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Hypokalemic Paralysis: A Hidden Card of Several Autoimmune Diseases

  • Yelitza Velarde-Mejía
    ,
  • Rocío Gamboa-Cárdenas
    ,
  • ,
  • César Pastor Asurza
  • Hospital Guillermo Almenara Irigoyen
    ,
  • ,
  • Universidad Científica del Sur
    ,
  • Universidad Nacional Mayor de San Marcos
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Journal (Volume, Issue Number)

Clinical Medicine Insights: Arthritis and Musculoskeletal Disorders (Volume 10)

Publication milestones

  • Published - 02/08/2017

Publication status

Published - 02/08/2017

Publication IDs

  • Scopus: 85044396056

Abstract

Acute hypokalemic paralysis is a rare and potentially fatal condition, with few related causes, one of which highlights distal renal tubular acidosis (dRTA). Distal renal tubular acidosis is a rare complication of several autoimmune diseases such as systemic lupus erythematosus, Sjögren’s syndrome, and Hashimoto thyroiditis. We report a case of a lupic patient who presented rapidly progressive quadriparesis in the context of active renal disease. Research revealed severe refractory hypokalemia, metabolic acidosis, and alkaline urine suggestive of dRTA. We diagnosed Sjögren’s syndrome based on sicca symptoms, an abnormal salivary glands’ nuclear scan and the presence of anti-Ro/SSA and anti-La/SSB. In addition, the finding of thyroid peroxidase, thyroglobulin antibodies, and hypothyroidism led us to the diagnosis of Hashimoto thyroiditis. Due to the active renal involvement on the context of systemic lupus erythematosus and Sjögren’s syndrome, the patient received immunosuppression with rituximab, resulting in a progressive and complete improvement.