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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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Epidemiology of systemic mastocytosis in Denmark
Mastocytosis is a heterogeneous group of diseases characterized by abnormal proliferation of mast cells. Systemic mastocytosis (SM), in which abnormal mast cells are present in tissues beyond the skin, is divided into seven subcategories with varying ...
Vestergaard, Hanne +7 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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An elderly woman presented with anaemia, thrombocytopenia and multifocal lytic and sclerotic bone lesions. Trephine bone marrow biopsy demonstrated widespread involvement by systemic mastocytosis (SM).
Kudela, Andrzej +4 more
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ANAESTHESIA IN PEDIATRIC PATIENTS WITH SYSTEMIC MASTOCYTOSIS
: Objective: To look at the anaesthesia in pediatric patients with systemic mastocytosis. Place and Time of study: Jinnah hospital, Lahore in June 2018 to May 2019. Methodology: Fundamental mastocytosis is an uncommon issue of pole cells which conveys
Haleema Abbas, Dr Waqas Ali Khan, Dr. Sana Rafiq
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Case Report of Systemic Mastocytosis with Cutaneous Involvement
Mastocytosis is a rare clonal disease of hematopoietic stem cells characterized by the accumulation of mast cells in the skin (cutaneous mastocytosis, CM) or in multiple organs such as the bone marrow, liver, spleen, and lymph nodes (systemic ...
YILMAZ, İNSU +2 more
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Interferon-α treatment in systemic mastocytosis
Patients with systemic mastocytosis are rare, constitute a heterogeneous clinical entity and some may not require treatment until long after diagnosis.
Bjerrum, Ole Weis
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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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Systemic mastocytosis following a malignant ovarian germ cell tumour.
Cases of mediastinal germ cell tumours associated with haematological disorders (two cases of systemic mastocytosis included) have been reported previously. This combination is more frequent than would be expected by chance alone. We report the case of a
Kurt, A.M. +6 more
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The elucidation of molecular mechanisms in systemic mastocytosis [PDF]
Mastocytosis, one of the subcategories of myeloproliferative neoplasms, results from a colonel, neoplastic proliferation of morphologically and immunophenotypically abnormal mast cells which accumulate primarily in the skin and bone marrow. Prevalence
Mcmullen, Amy Anne
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