杜宾约翰逊综合征伪装成新生儿胆道闭锁

Q4 Medicine
Avantika Dhanawat, Prashant Bachina, Santosh Kumar Panda
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引用次数: 0

摘要

胆道闭锁(BA)是新生儿胆汁淤积症的外科病因,需要及时干预。1例足月男新生儿,出生第3周表现为淡黄色,大便苍白,肝功能检查及肝胆亚胺二乙酸(HIDA)扫描怀疑BA。术中胆管造影正常,经全外显子组测序诊断为Dubin-Johnson综合征(DJS)。这个婴儿在接受降胆疗法后变得无黄疸。dj是BA的鉴别诊断之一;在这种情况下,可以考虑在进行有创胆管造影之前进行遗传评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dubin Johnson Syndrome Masquerading as Biliary Atresia in a Neonate
Biliary atresia (BA), a surgical cause of neonatal cholestasis, needs timely intervention. A term male neonate presented with yellowish discoloration and pale stool on the third week of life, suspected as BA based on the liver function test and hepatobiliary iminodiacetic acid (HIDA) scan. His intraoperative cholangiogram was normal and finally diagnosed as a case of Dubin-Johnson syndrome (DJS) by whole exome sequencing. The baby became anicteric with the cholestasis regimen. DJS is one of the differential diagnoses of BA; genetic evaluation may be considered prior to an invasive cholangiogram in such cases.
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来源期刊
Journal of Neonatology
Journal of Neonatology Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.30
自引率
0.00%
发文量
55
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