Results 161 to 170 of about 69,333 (214)

Clinical remission in allergy and clinical immunology practice: State of the art and World Allergy Organization (WAO) call to action. [PDF]

World Allergy Organ J
Morais-Almeida M, Canonica GW, Giavina-Bianchi P, Arasi S, Caminati M, Fiocchi A, Fonacier LS, Giavina-Bianchi M, Gómez RM, González-Diaz SN, Martin BL, Ortega Martell JA, Pitè H, Rouadi P, Sánchez Caraballo J, Villarreal-González RV, Virchow JC, Bachert C, Bernstein JA, Cianferoni A, Dávila I, Hanania NA, Heffler E, Nair P, Park HS, Saito H, Varricchi G, Yáñez A, Ansotegui IJ.   +28 more
europepmc   +1 more source

Mastocytosis with skin manifestations: current status

, 1999
Koumantaki-Mathioudaki, E, Karpouzis, AJ, Jorizzo, JL, Katsambas, AD   +3 more
core  

Diffuse Cutaneous Mastocytosis with Bullous Presentation: A Rare Case Report.

Indian J Dermatol
Mendiratta V, Bansal A, Singh S, Jain A.
europepmc   +1 more source

Mastocytosis

Primary Care - Clinics in Office Practice, 2016
Mastocytosis is a rare disease caused by excessive production of mast cells. Clinical presentation is variable, often based on the type of mastocytosis, but in all types of mastocytosis there seems to be an increase in the risk of anaphylaxis. Systemic mastocytosis is diagnosed based on bone marrow biopsy.
Ayesha, Abid, Michael A, Malone, Katherine, Curci   +2 more
exaly   +4 more sources

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Mastocytosis demystified

Hematology, 2023
Abstract Mastocytosis is a rare, clinically heterogenous clonal hematological neoplasm. Over 95% of patients harbor the driver KIT D816V mutation resulting in mast cell (MC) accumulation and proliferation in various organs, leading to variable symptom manifestations that result from MC mediator release in patients with systemic ...
Scott, Veitch, Deepti H, Radia
openaire   +2 more sources

Mastocytosis

Gastroenterology Nursing, 2018
Mastocytosis is a rare and underdiagnosed disorder characterized by mast cell proliferation in the tissues and organs of the body. The gastrointestinal manifestations of the disease can be noted in approximately 70%–80% of those patients diagnosed with the disorder.
openaire   +4 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