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[Renal amyloidosis: uncommon complication of sickle cell disease]. / L'amylose rénale: une complication inhabituelle de la drépanocytose.
Hadj Sadek, B; Radoui, A; Al Hamany, Z; Benamar, L; Bayahia, R; Ouzeddoun, N.
Affiliation
  • Hadj Sadek B; Service de Néphrologie-Dialyse et Transplantation Rénale, CHU Ibn Sina, Rabat, Maroc. bahaahadjsadek@yahoo.fr
Med Trop (Mars) ; 71(2): 185-6, 2011 Apr.
Article in Fr | MEDLINE | ID: mdl-21695882
ABSTRACT
Type AA amyloidosis is a rare complication of sickle cell anemia. The purpose of this report is to describe the case of a 30-year-old man with heterozygous sickle cell disease who was referred to our unit with nephritic syndrome and microscopic hematuria. Light microscopy on a renal biopsy specimen demonstrated AA amyloidosis. After elimination of other causes, it was concluded that amyloidosis was the result of recurrent acute inflammation secondary to sickle cell disease. To our knowledge, this is the fifth that renal amyloidosis as a complication of sickle cell disease has been described in the literature.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Amyloidosis / Anemia, Sickle Cell / Kidney Diseases Limits: Adult / Humans / Male Language: Fr Journal: Med Trop (Mars) Journal subject: MEDICINA TROPICAL Year: 2011 Type: Article Affiliation country: Morocco
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Collection: 01-internacional Database: MEDLINE Main subject: Amyloidosis / Anemia, Sickle Cell / Kidney Diseases Limits: Adult / Humans / Male Language: Fr Journal: Med Trop (Mars) Journal subject: MEDICINA TROPICAL Year: 2011 Type: Article Affiliation country: Morocco