Difficulties of primary diagnosis in patients with suspected systemic mastocytosis
Background. Mastocytosis is a rare myeloproliferative disease based on clonal hematopoiesis of mast cells, with accumulation of mast cells in various tissues and organs. The cutaneous mastocytosis is common in the pediatric population and, in general, progression to aggressive forms is not typical....
Saved in:
Main Authors: | Z. K. Abdulkhalikova, M. V. Barabanshchikova, V. V. Baykov, I. M. Barkhatov, E. V. Morozova, I. S. Moiseev |
---|---|
Format: | Article |
Language: | Russian |
Published: |
ABV-press
2024-09-01
|
Series: | Онкогематология |
Subjects: | |
Online Access: | https://oncohematology.abvpress.ru/ongm/article/view/946 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Targeted therapy for advanced forms of systemic mastocytosis in real clinical practice
by: D. I. Shikhbabaeva, et al.
Published: (2023-12-01) -
Treatment of indolent systemic mastocytosis with sarilumab is not supported in a randomized trial
by: Hirsh D. Komarow, MD, et al.
Published: (2025-08-01) -
Monomorphic type of maculopapular cutaneous mastocytosis: rationale for interdisciplinary collaboration
by: E. I. Kasikhina, et al.
Published: (2025-05-01) -
Assessment of skin manifestations under mastocytosis in adults and their associations with symptoms, level of tryptase and subtype of the disease
by: N. P. Teplyuk, et al.
Published: (2021-06-01) -
Mast cell activation syndrome: The overdiagnosis problems
by: N. V. Mikryukova, et al.
Published: (2025-06-01)