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Clinicopathologic analysis of 27 cases of cellular angiofibroma |
ZHANG Kang1 LI Xiangli2 JIANG Guoqing1 |
1.Department of Gynecology, the First Hospital of Tsinghua University, Beijing 100016, China;
2.Department of Pathology, the First Hospital of Tsinghua University, Beijing 100016, China
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Abstract Objective To investigate the clinical features, pathology, immunohistochemistry of cellular angiofibroma. Methods Clinical data of 26 cases reported in China from January 2000 to June 2022 in CNKI and Wanfang Data, and one case of cellular angiofibroma admitted to the First Hospital of Tsinghua University (hereinafter referred to as “our hospital”) on February 18, 2022 were collected. The characteristics of clinical, pathological, and immunohistochemical of the case were analyzed. Results The patient in our hospital was 44 years old, and was diagnosed with vulvar mass for three months, enlargement accompanied by tenderness for two weeks. The mass was located in the right medial lip of the minora, with a size of 9 cm. Pathologically, it showed short spindle cells with uniform distribution, more mitotic images, and large cell atypia. Small and medium blood vessels can be seen in the interstitium, and some blood vessels have thicker walls, accompanied by hyaline degeneration. Immunohistochemistry: CD34 (vessel +), Desimn (vessel +), Vimentin (+), SATA6 (-), S-100 (-), Ki-67 index (30%), SMA (vessel +), ER (+), PR (+). A total of 26 patients aged 16-78 years were reported, including 18 females and eight males. There were 21 cases with no pain and five cases with mild pain. The growth sites were the labia majora in 13 cases, the scrotum in four cases, the middle finger in two cases, the groin in two cases, the pubic mound in one case, the vulva in one case, the spermatocele in one case, the labia minora in one case, and the cervix in one case. The course of disease ranges from one week to ten years. The pathological features were composed of short spindle cells with the same morphology and abundant blood vessels. Immunohistochemistry showed that Vimentin was diffusion-positive, CD34, ER, PR, SMA were positive or partially positive, and Desimin, HMB45, S-100 were mostly negative. In the literatures, among the 26 patients who received surgical treatment, two patients were suspected to have relapsed, and one patient in our hospital did not have recurrence after surgery. Conclusion Cellular angiofibroma is a rare mesenchymal tumor, most common in the bisexual genital area. It is characterized by dense short spindle cells and abundant blood vessels under microscope. Surgical resection is the main treatment, and the patient has a good prognosis.
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[1] Nucci MR,Granter SR,Fletcher CD. Cellular angiofibroma:a benign neoplasm distinct from angiomyofibroblastoma and spindle cell lipoma [J]. Am J Surg Pathol,1997,21(6):636- 644.
[2] Val-Bernal JF,Azueta A,Parra A,et al. Paratesticular cellular angiofibroma with atypical(bizarre)cells:case report and literature review [J]. Pathol Res Pract,2013,209(6):388- 392.
[3] Iwasa Y,Fletcher CD. Cellular angiofibroma:clinicpathologic and immunohistochemical analysis of 51 cases [J]. Am J Surg Pathol,2004,28(11):1426-1435.
[4] Wyn I,Debiec-Rychter M,Van Cleynenbreugel B,et al. Cell- ular angiofibroma of the prostate:a rare tumor in an unusual location [J]. Case Rep Pathol,2014,2014:871530.
[5] 卢涌涌,陶利萍,卢山珊,等.精索富于细胞性血管纤维瘤1例并文献复习[J].中国现代医生,2011,49(36):119- 123.
[6] 姜惠峰,姜颖君.外阴富细胞性血管纤维瘤1例报道及文献复习[J].诊断病理学杂志,2001,8(1):327-332.
[7] 金行藻,孟奎.外阴富细胞性血管纤维瘤1例报道及文献复习[J].临床与实验病理学杂志,2003,19(1):104- 105.
[8] 唐涛,范娜娣.纤维母—肌纤维母细胞肿瘤6例临床病理分析[J].中国肿瘤临床,2003,30(9):645-651.
[9] 邓俊辉,余英豪,丁月琴,等.腹股沟富于细胞性血管纤维瘤1例报告并文献复习[J].中国误诊学杂,2007,7(17):3955-3957.
[10] 戴莉萍,赵妤,严常宝,等.大阴唇富于细胞性血管纤维瘤一例[J].中华病理学杂志,2009,38(12):847-848.
[11] 张滔,杨静.外阴富于细胞性血管纤维瘤一例[J].中华妇产科杂志,2011,46(5):397.
[12] 苏世强,翟保生,郭顺利,等.阴囊富于细胞性血管纤维瘤一例报告[J].中华泌尿外科杂志,2012,33(2):116-117.
[13] 刘益平,戴北飞.阴囊富于细胞性血管纤维瘤1例报告并文献复习[J].医学临床研究,2012,29(8):1612-1613.
[14] 许春月,杨静.外阴富于细胞性血管纤维瘤1例[J].实用妇产科杂志,2013,2(8):607-608.
[15] 都成,刘水策,齐跃,等.富于细胞性血管纤维瘤临床病理特点[J].现代肿瘤医学,2015,23(19):2831-2835.
[16] 张小伟,黄必飞,陈艳,等.左中指富于细胞性血管纤维瘤一例[J].中华手外科杂志,2015,31(6):412.
[17] 伍四春,赵明泽,张江红,等.富于细胞性血管纤维瘤临床病例特征分析[J].临床误诊误治,2016,29(1):34-35.
[18] 张协五,李腾,蒲小勇,等.原发性附睾富于细胞性血管纤维瘤1例报告并文献复习[J].现代泌尿生殖肿瘤杂志,2017,9(5):281-284.
[19] 程海霞,杨彬,何若冲,等.阴囊富于细胞性血管纤维瘤1例[J].山西医科大学学报,2017,48(4):396-397.
[20] 龚智泉,刘欣,王力夫,等.富于细胞性血管纤维瘤3例临床病理分析[J].临床与实验病理学杂志,2017,33(3):318-320.
[21] 曾煜鹏,王军,丁颖,等.腹股沟富于细胞性血管纤维瘤一例[J].中华病理学杂志,2019,48(12):974-976.
[22] 赵静,牛惠萍,任路平.大阴唇富于细胞性血管纤维瘤超声表现1例[J].中国超声医学杂志,2021,37(9):985.
[23] 苏婷,徐澄,张美华,等.富于细胞性血管纤维瘤四例[J].中华皮肤科杂志,2021,54(3):242-243.
[24] 李庆祝,张巍,魏鹏.右中指富于细胞性血管纤维瘤一例[J].中华显微外科杂志,2022,45(1):101-103.
[25] Hlaing T,Tse G. Angiomyofibroblastoma of the male pefineum:Anunusua location for a rare lesion [J]. Int J Surg Pathol,2000,8(1):79-82.
[26] Ayd?覦n ?譈,Terzi H,Turkay ?譈,et al. A giant vulvar mass:a case study of cellular angiofibroma [J]. Case Rep Obstet Gyn- ecol,2016,2016:2094818.
[27] McCluggage WG,Perenyei M,Irwin ST. Recurrent cellar ang- ifibroma of the vulva [J]. J Clin Pathol,2002,55(6):477- 479.
[28] Nucci MR,Fletcher CD. Vulvovaginal soft tissue tumours:Update and review [J]. Histoppathology,2000,36(2):97- 108.
[29] Ptaszyński K,Szumera-Cie■kiewicz A,Bartczak A. Cellular angiofibroma with atypia or sarcomatous transformation- case description with literature review [J]. Pol J Pathol,2012, 63(3):207-211.
[30] Magro G,Caltabiano R,Kacerovská D,et al. Vulvovaginal myofibroblastoma:expanding the morphological and immunohistochemical spectrum. A clinicopathologic study of 10 cases [J]. Hum Pathol,2012,43(2):243-253.
[31] Chien YC,Mokánszki A,Huang HY,et al. First Glance of Molecular Profile of Atypical Cellular Angiofibroma/Cellular Angiofibroma with Sarcomatous Transformation by Next Generation Sequencing [J]. Diagnostics,2020,10(1):35. |
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