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肛周浅表性CD34阳性纤维母细胞瘤:一例报告

Perianal superficial CD34-positive fibroblastic tumor: A case report.

作者信息

Long Chen-Yan, Wang Tao-Li

机构信息

The Second Department of General Surgery, Zhuzhou Hospital Affiliated to Xiangya School of Medicine, Central South University, Zhuzhou 412007, Hunan Province, China.

Department of Pathology, Zhuzhou Hospital Affiliated to Xiangya School of Medicine, Central South University, Zhuzhou 412007, Hunan Province, China.

出版信息

World J Clin Cases. 2021 Jul 16;9(20):5605-5610. doi: 10.12998/wjcc.v9.i20.5605.

Abstract

BACKGROUND

Superficial CD34-positive fibroblast tumors (SCPFTs) are newly recognized fibroblast and myofibroblast tumors representing intermediate tumors. To the best of our knowledge, fewer than 50 cases have been reported. Perianal SCPFT has not been previously reported.

CASE SUMMARY

A 55-year-old man was hospitalized upon discovering a painless perianal lump 10 d prior. Physical examination showed a lump of approximately 3 cm × 4 cm in the 7 to 8 o'clock direction in the perianal area. Perianal abscess was considered the primary diagnosis. Lump removal surgery was performed under epidural anesthesia. Postoperative pathology showed a well-circumscribed, soft tissue-derived, spindle-cell tumor with strong CD34 positivity by immunohistochemistry. The final diagnosis was perianal SCPFT. There were no complications, and the patient was followed for more than 8 mo without recurrence or metastasis.

CONCLUSION

We report a case of perianal superficial CD34-positive fibroblast tumor. This rare mesenchymal neoplasm has distinctive histomorphology, which is important for diagnosis. Comprehensive consideration of clinical information, imaging, histology, and immunohistochemistry is important for diagnosis.

摘要

背景

浅表性CD34阳性成纤维细胞瘤(SCPFTs)是新认识的成纤维细胞和肌成纤维细胞瘤,属于中间型肿瘤。据我们所知,报道的病例少于50例。肛周SCPFT此前未见报道。

病例摘要

一名55岁男性因10天前发现肛周无痛性肿块入院。体格检查显示肛周区域7至8点钟方向有一个约3 cm×4 cm的肿块。初步诊断为肛周脓肿。在硬膜外麻醉下进行肿块切除术。术后病理显示为边界清楚的软组织来源梭形细胞瘤,免疫组化显示CD34强阳性。最终诊断为肛周SCPFT。无并发症发生,对患者随访8个月以上无复发或转移。

结论

我们报告一例肛周浅表性CD34阳性成纤维细胞瘤。这种罕见的间叶性肿瘤具有独特的组织形态学,对诊断很重要。综合考虑临床信息、影像学、组织学和免疫组化对诊断很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0257/8281416/8daaf0087e23/WJCC-9-5605-g001.jpg

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