中华皮肤科杂志 ›› 2026, Vol. 59 ›› Issue (7): 675-677.doi: 10.35541/cjd.20240058

• 研究报道 • 上一篇    下一篇

单发纤维毛囊瘤15例临床病理分析

张淑媛    牛丰南    王益华   

  1. 南京大学医学院附属鼓楼医院病理科,南京  210008
    张淑媛现在铜陵市义安区人民医院病理科,铜陵  244100

  • 收稿日期:2024-01-29 修回日期:2024-12-18 发布日期:2026-07-03
  • 通讯作者: 王益华 E-mail:yihua8822@126.com

Clinicopathological analysis of 15 cases of solitary fibrofolliculoma

Zhang Shuyuan, Niu Fengnan, Wang Yihua   

  1. Department of Pathology, Nanjing Drum Tower Hospital, the Affiliated Hospital of Nanjing University Medical School, Nanjing 210008, China Zhang Shuyuan is now working at the Department of Pathology, People's Hospital of Yi'an District, Tongling 244100, China
  • Received:2024-01-29 Revised:2024-12-18 Published:2026-07-03
  • Contact: Wang Yihua E-mail:yihua8822@126.com

摘要: 【摘要】 目的 探讨单发性纤维毛囊瘤的临床和病理特征。方法 本研究为病例系列研究,回顾2008年4月至2023年12月于南京鼓楼医院经组织病理确诊的15例单发纤维毛囊瘤患者的临床资料,收集临床信息、病理学特征、免疫组化表现、随访信息。结果 15例患者年龄22 ~ 71岁,男9例,女6例;皮疹多数表现为黄色、白色的单发丘疹或结节,直径0.2 ~ 1.2 cm;发病部位包括鼻部(8例)、耳部(4例)、眼部(2例)、枕部(1例)。组织病理:真皮层内以发育良好的毛囊为中心,形成网状及分叶状结构;细胞一般无明显异形,有些可见毛鞘增生。7例行免疫组化染色检查:肿瘤上皮细胞p63、p40弥漫阳性,平滑肌肌动蛋白(SMA)阳性,S100、上皮细胞膜抗原局灶阳性,癌胚抗原阴性;肿瘤组织周围间叶细胞CD10阳性,CD34局灶阳性,SMA和结蛋白阴性;肿瘤内间叶细胞不表达CD10。所有患者均采取手术切除肿瘤,术后随访4 ~ 192个月,未见复发。结论 单发纤维毛囊瘤多为好发于面部与头颈的丘疹或结节,免疫组化特征为肿瘤组织周围间叶细胞CD10阳性,肿瘤内间叶细胞不表达CD10,对诊断具有一定帮助。

关键词: 错构瘤, 纤维毛囊瘤, 单发, 组织病理, 免疫组化

Abstract: 【Abstract】 Objective To investigate the clinical and pathological characteristics of solitary fibrofolliculoma. Methods This was a case series study. Clinical data were collected from 15 patients with histopathologically confirmed solitary fibrofolliculoma at Nanjing Drum Tower Hospital from April 2008 to December 2023. Clinical characteristics, histopathological features, immunohistochemical findings, and follow-up information were collected and analyzed. Results The 15 patients were aged from 22 to 71 years, including 9 males and 6 females. Skin lesions mostly presented as solitary yellowish or white papules or nodules measuring 0.2 ? 1.2 cm in diameter. The lesions were located on the nose (8 cases), ear (4 cases), periocular region (2 cases), and occipital region (1 case). Histopathologically, the lesions were centered on well-developed hair follicles within the dermis and exhibited reticular and lobulated architectures; cytologic atypia was generally absent, although outer root sheath hyperplasia was observed in some cases. Immunohistochemical study of 7 cases showed that the neoplastic epithelial cells were diffusely positive for p63 and p40, positive for smooth muscle actin (SMA), focally positive for S100 and epithelial membrane antigen, but negative for carcinoembryonic antigen; peritumoral mesenchymal cells were positive for CD10 and focally positive for CD34, but negative for SMA and desmin; intratumoral mesenchymal cells did not express CD10. All patients underwent surgical excision of the lesions. During a follow-up period of 4 - 192 months, no recurrence was observed. Conclusions Solitary fibrofolliculoma most commonly presents as papules or nodules on the face, head, and neck, and is immunohistochemically characterized by CD10 positivity in peritumoral mesenchymal cells and CD10 negativity in intratumoral mesenchymal cells, which may be helpful for the diagnosis.

Key words: Hamartoma, Fibrofolliculoma, Single, Organizational pathology, Immunohistochemistry

引用本文

张淑媛 牛丰南 王益华. 单发纤维毛囊瘤15例临床病理分析[J]. 中华皮肤科杂志, 2026,59(7):675-677. doi:10.35541/cjd.20240058

Zhang Shuyuan, Niu Fengnan, Wang Yihua. Clinicopathological analysis of 15 cases of solitary fibrofolliculoma[J]. Chinese Journal of Dermatology, 2026, 59(7): 675-677.doi:10.35541/cjd.20240058