Results 31 to 40 of about 6,446 (159)
KIT mutation analysis in mast cell neoplasms: recommendations of the European competence network on mastocytosis [PDF]
Although acquired mutations in KIT are commonly detected in various categories of mastocytosis, the methodologies applied to detect and quantify the mutant type and allele burden in cells and various tissues are poorly defined.
T. Haferlach +79 more
core +1 more source
Evaluation of Mast Cell Activation Syndromes: Impact of Pathology and Immunohistology [PDF]
Mast cell activation syndromes (MCAS) are clinically defined disease states with a largely unknown morphological background. Since mastocytosis may be associated with MCAS, it is crucial in every patient to document or exclude mastocytosis by appropriate
Horny, H. -P., Valent, P., Sotlar, K.
core +1 more source
Advanced systemic mastocytosis: from molecular and genetic progress to clinical practice
Systemic mastocytosis is a heterogeneous disease characterized by the accumulation of neoplastic mast cells in the bone marrow and other organ organs/tissues.
Celalettin Ustun +15 more
doaj +1 more source
Mastocytosis: Fertility and Pregnancy Management in a Rare Disease
Mastocytosis encompasses a subset of rare diseases, characterized by the presence and accumulation of abnormal neoplastic MC in various organ systems, including skin, bone marrow, spleen and gastrointestinal tract.
Jacqueline Ferrari +5 more
doaj +1 more source
Differential Diagnoses of Systemic Mastocytosis in Routinely Processed Bone Marrow Biopsy Specimens: A Review [PDF]
Diagnosis of systemic mastocytosis (SM) is mainly based on the morphological demonstration of compact mast cell infiltrates in various tissue sites. In almost all patients such infiltrates are detected in the bone marrow.
Horny, H. -P. +5 more
core +1 more source
Mastocytosis in children:A protocol for management
Mastocytosis is characterized by an increased number of mast cells with an abnormal growth and accumulation in one or more organs. In most children mastocytosis is limited to the skin (cutaneous mastocytosis) and often transient as compared with that in ...
Pasmans, SGMA +17 more
core +2 more sources
Phenotypic and genotypic characteristics of mastocytosis according to the age of onset. [PDF]
Adult's mastocytosis is usually associated with persistent systemic involvement and c-kit 816 mutation, while pediatrics disease is mostly limited to the skin and often resolves spontaneously.
Fanny Lanternier +26 more
doaj +1 more source
Abstract 1. A patient with splenic mastocytosis who had hypersplenism, periodic flushing and clotting defects is presented. 2. A correlation is shown between mastocytosis and elevated histamine and heparin levels in the spleen. 3. The patient is well nine months after splenectomy. 4.
N, ENDE, E I, CHERNISS
openaire +2 more sources
Background Pediatric Mastocytosis is a rare and heterogeneous disease, characterized by accumulation of mast cells in the skin (Cutaneous Mastocytosis) and/or, less frequently, in other organs, mainly liver, spleen, bone marrow, lymph nodes and ...
Grazia Bossi +9 more
doaj +1 more source
Background: Anaphylactic reactions are a well-known feature of mastocytosis, particularly in relation to hymenoptera venom stings. Although data on the frequency of drug hypersensitivity reactions is limited in mastocytosis, it is hypothesized that these
Jesper Jarkvist, Theo Gülen
doaj +1 more source

