Late Onset of Non-islet Cell Tumor Hypoglycemia Managed via Multidisciplinary Treatment in a Patient with a Solitary Fibrous Tumor

被引:2
|
作者
Takeuchi, Satoshi [1 ]
Goda, Tomohiro [1 ]
Taguchi, Jun [1 ]
Douhata, Yuichi [1 ]
Honma, Rio [1 ]
Ariga, Shin [1 ]
Ohhara, Yoshihito [1 ]
Shimizu, Yasushi [1 ]
Kinoshita, Ichiro [1 ]
Fukuda, Izumi [2 ]
Nagashima, Yoji [3 ]
Akita, Hirotoshi [1 ]
机构
[1] Hokkaido Univ, Grad Sch Med, Dept Med Oncol, Sapporo, Hokkaido, Japan
[2] Nippon Med Sch, Grad Sch Med, Dept Endocrinol Diabet & Metab, Tokyo, Japan
[3] Tokyo Womens Med Univ, Dept Pathol, Tokyo, Japan
关键词
non-islet cell tumor hypoglycemia; solitary fibrous tumor; high molecular weight IGF-2; paraneoplastic syndrome; multidisciplinary treatment; GROWTH-FACTOR-II; SOFT-TISSUE SARCOMA; PHASE-3; TRIAL; LEIOMYOSARCOMA; CHEMOTHERAPY; MULTICENTER; DACARBAZINE; LIPOSARCOMA; SECRETION; SERUM;
D O I
10.2169/internalmedicine.0231-17
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:2431 / 2436
页数:6
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