Results 41 to 50 of about 1,513 (156)

Scabies mimicking mastocytosis in two infants

open access: yesThe Turkish Journal of Pediatrics, 2013
Scabies is a common parasitic human infection in infants and children. However, diagnostic pitfalls are frequent in infants, in whom the clinical presentation is usually atypical and different from that in adults.
Emine Cölgeçen-Özel   +3 more
doaj  

Illuminating Immunity: A Systematic Review of Immune Cell Autofluorescence

open access: yesJournal of Biophotonics, Volume 18, Issue 6, June 2025.
ABSTRACT Immunophenotyping provides valuable prognostic and diagnostic information, but is technically complex and expensive. The assessment of autofluorescence is label‐free and provides complex information on cell identity. However, research on its application to immunophenotyping has been heterogenous.
Aline Knab   +4 more
wiley   +1 more source

The Report of a Very Rare Case of Peseudoxanthomatous Mastocytosis

open access: yesپزشکی بالینی ابن سینا, 2001
Diffuse cutaneous mastocytosis is very rare variety mast-cell disorder    which is called peseudoxanthomatous mastocytosis. Our case was a man    who was eighteen years old.
Mahmoud Farshchain   +2 more
doaj  

Urticaria Pigmentosa [PDF]

open access: yesThe Journal of Pediatrics, 2020
Avik Panigrahi   +2 more
openaire   +2 more sources

Clinical practice guidelines for the diagnosis and treatment of scabies

open access: yesInternational Journal of Dermatology, Volume 63, Issue 12, Page 1642-1656, December 2024.
Abstract Scabies, caused by the Sarcoptes scabiei var hominis mite burrowing into the skin, is a highly contagious disease characterized by intense nocturnal itching. Its global impact is considerable, affecting more than 200 million individuals annually and posing significant challenges to healthcare systems worldwide.
Soner Uzun   +24 more
wiley   +1 more source

Mastocitosis: urticaria pigmentosa

open access: yesRevista de Ciencias Médicas de Pinar del Río, 2015
La mastocitosis es una enfermedad rara. Se caracteriza por una proliferación benigna o en raras ocasiones maligna de mastocitos en los tejidos. Puede producir alteraciones tanto sistémicas como cutáneas.
Pedro Antonio Díaz Llanio   +4 more
doaj  

Subcellular expression of CD30 in cutaneous mastocytosis—An important factor for targeted treatment

open access: yesJournal of Cutaneous Pathology, Volume 51, Issue 11, Page 881-892, November 2024.
Abstract Background The subcellular distribution of CD30 on mast cells and the presence of eosinophils in cutaneous mastocytosis require further investigation, especially as the cell surface expression of CD30 is critical for the therapeutic response of systemic mastocytosis to brentuximab vedotin.
Christina Mitteldorf   +4 more
wiley   +1 more source

Spinal Adhesive Arachnoidopathy, the Disorder More Than Simply Adhesive Arachnoiditis: A Comprehensive Systematic Review of 510 Cases

open access: yesCNS Neuroscience &Therapeutics, Volume 30, Issue 10, October 2024.
ABSTRACT Background Spinal adhesive arachnoidopathy (SAA) is a chronic pathology associated with persistent inflammatory responses in the arachnoid. Adhesive arachnoiditis (AA) is one of the major forms of SAA, with accompanying secondary complications.
Weikang Zhang   +8 more
wiley   +1 more source

Urticaria pigmentosa en el adulto

open access: yesMedUNAB, 2012
La urticaria pigmentosa es una de las formas más comunes de las mastocitosis, las cuales corresponden a una serie de procesos caracterizados por un aumento anormal de los mastocitos en diversos órganos y tejidos corporales. En la urticaria pigmentosa
Jhon Alexander Ávila Rueda   +4 more
doaj  

Diagnosis of systemic mastocytosis with cryptic deletion of TET2 and DNMT3A resulting from unbalanced translocation

open access: yesBritish Journal of Haematology, Volume 205, Issue 3, Page 961-966, September 2024.
Summary Systemic mastocytosis (SM) is a rare haematological neoplasm associated with the gain of function mutation KIT D816V in 90% of adult patients. Classically, cytogenetic aberrations are not common except in cases of SM associated with another haematological neoplasm.
Signy Chow   +5 more
wiley   +1 more source

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