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Zollinger-Ellison Syndrome Associated with von Recklinghausen Disease: Case Report and Literature Review

机译:冯·瑞克林豪森病相关的佐林格-埃里森综合征:病例报告和文献复习

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Patient: Female, 28 Final Diagnosis: Gastrinoma Symptoms: Vomiting ? diarrhea ? epigastric soreness ? heartburn ? nausea ? significant weight loss Medication: — Clinical Procedure: Esophagogastroduodenoscopy ? blood tests ? abdomen CT scan ? surgery Specialty: Gastroenterology and Hepatology Objective: Rare co-existance of disease or pathology Background: Pancreatic endocrine tumors (PETs) are rare and can occur as part of neurofibromatosis type 1 (NF1). Gastrinomas are functional PETs that are rarely associated with NF1. Only two cases of their occurrence have been reported in the literature. Case Report: A 28-year-old woman was admitted for further evaluation of epigastric soreness, heartburn, nausea, vomiting, diarrhea, and a significant weight loss. Physical examination was remarkable for cutaneous findings (axillary freckling and multiple café-au-lait spots) as well as neurofibromas (dermal, plexiform). A diagnosis of NF1 was confirmed. Esophagogastroduodenoscopy (EGD) revealed multiple ulcers in the duodenum and the upper jejunum. A fasting gastrin level exceeded ten times the normal limit. An abdominal multi-slice 128 computed tomography (CT) scan revealed an oval mass of 26 mm in diameter adjacent to the second segment of the duodenum. The patient was examined carefully to rule out multiple endocrine neoplasia type 1 (MEN1). Surgical resection was performed and a gastrinoma, causing Zollinger-Ellison syndrome (ZES), was diagnosed by histological examinations of the extirpated mass. The serum gastrin level decreased to normal limits shortly after surgery. Continuous follow-up revealed that the symptoms and the EGD findings completely resolved without recurrences. Conclusions: Although NF1 has common skeletal, visual, neurological, and cardiovascular complications, it also has a rare association with duodenal or pancreatic gastrinomas. Vigilance for this possible association is important to promote timely and careful management to help eliminate serious and potentially life-threatening complications.
机译:患者:女,28岁最终诊断:胃泌素瘤症状:呕吐?腹泻?上腹酸痛?胃灼热 ?恶心?重大减肥药物:—临床程序:食管胃十二指肠镜检查?验血?腹部CT扫描外科专长:胃肠病学和肝病学目的:罕见的疾病或病理并存背景:胰腺内分泌肿瘤(PET)罕见,可作为1型神经纤维瘤病(NF1)的一部分发生。胃瘤是功能性PET,很少与NF1相关。文献中仅报道了其发生的两个案例。病例报告:一名28岁的妇女因进一步评估上腹酸痛,胃灼热,恶心,呕吐,腹泻和明显的体重减轻而入院。身体检查对于皮肤发现(腋窝雀斑和多个咖啡色斑点)以及神经纤维瘤(皮肤,丛状)非常显着。证实诊断为NF1。食管胃十二指肠镜检查(EGD)显示十二指肠和空肠上段有多个溃疡。空腹胃泌素水平超过正常极限的十倍。腹部多层128层计算机断层扫描(CT)扫描显示邻近十二指肠第二节段的直径为26 mm的椭圆形块。对该患者进行了仔细检查,以排除多发性内分泌肿瘤1型(MEN1)。进行手术切除,并通过组织学检查切除的肿块,诊断出引起Zollinger-Ellison综合征(ZES)的胃泌素瘤。手术后不久,血清胃泌素水平降至正常水平。持续的随访显示,症状和EGD的发现完全消失,没有复发。结论:尽管NF1具有常见的骨骼,视觉,神经和心血管并发症,但它与十二指肠或胰腺胃泌素瘤也很少见。对这种可能的关联保持警惕对于促进及时和谨慎的管理非常重要,有助于消除严重且可能危及生命的并发症。

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