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

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Clinical Cytology - Oral Presentations<br />

DIFFUSE LARGE B-CELL LYMPHOMA IN PATIENT AFTER TREATMENT OF<br />

ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA<br />

Džeko-Škugor N1 , Perić Z2 , Vrhovac R2 , Radić-Krišto D2 , Kardum-Skelin I3 , Jakšić B2 1 General Hospital Šibenik, Department of Cytology, Šibenik<br />

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

3Merkur University Hospital, Department of Medicine, Laboratory for Cytology and<br />

Hematology, Zagreb,Croatia<br />

Relatively few cases of Epstein-Barr (EBV)-positive B-cell lymphomas arising in patients<br />

with angioimmunoblastic T-cell lymphoma (AITL) have been reported, the most common<br />

of them diffuse large B-cell lymphoma (DLBCL).We report a case of angioimmunoblastic<br />

T-cell lymphoma in which diffuse large B-cell lymphoma arose 13 months after the<br />

initial diagnosis of AITL. A 36-year-old female patient was evaluated in March and April<br />

2008 with moderate leukocytosis, peripheral and abdominal lymphadenopathy. AITL was<br />

diagnosed after a fine-needle aspiration cytology (FNAC) of the enlarged cervical and<br />

supraclavicular lymph nodes was performed and confirmed by an immunophenotyping<br />

and biopsy of the cervical lymph nodes. The patient recieved chemotherapy regimen<br />

FED (fludarabine, endoxane, dexamethasone) and autologous hematopoietic stem cells<br />

transplantation was done. In April 2009 the patient was hospitalized because of fever,<br />

pancytopenia, hyperbilirubinemia and peripheral lymphadenopathy. A computed tomography<br />

(CT) study showed enlarged mediastinal and abdominal lymph nodes. A relapse of<br />

non-Hodgkin lymphoma (NHL) was suspected. The FNAC of the enlarged cervical lymph<br />

nodes was performed again, but this time the smears were composed of polymorphous<br />

population of lymphocytes with the predomination of large cells, CD20¬+ on immunocytochemical<br />

stains. The immunophenotyping confirmed a predomination of monoclonal<br />

mature B-cells. Serologic testing revealed increased titers of EBV VCA IgG and EBV<br />

EBNA IgG; the plasma EBV DNA levels were also increased. The patient showed a positive<br />

response to an additional chemotherapy regimen CHOP-R (cyclophosphamide, doxorubicin,<br />

vincristine, prednisone and rituximab) and there is the possibility of allogenic<br />

stem cell transplantation. AITL is a rare lymphoproliferative disorder in which the neoplastic<br />

T-cells represent the minority of the lymph node cell population and almost all<br />

cases harbor EBV-infected B-cells. Various authors postulated that immunodeficiency<br />

in AITL patients together with immunosupresive efects of cytotoxic drugs, may be responsible<br />

for EBV-induced proliferation of latently or newely EBV-infected B-cells with<br />

eventual clonal selection and proggresion to aggressive B-cell lymphoma.<br />

nivesdzeko@gmail.com<br />

77<br />

4 th <strong>Croatian</strong> <strong>Congress</strong> of Clinical Cytology / 1 st <strong>Croatian</strong> Symposium of Analytical Cytology / 2 nd <strong>Croatian</strong> Symposium of Cytotechnology

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