Hypokalemic Paralysis due to Primary Sjögren Syndrome: Case Report and Review of the Literature

Tubulointerstitial nephritis (TIN) is the main renal involvement associated with primary Sjögren syndrome (pSS). TIN can manifest as distal renal tubular acidosis (RTA), nephrogenic diabetes insipidus, proximal tubular dysfunction, and others. We present a 31-year-old female with hypokalemic paralys...

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Main Authors: A. Garza-Alpirez, A. C. Arana-Guajardo, J. A. Esquivel-Valerio, M. A. Villarreal-Alarcón, D. A. Galarza-Delgado
Format: Article
Language:English
Published: Wiley 2017-01-01
Series:Case Reports in Rheumatology
Online Access:http://dx.doi.org/10.1155/2017/7509238
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author A. Garza-Alpirez
A. C. Arana-Guajardo
J. A. Esquivel-Valerio
M. A. Villarreal-Alarcón
D. A. Galarza-Delgado
author_facet A. Garza-Alpirez
A. C. Arana-Guajardo
J. A. Esquivel-Valerio
M. A. Villarreal-Alarcón
D. A. Galarza-Delgado
author_sort A. Garza-Alpirez
collection DOAJ
description Tubulointerstitial nephritis (TIN) is the main renal involvement associated with primary Sjögren syndrome (pSS). TIN can manifest as distal renal tubular acidosis (RTA), nephrogenic diabetes insipidus, proximal tubular dysfunction, and others. We present a 31-year-old female with hypokalemic paralysis due to distal RTA (dRTA). She received symptomatic treatment and hydroxychloroquine with a good response. There is insufficient information on whether to perform a kidney biopsy in these patients or not. The evidence suggests that there is an inflammatory background and therefore a potential serious affection to these patients, such as hypokalemic paralysis. We found 52 cases of hypokalemic paralysis due to dRTA in pSS patients. The majority of those patients were treated only with symptomatic medication. Patients who received corticosteroids had stable evolution even though they did not have another symptomatology. With such heterogeneous information, prospective studies are needed to assess the value of adding corticosteroids as a standardized treatment of this manifestation.
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series Case Reports in Rheumatology
spelling doaj-art-ddd4a07b9e8e4a769b57f2a300ba7ef02025-02-03T06:08:28ZengWileyCase Reports in Rheumatology2090-68892090-68972017-01-01201710.1155/2017/75092387509238Hypokalemic Paralysis due to Primary Sjögren Syndrome: Case Report and Review of the LiteratureA. Garza-Alpirez0A. C. Arana-Guajardo1J. A. Esquivel-Valerio2M. A. Villarreal-Alarcón3D. A. Galarza-Delgado4Servicio de Reumatología, Departamento de Medicina Interna, Hospital Universitario “Dr. José Eleuterio González”, Universidad Autónoma de Nuevo León, Monterrey, NL, MexicoServicio de Reumatología, Departamento de Medicina Interna, Hospital Universitario “Dr. José Eleuterio González”, Universidad Autónoma de Nuevo León, Monterrey, NL, MexicoServicio de Reumatología, Departamento de Medicina Interna, Hospital Universitario “Dr. José Eleuterio González”, Universidad Autónoma de Nuevo León, Monterrey, NL, MexicoServicio de Reumatología, Departamento de Medicina Interna, Hospital Universitario “Dr. José Eleuterio González”, Universidad Autónoma de Nuevo León, Monterrey, NL, MexicoServicio de Reumatología, Departamento de Medicina Interna, Hospital Universitario “Dr. José Eleuterio González”, Universidad Autónoma de Nuevo León, Monterrey, NL, MexicoTubulointerstitial nephritis (TIN) is the main renal involvement associated with primary Sjögren syndrome (pSS). TIN can manifest as distal renal tubular acidosis (RTA), nephrogenic diabetes insipidus, proximal tubular dysfunction, and others. We present a 31-year-old female with hypokalemic paralysis due to distal RTA (dRTA). She received symptomatic treatment and hydroxychloroquine with a good response. There is insufficient information on whether to perform a kidney biopsy in these patients or not. The evidence suggests that there is an inflammatory background and therefore a potential serious affection to these patients, such as hypokalemic paralysis. We found 52 cases of hypokalemic paralysis due to dRTA in pSS patients. The majority of those patients were treated only with symptomatic medication. Patients who received corticosteroids had stable evolution even though they did not have another symptomatology. With such heterogeneous information, prospective studies are needed to assess the value of adding corticosteroids as a standardized treatment of this manifestation.http://dx.doi.org/10.1155/2017/7509238
spellingShingle A. Garza-Alpirez
A. C. Arana-Guajardo
J. A. Esquivel-Valerio
M. A. Villarreal-Alarcón
D. A. Galarza-Delgado
Hypokalemic Paralysis due to Primary Sjögren Syndrome: Case Report and Review of the Literature
Case Reports in Rheumatology
title Hypokalemic Paralysis due to Primary Sjögren Syndrome: Case Report and Review of the Literature
title_full Hypokalemic Paralysis due to Primary Sjögren Syndrome: Case Report and Review of the Literature
title_fullStr Hypokalemic Paralysis due to Primary Sjögren Syndrome: Case Report and Review of the Literature
title_full_unstemmed Hypokalemic Paralysis due to Primary Sjögren Syndrome: Case Report and Review of the Literature
title_short Hypokalemic Paralysis due to Primary Sjögren Syndrome: Case Report and Review of the Literature
title_sort hypokalemic paralysis due to primary sjogren syndrome case report and review of the literature
url http://dx.doi.org/10.1155/2017/7509238
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