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Severe diabetic ketoacidosis and autoimmune pancreatitis with SIRS in an adolescent with LRBA deficiency – A rare complication of a common primary immunodeficiency disease
Author(s) -
TarikereKrishnamurthy Shruthi,
Divya Ravindran,
RajavelSagul Ramanuja Mugunthan,
Dhaarani Jayaraman
Publication year - 2022
Publication title -
journal of family medicine and primary care
Language(s) - English
Resource type - Journals
eISSN - 2278-7135
pISSN - 2249-4863
DOI - 10.4103/jfmpc.jfmpc_1220_21
Subject(s) - common variable immunodeficiency , medicine , primary immunodeficiency , immunology , diabetic ketoacidosis , immunodeficiency , complication , pancreatitis , acute pancreatitis , autoimmunity , pediatrics , diabetes mellitus , immune system , antibody , endocrinology
Common variable immunodeficiency is the most common primary immunodeficiency disorder. Lipopolysaccharide (LPS)-responsive beige-like anchor protein (LRBA) deficiency is categorized as a common variable immunodeficiency associated with autoimmune manifestations and inflammatory bowel diseases. We report a rare case, an adolescent presenting with severe diabetic ketoacidosis (DKA) and acute pancreatitis with multiorgan dysfunction with common variable immunodeficiency (CVID) with homozygous LRBA mutation.

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