Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1111/cea.14608 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
How to Recognise Mastocytosis?
Clin Exp Allergy
January 2025
Department of Dermatology and Allergy Centre, Odense University Hospital, Odense, Denmark.
Current status and future directions in food protein-induced enterocolitis syndrome: An NIAID workshop report of the June 22, 2022, virtual meeting.
J Allergy Clin Immunol
November 2024
Allergy, Immunology and Transplantation, NIAID, National Institutes of Health, Rockville, Md.
Article Synopsis
- - Food Protein-Induced Enterocolitis (FPIES) is a type of food allergy that occurs primarily in children and is characterized by symptoms such as delayed vomiting, lethargy, and pale skin, typically emerging 1-4 hours after consuming the allergen.
- - Despite increasing recognition of FPIES, its exact causes remain unknown, and there are no specific tests to diagnose or track the condition's progress.
- - A recent workshop by the National Institute of Allergy and Infectious Diseases (NIAID) focused on FPIES, discussing current understanding, research gaps, and future priorities for improving diagnosis and management.
MASTering systemic mastocytosis: Lessons learned from a large patient cohort.
J Allergy Clin Immunol Glob
November 2024
Department of Allergy, Kaiser Permanente Medical Center, San Diego, Calif.
Article Synopsis
- Systemic mastocytosis (SM) is a rare disease affecting about 32,000 people in the U.S., often misdiagnosed due to vague symptoms and the necessity for invasive tests.
- A study of 116 patients revealed that the majority had indolent SM, with a significant average delay of 58.3 months for diagnosis, and some patients progressed to more advanced forms.
- The findings emphasize the need for better awareness and understanding of SM to improve diagnosis and treatment, suggesting that further studies are necessary to establish effective follow-up care for patients.
Beyond the Usual Suspects: Unraveling Spleen Mastocytosis in Hypersplenism Differential Diagnosis.
Cureus
August 2024
Hematology, Unidade Local de Saúde de Santo António, Porto, PRT.
Systemic mastocytosis (SM) poses a diagnostic challenge. This hematologic disorder involves abnormal mast cell proliferation and concurrent tissue infiltration. SM clinical presentation is not uniform, with patients displaying a wide array of symptoms related to different organ infiltration and mast cell mediators.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!