Behçet's Disease with Bilateral Renal Infarction Due to Mucormycosis
We herein report a case of Behçet's disease with renal infarction due to mucormycosis. A 76-year-old man with entero-Behçet's disease had been treated with glucocorticoid and tumor necrosis factor (TNF) inhibitors. His entero-Behçet's disease was refractory to these treatments, and il...
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| Veröffentlicht in: | Internal Medicine 2022/04/01, Vol.61(7), pp.1077-1083 |
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| creator | Shimoyama, Kumiko Niwa, Tomoyuki Furukawa, Shogo Morishita, Naomi Nagakura, Yuka Yonezawa, Haruka Hatakeyama, Masakazu Okubo, Yusuke Suzuki, Daisuki Kosugi, Isao Shiogama, Kazuya Ogawa, Noriyoshi |
| description | We herein report a case of Behçet's disease with renal infarction due to mucormycosis. A 76-year-old man with entero-Behçet's disease had been treated with glucocorticoid and tumor necrosis factor (TNF) inhibitors. His entero-Behçet's disease was refractory to these treatments, and ileocecal resection was performed. After the operation, renal infarction that was unresponsive to anticoagulation therapy developed. He ultimately died of renal failure due to renal infarction. At the autopsy, histopathology of abundant hyphae in the renal vessel wall revealed mucormycosis. Renal mucormycosis is an important cause of renal failure with renal infarction in immunocompromised patients. |
| doi_str_mv | 10.2169/internalmedicine.7462-21 |
| format | Article |
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A 76-year-old man with entero-Behçet's disease had been treated with glucocorticoid and tumor necrosis factor (TNF) inhibitors. His entero-Behçet's disease was refractory to these treatments, and ileocecal resection was performed. After the operation, renal infarction that was unresponsive to anticoagulation therapy developed. He ultimately died of renal failure due to renal infarction. At the autopsy, histopathology of abundant hyphae in the renal vessel wall revealed mucormycosis. Renal mucormycosis is an important cause of renal failure with renal infarction in immunocompromised patients.</description><identifier>ISSN: 0918-2918</identifier><identifier>EISSN: 1349-7235</identifier><identifier>DOI: 10.2169/internalmedicine.7462-21</identifier><identifier>PMID: 34544946</identifier><language>eng</language><publisher>Japan: The Japanese Society of Internal Medicine</publisher><subject>Aged ; Behcet Syndrome - complications ; Behcet Syndrome - diagnosis ; Case Report ; Glucocorticoids ; Humans ; immunocompromised hosts ; Infarction - etiology ; Male ; mucormycosis ; Mucormycosis - complications ; Mucormycosis - diagnosis ; renal infarction ; Tumor Necrosis Factor Inhibitors</subject><ispartof>Internal Medicine, 2022/04/01, Vol.61(7), pp.1077-1083</ispartof><rights>2022 by The Japanese Society of Internal Medicine</rights><rights>Copyright © 2022 by The Japanese Society of Internal Medicine</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c581t-6073d9482604db2f35e028ece98ab6d0902d8b624ce45d23afba56ab5c6b856d3</citedby><cites>FETCH-LOGICAL-c581t-6073d9482604db2f35e028ece98ab6d0902d8b624ce45d23afba56ab5c6b856d3</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/PMC9038466/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038466/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,1877,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34544946$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shimoyama, Kumiko</creatorcontrib><creatorcontrib>Niwa, Tomoyuki</creatorcontrib><creatorcontrib>Furukawa, Shogo</creatorcontrib><creatorcontrib>Morishita, Naomi</creatorcontrib><creatorcontrib>Nagakura, Yuka</creatorcontrib><creatorcontrib>Yonezawa, Haruka</creatorcontrib><creatorcontrib>Hatakeyama, Masakazu</creatorcontrib><creatorcontrib>Okubo, Yusuke</creatorcontrib><creatorcontrib>Suzuki, Daisuki</creatorcontrib><creatorcontrib>Kosugi, Isao</creatorcontrib><creatorcontrib>Shiogama, Kazuya</creatorcontrib><creatorcontrib>Ogawa, Noriyoshi</creatorcontrib><title>Behçet's Disease with Bilateral Renal Infarction Due to Mucormycosis</title><title>Internal Medicine</title><addtitle>Intern. Med.</addtitle><description>We herein report a case of Behçet's disease with renal infarction due to mucormycosis. A 76-year-old man with entero-Behçet's disease had been treated with glucocorticoid and tumor necrosis factor (TNF) inhibitors. His entero-Behçet's disease was refractory to these treatments, and ileocecal resection was performed. After the operation, renal infarction that was unresponsive to anticoagulation therapy developed. He ultimately died of renal failure due to renal infarction. At the autopsy, histopathology of abundant hyphae in the renal vessel wall revealed mucormycosis. Renal mucormycosis is an important cause of renal failure with renal infarction in immunocompromised patients.</description><subject>Aged</subject><subject>Behcet Syndrome - complications</subject><subject>Behcet Syndrome - diagnosis</subject><subject>Case Report</subject><subject>Glucocorticoids</subject><subject>Humans</subject><subject>immunocompromised hosts</subject><subject>Infarction - etiology</subject><subject>Male</subject><subject>mucormycosis</subject><subject>Mucormycosis - complications</subject><subject>Mucormycosis - diagnosis</subject><subject>renal infarction</subject><subject>Tumor Necrosis Factor Inhibitors</subject><issn>0918-2918</issn><issn>1349-7235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNplkU1uFDEQha0IlExCroC8C5sObv-1vUEifxApgBSRteV2V2cc9djBdoNyIg7CxfBkwijApryor96r8kMIt-SYtlK_9aFACnZaweCdD3DccUkb2u6gRcu4bjrKxAu0ILpVDa1lD-3nfEcIU52mu2iPccG55nKBzk9g-esnlKOMz3wGmwH_8GWJT_xkq4ed8DVUI3wZRptc8THgsxlwifjT7GJaPbiYfX6FXo52ynD49B6gm4vzr6cfm6svHy5P3181Tqi2NJJ0bNBcUUn40NORCSBUgQOtbC8HogkdVC8pd8DFQJkdeyuk7YWTvRJyYAfo3Ub3fu7r7Q5CqSua--RXNj2YaL35uxP80tzG70bX07mUVeDNk0CK32bIxax8djBNNkCcs6GiE6QjQqxRtUFdijknGLc2LTHrFMy_KZh1CrVVR18_X3M7-OfbK_B5A9zlYm9hC9hUvJvgf2XZmu6xbBy2oFvaZCCw33uYp7Y</recordid><startdate>20220401</startdate><enddate>20220401</enddate><creator>Shimoyama, Kumiko</creator><creator>Niwa, Tomoyuki</creator><creator>Furukawa, Shogo</creator><creator>Morishita, Naomi</creator><creator>Nagakura, Yuka</creator><creator>Yonezawa, Haruka</creator><creator>Hatakeyama, Masakazu</creator><creator>Okubo, Yusuke</creator><creator>Suzuki, Daisuki</creator><creator>Kosugi, Isao</creator><creator>Shiogama, Kazuya</creator><creator>Ogawa, Noriyoshi</creator><general>The Japanese Society of Internal Medicine</general><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><scope>5PM</scope></search><sort><creationdate>20220401</creationdate><title>Behçet's Disease with Bilateral Renal Infarction Due to Mucormycosis</title><author>Shimoyama, Kumiko ; Niwa, Tomoyuki ; Furukawa, Shogo ; Morishita, Naomi ; Nagakura, Yuka ; Yonezawa, Haruka ; Hatakeyama, Masakazu ; Okubo, Yusuke ; Suzuki, Daisuki ; Kosugi, Isao ; Shiogama, Kazuya ; Ogawa, Noriyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c581t-6073d9482604db2f35e028ece98ab6d0902d8b624ce45d23afba56ab5c6b856d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Aged</topic><topic>Behcet Syndrome - complications</topic><topic>Behcet Syndrome - diagnosis</topic><topic>Case Report</topic><topic>Glucocorticoids</topic><topic>Humans</topic><topic>immunocompromised hosts</topic><topic>Infarction - etiology</topic><topic>Male</topic><topic>mucormycosis</topic><topic>Mucormycosis - complications</topic><topic>Mucormycosis - diagnosis</topic><topic>renal infarction</topic><topic>Tumor Necrosis Factor Inhibitors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shimoyama, Kumiko</creatorcontrib><creatorcontrib>Niwa, Tomoyuki</creatorcontrib><creatorcontrib>Furukawa, Shogo</creatorcontrib><creatorcontrib>Morishita, Naomi</creatorcontrib><creatorcontrib>Nagakura, Yuka</creatorcontrib><creatorcontrib>Yonezawa, Haruka</creatorcontrib><creatorcontrib>Hatakeyama, Masakazu</creatorcontrib><creatorcontrib>Okubo, Yusuke</creatorcontrib><creatorcontrib>Suzuki, Daisuki</creatorcontrib><creatorcontrib>Kosugi, Isao</creatorcontrib><creatorcontrib>Shiogama, Kazuya</creatorcontrib><creatorcontrib>Ogawa, Noriyoshi</creatorcontrib><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Internal Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shimoyama, Kumiko</au><au>Niwa, Tomoyuki</au><au>Furukawa, Shogo</au><au>Morishita, Naomi</au><au>Nagakura, Yuka</au><au>Yonezawa, Haruka</au><au>Hatakeyama, Masakazu</au><au>Okubo, Yusuke</au><au>Suzuki, Daisuki</au><au>Kosugi, Isao</au><au>Shiogama, Kazuya</au><au>Ogawa, Noriyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Behçet's Disease with Bilateral Renal Infarction Due to Mucormycosis</atitle><jtitle>Internal Medicine</jtitle><addtitle>Intern. Med.</addtitle><date>2022-04-01</date><risdate>2022</risdate><volume>61</volume><issue>7</issue><spage>1077</spage><epage>1083</epage><pages>1077-1083</pages><artnum>7462-21</artnum><issn>0918-2918</issn><eissn>1349-7235</eissn><abstract>We herein report a case of Behçet's disease with renal infarction due to mucormycosis. A 76-year-old man with entero-Behçet's disease had been treated with glucocorticoid and tumor necrosis factor (TNF) inhibitors. His entero-Behçet's disease was refractory to these treatments, and ileocecal resection was performed. After the operation, renal infarction that was unresponsive to anticoagulation therapy developed. He ultimately died of renal failure due to renal infarction. At the autopsy, histopathology of abundant hyphae in the renal vessel wall revealed mucormycosis. Renal mucormycosis is an important cause of renal failure with renal infarction in immunocompromised patients.</abstract><cop>Japan</cop><pub>The Japanese Society of Internal Medicine</pub><pmid>34544946</pmid><doi>10.2169/internalmedicine.7462-21</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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| source | MEDLINE; J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese; PubMed Central; PubMed Central Open Access |
| subjects | Aged Behcet Syndrome - complications Behcet Syndrome - diagnosis Case Report Glucocorticoids Humans immunocompromised hosts Infarction - etiology Male mucormycosis Mucormycosis - complications Mucormycosis - diagnosis renal infarction Tumor Necrosis Factor Inhibitors |
| title | Behçet's Disease with Bilateral Renal Infarction Due to Mucormycosis |
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