Literature DB >> 998570

Oxalosis. An unusual cause of myelophthisis in childhood.

R W McKenna, L P Dehner.   

Abstract

In a child with renal failure and oliguria due to hyperoxaluria myelophthisis developed as a result of extensive bone-marrow replacement with calcium oxalate crystals and an accompanying fibrous proliferations. The histopathology associated with this metabolic disorder was demonstrated in posterior iliac crest bone-marrow trephine biopsies, renal biopsies, and nephrectomy specimens. Crystals were demonstrated in biopsy specimens of transplanted kidneys within six weeks following renal transplantation.

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Year:  1976        PMID: 998570     DOI: 10.1093/ajcp/66.6.991

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  3 in total

Review 1.  [Recurrence of the original disease in the transplanted kidney].

Authors:  E P Leumann; J Briner
Journal:  Klin Wochenschr       Date:  1984-04-02

Review 2.  Bone disease of primary hyperoxaluria in infancy.

Authors:  E Ring; H Wendler; M Ratschek; G Zobel
Journal:  Pediatr Radiol       Date:  1989

3.  A contribution to the formation mechanism of calcium oxalate urinary calculi. IV. Experimental investigations of the intrarenal crystallisation of calcium oxalate in rabbit.

Authors:  E Hienzsch; A Hesse; C Bothor; W Berg; J Roth
Journal:  Urol Res       Date:  1979-09
  3 in total

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