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Review and Updates on Systemic Mastocytosis and Related Entities

open access: yesCancers, 2023
Simple Summary Mast cells are specialized immune cells that mediate allergic and anaphylactic reactions, among other immunologic functions. The accumulation of abnormal mast cells can give rise to various disorders that range in severity of symptoms and ...
Julie Y. Li   +7 more
semanticscholar   +1 more source

New Insights Into the Pathogenesis of Mastocytosis: Emerging Concepts in Diagnosis and Therapy.

open access: yesAnnual Review of Pathology, 2022
Mastocytosis is a heterogeneous group of neoplasms defined by a numerical increase and accumulation of clonal mast cells (MCs) in various organ systems. The disease may present as cutaneous mastocytosis or systemic mastocytosis (SM).
P. Valent   +6 more
semanticscholar   +1 more source

Systemic Lymphadenopathic Mastocytosis with Eosinophilia

open access: yesDiagnostics, 2022
Systemic mastocytosis is a neoplastic proliferation of mast cells that most frequently involves cutaneous sites. Mastocytosis involves various extracutaneous sites, but the lymph node is rare.
Soyoung Im   +3 more
doaj   +1 more source

Recalcitrant Cutaneous Mastocytosis Treated With Genetically Informed Targeted Therapy: A Case Report

open access: yesInternational Journal of Dermatology and Venerology, 2023
Introduction:. Mastocytosis, a clonal proliferation of mast cells commonly involving the skin and bone marrow, has a varied clinical presentation ranging from cutaneous lesions to systemic disease.
Laura Gleason   +7 more
doaj   +1 more source

Mastocytosis [PDF]

open access: yesImmunology and Allergy Clinics of North America, 2014
Mastocytosis is a disorder of abnormal mast cell proliferation, with clinical features that include flushing, pruritus, abdominal pain, diarrhea, hypotension, syncope, and musculoskeletal pain. These features are the result of mast cell mediator release and infiltration into target organs.
Melody C, Carter   +2 more
openaire   +2 more sources

How “benign” is cutaneous mastocytosis? A Danish registry-based matched cohort study

open access: yesInternational Journal of Women's Dermatology, 2020
Background: There are limited estimates of the incidence rates (IRs) of mastocytosis, and only a few studies have addressed the long-term consequences of living with these diagnoses.
Line Kibsgaard, MD, PhD   +5 more
doaj   +1 more source

SWATH-MS identification of CXCL7, LBP, TGFβ1 and PDGFRβ as novel biomarkers in human systemic mastocytosis

open access: yesScientific Reports, 2022
Mastocytosis is a rare myeloproliferative disease, characterised by accumulation of neoplastic mast cells in one or several organs. It presents as cutaneous or systemic.
R. L. J. Graham   +5 more
doaj   +1 more source

KITD816V mutation in blood for the diagnostic screening of systemic mastocytosis and mast cell activation syndromes

open access: yesAllergy. European Journal of Allergy and Clinical Immunology, 2022
Current diagnostic algorithms for systemic mastocytosis (SM) rely on the detection of KITD816V in blood to trigger subsequent bone marrow (BM) investigations.
Paula Navarro-Navarro   +11 more
semanticscholar   +1 more source

Delayed Diagnosis of Indolent Systemic Mastocytosis as the Cause of Unexplained Skin Rash: A Case Report

open access: yesCase Reports in Oncology, 2023
Mastocytosis is a heterogeneous group of disorders in which mast cells exhibit clonal proliferation that infiltrates one or more organs. In cutaneous mastocytosis, the mast cells infiltrate the skin only, whereas systemic mastocytosis is diagnosed when ...
Awni Alshurafa   +4 more
doaj   +1 more source

Systemic Mastocytosis and Other Entities Involving Mast Cells: A Practical Review and Update

open access: yesCancers, 2022
Simple Summary In this article, we outline recent updates in systemic mastocytosis (SM) classification, including the bone marrow mastocytosis subtype; and discuss the mast cell leukemia subtype (acute or chronic), the rare variant of SM known as well ...
S. El Hussein   +4 more
semanticscholar   +1 more source

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