原发性高甘油三酯血症诱发的一组巴基斯坦儿童胰腺炎

S. Khan, Anusha Khan, M. Malik
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Results We found a cohort of 6 patients with primary hypertriglyceridemia after excluding secondary causes. Out of these 6 patients, 4 (66.6%) were male and 2 (33.3%) were female. Minimum age of our patient was 2 months and maximum was 17 years with a mean age of 6.5 years. Two patients presented less than one year of age. Mean triglyceride levels was 1,599 + 523 mg/dL. Four patients (66.6%) had acute pancreatitis, one each (16.6%) had recurrent and chronic pancreatitis. Family history was positive for hyperlipidaemia in two patients who had positive consanguinity. Patients with positive family history were symptomatic at earlier age. Conclusions This is the first study to highlight primary hypertriglyceridemia presenting as pancreatitis in paediatric population from Pakistan. 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摘要

摘要目的原发性高甘油三酯血症是一种罕见的儿童疾病。高甘油三酯血症诱发的胰腺炎最常见于成人,是继胆结石和饮酒之后的第三大常见病因。该研究的目的是强调高甘油三酯血症诱发的胰腺炎在三级护理医院的儿童队列的频率。方法对2013 - 2020年伊斯兰堡Shifa国际医院儿科胰腺炎患者进行回顾性分析。所有符合纳入标准的18岁以下患者均被纳入。检查了患者的医疗记录,包括症状、体征、年龄、生长参数和实验室检查。对HTG患者的胰腺炎或血脂异常家族史进行详细回顾。结果排除继发原因后,我们发现了6例原发性高甘油三酯血症患者。其中男性4例(66.6%),女性2例(33.3%)。患者最小年龄2个月,最大年龄17岁,平均年龄6.5岁。2例患者年龄不足1岁。平均甘油三酯水平为1599 + 523 mg/dL。急性胰腺炎4例(66.6%),复发性和慢性胰腺炎各1例(16.6%)。2例有血缘关系的患者高脂血症家族史呈阳性。家族史阳性的患者出现症状的年龄较早。结论:这是第一个在巴基斯坦儿童人群中强调原发性高甘油三酯血症表现为胰腺炎的研究。所有患者的甘油三酯水平均大于1000mg /dL。
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Primary hypertriglyceridemia induced pancreatitis in a cohort of Pakistani children
Abstract Objectives Primary hypertriglyceridemia is a rare condition in children. Hypertriglyceridemia induced pancreatitis is most commonly reported in adults, accounting for third most common cause after gallstones and alcohol consumption. The study aims to highlight the frequency of hypertriglyceridemia induced pancreatitis in a cohort of children presenting in a tertiary care hospital. Methods A retrospective review of paediatric patients with pancreatitis was conducted in Shifa International hospital, Islamabad, from 2013 to 2020. All patients under 18 years of age who fulfilled the inclusion criteria were included. Medical records of patients were checked for symptoms, signs, age, growth parameters and laboratory investigations. Patients who had HTG were reviewed in detail for family history of pancreatitis or dyslipidemias. Results We found a cohort of 6 patients with primary hypertriglyceridemia after excluding secondary causes. Out of these 6 patients, 4 (66.6%) were male and 2 (33.3%) were female. Minimum age of our patient was 2 months and maximum was 17 years with a mean age of 6.5 years. Two patients presented less than one year of age. Mean triglyceride levels was 1,599 + 523 mg/dL. Four patients (66.6%) had acute pancreatitis, one each (16.6%) had recurrent and chronic pancreatitis. Family history was positive for hyperlipidaemia in two patients who had positive consanguinity. Patients with positive family history were symptomatic at earlier age. Conclusions This is the first study to highlight primary hypertriglyceridemia presenting as pancreatitis in paediatric population from Pakistan. All patients had triglycerides level of greater than 1000 mg/dL.
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