Multiple myeloma with a previous diagnosis of focal segmental glomerulosclerosis: A case report and review of the literature

The presentation of focal segmental glomerulosclerosis (FSGS) and multiple myeloma (MM), either together or in succession, is extremely rare. Only nine studies have previously reported this poorly understood association. The present study reports the case of a 45-year-old male with FSGS that was dia...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Oncology letters 2015-11, Vol.10 (5), p.2821-2827
Hauptverfasser: DONG, ZHE-YI, XING, HAI-TAO, WANG, YUAN-DA, ZHANG, WEI, QIU, QIANG, CHEN, XIANG-MEI
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2827
container_issue 5
container_start_page 2821
container_title Oncology letters
container_volume 10
creator DONG, ZHE-YI
XING, HAI-TAO
WANG, YUAN-DA
ZHANG, WEI
QIU, QIANG
CHEN, XIANG-MEI
description The presentation of focal segmental glomerulosclerosis (FSGS) and multiple myeloma (MM), either together or in succession, is extremely rare. Only nine studies have previously reported this poorly understood association. The present study reports the case of a 45-year-old male with FSGS that was diagnosed by a renal biopsy performed for nephrotic syndrome (NS). The patient was admitted to the Chinese People's Liberation Army General Hospital one year later with a fever, anemia, unresolved NS and renal insufficiency. The patient was diagnosed with MM and a renal biopsy was repeated, the results of which suggested renal amyloidosis. The MM was treated with three cycles of vincristine, doxorubicin and dexamethasone chemotherapy. A review of the literature indicated that monoclonal gammopathy may lead to FSGS. It suggested that FSGS patients who are >40 years old should be routinely screened for plasma cell proliferative disorders to guide the treatment, determine a prognosis, achieve primary disease remission and avoid end-stage renal disease.
doi_str_mv 10.3892/ol.2015.3669
format Article
fullrecord <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4665327</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A439320256</galeid><sourcerecordid>A439320256</sourcerecordid><originalsourceid>FETCH-LOGICAL-c539t-ce8d34f5737dfa792a5f86a231bafb5de6a4841e0b595ac54266bbec4a9326193</originalsourceid><addsrcrecordid>eNptkk1v1DAQhiMEolXpjTOyBEIcyBI7sZP0gLSq-JIW9QJna-JMEldOHGynVSV-PA5bli7Cc_DIfuad8XiS5DnNNnlVs3fWbFhG-SYXon6UnNKyZinNKvb44JfFSXLu_XUWFxe0qsTT5ISJkjFWVKfJz6-LCXo2SMY7NHYEcqvDQIDMDm-0XTxpNfST9doT25HOKjDEYz_iFKLXxxB0i7FeGXQrdUG2RIFH4nC2LhCYWrJK4e0aHwYkRgd0EBaHz5InHRiP5_f7WfL944dvl5_T3dWnL5fbXap4XodUYdXmRcfLvGw7iM8C3lUCWE4b6BreooCiKihmDa85KF4wIZoGVQF1zgSt87Pk_V53XpoRWxVrd2Dk7PQI7k5a0PL4ZtKD7O2NLITgOSujwJt7AWd_LOiDHLVXaAxMGHskaRVTxhqYiOjLf9Bru7gpPk_StZyC0Zr_pXowKPXU2ZhXraJyW-SRyxhftTb_oaK1OGplJ-x0PD8KeP0gYEAwYfDWLEHbyR-Db_egip_mHXaHZtBMrpMlrZHrZMl1siL-4mEDD_CfOYrAqz3g5_jhurX-wFzt0izab51fa6zVeg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1932642195</pqid></control><display><type>article</type><title>Multiple myeloma with a previous diagnosis of focal segmental glomerulosclerosis: A case report and review of the literature</title><source>Spandidos Publications Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>DONG, ZHE-YI ; XING, HAI-TAO ; WANG, YUAN-DA ; ZHANG, WEI ; QIU, QIANG ; CHEN, XIANG-MEI</creator><creatorcontrib>DONG, ZHE-YI ; XING, HAI-TAO ; WANG, YUAN-DA ; ZHANG, WEI ; QIU, QIANG ; CHEN, XIANG-MEI</creatorcontrib><description>The presentation of focal segmental glomerulosclerosis (FSGS) and multiple myeloma (MM), either together or in succession, is extremely rare. Only nine studies have previously reported this poorly understood association. The present study reports the case of a 45-year-old male with FSGS that was diagnosed by a renal biopsy performed for nephrotic syndrome (NS). The patient was admitted to the Chinese People's Liberation Army General Hospital one year later with a fever, anemia, unresolved NS and renal insufficiency. The patient was diagnosed with MM and a renal biopsy was repeated, the results of which suggested renal amyloidosis. The MM was treated with three cycles of vincristine, doxorubicin and dexamethasone chemotherapy. A review of the literature indicated that monoclonal gammopathy may lead to FSGS. It suggested that FSGS patients who are &gt;40 years old should be routinely screened for plasma cell proliferative disorders to guide the treatment, determine a prognosis, achieve primary disease remission and avoid end-stage renal disease.</description><identifier>ISSN: 1792-1074</identifier><identifier>EISSN: 1792-1082</identifier><identifier>DOI: 10.3892/ol.2015.3669</identifier><identifier>PMID: 26722248</identifier><language>eng</language><publisher>Greece: D.A. Spandidos</publisher><subject>Biopsy ; Blood pressure ; Bone marrow ; Care and treatment ; Case reports ; Case studies ; Chemotherapy ; Diagnosis ; Drug dosages ; focal segmental glomerulosclerosis ; Immunoglobulins ; Kidney diseases ; Light ; Lymphoma ; Medical diagnosis ; monoclonal gammopathy of undetermined significance ; Multiple myeloma ; Oncology ; Patients ; Plasma ; plasma cell proliferative disorders ; Proteins ; Remission (Medicine) ; Stem cells ; Ultrasonic imaging ; Urine</subject><ispartof>Oncology letters, 2015-11, Vol.10 (5), p.2821-2827</ispartof><rights>Copyright: © Dong et al.</rights><rights>COPYRIGHT 2015 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2015</rights><rights>Copyright: © Dong et al. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c539t-ce8d34f5737dfa792a5f86a231bafb5de6a4841e0b595ac54266bbec4a9326193</citedby><cites>FETCH-LOGICAL-c539t-ce8d34f5737dfa792a5f86a231bafb5de6a4841e0b595ac54266bbec4a9326193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4665327/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4665327/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,5571,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26722248$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>DONG, ZHE-YI</creatorcontrib><creatorcontrib>XING, HAI-TAO</creatorcontrib><creatorcontrib>WANG, YUAN-DA</creatorcontrib><creatorcontrib>ZHANG, WEI</creatorcontrib><creatorcontrib>QIU, QIANG</creatorcontrib><creatorcontrib>CHEN, XIANG-MEI</creatorcontrib><title>Multiple myeloma with a previous diagnosis of focal segmental glomerulosclerosis: A case report and review of the literature</title><title>Oncology letters</title><addtitle>Oncol Lett</addtitle><description>The presentation of focal segmental glomerulosclerosis (FSGS) and multiple myeloma (MM), either together or in succession, is extremely rare. Only nine studies have previously reported this poorly understood association. The present study reports the case of a 45-year-old male with FSGS that was diagnosed by a renal biopsy performed for nephrotic syndrome (NS). The patient was admitted to the Chinese People's Liberation Army General Hospital one year later with a fever, anemia, unresolved NS and renal insufficiency. The patient was diagnosed with MM and a renal biopsy was repeated, the results of which suggested renal amyloidosis. The MM was treated with three cycles of vincristine, doxorubicin and dexamethasone chemotherapy. A review of the literature indicated that monoclonal gammopathy may lead to FSGS. It suggested that FSGS patients who are &gt;40 years old should be routinely screened for plasma cell proliferative disorders to guide the treatment, determine a prognosis, achieve primary disease remission and avoid end-stage renal disease.</description><subject>Biopsy</subject><subject>Blood pressure</subject><subject>Bone marrow</subject><subject>Care and treatment</subject><subject>Case reports</subject><subject>Case studies</subject><subject>Chemotherapy</subject><subject>Diagnosis</subject><subject>Drug dosages</subject><subject>focal segmental glomerulosclerosis</subject><subject>Immunoglobulins</subject><subject>Kidney diseases</subject><subject>Light</subject><subject>Lymphoma</subject><subject>Medical diagnosis</subject><subject>monoclonal gammopathy of undetermined significance</subject><subject>Multiple myeloma</subject><subject>Oncology</subject><subject>Patients</subject><subject>Plasma</subject><subject>plasma cell proliferative disorders</subject><subject>Proteins</subject><subject>Remission (Medicine)</subject><subject>Stem cells</subject><subject>Ultrasonic imaging</subject><subject>Urine</subject><issn>1792-1074</issn><issn>1792-1082</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNptkk1v1DAQhiMEolXpjTOyBEIcyBI7sZP0gLSq-JIW9QJna-JMEldOHGynVSV-PA5bli7Cc_DIfuad8XiS5DnNNnlVs3fWbFhG-SYXon6UnNKyZinNKvb44JfFSXLu_XUWFxe0qsTT5ISJkjFWVKfJz6-LCXo2SMY7NHYEcqvDQIDMDm-0XTxpNfST9doT25HOKjDEYz_iFKLXxxB0i7FeGXQrdUG2RIFH4nC2LhCYWrJK4e0aHwYkRgd0EBaHz5InHRiP5_f7WfL944dvl5_T3dWnL5fbXap4XodUYdXmRcfLvGw7iM8C3lUCWE4b6BreooCiKihmDa85KF4wIZoGVQF1zgSt87Pk_V53XpoRWxVrd2Dk7PQI7k5a0PL4ZtKD7O2NLITgOSujwJt7AWd_LOiDHLVXaAxMGHskaRVTxhqYiOjLf9Bru7gpPk_StZyC0Zr_pXowKPXU2ZhXraJyW-SRyxhftTb_oaK1OGplJ-x0PD8KeP0gYEAwYfDWLEHbyR-Db_egip_mHXaHZtBMrpMlrZHrZMl1siL-4mEDD_CfOYrAqz3g5_jhurX-wFzt0izab51fa6zVeg</recordid><startdate>20151101</startdate><enddate>20151101</enddate><creator>DONG, ZHE-YI</creator><creator>XING, HAI-TAO</creator><creator>WANG, YUAN-DA</creator><creator>ZHANG, WEI</creator><creator>QIU, QIANG</creator><creator>CHEN, XIANG-MEI</creator><general>D.A. Spandidos</general><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151101</creationdate><title>Multiple myeloma with a previous diagnosis of focal segmental glomerulosclerosis: A case report and review of the literature</title><author>DONG, ZHE-YI ; XING, HAI-TAO ; WANG, YUAN-DA ; ZHANG, WEI ; QIU, QIANG ; CHEN, XIANG-MEI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c539t-ce8d34f5737dfa792a5f86a231bafb5de6a4841e0b595ac54266bbec4a9326193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Biopsy</topic><topic>Blood pressure</topic><topic>Bone marrow</topic><topic>Care and treatment</topic><topic>Case reports</topic><topic>Case studies</topic><topic>Chemotherapy</topic><topic>Diagnosis</topic><topic>Drug dosages</topic><topic>focal segmental glomerulosclerosis</topic><topic>Immunoglobulins</topic><topic>Kidney diseases</topic><topic>Light</topic><topic>Lymphoma</topic><topic>Medical diagnosis</topic><topic>monoclonal gammopathy of undetermined significance</topic><topic>Multiple myeloma</topic><topic>Oncology</topic><topic>Patients</topic><topic>Plasma</topic><topic>plasma cell proliferative disorders</topic><topic>Proteins</topic><topic>Remission (Medicine)</topic><topic>Stem cells</topic><topic>Ultrasonic imaging</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DONG, ZHE-YI</creatorcontrib><creatorcontrib>XING, HAI-TAO</creatorcontrib><creatorcontrib>WANG, YUAN-DA</creatorcontrib><creatorcontrib>ZHANG, WEI</creatorcontrib><creatorcontrib>QIU, QIANG</creatorcontrib><creatorcontrib>CHEN, XIANG-MEI</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DONG, ZHE-YI</au><au>XING, HAI-TAO</au><au>WANG, YUAN-DA</au><au>ZHANG, WEI</au><au>QIU, QIANG</au><au>CHEN, XIANG-MEI</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multiple myeloma with a previous diagnosis of focal segmental glomerulosclerosis: A case report and review of the literature</atitle><jtitle>Oncology letters</jtitle><addtitle>Oncol Lett</addtitle><date>2015-11-01</date><risdate>2015</risdate><volume>10</volume><issue>5</issue><spage>2821</spage><epage>2827</epage><pages>2821-2827</pages><issn>1792-1074</issn><eissn>1792-1082</eissn><abstract>The presentation of focal segmental glomerulosclerosis (FSGS) and multiple myeloma (MM), either together or in succession, is extremely rare. Only nine studies have previously reported this poorly understood association. The present study reports the case of a 45-year-old male with FSGS that was diagnosed by a renal biopsy performed for nephrotic syndrome (NS). The patient was admitted to the Chinese People's Liberation Army General Hospital one year later with a fever, anemia, unresolved NS and renal insufficiency. The patient was diagnosed with MM and a renal biopsy was repeated, the results of which suggested renal amyloidosis. The MM was treated with three cycles of vincristine, doxorubicin and dexamethasone chemotherapy. A review of the literature indicated that monoclonal gammopathy may lead to FSGS. It suggested that FSGS patients who are &gt;40 years old should be routinely screened for plasma cell proliferative disorders to guide the treatment, determine a prognosis, achieve primary disease remission and avoid end-stage renal disease.</abstract><cop>Greece</cop><pub>D.A. Spandidos</pub><pmid>26722248</pmid><doi>10.3892/ol.2015.3669</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1792-1074
ispartof Oncology letters, 2015-11, Vol.10 (5), p.2821-2827
issn 1792-1074
1792-1082
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4665327
source Spandidos Publications Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Biopsy
Blood pressure
Bone marrow
Care and treatment
Case reports
Case studies
Chemotherapy
Diagnosis
Drug dosages
focal segmental glomerulosclerosis
Immunoglobulins
Kidney diseases
Light
Lymphoma
Medical diagnosis
monoclonal gammopathy of undetermined significance
Multiple myeloma
Oncology
Patients
Plasma
plasma cell proliferative disorders
Proteins
Remission (Medicine)
Stem cells
Ultrasonic imaging
Urine
title Multiple myeloma with a previous diagnosis of focal segmental glomerulosclerosis: A case report and review of the literature
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T13%3A41%3A06IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Multiple%20myeloma%20with%20a%20previous%20diagnosis%20of%20focal%20segmental%20glomerulosclerosis:%20A%20case%20report%20and%20review%20of%20the%20literature&rft.jtitle=Oncology%20letters&rft.au=DONG,%20ZHE-YI&rft.date=2015-11-01&rft.volume=10&rft.issue=5&rft.spage=2821&rft.epage=2827&rft.pages=2821-2827&rft.issn=1792-1074&rft.eissn=1792-1082&rft_id=info:doi/10.3892/ol.2015.3669&rft_dat=%3Cgale_pubme%3EA439320256%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1932642195&rft_id=info:pmid/26722248&rft_galeid=A439320256&rfr_iscdi=true