陷方面是一个高度异质性的群体。对于膀胱输尿管反流(VUR)等泌尿系统并发症的处理尚未在 MRCD 病例中讨论过。我们报告了一例因原发性和继发性膀胱输尿管反流(VUR)而导致反复尿路感染(UTI)的 MRCD 儿科病例。一名 6 个月大的男孩因发热性尿路感染(fUTI)转诊至我科,他患有多种畸形和吸入性肺炎病史。排尿膀胱尿道造影显示左侧尿道有高位膀胱返流,膀胱正常。由于没有观察到 VUR 自发消退,他在 1 岁 7 个月时接受了左侧输尿管再植术和左侧睾丸切除术。虽然他在术后立即出现了尿毒症,但出院后尿毒症没有复发。3 岁时,他因吸入性肺炎导致脓毒性休克和心脏骤停,心肺复苏后出现脑病。在这次事件中,通过肝活检确诊为 MRCD。自 4 岁起,他就反复出现膀胱尿道炎。VCUG 证实了膀胱畸形和右侧尿崩症。他在 6 岁时接受了膀胱切开术。术后恢复顺利。一年的随访未发现尿毒症复发。
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[MITOCHONDRIAL RESPIRATORY CHAIN DISORDERS WITH VESICOURETERAL REFLUX: A PEDIATRIC CASE REPORT].

Mitochondrial respiratory chain disorders (MRCD) constitute a highly heterogeneous group both with regard to clinical manifestations and underlying genetic/biochemical defects. Management of urological complications such as vesicoureteral reflux (VUR) has not been discussed in cases with MRCD. We report a pediatric case of MRCD with recurrent urinary tract infections (UTI) due to primary and secondary VUR.A 6-month-old boy with multiple malformations and a history of aspiration pneumonia was referred to our department for febrile UTI (fUTI). Voiding cystourethrography showed high-grade left VUR and a normal bladder. As a spontaneous resolution of VUR was not observed, he underwent left ureteral reimplantation concomitant with left orchidopexy at the age of 1 year and 7 months. Although he had fUTI immediately after surgery, no recurrence of the UTI occurred after discharge. At the age of 3 years, he had septic shock and cardiac arrest caused by aspiration pneumonia, as well as, encephalopathy following cardiopulmonary resuscitation. At this event, the diagnosis of MRCD was achieved by liver biopsy. Since the age of 4 years, he has had repeated fUTI. VCUG confirmed the bladder deformity and right VUR. He underwent vesico-cutaneostomy at the age of 6 years. The postoperative course was uneventful. No recurrence of UTI was observed at the one-year follow-up.

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