Results 21 to 30 of about 905 (194)
High burden of clonal mast cell disorders and hereditary α-tryptasemia in patients who need Hymenoptera venom immunotherapy. [PDF]
In this multicenter study, we have demonstrated that clonal mast cell disease and HαT are more prevalent among individuals who need VIT; one or both was found in 27% of individuals overall. Both diagnoses were highly concentrated among individuals with severe anaphylaxis.
Korošec P +24 more
europepmc +2 more sources
Mastocitosis sistémica con afectación de piel versus mastocitosis indolente [PDF]
El objetivo de trabajo es la presentación de los datos clínicos, analíticos, radiológicos, terapéuticos y de evolución de un caso de matocitosis sistémica (MS) con afectación de piel. Revisando la literatura ya que la mastocitosis sigue siendo una enfermedad de difídicl diagnóstico, sobre todo en los casos que no existen alteraciones cutáneas.
Tiberio,G. +5 more
openaire +4 more sources
A case of high‐risk AML in a patient with advanced systemic mastocytosis
Abstract Aggressive SM + AML has limited therapeutic options. Even a strong combination of decitabine–venetoclax–midostaurin has a transient effect on AML and a mitigated effect on SM. Larger series are required to identify the best therapeutic strategy.
Manlio Fazio +15 more
wiley +1 more source
Flow cytometry of duodenal intraepithelial lymphocytes improves diagnosis of celiac disease in difficult cases. [PDF]
Background Diagnosis of celiac disease is difficult when the combined results of serology and histology are inconclusive. Studies using flow cytometry of intraepithelial lymphocytes (IELs) have found that celiac patients have increased numbers of γδ IELs, along with a decrease in CD3‐CD103 + IELs.
Valle J +7 more
europepmc +2 more sources
Abstract Background Comorbidities are common in chronic inflammatory conditions, requiring multidisciplinary treatment approach. Understanding the link between a single disease and its comorbidities is important for appropriate treatment and management.
Pierandrea Morandini +10 more
wiley +1 more source
Sobre la Mastocitosis Sistémica [PDF]
La mastocitosis consiste en una serie de trastornos heterogéneos, caracterizados por la proliferación y acumulación de mastocitos en diferentes órganos y tejidos, siendo los más habituales: la piel, la médula ósea y el tracto gastrointestinal. La mayoría de los pacientes presentan síntomas relacionados con la liberación de mediadores del mastocito y ...
González Fernández, Mario +1 more
openaire +3 more sources
CUTANEOUS MASTOCYTOSIS IN THE ADULT: WHAT LIES BENEATH
Mastocytosis is a disorder characterized by clonal mast cell proliferation and accumulation within various organs, most commonly, the skin. Adult-onset mastocytosis is highly suggestive of a systemic involvement and the cases limited to the skin are ...
Liliana Torres +3 more
doaj +1 more source
Mastocitosis Cutánea: Revisión y actualización [PDF]
Realizar una revisión bibliográfica sobre Mastocitosis cutánea, sintetizando la información de las diferentes formas de manifestación, su clínica, diagnóstico, tratamiento y pronóstico, así como del estado actual de la investigación acerca de nuevos métodos diagnósticos y terapéuticos.
Bosque Blasco, Víctor +1 more
openaire +3 more sources
The usefulness of c-Kit in the immunohistochemical assessment of melanocytic lesions [PDF]
C-Kit (CD117), the receptor for the stem cell factor, a growth factor for melanocyte migra- tion and proliferation, has shown differential immunostaining in various benign and malig- nant melanocytic lesions. The purpose of this study is to compare c-Kit
Atzori L +9 more
core +1 more source
Urticaria pigmentosa de presentación atípica en la infancia: Reporte de un caso clínico
La Urticaria Pigmentosa es el tipo más frecuente de mastocitosis cutáneas de inicio en la edad pediátrica, representando el 75% de los casos. Se presenta con máculas y/o pápulas de color amarillo a café-rojizo, usualmente con signo de Darier positivo y ...
Catherina Moll-Manzur +2 more
doaj +1 more source

