Literature DB >> 2002265

Hematologic aspects of mastocytosis: II: management of hematologic disorders in association with systemic mast cell disease.

R I Parker1.   

Abstract

Individuals with systemic mast cell disease (SMCD) may develop various hematologic abnormalities, including cytopenias, myeloproliferative or myelodysplastic syndromes, lymphoproliferative syndromes, and primary or secondary leukemias. Management of those patients is often complicated by their associated hematologic abnormalities. In the case of non-malignant hematologic syndromes, the approach to management is supportive. At present, overt malignancies are managed with traditional chemotherapy. The presence of leukemia in patients with mast cell disease usually indicates a grave prognosis.

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Year:  1991        PMID: 2002265

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  2 in total

1.  Mast-cell phenotype in indolent forms of mastocytosis. Ultrastructural features, fluorescence detection of avidin binding, and immunofluorescent determination of chymase, tryptase, and carboxypeptidase.

Authors:  N Weidner; R F Horan; K F Austen
Journal:  Am J Pathol       Date:  1992-04       Impact factor: 4.307

2.  Systemic mastocytosis associated with splenic marginal zone lymphoma with villous lymphocytes.

Authors:  R Fernández-Torres; M M Verea; A Alvarez; P Torres; E Fonseca
Journal:  Dermatol Res Pract       Date:  2011-07-11
  2 in total

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