| Literature DB >> 18987258 |
Tung-Min Yu1, Shih-Hua Lin, Chuang Ya-Wen, Mei-Chin Wen, Yi-Hsing Chen, Chi-Hung Cheng, Cheng-Hsu Chen, Chung-Shi Chin, Kuo-Hsiung Shu.
Abstract
Acquired Bartter-like syndrome, albeit rare, has not been reported to be associated with sarcoidosis. We describe the case of a 32-year-old male patient who presented with progressive muscular weakness of both lower extremities. Profound hypokalaemia associated with renal (K(+)) wasting, bilateral nephrocalcinosis and high plasma renin activity resembled Bartter's syndrome (BS). Both mediastinal lymph node and renal biopsy demonstrated sarcoidosis with non-caseating granuloma. Genetic testing responsible for hereditary BS or Gitelman's syndrome (GS) was negative. Hypokalaemia was well controlled with the administration of spironolactone with oral steroids and KCl. Early recognition and prompt treatment of sarcoidosis-associated Bartter-like syndrome avoids unnecessary complications.Entities:
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Year: 2008 PMID: 18987258 DOI: 10.1093/ndt/gfn600
Source DB: PubMed Journal: Nephrol Dial Transplant ISSN: 0931-0509 Impact factor: 5.992