Results 31 to 40 of about 2,002 (144)

Challenging diagnosis of indolent systemic mastocytosis isolated to the GI tract. [PDF]

open access: yesBMJ Case Rep, 2021
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

open access: yesAnnals of Internal Medicine: Clinical Cases
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]

open access: yesInt J Surg Case Rep, 2020
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.

open access: yesIndian J Crit Care Med, 2018
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

Remission of indolent systemic mastocytosis in the absence of targeted therapy. [PDF]

open access: yesJ Allergy Clin Immunol Pract, 2022
Constantine GM   +7 more
europepmc   +3 more sources

Indolent systemic mastocytosis in a child: A rare and difficult diagnosis

open access: yesIndian Journal of Paediatric Dermatology, 2016
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]

open access: yesNEJM Evidence, 2023
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]

open access: yesAllergy: European Journal of Allergy and Clinical Immunology, 2020
Jakub Trizuljak   +2 more
exaly   +2 more sources

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