𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Translocation t(8;13)(p11;q11-12) in stem cell leukemia/lymphoma of t-cell and myeloid lineages

✍ Scribed by Rizwan Naeem; Samuel Singer; Jonathan A. Fletcher


Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
303 KB
Volume
12
Category
Article
ISSN
1045-2257

No coin nor oath required. For personal study only.

✦ Synopsis


An unusual hematologic neoplasia has been described recently in which the predominant clinical features include T-cell lymphoma, myeloid hyperplasia, and eosinophilia. The multilineage involvement in this disorder suggests transformation of a primitive stem cell. Abnormal karyotypes have been described in three such cases, including one case with t(8; I3)(p I I .2;q 12) and a second case with t(8; I 3)(p23;q 14). We report translocation of chromosomes 8 and I 3 in lymph node karyotypes from two patients with this syndrome. Fluorescence in situ hybridization confirmed an identical translocation, t(8; I 3)(p I I ;q I I -I2), in lymphoma cells from each patient. The translocation breakpoints are of particular interest because the FLJ3 receptor tyrosine kinase gene has been mapped to 13q 12. FLT3 is expressed highly in hematopoietic progenitor cells and in myeloid and lymphoid acute leukemias. Genes Chromosom Cancer 12: 148-15 I ( I 995);


πŸ“œ SIMILAR VOLUMES


t(10;11)(p13–14;q14–21): A New Recurrent
✍ Groupe FranΓ§ais de CytogΓ©nΓ©tique HΓ©matologique (GFCH) πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 412 KB

A workshop held by the "Groupe Frangais de Cytogenetique Hematologique" has identified a t ( I 0 I I)(p I 3-1 4;q 14-2 I) in four acute lyrnphoblastic leukemias of T-cell lineage. The immunophenotypes were consistent with immature thymocytes. This translocation is therefore a new candidate for a rec

Detection of 14q32.33 translocation and
✍ Teruyuki Takashima; Mototoshi Itoh; Yutaka Ueda; Kazuhiro Nishida; Toshiharu Tam πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 French βš– 178 KB πŸ‘ 1 views

Abnormalities of chromosome 14 involving band q32.33 are among the most commonly observed cytogenetic alterations in B-cell malignancies. To assess the incidence and pathogenetic implications of 14q32.33 translocation in chronic B-cell leukemia/lymphomas, we performed fluorescence in situ hybridizat

Human homeobox gene HOXC13 is the partne
✍ Roberta La Starza; Maurizio Trubia; Barbara Crescenzi; Caterina Matteucci; Massi πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 123 KB

## Abstract The chimeric gene __NUP98/HOXC13__ was detected in a patient with a de novo acute myeloid leukemia and a t(11;12)(p15;q13). Fluorescence in situ hybridization with PAC1173K1 identified the breakpoint on 11p15, indicating that the __NUP98__ gene was involved in the translocation. At 12q1

CBFB and MYH11 in inv(16)(p13q22) of acu
✍ Allison B. Weckerle; Madhumita Santra; Maggie C.Y. Ng; Patrick P. Koty; Yuh-Hwa πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 265 KB

## Abstract To gain a better understanding of the mechanism of chromosomal translocations in cancer, we investigated the spatial proximity between __CBFB__ and __MYH11__ genes involved in inv(16)(p13q22) found in patients with acute myeloid leukemia. Previous studies have demonstrated a role for sp

Characterization of the breakpoints in a
✍ Olga Chernova; Ivan Still; Matt Kalaycio; Gerald Hoeltge; John K. Cowell πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 199 KB πŸ‘ 1 views

We used fluorescence in situ hybridization to characterize the molecular position of the breakpoints in a t(8;13)(p11;q12) reciprocal translocation from a patient with an atypical myeloproliferative disorder. This structural chromosome abnormality is characteristic of this specific disease and occur