ABSTRACT
Between 1989 and 1995, 42 cases with acute lymphoblastic leukemia [18 males and 24 females] were diagnosed in our institution. Median age was 38.5 years [range, 16-88 years]. Leukocyte count was more than 30.10 9/l in 54 percent of cases. According to the French-American-British [FAB] criteria, 67 percent were classified L1 and 33 percent L2. Sixteen patients were treated with 12LA80 protocol, 14 patients with LALA 85 protocol, 6 patients with LALA 87 protocol and 6 patients with EORTC protocol. Complete remission was achieved in 22 cases [52 percent], 8 cases [20 percent] failed to respond and 12 [28 percent] died during induction. Relapse was observed in 10 cases. The 4-year survival rate was 28 percent confirming the worse prognosis of this leukemia when treated with standard chemotherapy
Subject(s)
Humans , Male , Female , Retrospective Studies , Precursor Cell Lymphoblastic Leukemia-Lymphoma , Precursor Cell Lymphoblastic Leukemia-Lymphoma , AdultABSTRACT
Between 1989 and 1996,21 cases with acute non lymphoblastic leukemia [11 males and 10 females] were diagnosed in our institution. Median age was 9 years [range, 2-15 years]. leukocyte count was more than 50.109/1 in 47% of cases. According to the French-American-British [FAB] criteria, 7 cases were classified M 1, 10 cases were classified M2, 1 classified M4Eo and 3 classified M5. All patients were treated with" 7+3 " protocol and complete remission was achieved in 17 cases [80%], 2 cases [10%] Failed to respond and 2 [10%] died during induction. Relapse was observed in 15 cases. The 3-year survival rate was 20% and the relapse-free survival rate was 12% confirming the worse prognosis of this leukemia when treated with standard chemotherapy
Subject(s)
Humans , Male , Female , Leukemia, Myeloid, Acute/classification , Leukemia, Myeloid, Acute/therapy , ChildABSTRACT
Between 1989 and 1996, 40 cases with acute leukemia [16 males and 24 females] were diagnosed in out institution. Median age was 65 years [range, 56- 88 years]. Leukocyte count was more than 30.109/1 in 42 percent of cases. According to the French-American-British [FAB] criteria, 11 cases were classified lymphoblastic and 29 myeloblastic. Sixteen patients have received palliative treatment because of there age and there bad performance status. Only 24 patients have received curative treatment. Complete remission was achieved in 12 cases [50 percent], 5 cases [20 percent] failed to respond and 7 [30 percent] died during induction. Relapse was observed in 8 cases. The 2-year survival rate was 10 percent confirming the worse prognosis of the acute leukemia in elderly
Subject(s)
Humans , Male , Female , Acute Disease , Leukemia/classification , Leukemia/therapy , AgedABSTRACT
Myelofibrosis is rarely associated with myelodysplastic syndrome. This association constitute a distinct clinicopathological entity which is difficult to be distinguished from other forms of myelofibrosis. We report six cases of this entity. Patients were aged between 50 and 79 years, with 3 males and 3 females. All these patients had similar clinical features consisting of pancytopenia and absent visceral enlargement. The analysis of bone marrow aspirate was difficult
Subject(s)
Humans , Male , Female , Primary Myelofibrosis/diagnosis , PancytopeniaABSTRACT
Pseudomonas aeruginosa is one of the most dangerous agents in neutropenic patients. Twenty two septicemia due to P. Aeruginosa occuring in neutropenic patients were analyzed. Fifty nine% of the patients had acute leukemia and more than two - thirds of the patients had severe neutropenia [less than 500 neutrophils / mm3]. The outcome was unfavorable with a high mortality rate