Insulinoma of Pancreas, Brief Experience at a Dedicated Surgical Oncology Department

A. Jamal, J. Mohsin, I. Haq, N. Mobeen, S. Begum, O. Shakeel, Syed Irfan Kabir, A. Syed, S. Khattak
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Abstract

Introduction: Insulinoma of pancreas is a rare neuroendocrine tumor (NET). Mostly insulinomas are benign and solitary. They can have association with multiple endocrine neoplasia 1 (MEN -1). Insulinomas presents with symptoms of hypoglycemia. Most of the times the symptoms are vague and result in delay in the diagnosis and hence management. After appropriate diagnostic and localization investigations along with metastatic workup, surgery is the treatment of choice. Surgery can offer cure. Minimally invasive surgery can offer potential benefits of minimal morbidity and at least equal oncological outcomes. Study Design: Case series. Place and Duration of Study: Department of Surgical Oncology, Shaukat Khanam Memorial Cancer Hospital & Research Center (SKMCH&RC), from January 2011 to March 2020. Methodology: We studied a total of five patients that presented to SKMCH&RC in the above-mentioned period. Detailed clinical information of these five patients, including sociodemographic variables, symptomatology, diagnostic and localization investigations, clinical and pathological staging, comprehensive details of surgery, postoperative course, oncological outcomes, postoperative resolution of symptoms, postoperative diabetes, prognosis and follow up duration were analysed. The record was being retrospectively retrieved from Hospital Information System (HIS) that is prospectively maintained. We are a paperless hospital and all data and record of the patient is maintained through HIS. Results: A total of five patients presented to SKMCH&RC with a mean age of 41 (18 -80) years. The median duration of symptoms was 24 (6-60) months. Symptomatic hypoglycemia was present in all 5 (100%) of the patients. Tumor distribution in the pancreas was as follows; uncinate 1 (20%), body 1 (20%) and tail 3 (60%). All five patients (100%) were treated by surgery. Resolution of symptoms occurred in all five (100%) of the patients. Conclusion: Insulinoma of pancreas is a rare disease with varied symptomatology, physicians shall have an index of suspicion for this disorder to aid early diagnosis that is pivotal for the management and prevention of possible fatal complications of hypoglycemia. Appropriate diagnostic and localizing investigations are required. Adequate surgery can offer cure. Minimally invasive surgery can be safely offered with equal oncological outcomes.
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胰腺胰岛素瘤,在专门外科肿瘤科的简短经验
简介:胰腺胰岛素瘤是一种罕见的神经内分泌肿瘤。大多数胰岛素瘤是良性和孤立的。它们可能与多发性内分泌肿瘤1 (MEN -1)有关。胰岛素缺乏表现为低血糖症状。大多数时候,症状是模糊的,导致延误诊断和治疗。经过适当的诊断和定位调查以及转移性检查,手术是治疗的选择。手术可以治愈。微创手术可以提供最小的发病率和至少相同的肿瘤结果的潜在好处。研究设计:病例系列。研究地点和时间:2011年1月至2020年3月,Shaukat Khanam纪念癌症医院和研究中心(SKMCH&RC)外科肿瘤科。方法:我们研究了在上述期间到SKMCH&RC就诊的5例患者。分析这5例患者的详细临床资料,包括社会人口学变量、症状、诊断和定位调查、临床和病理分期、手术综合细节、术后病程、肿瘤预后、术后症状缓解、术后糖尿病、预后和随访时间。从前瞻性维护的医院信息系统(HIS)中回顾性检索记录。我们是无纸化医院,病人的所有数据和记录都是通过HIS来维护的。结果:共有5例患者到SKMCH&RC就诊,平均年龄41岁(18 -80岁)。中位症状持续时间为24(6-60)个月。5例(100%)患者均出现症状性低血糖。胰腺肿瘤分布如下:钩肢1(20%),身体1(20%)和尾巴3(60%)。5例(100%)均行手术治疗。5例(100%)患者症状均得到缓解。结论:胰腺胰岛素瘤是一种罕见的疾病,其症状多样,医师应掌握该疾病的怀疑指数,以帮助早期诊断,这对低血糖并发症的处理和预防至关重要。需要适当的诊断和定位调查。适当的手术可以治愈。微创手术可以安全地提供,并具有相同的肿瘤预后。
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