Cargando…
A case of VEXAS syndrome presenting with unusual bone marrow granulomas: a diagnostic dilemma
BACKGROUND: VEXAS is a recently described inflammatory disease caused by mutations in the UBA1 gene. Symptoms are diverse and include fevers, cartilaginous inflammation, lung inflammation, vasculitis, neutrophilic dermatoses, and macrocytic anemia. Cytoplasmic inclusions in myeloid and erythroid pro...
Autores principales: | Vu, Khiem T., Wolfe, Rachel M., Lambird, Jonathan E., Maracaja, Danielle L. V. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10332027/ https://www.ncbi.nlm.nih.gov/pubmed/37430338 http://dx.doi.org/10.1186/s41927-023-00343-w |
Ejemplares similares
-
Diagnostic Dilemma: An Unusual Case of Angioimmunoblastic T-Cell Lymphoma Manifesting as Bone Marrow Non-Caseating Granuloma
por: Bhatlapenumarthi, Vineel, et al.
Publicado: (2020) -
Recovery of Bone Marrow Function in VEXAS Syndrome-potential Role for Romiplostim
por: Al-Hakim, Adam, et al.
Publicado: (2023) -
VEXAS syndrome: a diagnostic puzzle
por: Ruffer, Nikolas, et al.
Publicado: (2023) -
Management of an unusual peripheral giant cell granuloma: A diagnostic dilemma
por: Mannem, Satheesh, et al.
Publicado: (2012) -
VEXAS syndrome
por: Grayson, Peter C., et al.
Publicado: (2021)