Maharjan Prabir, Raut Sneha, Paudel Suman, Baral Arika, Maharjan Dhiresh Kumar, Thapa Prabin Bikram
Department of Gastrointestinal and General Surgery, Kathmandu Medical College and Teaching Hospital, Kathmandu, Nepal.
MBBS, Kathmandu Medical College and Teaching Hospital, Kathmandu, Nepal.
Int J Surg Case Rep. 2025 Jan;126:110805. doi: 10.1016/j.ijscr.2024.110805. Epub 2024 Dec 28.
Insulinomas are rare pancreatic neuroendocrine neoplasms with an incidence of one to four cases per million annually and a 5 % to 10 % association with hereditary multiple endocrine neoplasia type-1. While most insulinomas are benign and well-encapsulated, approximately 6 % may have malignant potential. Intraoperative localization remains a vital component of treatment, often facilitated by modern imaging techniques like intraoperative ultrasound and fluorescence modalities.
A 52-year-old woman was referred to Kathmandu Medical College with generalized weakness, recurrent headaches, and fatigue relieved by food intake. She had a history of hypoglycemia-induced abnormal body movements and loss of consciousness. After biochemical and imaging evaluations, she was diagnosed with pancreatic insulinoma. Based on the higher affinity of neuroendocrine tumoral cells for Indocyanine Green compared to normal pancreatic cells, the patient underwent Indocyanine Green-directed laparoscopic-assisted pancreaticoduodenectomy managed perioperatively with subcutaneous octreotide. She had an uneventful postoperative period and was discharged on the eighth day.
Insulinomas present a unique diagnostic and therapeutic challenge, especially in cases of sporadic occurrence. Surgical resection is the mainstay of treatment, with enucleation preferred for benign tumors. In this case, fluorescence-guided surgery and intraoperative ultrasound aided in accurate localization and successful excision.
Insulinomas, though rare, require prompt diagnosis and surgical intervention to prevent malignancy and metastasis.
胰岛素瘤是一种罕见的胰腺神经内分泌肿瘤,年发病率为百万分之一至四例,与1型遗传性多发性内分泌肿瘤的关联率为5%至10%。虽然大多数胰岛素瘤是良性的且包膜完整,但约6%可能具有恶性潜能。术中定位仍然是治疗的重要组成部分,现代成像技术如术中超声和荧光成像方式常常有助于实现这一点。
一名52岁女性因全身无力、反复头痛以及进食后疲劳缓解被转诊至加德满都医学院。她有低血糖诱发的异常身体运动和意识丧失病史。经过生化和影像学评估,她被诊断为胰腺胰岛素瘤。基于神经内分泌肿瘤细胞与正常胰腺细胞相比对吲哚菁绿具有更高的亲和力,该患者接受了吲哚菁绿引导下的腹腔镜辅助胰十二指肠切除术,并在围手术期皮下注射奥曲肽进行管理。她术后恢复顺利,于第八天出院。
胰岛素瘤带来了独特的诊断和治疗挑战,尤其是在散发性病例中。手术切除是主要的治疗方法,对于良性肿瘤首选摘除术。在本病例中,荧光引导手术和术中超声有助于准确的定位和成功切除。
胰岛素瘤虽然罕见,但需要及时诊断和手术干预以预防恶变和转移。