R. Beavers, Daphne Arena Goncharov, C. Degraffenreid, Mahmoud A. Abdelwahab, Xiao‐yan Du, E. Eyzaguirre, K. E. Lewis
{"title":"Angiomyofibroblastoma: A rare benign gynecologic tumor mistaken for a bartholin cyst","authors":"R. Beavers, Daphne Arena Goncharov, C. Degraffenreid, Mahmoud A. Abdelwahab, Xiao‐yan Du, E. Eyzaguirre, K. E. Lewis","doi":"10.15761/COGRM.1000308","DOIUrl":null,"url":null,"abstract":"Background: Angiomyofibroblastoma is a rare, benign superficial vulvar lesion of the middle-aged female. Most cases in the literature are initially misdiagnosed as Bartholin gland cysts with final diagnosis ascertained via pathology at the time of surgical excision. Case: A 45-year-old female presented with a large, painless vulvar mass. This mass had formed five years prior to presentation to our clinic, and the patient underwent a procedure to attempt to drain the mass 2-3 years following its initial formation. At her initial visit, a 15 X 10 cm mass was found on the posterior aspect of the right labia minora at the level of the vaginal vestibule. This mass extended inferiorly to the perineum. Needle aspiration was attempted in office but was unsuccessful. The mass was removed under general anesthesia in the operating room en bloc from the vulva without complication and the patient was discharged on postoperative day 0. The pathology of this mass was reported as angiomyofibroblastoma. Conclusion: Differentiating angiomyofibroblastoma from other potential soft tissue masses of the vulva, especially from the commonly mistaken Bartholin gland cyst or rare aggressive angiomyxoma, is essential for preventing unnecessary procedural workup or treatment miss of a malignant mass. Noting the key distinguishing pathological and clinical features of the tumor and considering risk factors for malignancy will aid in correct diagnosis without exposing the patient to extraneous procedures and potential harm.","PeriodicalId":87233,"journal":{"name":"Clinical obstetrics, gynecology and reproductive medicine","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical obstetrics, gynecology and reproductive medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15761/COGRM.1000308","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Angiomyofibroblastoma is a rare, benign superficial vulvar lesion of the middle-aged female. Most cases in the literature are initially misdiagnosed as Bartholin gland cysts with final diagnosis ascertained via pathology at the time of surgical excision. Case: A 45-year-old female presented with a large, painless vulvar mass. This mass had formed five years prior to presentation to our clinic, and the patient underwent a procedure to attempt to drain the mass 2-3 years following its initial formation. At her initial visit, a 15 X 10 cm mass was found on the posterior aspect of the right labia minora at the level of the vaginal vestibule. This mass extended inferiorly to the perineum. Needle aspiration was attempted in office but was unsuccessful. The mass was removed under general anesthesia in the operating room en bloc from the vulva without complication and the patient was discharged on postoperative day 0. The pathology of this mass was reported as angiomyofibroblastoma. Conclusion: Differentiating angiomyofibroblastoma from other potential soft tissue masses of the vulva, especially from the commonly mistaken Bartholin gland cyst or rare aggressive angiomyxoma, is essential for preventing unnecessary procedural workup or treatment miss of a malignant mass. Noting the key distinguishing pathological and clinical features of the tumor and considering risk factors for malignancy will aid in correct diagnosis without exposing the patient to extraneous procedures and potential harm.
背景:血管肌成纤维细胞瘤是一种罕见的中年女性外阴浅表良性病变。文献中大多数病例最初被误诊为Bartholin腺囊肿,最终在手术切除时通过病理确定诊断。病例:45岁女性,外阴肿块大,无痛性。该肿块在就诊前5年形成,患者在其最初形成后2-3年接受了手术,试图排出肿块。初次就诊时,在右侧小阴唇后部阴道前庭水平处发现一个15 X 10 cm的肿块。肿块向下延伸至会阴。在办公室尝试过针吸,但没有成功。在手术室全麻下将肿物整体从外阴取出,无并发症,术后第0天出院。病理报告为血管肌成纤维细胞瘤。结论:将血管肌成纤维细胞瘤与其他潜在的外阴软组织肿块鉴别,特别是与常被误诊为巴托林腺囊肿或罕见的侵袭性血管粘液瘤鉴别,对于避免恶性肿块的不必要检查或治疗遗漏至关重要。注意肿瘤的关键区别病理和临床特征,并考虑恶性肿瘤的危险因素将有助于正确诊断,而不会使患者暴露于外来手术和潜在伤害。