H Shineha, H Kimura, S Yanagisawa, R Abe, S Matsuda, T Uchida, S Kariyone
{"title":"Acute promyelocytic leukemia associated with insulinoma: a case report.","authors":"H Shineha, H Kimura, S Yanagisawa, R Abe, S Matsuda, T Uchida, S Kariyone","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>We report a case of acute promyelocytic leukemia (APL) coexisting with insulinoma in a 61-year-old female. Two years before the onset of APL, she was diagnosed as having insulinoma and underwent resection of the body and tail of the pancreas, but no insulinoma was found in the resected pancreas. The clinical symptoms of hyperinsulinism, however, continued after the operation and were treated with diazoxide (100 mg daily, 37 g in total) for about two years until the onset of APL. During the induction therapy for APL, she died of hemorrhage and infection; autopsy revealed the presence of insulinoma (13 X 9 mm in size) in the residual pancreas head. This is the first case report of coexistence of APL and insulinoma.</p>","PeriodicalId":76233,"journal":{"name":"Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society","volume":"53 1","pages":"57-61"},"PeriodicalIF":0.0000,"publicationDate":"1990-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
We report a case of acute promyelocytic leukemia (APL) coexisting with insulinoma in a 61-year-old female. Two years before the onset of APL, she was diagnosed as having insulinoma and underwent resection of the body and tail of the pancreas, but no insulinoma was found in the resected pancreas. The clinical symptoms of hyperinsulinism, however, continued after the operation and were treated with diazoxide (100 mg daily, 37 g in total) for about two years until the onset of APL. During the induction therapy for APL, she died of hemorrhage and infection; autopsy revealed the presence of insulinoma (13 X 9 mm in size) in the residual pancreas head. This is the first case report of coexistence of APL and insulinoma.
我们报告一例急性早幼粒细胞白血病(APL)并发胰岛素瘤在61岁的女性。在APL发病前两年,她被诊断为胰岛素瘤,并切除了胰腺体和尾部,但在切除的胰腺中未发现胰岛素瘤。然而,高胰岛素血症的临床症状在手术后持续存在,并使用二氮氧化合物(每天100 mg,共37 g)治疗约2年,直到APL发病。在APL诱导治疗期间,因出血、感染死亡;尸检显示胰脏残端有胰岛瘤(大小13 X 9mm)。这是首例APL与胰岛素瘤共存的病例报道。