Literature DB >> 8737563

Multiple myeloma presenting as proliferative (crescentic) glomerulonephritis.

R A Sirsat1, R B Deshpande.   

Abstract

Glomerular extracapillary cellular proliferation with crescent formation initially presenting as rapidly progressive glomerulonephritis is a rare clinical manifestation of multiple myeloma. We report here a case of a 58 year old female who initially presented with haematuria, loss of weight and appetite and history of febrile episodes and was diagnosed following renal biopsy as rapidly progressive glomerulonephritis. Haemodialysis was carried out a month later because of uremic symptoms and maintained with monitoring of serum, calcium, phosphate, alkaline phosphatase, albumin and iPTH levels. After 6 months, she complained of bone pains over anterior chest wall which persisted even with low calcium haemodialysis. Serum protein electrophoresis and bone marrow aspiration revealed multiple myeloma. On starting chemotherapy, bone pain subsided but the patient expired within 15 days of therapy.

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Year:  1994        PMID: 8737563

Source DB:  PubMed          Journal:  J Postgrad Med        ISSN: 0022-3859            Impact factor:   1.476


  4 in total

1.  Renal disorder preceding multiple myeloma.

Authors:  Metin Isik
Journal:  Med Oncol       Date:  2010-01-05       Impact factor: 3.064

2.  Plasma cell myeloma in a renal transplant recipient: A case report and review of literature.

Authors:  S Sharma; C Rana; P B Vinod; A Gupta
Journal:  Indian J Nephrol       Date:  2011-10

3.  Crescentic glomerulonephritis in IgA multiple myeloma: a case report.

Authors:  Grace T Moscoso-Solorzano; Marcus V Madureira-Silva; Carlos Balda; Marcello F Franco; Gianna Mastroianni-Kirsztajn
Journal:  Nephron Extra       Date:  2011-09-08

4.  Multiple Myeloma in a Patient with Focal Segmental Glomerulosclerosis: A Case Report.

Authors:  Ashraf O Oweis; Sameeha A Al Shelleh; Najla Aldaoud; Osama Mohammed Alshari; Mousa A Al-Abbadi
Journal:  Am J Case Rep       Date:  2018-08-13
  4 in total

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