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一名处女的非典型阴道侵袭性血管黏液瘤:来自约旦南部的病例报告

Atypical Vaginal Aggressive Angiomyxoma in a Virgin: A Case Report from South Jordan.

作者信息

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

机构信息

Department of Obstetrics and Gynecology, Faculty of Medicine, Mutah University, Alkarak, Jordan.

Department of Pathology, Faculty of Medicine, Mutah University, Alkarak, Jordan.

出版信息

Int J Womens Health. 2024 Jul 25;16:1257-1264. doi: 10.2147/IJWH.S465948. eCollection 2024.

Abstract

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 angiomyxoma 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.

摘要

侵袭性血管黏液瘤是一种具有局部侵袭性、很少被诊断出的间叶组织肿瘤,主要影响育龄期女性的会阴区域。它通常出现在阴道、外阴和其他盆腔软组织等部位,但其表现形式可能高度多样。我们描述了一例特别独特的侵袭性血管黏液瘤病例,该病例以非典型方式出现在一名31岁处女的阴道区域。该病例值得注意的是血管黏液瘤不寻常的生长模式——严格位于阴道上皮内,没有侵入周围组织的迹象,而这并不符合这类肿瘤通常具有的侵袭性特点。患者表现为一个肿块从处女膜突出,这种不常见的表现引发了对肿块性质的初步猜测。在对肿块进行手术切除后,通过细致的组织病理学检查做出了侵袭性血管黏液瘤的明确诊断。该病例强调了在阴道肿块的鉴别诊断中考虑侵袭性血管黏液瘤的至关重要性,尤其是那些不具有侵袭特征的肿块。该病例还凸显了临床医生需要提高对这种罕见肿瘤非典型表现可能性的认识,以便及时准确地诊断,并指导适当的管理策略。本报告为关于侵袭性血管黏液瘤的不断增多的文献做出了贡献,突出了其表现形式的多样性以及在非典型病例中提高怀疑程度的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/315f/11287368/302bd21962ab/IJWH-16-1257-g0001.jpg

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