Cholestasis caused by panhypopituitarism and acquired cytomegalovirus infection in a 2-month-old male infant A case report

被引:6
|
作者
Chan, U. [1 ]
Chan, Wai-Tao [1 ,2 ]
Ting, Wei-Hsin [3 ]
Ho, Che-Sheng [4 ]
Liu, Hsi-Che [5 ,6 ]
Lee, Hung-Chang [1 ]
机构
[1] MacKay Childrens Hosp, Dept Pediat, Div Gastroenterol & Nutr, 92,Sec 2,Zhongshan N Rd, Taipei 10449, Taiwan
[2] MacKay Jr Coll Med Nursing & Management, Taipei, Taiwan
[3] MacKay Childrens Hosp, Dept Pediat, Div Endocrinol & Metab, Taipei, Taiwan
[4] MacKay Childrens Hosp, Dept Pediat, Div Neurol, Taipei, Taiwan
[5] MacKay Childrens Hosp, Div Hematol Oncol, Dept Pediat, Taipei, Taiwan
[6] MacKay Med Coll, Taipei, Taiwan
关键词
cholestasis; cytomegalovirus; panhypopituitarism; septo-optic dysplasia; CONGENITAL HYPOPITUITARISM; NEONATAL CHOLESTASIS; DNA DETECTION; BREAST-MILK; DYSFUNCTION; ETIOLOGY; JAUNDICE;
D O I
10.1097/MD.0000000000006757
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale: Septo-optic dysplasia (SOD) is a rare congenital disorder that may cause jaundice in infants. However, it is usually prone to neglect and misdiagnosis in infants with cholestasis because endocrine disorder such as panhypopituitarism is rare in the cause of infantile cholestasis. We report a case of SOD concurrent with acquired cytomegalovirus (CMV) infection, who presented with prolonged jaundice as the first clinical sign. Patient concerns: The patient was a 2-month-old male infant who presented with cholestasis, combined with fever and panhypopituitarism. Diagnoses: He was diagnosed with SOD and acquired CMV infection. Interventions: He was treated with hormone replacement therapy and ganciclovir. Outcomes: After correction of the pituitary hormone deficiency and ganciclovir treatment, significant improvements of cholestasis, retinal lesions, and growth rate were seen in our patient. Lessons: Although an endocrine disorder such as panhypopituitarism is rare in the cause of neonatal or infantile cholestasis, we must keep this reason in mind.
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页数:4
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