| Literature DB >> 25017275 |
Feng-Ying Fang1, Chiung-Ru Lai2, Ming-Jie Yang1, Beng-Shian Huang3, Chih-Yao Chen1, Yiu-Tai Li4, Ming-Shyen Yen1, Peng-Hui Peter Wang5.
Abstract
OBJECTIVE: We present a case of primary cornual epithelioid trophoblastic tumor (ETT) because of its rarity and diagnostic and therapeutic challenge. CASE REPORT: A 28-year-old woman, gravida 1, para 1, who missed menstruation for 3 months, had an elevated β-human chorionic gonadotropin serum level of 2764 mIU/mL, an absence of intrauterine pregnancy, and the presence of an adnexal mass detected by transvaginal ultrasound. As an ectopic pregnancy was suspected, laparoscopic surgery was performed and showed a right corneal mass. Complete excision of the tumor was done through exploratory laparotomy. Frozen pathology favored the diagnosis of squamous cell carcinoma. Since there was no apparent tumor at other sites, no additional surgery was done. The final pathology showed ETT. Primary ETT is often misdiagnosed as an ectopic pregnancy, leading to delayed treatment, and poses a diagnostic challenge in distinguishing it from squamous cell carcinoma during pathological examination.Entities:
Keywords: epithelioid trophoblastic tumor; gestational trophoblastic neoplasm; immunohistochemistry
Mesh:
Year: 2014 PMID: 25017275 DOI: 10.1016/j.tjog.2014.03.002
Source DB: PubMed Journal: Taiwan J Obstet Gynecol ISSN: 1028-4559 Impact factor: 1.705