scholarly journals Successful Management of Refractory Type 1 Renal Tubular Acidosis with Amiloride

2017 ◽  
Vol 2017 ◽  
pp. 1-3
Author(s):  
Patrick Oguejiofor ◽  
Robert Chow ◽  
Kenneth Yim ◽  
Bernard G. Jaar

A 28-year-old female with history of hypothyroidism, Sjögren’s Syndrome, and Systemic Lupus Erythematosus (SLE) presented with complaints of severe generalized weakness, muscle pain, nausea, vomiting, and anorexia. Physical examination was unremarkable. Laboratory test showed hypokalemia at 1.6 mmol/l, nonanion metabolic acidosis with HCO3 of 11 mmol/l, random urine pH of 7.0, and urine anion gap of 8 mmol/l. CT scan of the abdomen revealed bilateral nephrocalcinosis. A diagnosis of type 1 RTA likely secondary to Sjögren’s Syndrome was made. She was started on citric acid potassium citrate with escalating dosages to a maximum dose of 60 mEq daily and potassium chloride over 5 years without significant improvement in serum K+ and HCO3 levels. She had multiple emergency room visits for persistent muscle pain, generalized weakness, and cardiac arrhythmias. Citric acid potassium citrate was then replaced with sodium bicarbonate at 15.5 mEq every 6 hours which was continued for 2 years without significant improvement in her symptoms and electrolytes. Amiloride 5 mg daily was added to her regimen as a potassium sparing treatment with dramatic improvement in her symptoms and electrolyte levels (as shown in the figures). Amiloride was increased to 10 mg daily and potassium supplementation was discontinued without affecting her electrolytes. Her sodium bicarbonate was weaned to 7.7 mEq daily.

2013 ◽  
Vol 191 (2) ◽  
pp. 608-613 ◽  
Author(s):  
Long Shen ◽  
Lakshmanan Suresh ◽  
Kishore Malyavantham ◽  
Przemek Kowal ◽  
Jingxiu Xuan ◽  
...  

Rheumatology ◽  
1989 ◽  
Vol 28 (6) ◽  
pp. 518-520 ◽  
Author(s):  
A. BINDER ◽  
P. J. MADDISON ◽  
P. SKINNER ◽  
A. KURTZ ◽  
D. A. ISENBERG

2011 ◽  
Vol 96 (11) ◽  
pp. 3302-3307 ◽  
Author(s):  
Ambika P. Ashraf ◽  
Timothy Beukelman ◽  
Valerie Pruneta-Deloche ◽  
David R. Kelly ◽  
Abhimanyu Garg

Abstract Context: Type 1 hyperlipoproteinemia (T1HLP) in childhood is most often due to genetic deficiency of lipoprotein lipase (LPL) or other related proteins. Objective: The aim was to report a case of marked hypertriglyceridemia and recurrent acute pancreatitis due to the presence of LPL autoantibody in a young girl who was subsequently diagnosed with Sjögren's syndrome. Subject and Methods: A 9-yr-old African-American girl presented with acute pancreatitis and serum triglycerides of 4784 mg/dl. Strict restriction of dietary fat reduced serum triglycerides, but she continued to experience recurrent pancreatitis. Approximately 18 months thereafter, she developed transient pauciarticular arthritis with elevated serum antinuclear antibody (>1:1280). Minor salivary gland biopsy revealed chronic sialadenitis with a dense periductal lymphocytic aggregate suggestive of Sjögren's syndrome. Genomic DNA was analyzed for LPL, GPIHBP1, APOA5, APOC2, and LMF1. Immunoblotting was performed to detect serum LPL autoantibody. Results: The patient had no disease-causing variants in LPL, GPIHBP1, APOA5, APOC2, or LMF1. Immunoblotting revealed serum LPL antibody. The patient responded to immunosuppressive therapy for Sjögren's syndrome with resolution of hypertriglyceridemia. Conclusions: Unexplained T1HLP in childhood could be secondary to LPL deficiency induced by autoantibodies. Therefore, diagnosis of autoimmune T1HLP should be entertained if clinical features are suggestive of an autoimmune process.


2019 ◽  
Vol 12 (8) ◽  
pp. e229611 ◽  
Author(s):  
Elizabeth A Kitsis ◽  
Fabreena Napier ◽  
Viral Juthani ◽  
Howard L Geyer

A 47-year-old woman presented with sicca symptoms, polyarthralgias, polymyalgias and dysphagia. She was found to have positive antinuclear, anti-SSA-Ro and anti-SSB-La antibodies. Slit lamp exam confirmed the presence of keratoconjunctivitis sicca, and the patient was diagnosed with Sjögren’s syndrome. Three years later, she was referred for evaluation of gait instability associated with recent falls. On physical examination, the patient was found to have bilateral ptosis, percussion myotonia, distal upper and lower extremity weakness, and a steppage gait. Electromyography demonstrated electrical myotonia. Genetic testing revealed expanded CTG repeats (733 and 533) in the myotonic dystrophy type 1 (DM1) protein kinase gene, confirming the diagnosis of DM1. Dysphagia, pain and eye discomfort may occur in both Sjögren’s syndrome and DM1, and in this case, may have delayed the diagnosis of muscular dystrophy.


2012 ◽  
Vol 19 (4) ◽  
pp. 220
Author(s):  
Ho-Jun Lee ◽  
Sung-Ji Lee ◽  
Seong-Chang Park ◽  
Dong-Jin Park ◽  
Tae-Jong Kim ◽  
...  

2021 ◽  
pp. 147-151
Author(s):  
Mansour Mbengue ◽  
Cedric Ouanekpone ◽  
Seynabou Diagne ◽  
Abdou Niang

Renal involvement occurs in approximately 5% of patients with Sjögren’s syndrome (SS). We reported the case of a 20-year-old African woman who was received for paralysis of 4 limbs secondary to hypokalemia. The diagnosis of renal tubular acidosis type 1 complicated by hypokalemia was retained. In the etiologic research of renal tubular acidosis type 1, primary SS was retained. The patient received symptomatic treatment based on potassium chloride, sodium bicarbonate, hydration, and a low protein diet. In terms of etiological treatment, she was put on corticosteroid and hydroxychloroquine. The outcome was favorable with correction of acidosis and hypokalemia.


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