腹腔镜成功切除一罕见局灶性先天性高胰岛素血症:个案报告及文献复习

A. Sukhotskaya, I. Kagantsov, V. Bairov, M. G. Vitovshchik, I. Nikitina, D. Ryzhkova, L. Mitrofanova, L. R. Sarakaeva
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摘要

先天性高胰岛素血症是一种严重的疾病,会对大脑皮层造成不可逆转的损害。这篇文章提出了一个临床观察成功的手术治疗儿童与一个极其罕见的形式高胰岛素血症伴有两个灶在胰腺的两端。由于反复出现低血糖,孩子从出生起就处于极度危急的状态,两周大时被诊断为高胰岛素血症。开始使用二氮氧化物和奥曲肽进行特异性治疗,但被证明无效(仍需要静脉注射葡萄糖,奥曲肽仅提供部分结果)。当患儿1个月大时,行正电子发射断层扫描- 18F-DOPA计算机断层扫描,发现胰腺尾部和头部的放射性药物局灶性过度固定。这一发现表明存在两个病理性病灶或一个病灶在尾部和放射性药物在头部的生理积累。在1个月零20天的时候,孩子接受了腹腔镜胰腺翻修术,通过活检证实了胰腺尾部的病灶。在确认切除边缘清晰的情况下切除尾部(15%)。在进一步的复习中,在头部检测到一个焦点。组织学证实完全切除后再次行手术切除。术后第12天患儿未经治疗出院,临床痊愈。目前正在对该儿童进行监测(超过6个月),根据年龄进行生长发育。进行了空腹检查,排除了高胰岛素血症的复发。本文详细介绍临床和影像学检查结果、患者病史、手术技术和干预结果。作为讨论的一部分,对先天性高胰岛素血症儿童腹腔镜胰腺切除术的行为进行了文献回顾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful laparoscopic resection of a rare focal form of congenital hyperinsulinism: Case report and literature review
Congenital hyperinsulinism is a severe disease that causes irreversible damage to the cerebral cortex. This article presents a clinical observation of successful surgical treatment for a child with an extremely rare form of hyperinsulinism accompanied by two foci in the opposite ends of the pancreas. The child was in extremely critical condition from birth due to recurrent hypoglycemia and was diagnosed with hyperinsulinism at the age of two weeks. Specific therapy with diazoxide and octreotide was initiated but proven to be ineffective (parenteral glucose administration was still needed, and octreotide only provided partial results). When the child was one month old, positron emission tomography-computed tomography with 18F-DOPA was performed and revealed the focal hyperfixation of the radiopharmaceutical in the tail and head of the pancreas. This finding indicated the presence of two pathological foci or a focus in the tail and the physiological accumulation of the radiopharmaceutical in the head. At the age of one month and 20 days, the child underwent laparoscopic revision of the pancreas to visualize a focus in the tail that was confirmed by express biopsy. The resection of the tail (15%) was performed with confirmation of clear resection margins. During further revision, a focus was detected in the head. Resection was again performed with histological confirmation of complete resection. On the 12th day after the operation, the child was discharged without therapy with clinical recovery. The child is currently being monitored (for over six months), growing and developing according to age. A fasting test was performed, and the recurrence of hyperinsulinism was ruled out. This article presents a detailed description of the clinical and radiological examination results, the patients history, the surgical techniques, and the intervention results. As part of the discussion, a literature review on the behavior of laparoscopic resections of the pancreas in children with congenital hyperinsulinism was carried out.
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