An infantile case of Hinman syndrome with severe acute renal failure

被引：3

作者：

Chaichanamongkol, Vorapong ^{[1
]}

Ikeda, Masahiro ^{[1
]}

Ishikura, Kenji ^{[1
]}

Hamasaki, Yuko ^{[1
]}

Hataya, Hiroshi ^{[1
]}

Satoh, Hiroyuki ^{[2
]}

Asanuma, Hiroshi ^{[2
]}

Shishido, Seiichiro ^{[2
]}

Honda, Masataka ^{[1
]}

机构：

[1] Tokyo Metropolitan Kiyose Childrens Hosp, Dept Pediat Nephrol, Tokyo 2048567, Japan

[2] Tokyo Metropolitan Kiyose Childrens Hosp, Dept Pediat Urol, Tokyo, Japan

来源：

CLINICAL AND EXPERIMENTAL NEPHROLOGY | 2008年 / 12卷 / 04期

关键词：

Hinman syndrome; non-neurogenic neurogenic bladder; acute renal failure; chronic renal failure; detrusor-sphincter dyssynergia; infant; urinary tract infection;

D O I：

10.1007/s10157-008-0048-3

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

A 1-year-6-month-old Japanese girl with Hinman syndrome manifested urosepsis and severe obstructive nephropathy. Her voiding cystourethrogram (VCUG) revealed high-grade vesicoureteral reflux with hydronephrosis; urodynamic study was compatible with detrusor-sphincter dyssynergia. She was treated conservatively, including clean intermittent catheterization. At 3 years old, bladder function had not improved, and estimated creatinine clearance was in the subnormal range. Hinman syndrome is a potential cause of acute and chronic renal failure in infancy. Taking account of the possibility of this condition in any neonates or infants who present urinary tract infection ( UTI) appears to be necessary, since early recognition and proper management of this syndrome may prevent serious complications.

引用

页码：309 / 311

页数：3

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