A case of primary T cell lymphoma of the liver presented as FUO / 대한내과학회지
Korean Journal of Medicine
;
: 260-265, 2001.
Artigo
em Coreano
| WPRIM
| ID: wpr-99485
ABSTRACT
Primary non-Hodgkin's lymphoma of the liver, an organ normally devoid of a native lymphoid tissue, is very rare. We report a case of primary hepatic T-cell lymphoma in a 18-year-old girl, with review of literature. The pateint admitted with fever for 5 months. The ultrasonography revealed a 10 x 7 cm sized mass in the left lobe of the liver. On abdominal CT, the mass was poorly enhancing and low attenuated. On MRI, the signal intensity of the mass was low in T1 weighted image, heterogeneously high in T2 weighted image, and peripherally enhanced in contrast enhancing T1 weighted image. The biopsy specimen obtained by laparatomy showed anaplastic tumor. The malignant cells were positive for T-cell lineage (CD3, CD44, CD45RO). There was no evidence of the lymphoma in other regions. The patient was treated with CHOP (cyclophosphamide, adriamycin, vincristine and prednisolone) chemotherapy without objective response. The patient died of sudden cardiogenic shock.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Choque Cardiogênico
/
Vincristina
/
Biópsia
/
Linfoma não Hodgkin
/
Imageamento por Ressonância Magnética
/
Linfócitos T
/
Doxorrubicina
/
Tomografia Computadorizada por Raios X
/
Linfoma de Células T
/
Ultrassonografia
Tipo de estudo:
Estudo diagnóstico
Limite:
Adolescente
/
Feminino
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Medicine
Ano de publicação:
2001
Tipo de documento:
Artigo
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