Rare pediatric SM case presents as skull lesion
Systemic mastocytosis is rare in children, and this case was particularly rare because of its lone symptom.
Systemic mastocytosis is rare in children, and this case was particularly rare because of its lone symptom.
A case report describes a woman diagnosed with and treated for systemic mastocytosis despite vague symptoms such as atypical skin lesions.
A recent article proposed unifying the 2001 WHO SM diagnostic criteria and revised criteria of the 2021 International Consensus Classification Group.
A new review recommended the use of sensitive mutation detection methods to better diagnose systemic mastocytosis (SM).
A new study suggests that the phenotype of advanced systemic mastocytosis patients might provide clinicians with tools to offer diagnoses and prognoses.
A recent report shows two specific prognostic scoring systems have the most accurate predictive value for advanced SM outcomes.
Data from part 1 of a phase 2 trial showed bezuclastinib resulted in an overall improvement of quality of life for non-advanced SM patients.
A recent study showed cellular markers CD25, CD30 and CD25 could help predict prognosis in patients with systemic mastocytosis.
In a recently published case study, a patient was diagnosed with SM via the Spanish Network on Mastocytosis (REMA) score.
Findings from the phase 2 PATHFINDER study presented at SOHO 2024 showed avapritinib had an overall positive effect in SM patients.