Challenging diagnosis of indolent systemic mastocytosis isolated to the GI tract. [PDF]
Mastocytosis is a rare group of disorders that presents with heterogenous phenotypes depending on the organ system involved. In the absence of cutaneous involvement—mast cell aggregates that may present as papules, nodules or plaques—classically associated with indolent systemic mastocytosis (SM), the diagnosis of this rare condition is particularly ...
Horton L +3 more
europepmc +3 more sources
Indolent Systemic Mastocytosis: An Incidental Diagnosis
Indolent systemic mastocytosis (ISM) is the most prevalent subtype of systemic mastocytosis, characterized by a clinical course progressing over several years to decades.
Ayesha Khalid, Arfa Faiz, Alan Kaell
doaj +2 more sources
Pancreatic neuroendocrine tumor presenting in indolent systemic mastocytosis: A case report. [PDF]
Abstract Introduction Systemic mastocystosis, a disorder of clonal mast cell expansion presents with symptoms of flushing, pruritus, musculoskeletal pain, gastrointestinal cramping and vascular instability. Patients with neuroendocrine tumors may present with similar symptoms due to the release
Sacco K +4 more
europepmc +3 more sources
Indolent Systemic Mastocytosis Manifesting as Protracted Anaphylactic Shock.
Systemic mastocytosis is a rare disease due to abnormal proliferation of mast cells (MCs). A case of indolent systemic mastocytosis is presented here. After anesthetic induction for elective thyroid swelling with propofol and atracurium followed by endotracheal intubation, a 57-year-old female patient developed acute hypotension, sinus tachycardia, red
Chatterjee M +6 more
europepmc +3 more sources
Indolent systemic mastocytosis and aleukemic mast cell leukemia: Subtle diagnostic differences with distinct management approaches [PDF]
Sara Yumeen, Elie Saliba
exaly +2 more sources
Remission of indolent systemic mastocytosis in the absence of targeted therapy. [PDF]
Constantine GM +7 more
europepmc +3 more sources
Indolent systemic mastocytosis in a child: A rare and difficult diagnosis
Mastocytosis is a sporadic disease characterized by an abnormal accumulation of mast cells (MCs) in single or multiple organs. A 5-year-old girl who was diagnosed as cutaneous mastocytosis by our Dermatology Department when she was 4 months of age was ...
Yasemin Altuner Torun +4 more
doaj +2 more sources
Avapritinib versus Placebo in Indolent Systemic Mastocytosis [PDF]
BACKGROUND: Indolent systemic mastocytosis (ISM) is a clonal mast-cell disease driven by the KIT D816V mutation. We assessed the efficacy and safety of avapritinib versus placebo, both with best supportive care, in patients with ISM. METHODS: We randomized patients with moderate to severe ISM (total symptom score [TSS] of ≥28; scores range from 0 to ...
van Daele, Paul +53 more
openaire +5 more sources
Clinical features and survival of patients with indolent systemic mastocytosis defined by the updated WHO classification [PDF]
Jakub Trizuljak +2 more
exaly +2 more sources
Case Report: Multidisciplinary management of a patient with indolent systemic mastocytosis and refractory symptoms [PDF]
Matthew J Hamilton +2 more
exaly +2 more sources

