Case report highlights complex genomic changes in mast cell leukemia
An older man developed MCL with complex genomic alterations, highlighting the challenges of diagnosing this rare subtype of SM.
An older man developed MCL with complex genomic alterations, highlighting the challenges of diagnosing this rare subtype of SM.
Mastocytosis itch is driven by more than histamine; a new review explores how crosstalk between mast cells and neurons drives this symptom.
A case series of five postmenopausal women with SM-associated osteoporosis found that denosumab may improve bone mass and quality of life.
A recent case report highlights that repeated bone fractures can be a warning sign of systemic mastocytosis (SM).
A review examines decades of research on mast cells and their diversity, explaining why these key cells in SM are hard to study.
Though uncommon, advanced SM can cause severe gastrointestinal distress with no skin issues, making diagnosis a challenge.
A small-scale study in Turkey evaluated sleep studies of nine patients with SM, observing potential sleep-related burden in some individuals.
An 81-year old woman with a highly complex case of mast cell leukemia demonstrated the importance of tailored care.
Extensive evaluation helped doctors distinguish between exercise-induced anaphylaxis and mast cell disorders like SM and MCAS.
A PROSPECTOR analysis found that tryptase levels in clonal mast cell disease often fell below the cutoff used to support an SM diagnosis.