Results 31 to 40 of about 69,333 (214)

Cutaneous mastocytosis. a dermatological perspective

open access: yes, 2021
Mastocytosis is a rare disease characterised by expansion and collection of clonal mast cells in various organs including the skin, bone marrow, spleen, lymph nodes and gastrointestinal tract.
Campione E.   +9 more
core   +2 more sources

Treatment of Mastocytosis: A Literature Review

open access: yesКлиническая онкогематология, 2021
The term “mastocytosis” refers to a group of rare heterogeneous disorders resulting from proliferation and accumulation of neoplastic mast cells in various organs.
Karina Maksimovna Chernavina   +2 more
doaj   +1 more source

Fatal anaphylactic sting reaction in a patient with mastocytosis [PDF]

open access: yes, 2008
We report on a 33-year-old female patient with indolent systemic mastocytosis and urticaria pigmentosa who died of an anaphylactic reaction after a yellow jacket sting.
Rueff, F.   +4 more
core   +1 more source

KIT mutation analysis in mast cell neoplasms: recommendations of the European competence network on mastocytosis [PDF]

open access: yes, 2015
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   +74 more
core   +1 more source

Differential Diagnoses of Systemic Mastocytosis in Routinely Processed Bone Marrow Biopsy Specimens: A Review [PDF]

open access: yes, 2010
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

Advanced systemic mastocytosis: from molecular and genetic progress to clinical practice

open access: yesHaematologica, 2016
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

Definitions, Criteria and Global Classification of Mast Cell Disorders with Special Reference to Mast Cell Activation Syndromes: A Consensus Proposal [PDF]

open access: yes, 2011
Activation of tissue mast cells (MCs) and their abnormal growth and accumulation in various organs are typically found in primary MC disorders also referred to as mastocytosis.
Triggiani, Massimo   +37 more
core   +1 more source

Evaluation of Mast Cell Activation Syndromes: Impact of Pathology and Immunohistology [PDF]

open access: yes, 2012
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

Phenotypic and genotypic characteristics of mastocytosis according to the age of onset. [PDF]

open access: yesPLoS ONE, 2008
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

Mastocytosis: Fertility and Pregnancy Management in a Rare Disease

open access: yesFrontiers in Oncology, 2022
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

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