A Case of Metastatic Vulvar Choriocarcinoma Misdiagnosed as Vulvar Abscess: A Case Report.

IF 0.6 Q4 OBSTETRICS & GYNECOLOGY
Case Reports in Obstetrics and Gynecology Pub Date : 2024-08-27 eCollection Date: 2024-01-01 DOI:10.1155/2024/9918452
Alita Mrema, Prudence H Kiwia, Shaban J Shaban, Anwar Z Mohamed, Latifa Rajab Abdallah, Rajabu Kiaratu, John Mahoyogo, Agapiti Chuwa, David H Mvunta
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引用次数: 0

Abstract

Background: Metastatic vulvar choriocarcinoma, a rare ectopic gestational trophoblastic neoplasia (GTN), often presents a diagnostic challenge due to its mimicry of other conditions, particularly in resource-limited settings. Its primary symptom is abnormal vaginal bleeding without a clear cause. Consequently, diagnosing and managing it poses difficulties for many low-resource health facilities, as evidenced by the current case. Case Presentation: We present the case of a 25-year-old, P2+2+2L2, who had a large painless, bleeding vulva mass for nearly 5 months. This followed a spontaneous abortion the month prior. The mass gradually increased in size and was accompanied by fever, pus discharge, and weight loss. Despite being treated at multiple health facilities for a vulvar abscess, there was no improvement. A diagnosis was finally made at a tertiary facility where elevated quantitative serum beta-human chorionic gonadotropin (hCG) (β-hCG) was noted. Due to uncontrollable vulva bleeding, she was referred to another tertiary facility for emergency radiotherapy. Following stabilization, chemotherapy was administered using the EMA-CO protocol. Conclusion: The report highlights the difficulty in diagnosing vulvar choriocarcinoma, underscoring the importance of a high index of suspicion. Clinical tests such as serum (β-hCG) and imaging studies are crucial for diagnosis. In resource-limited settings, a simple strip-based urine pregnancy test with serial dilutions can be sufficient for diagnosing and managing vulvar choriocarcinoma.

一例被误诊为外阴脓肿的转移性外阴绒毛膜癌:病例报告。
背景:转移性外阴绒毛膜癌是一种罕见的异位妊娠滋养细胞肿瘤(GTN),因其与其他疾病相似,常常给诊断带来挑战,尤其是在资源有限的环境中。其主要症状是无明确病因的异常阴道出血。因此,对许多资源匮乏的医疗机构来说,诊断和处理这种病症都很困难,本病例就是一个很好的例子。病例介绍:本病例患者 25 岁,P2+2+2L2,外阴大块无痛性出血近 5 个月。在此之前的一个月,她进行了自然流产。肿块逐渐增大,并伴有发烧、脓性分泌物和体重减轻。尽管曾在多家医疗机构接受过外阴脓肿治疗,但情况没有任何好转。最后在一家三级医疗机构确诊,发现血清中的β-人绒毛膜促性腺激素(hCG)(β-hCG)定量升高。由于外阴出血无法控制,她被转到另一家三级医院接受紧急放射治疗。病情稳定后,采用 EMA-CO 方案进行了化疗。结论:该报告强调了诊断外阴绒毛膜癌的难度,突出了高度怀疑的重要性。血清(β-hCG)等临床检验和影像学检查是诊断的关键。在资源有限的情况下,简单的条状尿妊娠试验和连续稀释就足以诊断和处理外阴绒毛膜癌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Case Reports in Obstetrics and Gynecology
Case Reports in Obstetrics and Gynecology Medicine-Obstetrics and Gynecology
CiteScore
1.30
自引率
0.00%
发文量
64
审稿时长
12 weeks
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