Results 151 to 160 of about 917,566 (209)

Hereditary Alpha-Tryptasemia and Mastocytosis: What We Know and What We Need To Learn. [PDF]

Curr Allergy Asthma Rep
Rama TA, Gulen T.
europepmc   +1 more source

Mast cell burden and immunophenotype of Chinese patients with cutaneous mastocytosis: a 10-year study with focus on the easily neglected pathogenic features. [PDF]

Front Med (Lausanne)
Jia Q, Li X, Fan A, Zheng D, Li S, Wang W, Li S, Li J.   +7 more
europepmc   +1 more source

Systemic Mastocytosis [PDF]

Hematology/Oncology Clinics of North America, 2010
An unusual disease, mastocytosis challenges the pathologist with a variety of morphologic appearances and heterogeneous clinical presentations ranging from skin manifestations (pruritus, urticaria, dermatographism) to systemic signs and symptoms indicative of mast cell mediator release, including flushing, hypotension, headache, and anaphylaxis among ...
Tracy I, George, Hans-Peter, Horny
openaire   +4 more sources

Systemic Mastocytosis

The American Journal of the Medical Sciences, 2011
Systemic mastocytosis (SM) is a clonal disorder of hematopoietic system characterized by abnormal growth and accumulation of mast cells in various tissues. Its clinical spectrum ranges from mild disease to an aggressive course with life-threatening conditions.
Erbas, Tomris, DAĞDELEN, SELÇUK, Ozdemir, Didem   +2 more
core   +5 more sources

Systemic mastocytosis

Blood, 2013
The term mastocytosis encompasses a heterogeneous group of clonal diseases characterized by proliferation and accumulation of mast cells (MC) in different tissues, mainly skin and bone marrow (BM).
Bouvier, Sylvie, Arnaud, Anne
core   +6 more sources

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Avapritinib for Systemic Mastocytosis

Expert Review of Hematology, 2021
Systemic mastocytosis (SM) is a rare myeloid neoplasm driven in ≈95% of cases by activating KIT mutations, usually D816V. SM can be indolent (ISM), smoldering (SSM) and advanced (AdvSM), the latter characterized by organ damage resulting from infiltrating neoplastic mast cells.
Prithviraj Bose, Srdan Verstovsek
openaire   +2 more sources

Systemic Mastocytosis and the Mastocytosis Syndrome

Journal of Cutaneous Pathology, 1979
A patient with extensive systemic mastocytosis and the mastocytosis syndrome was studied by light and electron microscopy. Mast cell proliferation was found in the bone marrow, the liver, spleen and lymph node. In addition, the patient had telangiectasia macularis eruptiva perstans and elevated histamine levels.
G D, Monheit, T, Murad, M, Conrad
openaire   +2 more sources