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