A. Jamal, J. Mohsin, I. Haq, N. Mobeen, S. Begum, O. Shakeel, Syed Irfan Kabir, A. Syed, S. Khattak
{"title":"Insulinoma of Pancreas, Brief Experience at a Dedicated Surgical Oncology Department","authors":"A. Jamal, J. Mohsin, I. Haq, N. Mobeen, S. Begum, O. Shakeel, Syed Irfan Kabir, A. Syed, S. Khattak","doi":"10.31487/j.cor.2020.08.10","DOIUrl":null,"url":null,"abstract":"Introduction: Insulinoma of pancreas is a rare neuroendocrine tumor (NET). Mostly insulinomas are\nbenign and solitary. They can have association with multiple endocrine neoplasia 1 (MEN -1). Insulinomas\npresents with symptoms of hypoglycemia. Most of the times the symptoms are vague and result in delay in\nthe diagnosis and hence management. After appropriate diagnostic and localization investigations along\nwith metastatic workup, surgery is the treatment of choice. Surgery can offer cure. Minimally invasive\nsurgery can offer potential benefits of minimal morbidity and at least equal oncological outcomes.\nStudy Design: Case series.\nPlace and Duration of Study: Department of Surgical Oncology, Shaukat Khanam Memorial Cancer\nHospital & Research Center (SKMCH&RC), from January 2011 to March 2020.\nMethodology: We studied a total of five patients that presented to SKMCH&RC in the above-mentioned\nperiod. Detailed clinical information of these five patients, including sociodemographic variables,\nsymptomatology, diagnostic and localization investigations, clinical and pathological staging,\ncomprehensive details of surgery, postoperative course, oncological outcomes, postoperative resolution of\nsymptoms, postoperative diabetes, prognosis and follow up duration were analysed. The record was being\nretrospectively retrieved from Hospital Information System (HIS) that is prospectively maintained. We are\na paperless hospital and all data and record of the patient is maintained through HIS.\nResults: A total of five patients presented to SKMCH&RC with a mean age of 41 (18 -80) years. The\nmedian duration of symptoms was 24 (6-60) months. Symptomatic hypoglycemia was present in all 5\n(100%) of the patients. Tumor distribution in the pancreas was as follows; uncinate 1 (20%), body 1 (20%)\nand tail 3 (60%). All five patients (100%) were treated by surgery. Resolution of symptoms occurred in all\nfive (100%) of the patients.\nConclusion: Insulinoma of pancreas is a rare disease with varied symptomatology, physicians shall have\nan index of suspicion for this disorder to aid early diagnosis that is pivotal for the management and\nprevention of possible fatal complications of hypoglycemia. Appropriate diagnostic and localizing\ninvestigations are required. Adequate surgery can offer cure. Minimally invasive surgery can be safely\noffered with equal oncological outcomes.","PeriodicalId":10487,"journal":{"name":"Clinical Oncology and Research","volume":"140 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Oncology and Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31487/j.cor.2020.08.10","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
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.