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Cytology and flow cytometry of angioimmunoblastic T-cell lymphoma


Trutin Ostović, Karmen; Hariš, Višnja; Miletić, Zorana; Lukšić, Ivica; Pandžić Jakšić, Vlatka; Jakšić, Ozren
Cytology and flow cytometry of angioimmunoblastic T-cell lymphoma // Abstracts of the 36th European Congress of Cytology ; u: Cytopathology 22 (2011) (S1) 1-194 ; Posters 55-183
Istanbul, Turska, 2011. str. 157-157 (poster, međunarodna recenzija, sažetak, stručni)


Naslov
Cytology and flow cytometry of angioimmunoblastic T-cell lymphoma

Autori
Trutin Ostović, Karmen ; Hariš, Višnja ; Miletić, Zorana ; Lukšić, Ivica ; Pandžić Jakšić, Vlatka ; Jakšić, Ozren

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni

Izvornik
Abstracts of the 36th European Congress of Cytology ; u: Cytopathology 22 (2011) (S1) 1-194 ; Posters 55-183 / - , 2011, 157-157

Skup
European Congress of Cytology (36 ; 2011)

Mjesto i datum
Istanbul, Turska, 22.-25.09.2011

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
Angioimmunoblastic T-cell lymphoma; cytopathology; flow-cytometry

Sažetak
Aim was to present angioimmunoblastic T-cell lymphoma (AILT). According to WHO classification it is a peripheral T-cell lymphoma characterised by systemic disease, a polymorphous inflitrate involving lymph nodes with a prominent proliferation of high endothelial venules and follicular dendritic cells. It is usually a challenge for cytologists due to its heterogeneity and morphological similarity to reactive lymphadenopathia. 63-years old male suffered from generalised limphadenopathia, rash, dysproteinaemia and hepatosplenomegaly. Fine needle aspiration cytology of nodes on the neck and arm was performed. One part was used for cytological analysis and another one for DNA analysis and immunophenotyping by flow-cytometry. The smears consists of lots of mixed polymorphic cells: immunoblasts, plasma cells, eosinophilic granulocytes, histiocytes, endothelial cells, mastocytes and small to medium-sized lymphocytes with clear to pale cytoplasm and distinct cell membranes and minimal cytological atypia or reactive lymphocytes. DNA analysis done by flow cytometry showed aneuploidy with high proliferation, and immunophenotyping showed high CD5, CD3, CD2, CD10 and HLA-DR. Bone marrow aspirate was inflitrated by the same population of cells detected in lymph nodes' aspirates. Cytological diagnosis of possible AILT was established and confirmed by histopathology. The patient has been treated for 7 years in Germany because of lymphogranulomatosis X before arriving to our hospital. In our hospital he got chemotherapy and enlarged lymph nodes were cured. Despite that after 17 months the patient died in IV B stage of the disease. Cytology with flow cytometry and clinical data can put the exact diagnosis and follow-up of angioimmunoblastic lymphoma.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti

Napomena
DOI: 10.1111/j.1365-2303.2011.00911.x



POVEZANOST RADA


Ustanove
Klinička bolnica "Dubrava",
Zdravstveno veleučilište, Zagreb

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE