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Aggressive Clinicopathological Course of Myeloma with t(3;16) (q21;q22) Cytogenetic Abnormality
Multiple myeloma (MM) is a heterogeneous disease and patients present with a wide variety of cytogenetic anomalies reflecting the nature of the disease [1]. The aim of this letter is to report a rare karyotypic abnormality with an aggressive clinical course of MM. A 56-year-old male patient was admi...
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Published in: | Turkish journal of haematology 2019-02, Vol.36 (1), p.62-63 |
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container_title | Turkish journal of haematology |
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creator | Bozkurt, Süreyya Okay, Müfide Haznedaroğlu, İbrahim |
description | Multiple myeloma (MM) is a heterogeneous disease and
patients present with a wide variety of cytogenetic anomalies
reflecting the nature of the disease [1]. The aim of this letter
is to report a rare karyotypic abnormality with an aggressive
clinical course of MM.
A 56-year-old male patient was admitted to the neurosurgery
clinic with dorsal shoulder pain and inability to walk in April 2011.
He underwent thoracic and lumbar spinal magnetic resonance
imaging. Laminectomy was performed on the patient upon
detecting masses at the levels of the first and seventh thoracic
vertebrae. The patient was referred to our center when he was
determined to have “lymphoma” based on the first evaluation of his biopsy material. |
doi_str_mv | 10.4274/tjh.galenos.2018.2018.0049 |
format | article |
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patients present with a wide variety of cytogenetic anomalies
reflecting the nature of the disease [1]. The aim of this letter
is to report a rare karyotypic abnormality with an aggressive
clinical course of MM.
A 56-year-old male patient was admitted to the neurosurgery
clinic with dorsal shoulder pain and inability to walk in April 2011.
He underwent thoracic and lumbar spinal magnetic resonance
imaging. Laminectomy was performed on the patient upon
detecting masses at the levels of the first and seventh thoracic
vertebrae. The patient was referred to our center when he was
determined to have “lymphoma” based on the first evaluation of his biopsy material.</description><identifier>ISSN: 1300-7777</identifier><identifier>EISSN: 1308-5263</identifier><identifier>DOI: 10.4274/tjh.galenos.2018.2018.0049</identifier><identifier>PMID: 29726398</identifier><language>eng</language><publisher>Turkey: Türk Hematoloji Derneği</publisher><subject>cytogenetic abnormality ; Letters to the Editor ; multiple myeloma ; rare translocations ; Tıp</subject><ispartof>Turkish journal of haematology, 2019-02, Vol.36 (1), p.62-63</ispartof><rights>Copyright 2019 by Turkish Society of Hematology / Turkish Journal of Hematology, Published by Galenos Publishing House. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-1765-9894 ; 0000-0001-8028-9462 ; 0000-0001-5317-0597</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6373501/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6373501/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29726398$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Küçükkaya,Reyhan</contributor><creatorcontrib>Bozkurt, Süreyya</creatorcontrib><creatorcontrib>Okay, Müfide</creatorcontrib><creatorcontrib>Haznedaroğlu, İbrahim</creatorcontrib><title>Aggressive Clinicopathological Course of Myeloma with t(3;16) (q21;q22) Cytogenetic Abnormality</title><title>Turkish journal of haematology</title><addtitle>Turk J Haematol</addtitle><description>Multiple myeloma (MM) is a heterogeneous disease and
patients present with a wide variety of cytogenetic anomalies
reflecting the nature of the disease [1]. The aim of this letter
is to report a rare karyotypic abnormality with an aggressive
clinical course of MM.
A 56-year-old male patient was admitted to the neurosurgery
clinic with dorsal shoulder pain and inability to walk in April 2011.
He underwent thoracic and lumbar spinal magnetic resonance
imaging. Laminectomy was performed on the patient upon
detecting masses at the levels of the first and seventh thoracic
vertebrae. The patient was referred to our center when he was
determined to have “lymphoma” based on the first evaluation of his biopsy material.</description><subject>cytogenetic abnormality</subject><subject>Letters to the Editor</subject><subject>multiple myeloma</subject><subject>rare translocations</subject><subject>Tıp</subject><issn>1300-7777</issn><issn>1308-5263</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkU1v1DAQhi0EoqXwF1DEhfaQxR-JY1Op0ioUWGkRFzhbjjPOeuWNt3ZatP8e76ZU1IfxyJ55Z_Q-CH0geFHRpvo0bTeLQXsYQ1pQTMQcMK7kC3ROGBZlTTl7ecpx2eRzht6ktMWYCk7xa3RGZZMrpDhHajkMEVJyD1C03o3OhL2eNsGHwRntizbcxwRFsMWPA_iw08UfN22K6ZJdE35VXN5Rcn1H6VXRHqYwwAiTM8WyG0Pcae-mw1v0ymqf4N3jfYF-f7391X4v1z-_rdrlujQVq6ayJ7iupaEUhKhrxgSxxnAmKiEp0ZLzDiTmQncGg6RMWyuFYRKbBoS1YNkFWs26fdBbtY9up-NBBe3U6SHEQemYd_OgOFTWioZKLXHFeZ5ghBaUyL7DhGOStW5mrf19t4PewDhF7Z-JPv8Z3UYN4UFx1rD6JPBxFnA9aB_G7CuobXZyzBao1Zfb5VoJVjU4V36eK00MKUWwT1MIVkfYKsNWj7DVkfMcjrBz8_v_93xq_UeX_QVbxaih</recordid><startdate>20190207</startdate><enddate>20190207</enddate><creator>Bozkurt, Süreyya</creator><creator>Okay, Müfide</creator><creator>Haznedaroğlu, İbrahim</creator><general>Türk Hematoloji Derneği</general><general>Galenos Publishing</general><general>Galenos Publishing House</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IEBAR</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-1765-9894</orcidid><orcidid>https://orcid.org/0000-0001-8028-9462</orcidid><orcidid>https://orcid.org/0000-0001-5317-0597</orcidid></search><sort><creationdate>20190207</creationdate><title>Aggressive Clinicopathological Course of Myeloma with t(3;16) (q21;q22) Cytogenetic Abnormality</title><author>Bozkurt, Süreyya ; Okay, Müfide ; Haznedaroğlu, İbrahim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-d10559c22e88553381fcc63848921a966be9068abc0e923aff98c390c7e8ffef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>cytogenetic abnormality</topic><topic>Letters to the Editor</topic><topic>multiple myeloma</topic><topic>rare translocations</topic><topic>Tıp</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bozkurt, Süreyya</creatorcontrib><creatorcontrib>Okay, Müfide</creatorcontrib><creatorcontrib>Haznedaroğlu, İbrahim</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Idealonline online kütüphane - Journals</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Turkish journal of haematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bozkurt, Süreyya</au><au>Okay, Müfide</au><au>Haznedaroğlu, İbrahim</au><au>Küçükkaya,Reyhan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aggressive Clinicopathological Course of Myeloma with t(3;16) (q21;q22) Cytogenetic Abnormality</atitle><jtitle>Turkish journal of haematology</jtitle><addtitle>Turk J Haematol</addtitle><date>2019-02-07</date><risdate>2019</risdate><volume>36</volume><issue>1</issue><spage>62</spage><epage>63</epage><pages>62-63</pages><issn>1300-7777</issn><eissn>1308-5263</eissn><abstract>Multiple myeloma (MM) is a heterogeneous disease and
patients present with a wide variety of cytogenetic anomalies
reflecting the nature of the disease [1]. The aim of this letter
is to report a rare karyotypic abnormality with an aggressive
clinical course of MM.
A 56-year-old male patient was admitted to the neurosurgery
clinic with dorsal shoulder pain and inability to walk in April 2011.
He underwent thoracic and lumbar spinal magnetic resonance
imaging. Laminectomy was performed on the patient upon
detecting masses at the levels of the first and seventh thoracic
vertebrae. The patient was referred to our center when he was
determined to have “lymphoma” based on the first evaluation of his biopsy material.</abstract><cop>Turkey</cop><pub>Türk Hematoloji Derneği</pub><pmid>29726398</pmid><doi>10.4274/tjh.galenos.2018.2018.0049</doi><tpages>2</tpages><orcidid>https://orcid.org/0000-0002-1765-9894</orcidid><orcidid>https://orcid.org/0000-0001-8028-9462</orcidid><orcidid>https://orcid.org/0000-0001-5317-0597</orcidid><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | NCBI_PubMed Central(免费); DOAJ Directory of Open Access Journals; ProQuest - Publicly Available Content Database |
subjects | cytogenetic abnormality Letters to the Editor multiple myeloma rare translocations Tıp |
title | Aggressive Clinicopathological Course of Myeloma with t(3;16) (q21;q22) Cytogenetic Abnormality |
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