Coexistent systemic mastocytosis and essential thrombocythemia complicated with monoclonal gammopath...
Coexistent systemic mastocytosis and essential thrombocythemia complicated with monoclonal gammopathy and hypocomplementaemia
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Heidelberg: SP Versita
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Language
English
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Heidelberg: SP Versita
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Hematological neoplasms associated with systemic mast cell disease are most frequently of myeloid origin. There are a few reports, however, of systemic mastocytosis (SM) cases associated with lymphoid or plasma cell neoplasms as well. In this report, the authors present a case of SM (with D816V mutation in the c-KIT gene) associated with JAK2 V617F...
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Coexistent systemic mastocytosis and essential thrombocythemia complicated with monoclonal gammopathy and hypocomplementaemia
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TN_cdi_proquest_journals_1095626265
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1095626265
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ISSN
1895-1058,2391-5463
E-ISSN
1644-3640,2391-5463
DOI
10.2478/s11536-012-0065-1
