Results 11 to 20 of about 10,225 (204)

Cutaneous mastocytosis [PDF]

open access: yesAtlas of Genetics and Cytogenetics in Oncology and Haematology, 2020
Review on cutaneous mastocytosis, with data on clinics, pathology, and involved ...
Chisholm, Karen M
core   +8 more sources

Cutaneous mastocytosis. a dermatological perspective

open access: yesAustralasian Journal of Dermatology, 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   +7 more sources

Diffuse cutaneous mastocytosis (pigmented maculopapular cutaneous mastocytosis) in a cat

open access: yesMacedonian Veterinary Review, 2020
Diffuse cutaneous mastocytosis was diagnosed in a 6-year-old, indoor, neutered female domestic European shorthair cat. Marked pruritus located mainly on the head and neck was noticed in the cat and in this area the animal had developed alopecia, crusts ...
Marcin Szczepanik   +3 more
doaj   +2 more sources

French guidelines for the management of nonadvanced mastocytosis in adults. [PDF]

open access: yesOrphanet J Rare Dis
Mastocytosis is a rare disease caused by abnormal mast cell accumulation/proliferation in various organs/tissues. Its clinical features exhibit significant variability irrespective of its clinical presentation, classification, global survival or impact ...
Bulai Livideanu C   +5 more
europepmc   +2 more sources

Bullous mastocytosis

open access: yesIndian Journal of Dermatology, 2007
Mastocytosis is a condition characterized by the disorderly infiltration of mast cells in several tissues and comprises many different clinical situations varying from indolent cutaneous forms to malignant and systemic conditions. Bullous mastocytosis is
Devi Basanti   +3 more
core   +1 more source

Rare Clinical Image of Cutaneous Mastocytosis

open access: yesJournal of Clinical and Diagnostic Research
Mastocytosis, a rare condition also referred to as a clonal bone marrow disorder, is characterised by an excessive presence of CD34+ mast cell progenitors and functionally impaired mast cells. This disorder can affect both adults and children, leading to
Keyur Dudhat   +3 more
core   +2 more sources

Cutaneous mastocytosis - clinical heterogeneity

open access: yesInternational Archives of Allergy and Immunology, 2002
Cutaneous mastocytosis (CM) encompasses several distinct patterns of disease which can be distinguished by the type of skin lesions, age of onset, familial occurrence, noncutaneous involvement, associated c-kit mutations, and prognosis.
Henz, Beate M., Hartmann, Karin
core   +4 more sources

Mastocytosis. General concepts, view on patient management, examples of clinical course of the disease

open access: yesZdorovʹe Rebenka, 2022
Background. Mastocytosis is a disease characterized by the presence of mast cells in various organs. The skin is affected most often. Almost every patient diagnosed with mastocytosis has skin lesions.
O.L. Statkevych, T.V. Sviatenko
doaj   +1 more source

Characteristics and outcomes of patients with pediatric-onset non-mastocytosis mast cell activation disorders: A CEREMAST study. [PDF]

open access: yesPediatr Allergy Immunol
Abstract Background Mast cell (MC) activation (MCA) disorders (MCAD) include diseases in which MCs excessively release mediators leading to recurrent manifestations of MCA. MCAD encompasses MCA syndrome (MCAS) which is defined by (i) documented systemic symptoms of MCA, (ii) a 20% increase in serum tryptase level from the individual's baseline plus 2 ...
Weiss M   +25 more
europepmc   +2 more sources

Cutaneous mastocytosis in childhood

open access: yesAllergologie select, 2022
Mastocytoses are characterized by clonal proliferation of mast cells in various tissues. In childhood, cutaneous mastocytosis (CM) occurs almost exclusively. It is confined to the skin, and has a good prognosis. The most common form is the maculopapular cutaneous mastocytosis (MPCM), formerly called urticaria pigmentosa. A distinction is made between a
Nemat, Katja, Abraham, Susanne
openaire   +3 more sources

Home - About - Disclaimer - Privacy