Саse reроrt оf fetal liver cirrhosis due to gestational alloimmune liver disease in а primigravida femаle, in north east region of India

Authors

  • Priya Gupta Department of Obstetrics and Gynecology, Baptist Christian Hospital, Tezpur, Assam, India
  • Sandip Maheshwari Department of Radiodiagnosis, 155 Base Hospital, Tezpur, Assam, India

DOI:

https://doi.org/10.18203/2320-1770.ijrcog20220199

Keywords:

Neonatal hemochromatosis, Fetal liver failure, Gestational alloimmune liver disease

Abstract

Fetal liver failure is a major cause of neonatal morbidity and mortality, presenting as acute liver failure and/or congenital cirrhosis. There are several causes of fetal liver failure and early diagnosis is mandatory to elucidate the etiology and determine a specific treatment or the best management strategy. Gestational alloimmune liver disease associated with neonatal hemochromatosis (GALD-NH) is a rare cause of fetal liver failure. It should be considered in any neonate with fetal signs of liver failure with no other identifiable causes. GALD-NH is often diagnosed late and patients are therefore referred late to specialized centers, delaying treatment. This case highlighted the consequences of late diagnosis and treatment of GALD-NH and emphasizes the importance of a high grade of suspicion of this disease in order to refer the patient to a specialized center soon enough to perform the appropriate treatment.

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Published

2022-01-28

Issue

Section

Case Reports