一名处女的非典型阴道侵袭性血管瘤:来自南约旦的病例报告

Ahlam M Al-Kharabsheh, Bushra AlTarawneh, Seham M Abufraijeh, Omar Abu Azzam
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摘要

:侵袭性血管肌瘤是一种局部浸润性间质肿瘤,很少确诊,主要侵犯育龄妇女的会阴部。它通常出现在阴道、外阴和其他盆腔软组织等部位,但其表现可千变万化。我们描述了一个特别独特的侵袭性血管肌瘤病例,它以非典型的方式出现在一名 31 岁处女的阴道区域。值得注意的是,该病例的血管肌瘤生长模式不同寻常--严格位于阴道上皮内,没有向周围组织侵犯的迹象,这在此类肿瘤的侵袭性中并不典型。患者的肿块突出于处女膜,这种表现并不常见,因此患者最初对肿块的性质有所猜测。手术切除肿块后,通过细致的组织病理学检查,最终确诊为侵袭性血管肌瘤。本病例强调了在阴道肿块的鉴别诊断中考虑侵袭性血管肌瘤的重要性,尤其是那些没有表现出侵袭性特征的肿块。该病例还强调,临床医生需要提高对这种罕见肿瘤潜在非典型表现的认识,以便及时准确地做出诊断,并指导适当的治疗策略。关于侵袭性血管肌瘤的文献越来越多,本报告为这方面的研究做出了贡献,它强调了血管肌瘤表现的多变性以及对不典型病例加强怀疑的必要性。
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Atypical Vaginal Aggressive Angiomyxoma in a Virgin: A Case Report from South Jordan
: Aggressive angiomyxoma is a locally invasive, rarely diagnosed mesenchymal tumor that predominantly affects the perineal region of women in their reproductive years. It is typically found in areas such as the vagina, vulva, and other pelvic soft tissues, but its presentation can be highly variable. We describe a particularly unique case of aggressive angiomyxoma, presenting in an atypical manner within the vaginal region of a 31-year-old virgin woman. This case is noteworthy for the unusual growth pattern of the angiomyxoma—located strictly within the vaginal epithelium, showing no signs of invasion into surrounding tissues, which is not typical of the aggressive nature of this type of tumor. The patient presented with a mass that protruded through the hymen, an uncommon presentation that led to initial speculation about the nature of the mass. The definitive diagnosis of aggressive angiomyx-oma was made by meticulous histopathological examination after surgical excision of the mass. This case emphasizes the critical importance of considering aggressive angiomyxoma in the differential diagnosis of vaginal masses, particularly those that do not exhibit invasive characteristics. The case also highlights the need for increased awareness among clinicians about the potential for atypical presentations of this rare tumor, to facilitate timely and accurate diagnosis, and to guide appropriate management strategies. This report contributes to the growing body of literature on aggressive angiomyxoma, highlighting the variability in its presentation and the need to heighten suspicion in atypical cases.
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