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Complete Hypokalemic Quadriparesis as a First Presentation of Sjögren Syndrome

RATIONALE: We hope to increase awareness that hypokalemic paralysis may be the first presentation of Sjögren syndrome, for which potassium-sparing diuretics can be an effective adjunct to potassium replenishment. PRESENTING CONCERNS: A 73-year-old female presented to a peripheral hospital with quadr...

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Autores principales: An, Jason, Braam, Branko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952274/
https://www.ncbi.nlm.nih.gov/pubmed/29774167
http://dx.doi.org/10.1177/2054358118774536
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author An, Jason
Braam, Branko
author_facet An, Jason
Braam, Branko
author_sort An, Jason
collection PubMed
description RATIONALE: We hope to increase awareness that hypokalemic paralysis may be the first presentation of Sjögren syndrome, for which potassium-sparing diuretics can be an effective adjunct to potassium replenishment. PRESENTING CONCERNS: A 73-year-old female presented to a peripheral hospital with quadriparesis and a critically low serum potassium of 1.6 mmol/L with U waves on the electrocardiogram (ECG). The initial arterial blood gas showed a pH of 7.19, bicarbonate of 13 mEq/L, and a CO(2) of 35 mm Hg. Over the next 6 days, she was administered a total of 450 mEq of potassium supplements. Despite this, her potassium never increased above 2.9 mmol/L and was thus transferred to the University Hospital for further management. On arrival, her vital signs were within normal limits. Her only other symptoms were fatigue and ocular dryness. Physical exam showed slightly weakened quadriceps muscles bilaterally, graded 4/5. Examination was otherwise unremarkable. Admission investigations included a potassium of 2.8 mmol/L, chloride 118 mmol/L, sodium 136 mmol/L, and eGFR 48 mL/min/1.73 m(2). Renin aldosterone ratio was normal. DIAGNOSES: Distal renal tubular acidosis (RTA) was diagnosed based on a normal anion gap metabolic acidosis, positive urine anion gap, and elevated urine potassium to creatinine ratio. Investigation of underlying causes revealed a positive Antinuclear antibody (ANA), elevated rheumatoid factor, and high anti-Ro/SSA titre which directed us toward a unifying diagnosis of Sjögren syndrome. A renal biopsy was undertaken as an outpatient and demonstrated severe interstitial nephritis with acute and chronic components, parenchymal scarring, atrophy, and small vessel arteriosclerosis. INTERVENTIONS: In the acute setting, the patient was treated with bicarbonate and amiloride in addition to potassium supplementation. OUTCOMES: The patient’s hypokalemic paralysis and metabolic acidosis were corrected. LESSONS LEARNED: Severe hypokalemic paralysis in distal RTA associated with Sjögren syndrome can be successfully treated with amiloride in addition to potassium supplementation. We also review the literature on the aberrancies seen in H(+)ATPase, Band 3, Pendrin, and carbonic anhydrase that may underlie the pathogenesis of distal RTA in Sjögren syndrome.
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spelling pubmed-59522742018-05-17 Complete Hypokalemic Quadriparesis as a First Presentation of Sjögren Syndrome An, Jason Braam, Branko Can J Kidney Health Dis Case Analysis RATIONALE: We hope to increase awareness that hypokalemic paralysis may be the first presentation of Sjögren syndrome, for which potassium-sparing diuretics can be an effective adjunct to potassium replenishment. PRESENTING CONCERNS: A 73-year-old female presented to a peripheral hospital with quadriparesis and a critically low serum potassium of 1.6 mmol/L with U waves on the electrocardiogram (ECG). The initial arterial blood gas showed a pH of 7.19, bicarbonate of 13 mEq/L, and a CO(2) of 35 mm Hg. Over the next 6 days, she was administered a total of 450 mEq of potassium supplements. Despite this, her potassium never increased above 2.9 mmol/L and was thus transferred to the University Hospital for further management. On arrival, her vital signs were within normal limits. Her only other symptoms were fatigue and ocular dryness. Physical exam showed slightly weakened quadriceps muscles bilaterally, graded 4/5. Examination was otherwise unremarkable. Admission investigations included a potassium of 2.8 mmol/L, chloride 118 mmol/L, sodium 136 mmol/L, and eGFR 48 mL/min/1.73 m(2). Renin aldosterone ratio was normal. DIAGNOSES: Distal renal tubular acidosis (RTA) was diagnosed based on a normal anion gap metabolic acidosis, positive urine anion gap, and elevated urine potassium to creatinine ratio. Investigation of underlying causes revealed a positive Antinuclear antibody (ANA), elevated rheumatoid factor, and high anti-Ro/SSA titre which directed us toward a unifying diagnosis of Sjögren syndrome. A renal biopsy was undertaken as an outpatient and demonstrated severe interstitial nephritis with acute and chronic components, parenchymal scarring, atrophy, and small vessel arteriosclerosis. INTERVENTIONS: In the acute setting, the patient was treated with bicarbonate and amiloride in addition to potassium supplementation. OUTCOMES: The patient’s hypokalemic paralysis and metabolic acidosis were corrected. LESSONS LEARNED: Severe hypokalemic paralysis in distal RTA associated with Sjögren syndrome can be successfully treated with amiloride in addition to potassium supplementation. We also review the literature on the aberrancies seen in H(+)ATPase, Band 3, Pendrin, and carbonic anhydrase that may underlie the pathogenesis of distal RTA in Sjögren syndrome. SAGE Publications 2018-05-10 /pmc/articles/PMC5952274/ /pubmed/29774167 http://dx.doi.org/10.1177/2054358118774536 Text en © The Author(s) 2018 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Analysis
An, Jason
Braam, Branko
Complete Hypokalemic Quadriparesis as a First Presentation of Sjögren Syndrome
title Complete Hypokalemic Quadriparesis as a First Presentation of Sjögren Syndrome
title_full Complete Hypokalemic Quadriparesis as a First Presentation of Sjögren Syndrome
title_fullStr Complete Hypokalemic Quadriparesis as a First Presentation of Sjögren Syndrome
title_full_unstemmed Complete Hypokalemic Quadriparesis as a First Presentation of Sjögren Syndrome
title_short Complete Hypokalemic Quadriparesis as a First Presentation of Sjögren Syndrome
title_sort complete hypokalemic quadriparesis as a first presentation of sjögren syndrome
topic Case Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952274/
https://www.ncbi.nlm.nih.gov/pubmed/29774167
http://dx.doi.org/10.1177/2054358118774536
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