Results 41 to 50 of about 2,935 (197)
Development of the autoinflammatory disease damage index (ADDI) [PDF]
OBJECTIVES: Autoinflammatory diseases cause systemic inflammation that can result in damage to multiple organs. A validated instrument is essential to quantify damage in individual patients and to compare disease outcomes in clinical studies.
Al-Mayouf, SM +48 more
core +6 more sources
Mastocytosis in Children: Literature Review and Own Clinical Observation
The review of literature presents the data on neoplastic disease — mastocytosis. We provide the modern information of the etiopathogenesis, classification, clinical presentation, methods of diagnosis and treatment in children. We presented own experience
N.V. Nagornaya +3 more
doaj +1 more source
Mastocytosis is an accumulation of clonal mast cells within tissues and it is most commonly caused by an activating mutation in the KIT gene. In this study, we report a neonatal case who presented with diffuse cutaneous mastocytosis (CM) at birth.
Yanfang Li +4 more
doaj +1 more source
Mastocytosis is a heterogeneous group of disorders in which mast cells exhibit clonal proliferation that infiltrates one or more organs. In cutaneous mastocytosis, the mast cells infiltrate the skin only, whereas systemic mastocytosis is diagnosed when ...
Awni Alshurafa +4 more
doaj +1 more source
Summary Mastocytosis is categorized into cutaneous mastocytosis (CM), mast cell sarcoma and systemic mastocytosis (SM). Within SM, indolent SM (ISM) is the more frequent subtype. Adult patients with CM but without an extracutaneous biopsy are classified as having mastocytosis in the skin (MIS), a provisional diagnosis.
Julien Rossignol +15 more
wiley +1 more source
Mastocitosis cutánea maculopapular infantil: reporte de un caso
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
Co-Occurrence of neurofibromatosis-1 with urticaria pigmentosa: A Coincidental association?
Neurofibromatosis-1 (NF-1) is a neuroectodermal abnormality characterized by multiple neurofibromas, café-au-lait macules, axillary freckling, and Lisch nodules.
Nazneen Zulfikar Arsiwala +2 more
doaj +1 more source
Systemic Mastocytosis: Predominantly Involving the Bone, A Case Report [PDF]
Systemic mastocytosis (SM) is a rare clonal disorder of mast cells that can range from chronic smouldering type to aggressive mast cell leukaemia. It presents with non–specific symptoms like urticaria pigmentosa, unexplained flushing, hypotension and ...
Ketan P Mallya +4 more
doaj +1 more source
Mastocitosis cutáneas : a propósito de tres casos de urticaria pigmentosa [PDF]
Las mastocitosis son un grupo de enfermedades que tienen en común la proliferación y acumulación de mastocitos en la piel y tejidos extracutáneos. El 65% de ellas se inicia en la infancia.
Innocenti, Carolina +3 more
core
A Perspective on the Use of NB-UVB Phototherapy vs. PUVA Photochemotherapy [PDF]
Narrowband UVB (NB-UVB) phototherapy and psoralen-UVA (PUVA) photochemotherapy are widely used phototherapeutic modalities for a range of skin diseases.
Ahmad +119 more
core +3 more sources

