INTRODUCTIONAcute leukemias are one of the most common malignancies in children aged <15 years, accounting for nearly 30%. Though several risk factors have been proposed, a specific etiology has not been determined till date. Fortunately, it is one of the curable malignancies in children and hence early diagnosis is essential.Studies from India have reported variable outcomes, with few specialized centers showing a favourable outcome in more than 70%.1 Not all children have access to the regional Cancer Institutes of India. Children managed at other centers must also receive a minimum standard of care. Multiple poor prognostic factors are described in ALL such as age <1 year or >10 years, male sex, very high leukocyte count, mature B-cell type and T-cell type of ALL, chromosomal abnormalities {ex: t (9;22) or t (4;11)}, which when present have a high chance of relapse and mortality. Whether the risk factors in our population are similar or any other unique risk factor operates in our patients, has to be confirmed.Flowcytometry has now become a standard tool for diagnosing and monitoring acute as well as chronic leukemia. Immunophenotyping by flow cytometry enables accurate diagnosis and treatment on the basis of which further treatment is planned. Immunophenotyping ABSTRACT Background: Acute leukemia contributes to nearly one third of the pediatric malignancies. For effective management of a curable malignancy, the epidemiology of childhood leukemias and audit of previously treated patients would be required. The objective was to study the clinical and immunophenotypic pattern of acute leukemia in children <12 years of age admitted in a tertiary centre. Methods: Prospective study done on 31 children, diagnosed as leukemia and treated over a period of 3 years in GRH, Madurai. Detailed history analysis, clinical examination, lab investigations including flowcytometry were done. Results: ALL was the most common acute leukemia in children (90.3%). 85.7% were identified as B-cell and 14.3% as T-cell. Of the B-ALL, 87.5% was pre-B, 8.3% pro-B and 4.2% mature B ALL. Myeloid antigen co-expression was seen in 35.7%. Fever was the most common symptom (87%) and hepatosplenomegaly was the most common sign (>90%). Poor outcome was noted in 42.3%. T-cell appeared to have worse prognosis than B-cell but did not retain independent prognostic significance in univariate analysis. Conclusions: B-ALL was more common than T-ALL. Extra medullary organ involvement indicates increased tumor burden and poor outcome. None of the clinical or laboratory parameters appeared to predict poor outcomes in our study and this may be due to small sample size. This study provides an insight into the data regarding the epidemiology, clinicopathologic feature and outcome of acute leukemia in a center with low resource settings.