[A particular presentation of a T cell large granular lymphocytic leukaemia]. / Une présentation particulière de leucémie à grands lymphocytes granuleux.
Ann Pathol
; 43(1): 52-56, 2023 Jan.
Article
en Fr
| MEDLINE
| ID: mdl-36494259
ABSTRACT
T cell prolymphocytic leukemia (T-PLL) is a rare, aggressive neoplasm derived from post-thymic T cells. Patients are typically middle-aged with a slight male predominance who present with a high white blood cell count, hepatosplenomegaly, lymphadenopathy, and other symptoms typically associated with leukemia. Although cutaneous involvement has been reported in up to 30% of cases of T-PLL, to our knowledge, none have presented with a presentation resembling livedoid vasculopathy. In the correct clinical context, an underlying hematolymphoid neoplasm should be included in the differential diagnosis of a patient presenting with livedoid vasculopathy.
Palabras clave
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Leucemia Linfocítica Granular Grande
/
Vasculopatía Livedoide
Límite:
Female
/
Humans
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Male
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Middle aged
Idioma:
Fr
Revista:
Ann Pathol
Año:
2023
Tipo del documento:
Article