T-Cell Lymphoma with Rosai-Dorfman Syndrome-Like Feature / 대한혈액학회지
Korean Journal of Hematology
;
: 153-156, 1999.
Artigo
em 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:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Vincristina
/
Biópsia
/
Fibrose
/
Linfócitos T
/
Doxorrubicina
/
Histiocitose Sinusal
/
Linfoma de Células T
/
Tratamento Farmacológico
/
Anemia Hemolítica
/
Linfonodos
Limite:
Feminino
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Hematology
Ano de publicação:
1999
Tipo de documento:
Artigo
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