inv(18)(p11q21)
2008-06-01 Jean-Loup Huret   Affiliation1.Genetics, Dept Medical Information, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France
Clinics and Pathology
Disease
Myelodysplastic syndrome and non Hodgkin lymphoma.
Epidemiology
Four cases are available to date: an indolent B-cell follicular lymphoma, a non Hodgkin lymphoma (NHL) not otherwise specified (NOS), a refractory anemia (RA) possibly related to the treatment of a multiple myeloma diagnosed 4 years before, and a refractory anemia with excess of blasts in transformation (RAEB-t) evolving rapidly towards an acute myeloid leukemia (AML). There were 2 male and 2 female patients, aged 70, 70, 76 and ? (Fan et al., 1988; Avanzi et al., 1989; Fan and Rizkalla, 2003; Adeyinka et al., 2007).
Prognosis
Data on (short term) evolution is only available in the two myeloid cases: the RA case remained well 4 months after diagnosis, while the RAEB-t/AML case died shortly after diagnosis.
Genes Involved and Proteins
Note
Genes involved in this structural anomaly are unknown.
Article Bibliography
| Pubmed ID | Last Year | Title | Authors |
|---|---|---|---|
| 17321329 | 2007 | Loss of 17p is a major consequence of whole-arm chromosome translocations in hematologic malignancies. | Adeyinka A et al |
| 2792325 | 1989 | Trisomy 11 in myelodysplastic syndrome-derived acute myeloblastic leukaemias. | Avanzi GC et al |
| 3422038 | 1988 | An acquired Robertsonian translocation dic(14;14)(p11;p11) in a patient with a myelodysplastic syndrome following treatment of multiple myeloma. | Fan YS et al |
| 12742158 | 2003 | Comprehensive cytogenetic analysis including multicolor spectral karyotyping and interphase fluorescence in situ hybridization in lymphoma diagnosis. a summary of 154 cases. | Fan YS et al |
Summary
Note
The anomaly is found in heterogeneous diseases, but the cases present some surprisingly similar cytogenetic features.
Citation
Jean-Loup Huret
inv(18)(p11q21)
Atlas Genet Cytogenet Oncol Haematol. 2008-06-01
Online version: http://atlasgeneticsoncology.org/haematological/1545/inv(18)(p11q21)
