Literature DB >> 19762388

Gelatinous transformation of the bone marrow in systemic lupus erythematosus.

M Yamamoto1, H M Belmont, M Utsunomiya, Y Hidaka, M Kishimoto.   

Abstract

Gelatinous transformation of the bone marrow is a rare disease characterised by a focal marrow hypoplasia, fat atrophy and accumulation of extracellular mucopolysaccharides abundant in hyaluronic acid, which is often associated with extreme malnutrition and weight loss. There are only two reports describing its association with systemic lupus erythematosus (SLE). One described underlying diseases in 155 cases of gelatinous transformation of the bone marrow and found one case with clinical diagnosis of SLE, but no clinical details were provided. The other described three SLE patients with gelatinous transformation of the bone marrow; however, two of these were cachectic and one was diagnosed with concomitant tuberculosis. We describe one active SLE patient without other comorbidities whose pancytopaenia was histologically confirmed as gelatinous transformation. The combination of high-dose steroid, intravenous immunoglobulin and mycophenolate mofetil improved the peripheral blood cytopaenia and reversed the bone marrow abnormalities.

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Year:  2009        PMID: 19762388     DOI: 10.1177/0961203309106344

Source DB:  PubMed          Journal:  Lupus        ISSN: 0961-2033            Impact factor:   2.911


  3 in total

1.  Gelatinous Transformation of Bone Marrow: A Prospective Tertiary Center Study, Indicating Varying Trends in Epidemiology and Pathogenesis.

Authors:  Sneh Singh; Monica Gupta; Gajender Singh; Ashima Batra; Pratibha Dhiman; Sonia Chhabra; Rajeev Sen
Journal:  Indian J Hematol Blood Transfus       Date:  2015-02-17       Impact factor: 0.900

Review 2.  Gelatinous transformation of bone marrow: rare or underdiagnosed?

Authors:  Khushdeep Kaur Shergill; Gagandeep Singh Shergill; Hari Janardanan Pillai
Journal:  Autops Case Rep       Date:  2017-12-08

3.  Gelatinous transformation of bone marrow.

Authors:  Flavia Fazzio Barbin; Cristiano Claudino Oliveira
Journal:  Autops Case Rep       Date:  2017-06-30
  3 in total

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