{"title":"Pediatric pancreatic perineurioma: A case report","authors":"Eakes A , Hill B , Beierle EA","doi":"10.1016/j.epsc.2025.102959","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Perineuriomas are rare, benign, peripheral nerve sheath tumors that are distinguished from other lesions such as neurofibroma with specific immunohistochemical stains.</div></div><div><h3>Case presentation</h3><div>The patient was an 18-year-old female with a history of spina bifida and neuroblastoma. She was asymptomatic but at a follow up visit for urinary issues related to her spina bifida, an ultrasound of the kidneys revealed a retroperitoneal mass near the left kidney. Cross sectional imaging was completed and identified a left paraspinous mass measuring 13.3 x 10.1 × 11.2 cm, arising from the pancreas. Laboratory evaluations including liver function tests, complete blood count, renal panel, urine metanephrines, alpha fetoprotein and beta-hCg were normal. Complete resection of the mass required a distal pancreatectomy and splenectomy performed via laparotomy. Histologic evaluation of the mass was consistent with perineurioma. Postoperative recovery was unremarkable and the patient remains free of disease at one year followup with ultrasound imaging.</div></div><div><h3>Conclusion</h3><div>Perineurioma, a rare peripheral nerve sheath neoplasm, should be considered in the differential diagnosis for retroperitoneal masses in the pediatric population.</div></div>","PeriodicalId":45641,"journal":{"name":"Journal of Pediatric Surgery Case Reports","volume":"114 ","pages":"Article 102959"},"PeriodicalIF":0.2000,"publicationDate":"2025-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pediatric Surgery Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2213576625000041","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction
Perineuriomas are rare, benign, peripheral nerve sheath tumors that are distinguished from other lesions such as neurofibroma with specific immunohistochemical stains.
Case presentation
The patient was an 18-year-old female with a history of spina bifida and neuroblastoma. She was asymptomatic but at a follow up visit for urinary issues related to her spina bifida, an ultrasound of the kidneys revealed a retroperitoneal mass near the left kidney. Cross sectional imaging was completed and identified a left paraspinous mass measuring 13.3 x 10.1 × 11.2 cm, arising from the pancreas. Laboratory evaluations including liver function tests, complete blood count, renal panel, urine metanephrines, alpha fetoprotein and beta-hCg were normal. Complete resection of the mass required a distal pancreatectomy and splenectomy performed via laparotomy. Histologic evaluation of the mass was consistent with perineurioma. Postoperative recovery was unremarkable and the patient remains free of disease at one year followup with ultrasound imaging.
Conclusion
Perineurioma, a rare peripheral nerve sheath neoplasm, should be considered in the differential diagnosis for retroperitoneal masses in the pediatric population.
导读:神经鞘瘤是一种少见的、良性的周围神经鞘肿瘤,可通过特异性免疫组化染色与神经纤维瘤等其他病变区分开来。患者为18岁女性,既往有脊柱裂和神经母细胞瘤病史。患者无症状,但在脊柱裂泌尿系统问题的随访中,肾脏超声检查显示左肾附近有腹膜后肿块。完成横断成像,发现左侧棘旁肿块,尺寸为13.3 x 10.1 x 11.2 cm,起源于胰腺。实验室检查包括肝功能检查、全血细胞计数、肾脏检查、尿肾上腺素、甲胎蛋白和- hcg均正常。完全切除肿块需要经剖腹手术行远端胰腺切除术和脾切除术。肿块的组织学检查符合神经会阴瘤。术后恢复不明显,患者在超声成像随访一年后仍无疾病。结论小儿腹膜后肿物是一种少见的周围神经鞘肿瘤,应作为鉴别诊断的参考。