T-Cell Lymphoma with Rosai-Dorfman Syndrome-Like Feature / 대한혈액학회지
Korean Journal of Hematology
;
: 153-156, 1999.
Artículo
en Coreano
| WPRIM
| ID: wpr-720244
ABSTRACT
T-cell lymphoma is heterogeneous with respect to clinical presentation, course, and morphology, but it is rarely associated with sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Syndrome). We report a case of T-cell lymphoma with Rosai-Dorfman Syndrome like feature in a 31-years-old woman who presented severe non-immune hemolytic anemia and massive retroperitoneal and cervical lymphadenopathy. Her cervical lymph node biopsy revealed histiocytic infiltration showing erythrophagocytosis without marked fibrosis in the capsular and pericapsular areas and distension of sinusoids. After 6 cycles of CHOP (Cyclophosphamide, Adriamycin, Vincristine, and Prednisolone) chemotherapy, cervical and retroperitoneal lymphadenopathy was completely disappeared and according to the resolution of lymphadenopathy hemolytic anemia was also improved.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Vincristina
/
Biopsia
/
Fibrosis
/
Linfocitos T
/
Doxorrubicina
/
Histiocitosis Sinusal
/
Linfoma de Células T
/
Quimioterapia
/
Anemia Hemolítica
/
Ganglios Linfáticos
Límite:
Femenino
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Hematology
Año:
1999
Tipo del documento:
Artículo
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