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VOLUME 19 , ISSUE 9 ( 2015 ) > List of Articles

CASE REPORT

An unusually dry story

Gurukiran Danigeti, Dharanipragada Subrahmanyan

Keywords : Acute demyelinating encephalomyelitis, distal renal tubular acidosis, hypokalemic paralysis, nephrocalcinosis, neuromyelitis optica, Sjogren′s syndrome

Citation Information : Danigeti G, Subrahmanyan D. An unusually dry story. Indian J Crit Care Med 2015; 19 (9):550-553.

DOI: 10.4103/0972-5229.164808

License: CC BY-ND 3.0

Published Online: 00-09-2015

Copyright Statement:  Copyright © 2015; Jaypee Brothers Medical Publishers (P) Ltd.


Abstract

We present a middle-aged woman with a prior history of central nervous system (CNS) demyelinating disorder who presented with an acute onset quadriparesis and respiratory failure. The evaluation revealed distal renal tubular acidosis with hypokalemia and medullary nephrocalcinosis. Weakness persisted despite potassium correction, and ongoing evaluation confirmed recurrent CNS and long-segment spinal cord demyelination with anti-aquaporin-4 antibodies. There was no history of dry eyes or dry mouth. Anti-Sjogren′s syndrome A antigen antibodies were elevated, and there was reduced salivary flow on scintigraphy. Coexistent antiphospholipid antibody syndrome with inferior vena cava thrombosis was also found on evaluation. The index patient highlights several rare manifestations of primary Sjogren′s syndrome (pSS) as the presenting features and highlights the differential diagnosis of the clinical syndromes in which pSS should be considered in the Intensive Care Unit.


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