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4. Hrvatski kongres kliniËke citologije 4th Croatian Congress ... - Penta

4. Hrvatski kongres kliniËke citologije 4th Croatian Congress ... - Penta

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<strong>4.</strong> <strong>Hrvatski</strong> <strong>kongres</strong> <strong>kliniËke</strong> <strong>citologije</strong> / 1. <strong>Hrvatski</strong> simpozij analitiËke <strong>citologije</strong> / 2. <strong>Hrvatski</strong> simpozij citotehnologije<br />

90<br />

Klinička citologija - Usmena predavanja<br />

T LYMPHOBLASTIC LEUKEMIA WITH AN UNUSUAL BURKITT LYMPHOMA<br />

MORPHOLOGY - A CASE REPORT<br />

Milas M1 , Jelić Puškarić B1 , Planinc-Peraica A2 , Šiftar Z3 , Kardum-Skelin I1 , Jakšić B2 1Merkur University Hospital, Department of Medicine, Laboratory for Cytology and<br />

Hematology, Zagreb, Croatia<br />

2 Merkur University Hospital, Department of Medicine, Zagreb, Croatia<br />

3 Merkur University Hospital, Institute of Clinical Chemistry, Zagreb, Croatia<br />

Precursor T- cell acute lymphoblastic leukaemia (T-ALL)/lymphoma (T-LBL) is a neoplasm<br />

committed to the T-cell lineage. It comprises about 20 – 25% of adult cases of<br />

ALL and about 85 - 90% of LBL. In adults it is still a disease with poor prognosis with<br />

median survival to 12 months in spite of progress made in understanding its pathogenesis<br />

and treatment. Complications such as infections, sepsis, meningeal involvement<br />

can occur at any time during treatment and be the cause of fatal outcome. We report a<br />

case of a 56-year-old male who was hospitalized due to high fever and kidney infection.<br />

Further examination showed anemia, thrombocytopenia, normal level of white blood<br />

cells and high level of lactat-dehidrogenase (LDH). Bone marrow aspiration revealed<br />

87% and peripheral blood 41% of lymphoblasts with cytoplasmic vacuoles which suggested<br />

Burkitt lymphoma morphology. Patient’s karyotype showed no chromosomal aberations.<br />

Identification of immunophenotype discovered cells which were CD2 positive<br />

and CD20 negative with focal acid phosphatase activity in 67% of blasts. This excluded<br />

Burkitt lymphoma and led to diagnosis of T-ALL. Patient was submitted to a numerous<br />

chemotherapy treatments and autologous stem cell transplantation. Despite these<br />

efforts, complicatons of disease (infection and pleural effusion) led to fatal outcome<br />

after 10 months from diagnosis. Our case report showed how morphology alone can be<br />

misleading and is not enough in diagnosing ALL. Beside morphologic criteria, setting<br />

correct diagnosis depends on identification of immunophenotype by flow cytometry and<br />

cytogenetic-molecular abnormalities. Further improvements in the molecular definition<br />

of ALL subtypes, development of new and targeted drugs will improve patient’s outcome<br />

and prognosis.<br />

marina.milas@gmail.com

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