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Idiopathic desmoid-type fibromatosis of the pancreatic head: case report and literature review

机译:胰头特发性类胶质样纤维瘤病:病例报告和文献复习

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摘要

Desmoid-type fibromatosis (DTF) is an uncommon nonmetastatic fibrous neoplasm. Sporadic intraperitoneal DTF is rarely described in current literature. We herein report a case of DTF of unknown cause involving the pancreatic head. A 41-year-old man presented with recurrent epigastric pain and weight loss. An abdominal computed tomography scan showed a well-delineated solid cystic mass inside the pancreatic head. Pylorus-preserving pancreaticoduodenectomy was performed due to the patient’s debilitating symptoms and suspected malignancy. The pathological examination revealed massive fibroblastic proliferation arising from the musculoaponeurotic tissues, consistent with a diagnosis of DTF. Immunohistochemical phenotyping determined positive immunoreactivity to vimentin and β-catenin, but negative immunoreactivity to smooth muscle actin, CD117, CD34, or S-100, confirming the diagnosis of DTF. No local recurrence or distant metastasis was found during a 24-month follow-up. Radical resection is recommended as first-line treatment for pancreatic DTF. Long-term follow-up studies are required to establish the prognosis of pancreatic DTF.
机译:类胶质纤维瘤病(DTF)是一种罕见的非转移性纤维性肿瘤。当前文献中很少描述偶发性腹膜内DTF。我们在此报告了一种不明原因的涉及胰头的DTF病例。一名41岁的男子出现上腹部反复疼痛和体重减轻。腹部计算机断层扫描显示胰头内部有良好的固态囊性肿块。保留幽门的胰十二指肠切除术是由于患者的虚弱症状和疑似恶性肿瘤而进行的。病理检查显示由肌肉海绵体组织引起的大量成纤维细胞增生,与DTF的诊断一致。免疫组织化学表型确定对波形蛋白和β-连环蛋白的阳性免疫反应,但对平滑肌肌动蛋白,CD117,CD34或S-100的阴性免疫反应,证实了DTF的诊断。在24个月的随访中未发现局部复发或远处转移。推荐根治性切除术作为胰腺DTF的一线治疗。需要长期的随访研究来确定胰腺DTF的预后。

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