Results 41 to 50 of about 61,997 (154)
Chronic myeloid leukemia and systemic mastocytosis are myeloid neoplasms sharing a number of pathogenetic and clinical features. In both conditions, an aberrantly activated oncoprotein with tyrosine kinase activity, namely BCR-ABL1 in chronic myeloid ...
Siham Bibi +9 more
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Mast cell leukemia is a rare and aggressive form of mastocytosis characterized by >20% mast cells found in the bone marrow aspirates of patients with signs of systemic mastocytosis-related organ damage.
James Bauer, MD, PhD +2 more
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Mastocytosis: One Word for Different Diseases
Mastocytosis is a neoplastic disease originating from tissue infiltration by transformed mast cells. The diagnosis requires a high grade of suspicion due to the large variety of presenting symptoms. The World Health Organization classification recognizes
Marianna Criscuolo +3 more
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Systemic Mastocytosis with Smoldering Multiple Myeloma: Report of a Case
Systemic mastocytosis (SM) is a disease characterized by a clonal infiltration of mast cells affecting various tissues of the body. It is grouped into six different subtypes according to the World Health Organization classification. It is called indolent
Sassine Ghanem +4 more
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Indolent systemic mastocytosis limited to the bone: a case report and review of the literature
CONTEXT Systemic mastocytosis is defined as a clonal disorder of mast cells and their precursor cells and is currently classified as a myeloproliferative neoplasm.
Pedro Pinto-Lopes +4 more
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Recurrent prosthetic mitral valve thrombosis: The first report of an unusual feature of systemic mastocytosis, a case report and review of the literature. [PDF]
Background: Mastocytosis is a systemic disease involving the clonal expansion of mast cells in multiple organs. Given that immune system overreaction and excessive histamine release are among the most prominent events in mastocytosis, the incidence of ...
Amirhossein Akbarzadehpasha +6 more
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Systemic Mastocytosis Associated with Splenic Marginal Zone Lymphoma with Villous Lymphocytes
The development of a second haematological disease during the course of systemic mastocytosis is a well-known phenomenon. In most of the cases, they consist of myelodysplasia or myeloproliferative disorders.
R. Fernández-Torres +4 more
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Clinical features of 30 adult patients suffering from mastocytosis with skin lesion were compared with the duration of the disease, severity of skin and systemic symptoms, involvement of the internals in the pathologic process, level of tryptase in the ...
N. P. Teplyuk, P. M. Pyatilova
doaj
Systemic mastocytosis associated with chronic myelomonocytic leukemia and xanthogranuloma
A patient with a history of non-diagnostic bone marrow biopsies presented with a red to brown maculopapular rash on the back. Biopsies confirmed multiple xanthogranulomas as well as a mastocytosis.
Philipp Tschandl +2 more
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