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胰腺硬化性上皮样纤维肉瘤:一例报告。

Sclerosing epithelioid fibrosarcoma of the pancreas: A case report.

作者信息

Sun Meng-Qing, Guo Li-Na, You Yan, Qiu Yan-Yu, He Xiao-Dong, Han Xian-Lin

机构信息

Department of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China.

Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China.

出版信息

World J Clin Cases. 2024 Sep 16;12(26):5983-5989. doi: 10.12998/wjcc.v12.i26.5983.

Abstract

BACKGROUND

A sclerosing epithelioid fibrosarcoma (SEF) is a rare malignant fibroblastic soft tissue tumor that rarely occurs in intra-abdominal organs. A case of a SEF in the pancreatic head is reported herein, including its clinical manifestations, preoperative imaging features, gross specimen and pathological findings.

CASE SUMMARY

A 33-year-old male patient was admitted to Peking Union Medical College Hospital in December 2023 due to a one-year history of intermittent upper abdominal pain and the discovery of a pancreatic mass. The patient underwent an enhanced computed tomography scan of the abdomen, which revealed a well-defined, round mass with clear borders and calcifications in the pancreatic head. The mass exhibited progressive, uneven mild enhancement, measuring approximately 6.6 cm × 6.3 cm. The patient underwent laparoscopic pylorus-preserving pancreaticoduodenectomy. Postoperative pathological examination revealed that the lesion was consistent with a SEF. At the 3-month postoperative follow-up, the patient did not report any short-term complications, and there were no signs of tumor recurrence.

CONCLUSION

SEFs are rare malignant fibrous soft tissue tumors. SEFs rarely develop in the pancreas, and its preoperative diagnosis depends on imaging findings, with confirmation depending on pathological examination and immunohistochemistry. Currently, only four cases of pancreatic SEF have been reported in studies written in English. This case is the first reported case of a pancreatic SEF by a clinical physician.

摘要

背景

硬化性上皮样纤维肉瘤(SEF)是一种罕见的恶性成纤维细胞性软组织肿瘤,很少发生于腹腔内器官。本文报道一例胰头SEF病例,包括其临床表现、术前影像学特征、大体标本及病理结果。

病例摘要

一名33岁男性患者因间歇性上腹痛1年并发现胰腺肿物于2023年12月入住北京协和医院。患者接受了腹部增强计算机断层扫描,结果显示胰头有一个边界清晰、圆形、边界清楚且有钙化的肿物。该肿物呈渐进性、不均匀轻度强化,大小约为6.6 cm×6.3 cm。患者接受了腹腔镜保留幽门胰十二指肠切除术。术后病理检查显示病变符合SEF。术后3个月随访时,患者未报告任何短期并发症,也没有肿瘤复发迹象。

结论

SEF是罕见的恶性纤维性软组织肿瘤。SEF很少发生于胰腺,其术前诊断依赖于影像学表现,确诊依赖于病理检查及免疫组化。目前,英文文献报道的胰腺SEF病例仅有4例。本病例是临床医生首次报道的胰腺SEF病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/604e/11287511/0f96a49c76d0/WJCC-12-5983-g001.jpg

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