A Case of Kawasaki Disease Complicated With Cerebral Salt-Wasting Syndrome

被引:4
|
作者
Oshima, Masanari [1 ]
Fukuhara, Junji [1 ]
Noto, Takanori [1 ]
Noguchi, Teppei [1 ]
Murabayashi, Masao [1 ]
Ayusawa, Mamoru [2 ]
Morioka, Ichiro [2 ]
机构
[1] Numazu City Hosp, Dept Pediat, Shizuoka, Japan
[2] Nihon Univ, Dept Pediat & Child Hlth, Sch Med, Tokyo, Japan
来源
FRONTIERS IN PEDIATRICS | 2020年 / 8卷
关键词
Kawasaki disease; cerebral salt-wasting syndrome (CSWS); syndrome of inappropriate antidiuretic hormone secretion (SIADH); hyponatremia; fractional excretion of uric acid (FEUA); REVERSIBLE SPLENIAL LESION; MILD ENCEPHALOPATHY; HYPONATREMIA; CHILDREN; PATIENT;
D O I
10.3389/fped.2020.00325
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
We report the case of a 3-years-old boy who developed severe hyponatremia and unconsciousness during an episode of Kawasaki disease (KD). He was diagnosed with cerebral salt-wasting syndrome (CSWS), which has not previously been reported as a complication of KD. He was diagnosed with KD with fever and four clinical signs and received intravenous immunoglobulin (IVIG) on the day after onset. Hyponatremia had been observed, and it worsened after IVIG. At first, syndrome of inappropriate antidiuretic hormone secretion (SIADH) was suspected, but his hyponatremia did not improve by restriction of water intake. The patient's consciousness level decreased along with the worsening hyponatremia. Electroencephalography revealed abnormal electrical discharge concordant with acute encephalopathy. Laboratory data showed hypouricemia with high fractional excretion of uric acid (FEUA), in addition to a negative balance of both Na and water. We diagnosed KD complicated with CSWS. The patient improved promptly with appropriate Na supplementation and water correction.
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页数:6
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