Late Onset of Non-islet Cell Tumor Hypoglycemia Managed via Multidisciplinary Treatment in a Patient with a Solitary Fibrous Tumor
Solitary fibrous tumor (SFT) is a rare subtype of soft tissue sarcoma (STS). We herein describe a case of late onset of non-islet cell tumor hypoglycemia (NICTH) that was managed via multidisciplinary treatment in a patient with SFT. A 67-year-old man previously diagnosed with SFT 4 years prior to t...
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Veröffentlicht in: | Internal Medicine 2018/08/15, Vol.57(16), pp.2431-2436 |
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creator | Takeuchi, Satoshi Goda, Tomohiro Taguchi, Jun Douhata, Yuichi Honma, Rio Ariga, Shin Ohhara, Yoshihito Shimizu, Yasushi Kinoshita, Ichiro Fukuda, Izumi Nagashima, Yoji Akita, Hirotoshi |
description | Solitary fibrous tumor (SFT) is a rare subtype of soft tissue sarcoma (STS). We herein describe a case of late onset of non-islet cell tumor hypoglycemia (NICTH) that was managed via multidisciplinary treatment in a patient with SFT. A 67-year-old man previously diagnosed with SFT 4 years prior to this presentation and treated with several rounds of surgery, presented with massive tumors. Eighteen months following his prescribed chemotherapy, the patient developed hypoglycemia. He was diagnosed with NICTH, after confirming the presence of high molecular weight insulin-like growth factor-2. This case suggests that paraneoplastic syndrome can occur even in cases of rare cancers, such as STS. |
doi_str_mv | 10.2169/internalmedicine.0231-17 |
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We herein describe a case of late onset of non-islet cell tumor hypoglycemia (NICTH) that was managed via multidisciplinary treatment in a patient with SFT. A 67-year-old man previously diagnosed with SFT 4 years prior to this presentation and treated with several rounds of surgery, presented with massive tumors. Eighteen months following his prescribed chemotherapy, the patient developed hypoglycemia. He was diagnosed with NICTH, after confirming the presence of high molecular weight insulin-like growth factor-2. 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Med.</addtitle><description>Solitary fibrous tumor (SFT) is a rare subtype of soft tissue sarcoma (STS). We herein describe a case of late onset of non-islet cell tumor hypoglycemia (NICTH) that was managed via multidisciplinary treatment in a patient with SFT. A 67-year-old man previously diagnosed with SFT 4 years prior to this presentation and treated with several rounds of surgery, presented with massive tumors. Eighteen months following his prescribed chemotherapy, the patient developed hypoglycemia. He was diagnosed with NICTH, after confirming the presence of high molecular weight insulin-like growth factor-2. This case suggests that paraneoplastic syndrome can occur even in cases of rare cancers, such as STS.</description><subject>Case Report</subject><subject>Chemotherapy</subject><subject>high molecular weight IGF-2</subject><subject>Hypoglycemia</subject><subject>Insulin</subject><subject>Internal medicine</subject><subject>Molecular weight</subject><subject>multidisciplinary treatment</subject><subject>non-islet cell tumor hypoglycemia</subject><subject>Paraneoplastic syndrome</subject><subject>Patients</subject><subject>Sarcoma</subject><subject>Soft tissue sarcoma</subject><subject>solitary fibrous tumor</subject><subject>Surgery</subject><subject>Tumors</subject><issn>0918-2918</issn><issn>1349-7235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNplkcFuEzEQhleIiobCKyBLXLhs8Xht7_qChCJKkQKpRDhbzq43ceS1g-0typUnx9uECNrL2CN_83tm_qJAgK8JcPHeuKSDU3bQnWmN09eYVFBC_ayYQUVFWZOKPS9mWEBTkhwui5cx7jCumlqQF8UlEYxwQWFW_F6opNHSRZ2Q79E370oTbU7m2lq0Ggcf0O1h7zf20OrBKPRVObXRHbqf7qNNpjOxNXtrnAoHtApapUG7hIxDCt2pZKbkl0nbnH731qQJuzHr4Md41H9VXPTKRv36dF4VP24-rea35WL5-cv846JsOaOphJZxxnpFcK2Bsx6YqNY941DpmkDPiRCE1RSw6ChvQHdr2gtM61xFO9aJ6qr4cNTdj-u8uDY3FpSV-2CG3JP0ysj_X5zZyo2_lxxoAw3OAu9OAsH_HHVMcsiz5z0pp_M0kmCoAJOa1hl9-wjd-XFyLFOEclFhDhPVHKk2-BiD7s_NAJaT0fKx0XIyWj6Uvvl3mHPhX2czsDwCu5iyYWdAhWRaq58qs1oCn-LpizPZblWQ2lV_AG_Cx90</recordid><startdate>20180815</startdate><enddate>20180815</enddate><creator>Takeuchi, Satoshi</creator><creator>Goda, Tomohiro</creator><creator>Taguchi, Jun</creator><creator>Douhata, Yuichi</creator><creator>Honma, Rio</creator><creator>Ariga, Shin</creator><creator>Ohhara, Yoshihito</creator><creator>Shimizu, Yasushi</creator><creator>Kinoshita, Ichiro</creator><creator>Fukuda, Izumi</creator><creator>Nagashima, Yoji</creator><creator>Akita, Hirotoshi</creator><general>The Japanese Society of Internal Medicine</general><general>Japan Science and Technology Agency</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180815</creationdate><title>Late Onset of Non-islet Cell Tumor Hypoglycemia Managed via Multidisciplinary Treatment in a Patient with a Solitary Fibrous Tumor</title><author>Takeuchi, Satoshi ; Goda, Tomohiro ; Taguchi, Jun ; Douhata, Yuichi ; Honma, Rio ; Ariga, Shin ; Ohhara, Yoshihito ; Shimizu, Yasushi ; Kinoshita, Ichiro ; Fukuda, Izumi ; Nagashima, Yoji ; Akita, Hirotoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c654t-1c5655fa207e165f1593bf5613e721f62992574109d4681edb4f90475654d5d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Case Report</topic><topic>Chemotherapy</topic><topic>high molecular weight IGF-2</topic><topic>Hypoglycemia</topic><topic>Insulin</topic><topic>Internal medicine</topic><topic>Molecular weight</topic><topic>multidisciplinary treatment</topic><topic>non-islet cell tumor hypoglycemia</topic><topic>Paraneoplastic syndrome</topic><topic>Patients</topic><topic>Sarcoma</topic><topic>Soft tissue sarcoma</topic><topic>solitary fibrous tumor</topic><topic>Surgery</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takeuchi, Satoshi</creatorcontrib><creatorcontrib>Goda, Tomohiro</creatorcontrib><creatorcontrib>Taguchi, Jun</creatorcontrib><creatorcontrib>Douhata, Yuichi</creatorcontrib><creatorcontrib>Honma, Rio</creatorcontrib><creatorcontrib>Ariga, Shin</creatorcontrib><creatorcontrib>Ohhara, Yoshihito</creatorcontrib><creatorcontrib>Shimizu, Yasushi</creatorcontrib><creatorcontrib>Kinoshita, Ichiro</creatorcontrib><creatorcontrib>Fukuda, Izumi</creatorcontrib><creatorcontrib>Nagashima, Yoji</creatorcontrib><creatorcontrib>Akita, Hirotoshi</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</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>Takeuchi, Satoshi</au><au>Goda, Tomohiro</au><au>Taguchi, Jun</au><au>Douhata, Yuichi</au><au>Honma, Rio</au><au>Ariga, Shin</au><au>Ohhara, Yoshihito</au><au>Shimizu, Yasushi</au><au>Kinoshita, Ichiro</au><au>Fukuda, Izumi</au><au>Nagashima, Yoji</au><au>Akita, Hirotoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Late Onset of Non-islet Cell Tumor Hypoglycemia Managed via Multidisciplinary Treatment in a Patient with a Solitary Fibrous Tumor</atitle><jtitle>Internal Medicine</jtitle><addtitle>Intern. Med.</addtitle><date>2018-08-15</date><risdate>2018</risdate><volume>57</volume><issue>16</issue><spage>2431</spage><epage>2436</epage><pages>2431-2436</pages><issn>0918-2918</issn><eissn>1349-7235</eissn><abstract>Solitary fibrous tumor (SFT) is a rare subtype of soft tissue sarcoma (STS). We herein describe a case of late onset of non-islet cell tumor hypoglycemia (NICTH) that was managed via multidisciplinary treatment in a patient with SFT. A 67-year-old man previously diagnosed with SFT 4 years prior to this presentation and treated with several rounds of surgery, presented with massive tumors. Eighteen months following his prescribed chemotherapy, the patient developed hypoglycemia. He was diagnosed with NICTH, after confirming the presence of high molecular weight insulin-like growth factor-2. 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subjects | Case Report Chemotherapy high molecular weight IGF-2 Hypoglycemia Insulin Internal medicine Molecular weight multidisciplinary treatment non-islet cell tumor hypoglycemia Paraneoplastic syndrome Patients Sarcoma Soft tissue sarcoma solitary fibrous tumor Surgery Tumors |
title | Late Onset of Non-islet Cell Tumor Hypoglycemia Managed via Multidisciplinary Treatment in a Patient with a Solitary Fibrous Tumor |
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