Minimal change disease as the etiology of the nephrotic syndrome in a patient with angioimmunoblastic lymphadenopathy.
Publication/Presentation Date
1-1-1988
Abstract
Glomerular lesions have rarely been reported with angioimmunoblastic lymphadenopathy (AILD). A patient with histologically documented AILD developed the nephrotic syndrome. Renal biopsy demonstrated minimal change disease. Both the lymphadenopathy and the nephrotic syndrome spontaneously remitted in this patient. Prior reports of renal disease in AILD and atypical lymphoproliferative disorders are discussed. An association between the minimal change lesions and AILD is suggested.
Volume
16
Issue
3
First Page
206
Last Page
209
ISSN
0098-1532
Published In/Presented At
Staszewski, H., Kumar, G., & Mishriki, Y. (1988). Minimal change disease as the etiology of the nephrotic syndrome in a patient with angioimmunoblastic lymphadenopathy. Medical and pediatric oncology, 16(3), 206–209. https://doi.org/10.1002/mpo.2950160311
Disciplines
Medicine and Health Sciences
PubMedID
3380062
Department(s)
Department of Medicine
Document Type
Article