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Case Reports
. 2022 May;197(4):e53-e55.
doi: 10.1111/bjh.18050. Epub 2022 Feb 10.

Multiple myeloma occurring in a case of Niemann-Pick disease Type B: A pathophysiological link?

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Case Reports

Multiple myeloma occurring in a case of Niemann-Pick disease Type B: A pathophysiological link?

Elodie Portier et al. Br J Haematol. 2022 May.
No abstract available

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References

REFERENCES

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    1. Schuchman EH. The pathogenesis and treatment of acid sphingomyelinase-deficient Niemann-pick disease. J Inherit Metab Dis. 2007;30:654-63.
    1. Lidove O, Belmatoug N, Froissart R, Lavigne C, Durieu I, Mazodier K, et al. Déficit en sphingomyélinase acide (maladie de Niemann-Pick B): une étude rétrospective multicentrique de 28 patients adultes. La Revue de Médecine Interne. 2017;38:291-9.
    1. Arends M, van Dussen L, Biegstraaten M, Hollak CEM. Malignancies and monoclonal gammopathy in Gaucher disease; a systematic review of the literature. Br J Haematol. 2013;161:832-42.
    1. de Fost M, Vom Dahl S, Weverling GJ, Brill N, Brett S, Häussinger D, et al. Increased incidence of cancer in adult Gaucher disease in Western Europe. Blood Cells Mol Dis. 2006;36:53-8.

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