Literature DB >> 8044308

A case of sarcoidosis revealed in the course of IgA nephropathy.

S Tateno1, Y Kobayashi, F Kobayashi.   

Abstract

A 36 year old man, who had been proteinuric for 14 years due to immunoglobulin A (IgA) nephropathy, was admitted because of an acute exacerbation in renal dysfunction with hypercalcemia. He had presented with aortic regurgitation and increased pulmonary marking by chest X-ray, but laboratory examinations had failed to make an exact diagnosis. On admission, noncaseating epithelioid granulomas were disclosed by muscle and skin biopsies. Ophthalmological evaluation revealed old uveitis and retinal changes consistent with sarcoidosis. In this case, IgA nephropathy was thought to be the initial manifestation of sarcoidosis that developed latently. Sarcoidosis should be considered in a differential diagnosis of IgA nephropathy.

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Year:  1994        PMID: 8044308     DOI: 10.1111/j.1440-1827.1994.tb02939.x

Source DB:  PubMed          Journal:  Pathol Int        ISSN: 1320-5463            Impact factor:   2.534


  2 in total

1.  Case of summer-type hypersensitivity pneumonitis complicated with IgA nephropathy.

Authors:  Tomoki Maetani; Hiroshi Shima; Yusuke Shiraishi; Satoshi Marumo
Journal:  BMJ Case Rep       Date:  2019-06-18

2.  Clinicopathological study of glomerular diseases associated with sarcoidosis: a multicenter study.

Authors:  Thomas Stehlé; Dominique Joly; Philippe Vanhille; Jean-Jacques Boffa; Philippe Rémy; Laurent Mesnard; Maxime Hoffmann; Philippe Grimbert; Gabriel Choukroun; François Vrtovsnik; Jérôme Verine; Dominique Desvaux; Francine Walker; Philippe Lang; Matthieu Mahevas; Dil Sahali; Vincent Audard
Journal:  Orphanet J Rare Dis       Date:  2013-04-30       Impact factor: 4.123

  2 in total

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