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...
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Veröffentlicht in: | Oncology letters 2015-11, Vol.10 (5), p.2821-2827 |
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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. |
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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.</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 >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 & 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 & Medical Complete (Alumni)</collection><collection>Health & 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 >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. 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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 |
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