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1.
Korean Journal of Hematology ; : 153-156, 1999.
Article in Korean | 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.


Subject(s)
Female , Humans , Anemia, Hemolytic , Biopsy , Doxorubicin , Drug Therapy , Fibrosis , Histiocytosis, Sinus , Lymph Nodes , Lymphatic Diseases , Lymphoma, T-Cell , T-Lymphocytes , Vincristine
2.
Korean Journal of Nephrology ; : 788-792, 1997.
Article in Korean | WPRIM | ID: wpr-124259

ABSTRACT

We present a case of liposarcoma related with minimal change nephrotic syndrome. A 49-year-old woman was admitted due to generalized edema and a palpable mass at epigastric area. Her laboratory data were as follows : serum creatinine 0.6mg/dl, BUN 7mg/dl, serum total protein 3.6g/dl(albumin 0.6 g/dl) serum total cholesterol 299mg/dl, 24 hour-urine protein 5.1g. A CT scan of the abdomen revealed huge adult head sized mass(15X10X15cm) consisted with mixed pattern of well enhancing solid, cystic and fat portion which is located between the liver and the stomach. A kidney biopsy showed minimal change nephropathy. At explo-laparostomy the tumor was well differentiated liposarcoma. After operation and steroid therapy, her proteinuria and hypoalbuminemia were a little improved. And then radiation therapy(daily 180 cGy, 5 fx/wk, upto 5040cGy/28 fx/42 day) was done. Complete remission of liposarcoma was followed by regression of the nephrotic syndrome. After radiation therapy, her laboratory data were serum total protein 6.7g/dl (albumin 4.3g/dl), total cholesterol 170mg/dl, 24 hour-urine protein 0.3g. She has been maintained complete remission of the nephrotic syndrome by steroid maintenance dose.


Subject(s)
Adult , Female , Humans , Middle Aged , Abdomen , Biopsy , Cholesterol , Creatinine , Edema , Head , Hypoalbuminemia , Kidney , Liposarcoma , Liver , Nephrosis, Lipoid , Nephrotic Syndrome , Proteinuria , Stomach , Tomography, X-Ray Computed
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