| Literature DB >> 32499473 |
Durga Shankar Meena1, Deepak Kumar1, Gopal Krishana Bohra1, Sunil Kumar Bhambu1.
Abstract
Sjogren syndrome (SS) is a systemic autoimmune disorder with predominant exocrine gland involvement leading to sicca symptoms. Among extraglandular manifestations, renal disease is the most common. Tubular interstitial nephritis and renal tubular acidosis (RTA) are the common presentations. Mild hypokalemia associated with distal RTA is common in SS, however, severe hypokalemia causing paralysis is unusual. We report the case of a 26-year-old female who presented with hypokalemic paralysis. On evaluation, distal RTA was diagnosed. Further evaluation showed positive SS-a/SS-b antibodies in high titer, which confirms the diagnosis of primary SS. Our report illustrates that SS is a rare but important cause of hypokalemic paralysis.Entities:
Keywords: Hypokalemic paralysis; Sjogren syndrome; renal tubular acidosis
Year: 2020 PMID: 32499473 DOI: 10.4103/aam.aam_34_19
Source DB: PubMed Journal: Ann Afr Med ISSN: 0975-5764