特发性甲状旁腺功能减退合并原发性甲状旁腺功能减退合并糖尿病1例。

Y Sumida, M Matsumura, H Goto, K Murata, K Tsuchihashi, M Misaki, T Shima
{"title":"特发性甲状旁腺功能减退合并原发性甲状旁腺功能减退合并糖尿病1例。","authors":"Y Sumida,&nbsp;M Matsumura,&nbsp;H Goto,&nbsp;K Murata,&nbsp;K Tsuchihashi,&nbsp;M Misaki,&nbsp;T Shima","doi":"10.1507/endocrine1927.70.6_609","DOIUrl":null,"url":null,"abstract":"<p><p>A 50-year-old man was admitted to our hospital for the evaluation of hypocalcemia and the treatment of diabetes mellitus. Seven months before admission, he sometimes felt thirst and polyuria, and 4 months before admission, he went to a doctor to check his blood glucose and was diagnosed as having diabetes mellitus which had suddenly developed. At that time he was treated with sulfonylurea, but his diabetic control was very poor. At the time of admission to our hospital, the patient's serum calcium (Ca) level was 5.7 mg/dl, phosphorus (P) 5.0 mg/dl, and fasting blood glucose 308 mg/dl, but urinary ketone bodies were not detected. High sensitive assay of parathyroid hormone (HS-PTH), intact PTH and C-terminus PTH concentrations were under the level of detection. TSH level was slightly high (6.1 mu U/ml) with positive antimicrosomal and antithyroglobulin antibodies but thyroid hormone levels were within normal limits. TRH test showed over-response of TSH. Based on Ellsworth-Howard test, we made the diagnosis of idiopathic hypoparathyroidism associated with primary hypothyroidism and diabetes mellitus. He was treated with insulin twice a day and reached good control, and he was also administered 1 alpha-OH-D3 and calcium lactate resulting in an increase of serum Ca level after 2 weeks. These findings suggest that this case may be a polyglandular autoimmune (PGA) syndrome type 1 reported by Neufeld, which is very rare in Japan. The type of diabetes mellitus of this case is controversial. It is, however, necessary to pay attention to the decrease of the patient's insulin-secreting activity because autoimmune disorders are accompanied by this case.</p>","PeriodicalId":19249,"journal":{"name":"Nihon Naibunpi Gakkai zasshi","volume":"70 6","pages":"609-14"},"PeriodicalIF":0.0000,"publicationDate":"1994-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1507/endocrine1927.70.6_609","citationCount":"1","resultStr":"{\"title\":\"[A case of idiopathic hypoparathyroidism associated with primary hypothyroidism and diabetes mellitus].\",\"authors\":\"Y Sumida,&nbsp;M Matsumura,&nbsp;H Goto,&nbsp;K Murata,&nbsp;K Tsuchihashi,&nbsp;M Misaki,&nbsp;T Shima\",\"doi\":\"10.1507/endocrine1927.70.6_609\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A 50-year-old man was admitted to our hospital for the evaluation of hypocalcemia and the treatment of diabetes mellitus. Seven months before admission, he sometimes felt thirst and polyuria, and 4 months before admission, he went to a doctor to check his blood glucose and was diagnosed as having diabetes mellitus which had suddenly developed. At that time he was treated with sulfonylurea, but his diabetic control was very poor. At the time of admission to our hospital, the patient's serum calcium (Ca) level was 5.7 mg/dl, phosphorus (P) 5.0 mg/dl, and fasting blood glucose 308 mg/dl, but urinary ketone bodies were not detected. High sensitive assay of parathyroid hormone (HS-PTH), intact PTH and C-terminus PTH concentrations were under the level of detection. TSH level was slightly high (6.1 mu U/ml) with positive antimicrosomal and antithyroglobulin antibodies but thyroid hormone levels were within normal limits. TRH test showed over-response of TSH. Based on Ellsworth-Howard test, we made the diagnosis of idiopathic hypoparathyroidism associated with primary hypothyroidism and diabetes mellitus. He was treated with insulin twice a day and reached good control, and he was also administered 1 alpha-OH-D3 and calcium lactate resulting in an increase of serum Ca level after 2 weeks. These findings suggest that this case may be a polyglandular autoimmune (PGA) syndrome type 1 reported by Neufeld, which is very rare in Japan. The type of diabetes mellitus of this case is controversial. It is, however, necessary to pay attention to the decrease of the patient's insulin-secreting activity because autoimmune disorders are accompanied by this case.</p>\",\"PeriodicalId\":19249,\"journal\":{\"name\":\"Nihon Naibunpi Gakkai zasshi\",\"volume\":\"70 6\",\"pages\":\"609-14\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1994-08-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1507/endocrine1927.70.6_609\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nihon Naibunpi Gakkai zasshi\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1507/endocrine1927.70.6_609\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nihon Naibunpi Gakkai zasshi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1507/endocrine1927.70.6_609","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

一位50岁男性因评估低钙血症及治疗糖尿病而入院。入院前7个月,他有时感到口渴和多尿,入院前4个月,他去看医生检查血糖,诊断为突然发生的糖尿病。当时他接受磺脲类药物治疗,但他的糖尿病控制很差。入院时患者血钙(Ca) 5.7 mg/dl,血磷(P) 5.0 mg/dl,空腹血糖308 mg/dl,未检出尿酮体。甲状旁腺激素(HS-PTH)、完整甲状旁腺激素和c端甲状旁腺激素的高灵敏度检测均低于检测水平。TSH水平略高(6.1 mu U/ml),抗甲状腺球蛋白抗体阳性,但甲状腺激素水平在正常范围内。TRH试验显示TSH反应过度。根据Ellsworth-Howard试验,我们诊断为特发性甲状旁腺功能减退症合并原发性甲状腺功能减退症和糖尿病。每日2次胰岛素治疗,病情得到良好控制,同时给予1 α - oh - d3和乳酸钙治疗,2周后血清钙水平升高。这些结果提示该病例可能是Neufeld报道的1型多腺体自身免疫(PGA)综合征,在日本非常罕见。该病例的糖尿病类型存在争议。然而,有必要注意患者胰岛素分泌活性的降低,因为本病例伴有自身免疫性疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A case of idiopathic hypoparathyroidism associated with primary hypothyroidism and diabetes mellitus].

A 50-year-old man was admitted to our hospital for the evaluation of hypocalcemia and the treatment of diabetes mellitus. Seven months before admission, he sometimes felt thirst and polyuria, and 4 months before admission, he went to a doctor to check his blood glucose and was diagnosed as having diabetes mellitus which had suddenly developed. At that time he was treated with sulfonylurea, but his diabetic control was very poor. At the time of admission to our hospital, the patient's serum calcium (Ca) level was 5.7 mg/dl, phosphorus (P) 5.0 mg/dl, and fasting blood glucose 308 mg/dl, but urinary ketone bodies were not detected. High sensitive assay of parathyroid hormone (HS-PTH), intact PTH and C-terminus PTH concentrations were under the level of detection. TSH level was slightly high (6.1 mu U/ml) with positive antimicrosomal and antithyroglobulin antibodies but thyroid hormone levels were within normal limits. TRH test showed over-response of TSH. Based on Ellsworth-Howard test, we made the diagnosis of idiopathic hypoparathyroidism associated with primary hypothyroidism and diabetes mellitus. He was treated with insulin twice a day and reached good control, and he was also administered 1 alpha-OH-D3 and calcium lactate resulting in an increase of serum Ca level after 2 weeks. These findings suggest that this case may be a polyglandular autoimmune (PGA) syndrome type 1 reported by Neufeld, which is very rare in Japan. The type of diabetes mellitus of this case is controversial. It is, however, necessary to pay attention to the decrease of the patient's insulin-secreting activity because autoimmune disorders are accompanied by this case.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信