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Coexistence of immunoglobulin M nephropathy and autoimmune hemolytic anemia: 2 rare entities.

Abstract
Immunoglobulin M (IgM) nephropathy is described as mesengial proliferative glomerulonephritis with diffuse mesengial IgM deposition. We report a patient diagnosed with IgM nephropathy and concomitant autoimmune hemolytic anemia syndrome associated with cold-reacting autoantibodies. Complete remission was achieved with systemic corticosteroid and plasmapheresesis.
AuthorsNergiz Bayrakci, Nihal Ozkayar, Muge Erek Ersozen, Aysel Colak, Ebru Gok Oguz, Fatih Dede
JournalIranian journal of kidney diseases (Iran J Kidney Dis) Vol. 9 Issue 6 Pg. 472-4 (Nov 2015) ISSN: 1735-8604 [Electronic] Iran
PMID26552355 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Immunoglobulin M
Topics
  • Aged
  • Anemia, Hemolytic, Autoimmune (complications, diagnosis)
  • Female
  • Glomerulonephritis (complications, immunology, pathology)
  • Humans
  • Immunoglobulin M (analysis)

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