Pregled bibliografske jedinice broj: 467439
T-Lymphoblastic Lymphoma With an Unusual t(8 ; 14)(q24 ; q11) - Case Report
T-Lymphoblastic Lymphoma With an Unusual t(8 ; 14)(q24 ; q11) - Case Report // Knjiga sažetaka, 4. Hrvatski kongres kliničke citologije, 1. Hrvatski simpozij analitičke citologije i 2. Hrvatski simpozij citotehnologije s međunarodnim sudjelovanjem / Kardum-Skelin, Ika ; Batinić, Drago ; Anić, Veronika (ur.).
Zagreb: Hrvatsko društvo za kliničku citologiju ; Hrvatska udruga citotehnologa, 2009. (predavanje, međunarodna recenzija, sažetak, stručni)
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Naslov
T-Lymphoblastic Lymphoma With an Unusual t(8 ; 14)(q24 ; q11) - Case Report
Autori
Mandac, Inga ; Ostojić-Kolonić, Slobodanka ; Vrhovac, Radovan ; Lasan-Trčić, Ruživa ; Jakelić-Piteša, Jasminka ; ardum-Skelin, Ika
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
Knjiga sažetaka, 4. Hrvatski kongres kliničke citologije, 1. Hrvatski simpozij analitičke citologije i 2. Hrvatski simpozij citotehnologije s međunarodnim sudjelovanjem
/ Kardum-Skelin, Ika ; Batinić, Drago ; Anić, Veronika - Zagreb : Hrvatsko društvo za kliničku citologiju ; Hrvatska udruga citotehnologa, 2009
Skup
4. Hrvatski kongres kliničke citologije, 1. Hrvatski simpozij analitičke citologije i 2. Hrvatski simpozij citotehnologije s međunarodnim sudjelovanjem
Mjesto i datum
Split, Hrvatska, 11.10.2009. - 14.10.2009
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
T-lymphoblastic lymphoma; cytogenetics; t(8; 14)(q24; q11.2)
Sažetak
Cytogenetic abnormalities seen at presentation of acute lymphoblastic leukemia or lymphoblastic lymphoma (ALL/ LBL) are associated with distinct clinical and hematologic disease entities. T-ALL/LBL are morphologically indistinguishable from those of B-ALL/LBL. An abnormal kariotype is found in 50–70% of cases of T-ALL/LBL. We present a 35-year old male patient with T-ALL/LBL and t(8 ; 14)(q24 ; q11.2). Our patient presented with B-symptoms, bulky mediastinal disease and CNS infiltration. Bone marrow was morphologically normal and cytogenetically without clonal aberrations. ytological findings of the supraclavicular lymph node showed numerous CD3 positive (100%) and CD2 positive (88%) lymphoblasts, negative for CD34 and CD10. Flow cytometry of lymph node revealed T cell phenotype of immature cells: CD45+CD2+CD5+CD7+CD4+CD8+CD3cyt +CD3TdT+CD10-CD34-HLAD/DR-. Cytogenetic analysis of lymph node showed translocation t(1 ; 4)(p32 ; p12), t(8 ; 14)(q24 ; q11.2). Southern blot analysis of extracted DNA from the supraclavicular lymph node demonstrated clonal rearrangement of the T cell antigen receptor (TCR/J) gene (region Vb+Jb2). Based on these findings, diagnosis of T lymphoblastic non Hodgkin lymphoma was established. Cerebrospinal fluid analysis showed CNS infiltration with 49% lymphoblasts positive for CD4 and CD8. The disease progressed rapidly with poor response to therapy. T-ALL/LBL with an unusual t(8 ; 14)(q24 ; q11.2) is a very rare hematologic disorder with rapid disease progression and poor response to conventional therapy because of frequent central nervous system involvement and early relapses.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
108-1081873-1893 - Prognostički faktori, dijagnostika i terapija hemoblastoza (Jakšić, Branimir, MZOS ) ( CroRIS)
198-1980955-0953 - Imunobiologija kronične B-limfocitne leukemije i mikrookoliš (Jakšić, Ozren, MZOS ) ( CroRIS)
Ustanove:
Klinička bolnica "Merkur",
Medicinski fakultet, Zagreb,
Medicinski fakultet, Split
Profili:
Jasminka Jakelić-Piteša
(autor)
Inga Mandac Smoljanović
(autor)
Slobodanka Ostojić Kolonić
(autor)
Radovan Vrhovac
(autor)