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胰岛细胞增生症和胰岛素瘤:罕见共存与治疗挑战。

Nesidioblastosis and Insulinoma: A Rare Coexistence and a Therapeutic Challenge.

机构信息

Section of Diabetes and Metabolic Disease, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Division of General and Transplant Surgery, University of Pisa, Pisa, Italy.

出版信息

Front Endocrinol (Lausanne). 2020 Jan 24;11:10. doi: 10.3389/fendo.2020.00010. eCollection 2020.

Abstract

Nesidioblastosis and insulinoma are disorders of the endocrine pancreas causing endogenous hyperinsulinemic hypoglycemia. Their coexistence is very unusual and treatment represents a still unresolved dilemma. The patient was a 43-year-old Caucasian woman, with a 2-year history of repeated severe hypoglycemic events. The diagnostic work-up was strongly suggestive of insulinoma and the patient was submitted to surgical treatment carried out laparoscopically under robotic assistance. However, surgical exploration and intraoperative ultrasonography failed to detect a pancreatic tumor. Resection was therefore carried out based on the results of selective intra-arterial calcium stimulation test, following a step-up approach, eventually leading to a pancreatoduodenectomy at the splenic artery. The histopathology examination and the immunohistochemical staining were consistent with adult-onset nesidioblastosis. After surgery, the patient continued to experience hypoglycemia with futile response to medical treatments (octreotide, calcium antagonists, diazoxide, and prednisone). Following multidisciplinary evaluation and critical review of a repeat abdominal computed tomography scan, a small nodular lesion was identified in the tail of the pancreas. The nodule was enucleated laparoscopically and the pathological examination revealed an insulinoma. In spite of the insulinoma resection, glycemic values were only partially restored, with residual nocturnal hypoglycemia. Administration of uncooked cornstarch (1.25 g/kg body weight) at bedtime was associated with significant improvement of interstitial glucose levels ( < 0.0001) and reduction of nocturnal hypoglycemia episodes ( = 0.0002). This report describes a rare coexistence of adult-onset nesidioblastosis and insulinoma, suggesting the existence of a wide and continuous spectrum of proliferative β-cell changes. Moreover, we propose that uncooked cornstarch may offer an additional approach to alleviate the hypoglycemic episodes when surgery is impracticable/unaccepted.

摘要

胰岛细胞瘤和胰岛素瘤是引起内源性高胰岛素血症低血糖的内分泌胰腺疾病。它们的共存非常罕见,治疗代表了一个尚未解决的难题。患者为 43 岁白人女性,有 2 年反复发作严重低血糖事件史。诊断工作强烈提示为胰岛素瘤,患者接受了腹腔镜机器人辅助下的手术治疗。然而,手术探查和术中超声未能发现胰腺肿瘤。因此,根据选择性动脉内钙刺激试验的结果进行了逐步切除,最终在脾动脉处行胰十二指肠切除术。组织病理学检查和免疫组织化学染色与成人发病的胰岛细胞瘤一致。手术后,患者继续出现低血糖,尽管进行了药物治疗(奥曲肽、钙通道阻滞剂、二氮嗪和泼尼松)但无济于事。经过多学科评估和对重复腹部 CT 扫描的仔细审查,在胰腺尾部发现了一个小结节性病变。通过腹腔镜进行了结节切除术,病理检查显示为胰岛素瘤。尽管切除了胰岛素瘤,但血糖值仅部分恢复,仍存在夜间低血糖。睡前给予未煮过的玉米淀粉(1.25 g/kg 体重)可显著改善间质葡萄糖水平(<0.0001)并减少夜间低血糖发作(=0.0002)。本报告描述了一种罕见的成人发病的胰岛细胞瘤和胰岛素瘤共存,提示存在广泛连续的β细胞增殖变化谱。此外,我们提出未煮过的玉米淀粉在手术不可行/不可接受时可能提供一种额外的缓解低血糖发作的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5d8/6996476/0fc90e9d3f90/fendo-11-00010-g0001.jpg

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