成人发病的特发性肾母细胞病的功能定位。

IF 0.9 Q4 ENDOCRINOLOGY & METABOLISM
Case Reports in Endocrinology Pub Date : 2022-10-07 eCollection Date: 2022-01-01 DOI:10.1155/2022/2802975
Jess C Hercus, Pouneh Pasha, Sadiq Al Lawati, Peter Kim, Andre Mattman, Douglas Webber, David M Thompson
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引用次数: 0

摘要

Nesidioblastosis是一种罕见的胰腺疾病,涉及整个胰腺的β细胞增大,导致胰岛素分泌升高。我们提出的情况下,一个53岁的妇女与最初的症状空腹低血糖。计算机断层扫描和磁共振成像扫描未发现胰腺病变,奥曲肽扫描未发现胰岛素瘤。选择性动脉钙刺激(SACST)显示,5条动脉中有3条的胰岛素分泌增加。SACST结果提示为nesidioblastosis的诊断,在远端胰腺次全切除术后通过组织病理学证实。患者术后糖耐量正常,无进一步低血糖问题,提示这是一例罕见的仅部分穿过胰腺的成肾细胞病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Functional Localization of Adult-Onset Idiopathic Nesidioblastosis.

Functional Localization of Adult-Onset Idiopathic Nesidioblastosis.

Functional Localization of Adult-Onset Idiopathic Nesidioblastosis.

Nesidioblastosis is a rare pancreatic disorder involving enlarged beta cells throughout the pancreas, causing elevated insulin production. We present the case of a 53-year-old woman with the initial symptom of fasting hypoglycemia. No pancreatic lesions were indicated on computed tomography and magnetic resonance imaging scans, and an octreotide scan was negative for insulinoma. Selective arterial calcium stimulation (SACST) showed increased insulin production from the stimulation of 3 out of 5 arteries. The SACST results suggested a diagnosis of nesidioblastosis, which was confirmed by histopathology after a subtotal distal pancreatectomy. The patient has normal glucose tolerance after surgery with no further problems of hypoglycemia, indicating that this is a rare case of nesidioblastosis extending only partially through the pancreas.

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来源期刊
Case Reports in Endocrinology
Case Reports in Endocrinology ENDOCRINOLOGY & METABOLISM-
CiteScore
2.10
自引率
0.00%
发文量
45
审稿时长
13 weeks
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