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Синдром VEXAS

ORPHA:596753· ICD-10 M35.8· VEXAS syndrome

Визначення(English summary)

A rare autoinflammatory syndrome characterized by adult onset of rheumatologic manifestations such as recurrent fever, skin and pulmonary inflammation, ear and nose chondritis, vasculitis, deep vein thrombosis, and arthralgia. Laboratory examination reveals progressive hematologic abnormalities including macrocytic anemia and thrombocytopenia, as well as elevated inflammatory markers. Bone marrow biopsy shows hypercellularity and signs of bone marrow dysplasia. The disease primarily occurs in males and is caused by somatic mutations on chromosome Xp11.

Поширеність
<1 / 1 000 000
Успадкування
Not applicable
Вік початку
Adult, Elderly