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Unusual chromosome aberration, t(13;14)(q32;q32.3), in a case of essential thrombocythemia with extreme thrombocytosis
A case of essential thrombocythemia (ET) with extreme thrombocytosis in a 70-year-old male patient is described. The cytogenetic analysis revealed a pathologic clone with the following previously unreported, unusual karyotype: 46,XY,t(13;14)(q32;q32.3) and pericentric inversion of chromosome 9. The...
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| Published in: | Cancer genetics and cytogenetics 1996-10, Vol.91 (1), p.68-70 |
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| Main Authors: | , , , |
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| Language: | English |
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| cited_by | cdi_FETCH-LOGICAL-c389t-3432dce431bbefb3a26d7368fb8df86f39d7c0d38620a17d67ee03ec436ceb523 |
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| cites | cdi_FETCH-LOGICAL-c389t-3432dce431bbefb3a26d7368fb8df86f39d7c0d38620a17d67ee03ec436ceb523 |
| container_end_page | 70 |
| container_issue | 1 |
| container_start_page | 68 |
| container_title | Cancer genetics and cytogenetics |
| container_volume | 91 |
| creator | Mitev, Lubomir Georgiev, George Petrov, Angel Manolova, Yanka |
| description | A case of essential thrombocythemia (ET) with extreme thrombocytosis in a 70-year-old male patient is described. The cytogenetic analysis revealed a pathologic clone with the following previously unreported, unusual karyotype: 46,XY,t(13;14)(q32;q32.3) and pericentric inversion of chromosome 9. The possible association of t(13;14) with the high platelet count is discussed. |
| doi_str_mv | 10.1016/S0165-4608(96)00153-7 |
| format | article |
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The cytogenetic analysis revealed a pathologic clone with the following previously unreported, unusual karyotype: 46,XY,t(13;14)(q32;q32.3) and pericentric inversion of chromosome 9. The possible association of t(13;14) with the high platelet count is discussed.</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Chromosome Aberrations - genetics</subject><subject>Chromosome Inversion</subject><subject>Chromosomes, Human, Pair 13 - genetics</subject><subject>Chromosomes, Human, Pair 14 - genetics</subject><subject>Chromosomes, Human, Pair 9 - genetics</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Karyotyping</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Platelet diseases and coagulopathies</subject><subject>Thrombocythemia, Essential - complications</subject><subject>Thrombocythemia, Essential - genetics</subject><subject>Thrombocytosis - complications</subject><subject>Thrombocytosis - genetics</subject><subject>Translocation, Genetic - genetics</subject><issn>0165-4608</issn><issn>1873-4456</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNqFkM1q3DAURkVpSSdpHyGgRSkzEKeSJUsyWZQS-geBLtqshSxfMyq2lejKafP20WSG6bILSYvv3O-KQ8g5Z5eccfXhZ7maSipm1q3aMMYbUekXZMWNFpWUjXpJVkfkNTlF_M0Y03WrTsiJaZnhmq3Iw-284OJG6rcpThHjBNR1kJLLIc4XNK-5uOJys74X9VU5l2JzQcNMHfUOgcaBAiLMOZSKvKvoon_MW5iCo39C3lL4mxOU0n9hxIBvyKvBjQhvD-8Zuf3y-df1t-rmx9fv159uKi9MmyshRd17kIJ3HQydcLXqtVBm6Ew_GDWIttee9cKomjmue6UBmAAvhfLQNbU4I-_3vXcp3i-A2U4BPYyjmyEuaLVpeKO5LGCzB32KiAkGe5fC5NKj5czufNtn33Yn07bKPvu2usydHxYs3QT9ceoguOTvDrlD78YhudkHPGK11LJlomAf9xgUGQ8BkkUfYPbQhwQ-2z6G_3zkCY_1nGI</recordid><startdate>19961001</startdate><enddate>19961001</enddate><creator>Mitev, Lubomir</creator><creator>Georgiev, George</creator><creator>Petrov, Angel</creator><creator>Manolova, Yanka</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19961001</creationdate><title>Unusual chromosome aberration, t(13;14)(q32;q32.3), in a case of essential thrombocythemia with extreme thrombocytosis</title><author>Mitev, Lubomir ; Georgiev, George ; Petrov, Angel ; Manolova, Yanka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-3432dce431bbefb3a26d7368fb8df86f39d7c0d38620a17d67ee03ec436ceb523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Chromosome Aberrations - genetics</topic><topic>Chromosome Inversion</topic><topic>Chromosomes, Human, Pair 13 - genetics</topic><topic>Chromosomes, Human, Pair 14 - genetics</topic><topic>Chromosomes, Human, Pair 9 - genetics</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Karyotyping</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Platelet diseases and coagulopathies</topic><topic>Thrombocythemia, Essential - complications</topic><topic>Thrombocythemia, Essential - genetics</topic><topic>Thrombocytosis - complications</topic><topic>Thrombocytosis - genetics</topic><topic>Translocation, Genetic - genetics</topic><toplevel>online_resources</toplevel><creatorcontrib>Mitev, Lubomir</creatorcontrib><creatorcontrib>Georgiev, George</creatorcontrib><creatorcontrib>Petrov, Angel</creatorcontrib><creatorcontrib>Manolova, Yanka</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer genetics and cytogenetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mitev, Lubomir</au><au>Georgiev, George</au><au>Petrov, Angel</au><au>Manolova, Yanka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Unusual chromosome aberration, t(13;14)(q32;q32.3), in a case of essential thrombocythemia with extreme thrombocytosis</atitle><jtitle>Cancer genetics and cytogenetics</jtitle><addtitle>Cancer Genet Cytogenet</addtitle><date>1996-10-01</date><risdate>1996</risdate><volume>91</volume><issue>1</issue><spage>68</spage><epage>70</epage><pages>68-70</pages><issn>0165-4608</issn><eissn>1873-4456</eissn><coden>CGCYDF</coden><abstract>A case of essential thrombocythemia (ET) with extreme thrombocytosis in a 70-year-old male patient is described. The cytogenetic analysis revealed a pathologic clone with the following previously unreported, unusual karyotype: 46,XY,t(13;14)(q32;q32.3) and pericentric inversion of chromosome 9. The possible association of t(13;14) with the high platelet count is discussed.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>8908170</pmid><doi>10.1016/S0165-4608(96)00153-7</doi><tpages>3</tpages></addata></record> |
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| identifier | ISSN: 0165-4608 |
| ispartof | Cancer genetics and cytogenetics, 1996-10, Vol.91 (1), p.68-70 |
| issn | 0165-4608 1873-4456 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_78515714 |
| source | ScienceDirect Freedom Collection |
| subjects | Aged Biological and medical sciences Chromosome Aberrations - genetics Chromosome Inversion Chromosomes, Human, Pair 13 - genetics Chromosomes, Human, Pair 14 - genetics Chromosomes, Human, Pair 9 - genetics Hematologic and hematopoietic diseases Humans Karyotyping Male Medical sciences Platelet diseases and coagulopathies Thrombocythemia, Essential - complications Thrombocythemia, Essential - genetics Thrombocytosis - complications Thrombocytosis - genetics Translocation, Genetic - genetics |
| title | Unusual chromosome aberration, t(13;14)(q32;q32.3), in a case of essential thrombocythemia with extreme thrombocytosis |
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