Case report: Initial presentation of pancreatic schwannoma as cystic pancreatic mass treated with classic Whipple's procedure.

Zekewos Demissie Jemaneh, Nahom Zemedkun, Serkalem Nurlegn, Amanuel Mamuye Woldeamanuel, Henok Seife, Yohannes Birhanu, Bethelhem Berhanu Belachew
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Abstract

Pancreatic schwannomas are exceedingly rare tumors arising from Schwann cells of the peripheral nerve sheath within the pancreas. Often asymptomatic or presenting with nonspecific symptoms, these tumors pose a diagnostic challenge due to their mimicry of other pancreatic neoplasms on imaging studies. Histologically, pancreatic schwannomas demonstrate spindle cell proliferation with a distinct Immunohistochemical profile, including positive staining for S-100 protein. Surgical resection remains the cornerstone of treatment, with excellent long-term prognosis following complete excision. Here, we present a case report of a pancreatic schwannoma in a woman presenting with a cystic pancreatic mass, underscoring the importance of considering this rare entity in the differential diagnosis of pancreatic lesions.

Abstract Image

病例报告:胰腺神经鞘瘤最初表现为囊性胰腺肿块,采用经典惠普尔手术治疗。
胰腺神经鞘瘤是一种极为罕见的肿瘤,起源于胰腺周围神经鞘的雪旺细胞。这些肿瘤通常无症状或表现为非特异性症状,由于其影像学检查与其他胰腺肿瘤相似,因此对诊断构成挑战。组织学上,胰腺神经鞘瘤表现出梭形细胞增生,具有独特的免疫组化特征,包括S-100蛋白阳性染色。手术切除仍然是治疗的基石,完全切除后具有良好的长期预后。在此,我们报告一女性胰腺神经鞘瘤的病例报告,其表现为胰腺囊性肿块,强调在胰腺病变鉴别诊断中考虑这种罕见实体的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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