Results 21 to 30 of about 9,543 (174)

An intriguing coexistence of cutaneous and systemic mastocytosis with atypical chronic myeloid leukemia: An associated hematologic neoplasm (SM-AHN)

open access: yesJournal of Applied Hematology, 2021
Systemic mastocytosis (SM) characterized by focal or diffuse infiltrates of neoplastic mast cells can range from indolent cutaneous disease to aggressive systemic disease.
B R Rajalakshmi, Vijaya Basavaraj
doaj   +1 more source

Mastocitosis cutánea maculopapular infantil: reporte de un caso

open access: yesRevista Médica Clínica Las Condes, 2019
Resumen: Objetivo: Reportar un caso de mastocitosis cutánea maculopapular de inicio en la infancia y realizar una revisión bibliográfica con énfasis en el diagnóstico, estudio, pronóstico y tratamiento.
Renatta de Grazia   +3 more
doaj   +1 more source

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   +1 more source

PD-1 Regulates the Growth of Human Mastocytosis Cells

open access: yesAllergology International, 2013
Background: Programmed death-1 (PD-1) is a marker for human neoplastic T cells. Here, we evaluated whether or not PD-1 was also a marker for human mastocytosis, and explored the role of PD-1 in human mastocytosis cells.
Tatsuki R. Kataoka   +9 more
doaj   +1 more source

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   +1 more source

A case report of primary cutaneous marginal zone B-cell lymphoma with mastocytosis

open access: yesSAGE Open Medical Case Reports, 2021
A 53-year-old man presented with asymptomatic, dusky reddish nodules on his trunk, which had persisted for 7 years. Histological findings showed nodular to diffuse dermal infiltration of lymphocytes with irregular nuclei, eosinophils, plasma cells, and ...
Hyun Yi Lee, Joong Sun Lee, Dae Won Koo
doaj   +1 more source

Mastocytosis in the Skin: Disease Heterogeneity among Children and Adults

open access: yesActa Dermato-Venereologica, 2023
is missing (Short communication)
Christos Fokoloros   +7 more
doaj   +1 more source

Clinical Scoring of Cutaneous Mastocytosis

open access: yesActa Dermato-Venereologica, 2001
There are still many controversies in defining and evaluating mastocytosis. One of the aspects that is missing is a system for clinical evaluation of mastocytosis of the skin. A calculation based on a semi-quantitative analysis of three aspects of mastocytosis was designed. The method is called the scoring index of mastocytosis (SCORMA).
Heide, R.   +3 more
openaire   +3 more sources

Pseudoxanthomatous mastocytosis in a 2-month female infant

open access: yesIndian Journal of Dermatology, 2022
Mastocytosis is a rare disease characterized by infiltration of mast cells in various tissues like skin, bone marrow, liver, spleen, and gastrointestinal tract. Here, we present a case report of diffuse cutaneous mastocytosis (pseudoxanthomatous type) in
Tulika Rai   +3 more
doaj   +1 more source

Successful treatment of provisional cutaneous mastocytosis with interferon alpha

open access: yesIndian Journal of Dermatology, 2016
Mastocytosis is a disorder characterized by the clonal proliferation of mast cells and their accumulation in skin, bone marrow, liver, and spleen. Cutaneous mastocytosis presents in children in over 90% of the cases and any cutaneous manifestation in an ...
Andrea Rosario, Ramesh M Bhat
doaj   +1 more source

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