Results 11 to 20 of about 6,446 (159)

Cutaneous types of mastocytosis in paediatry. Case report of maculopapular cutaneous mastocytosis in an infant

open access: yesКлинический разбор в общей медицине, 2020
Mastocytosis is a heterogeneous group of neoplasms characterized by increased mast cells proliferation and accumulation in various organs and tissues. The paper introduces the newest mastocytosis classification and diagnosis principles.
Olga B. Tamrazova, Evgeniya A. Glukhova
doaj   +2 more sources

Review papers The role of KIT gene mutations in pathogenesis of pediatric mastocytosis

open access: yesPrzegląd Dermatologiczny, 2015
Mastocytosis is characterized by excessive proliferation and accumulation of mast cells in skin and/or other organs. Two forms of the disease, cutaneous and systemic mastocytosis, differ significantly in symptomatology and clinical course.
Joanna Dawicka   +5 more
doaj   +2 more sources

Diffuse cutaneous mastocytosis in an infant

open access: yesIndian Journal of Paediatric Dermatology, 2016
Mastocytosis is a group of a disorder characterized by infiltration of mast cell in various organs, e.g. skin, bone marrow, liver, spleen, gastrointestinal tract, lymph node, etc., The term bullous mastocytosis is generally used to describe the varieties
Sitangshu Chatterjee   +2 more
doaj   +2 more sources

Drug hypersensitivity reactions and allergy in patients with mastocytosis [PDF]

open access: yesPrzegląd Dermatologiczny, 2017
Mastocytosis is a rare myeloproliferative disease caused by excessive proliferation and accumulation of mast cells in the skin and internal organs. The most common variant of mastocytosis in children is cutaneous mastocytosis.
Justyna H. Czarny   +7 more
doaj   +2 more sources

Cutaneous mastocytosis: Clinical Case

open access: yesПедиатрическая фармакология
Skin syndrome is common in the practice of allergologist-immunologist, and it requires differential diagnosis. One of the rare skin diseases among children is mastocytosis caused by excessive accumulation of mast cells in various organs.
Aset Kh. Ibisheva   +5 more
doaj   +2 more sources

Systemic mastocytosis

open access: yesThe American Journal of the Medical Sciences, 2011
Mastocytosis is a heterogeneous group of rare disorders characterized by the abnormal growth and accumulation of mast cells in one or more organs. Mast cells are myeloid lineage cells that express the CD117 (KIT), CD45, and Fcε‎RI cell surface markers ...
Tomás Ahern, Donal O’Shea
core   +4 more sources

Biochemical markers predictive for bone marrow involvement in systemic mastocytosis [PDF]

open access: yesHaematologica, 2008
Systemic mastocytosis is characterized by bone marrow involvement, which requires a bone marrow biopsy for diagnostic work-up. We questioned whether bone marrow involvement could be predicted using biochemical markers.
Marjolein L. Donker   +7 more
doaj   +2 more sources

Clinical features of mastocytosis at pediatric patients

open access: yesVestnik Dermatologii i Venerologii, 2017
Mastocytosis is relevant to heterogeneous disease group characterized with redundant accumulation and proliferation of mast cells in tissues. The skin form of mastocytosis is mainly occurs in children.
D. V. Proshutinskaya, O. S. Makoveckaya
doaj   +2 more sources

Mastocytosis

open access: yesPrimary Care: Clinics in Office Practice, 2016
Mastocytosis is a heterogeneous disease with an increased number and activation of mast cells. Subtypes range from benign to rare aggressive forms, and the disease may affect people of all ages. The pathogenesis involves mutations in the KIT gene in both
Havelund, Troels   +9 more
core   +3 more sources

Nodular mastocytosis: a case study

open access: yesVestnik Dermatologii i Venerologii, 2017
A case study of nodular mastocytosis is described. Tacrolimus was used to treat skin manifestations of mastocytosis.
E. V. Pavlova   +4 more
doaj   +2 more sources

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