Ovarian mucinous adenoma with a malignant component in an adolescent: a case report

IF 0.3 Q4 PEDIATRICS
John Paul Bustamante , Shaban Gheith , Mohammad Fadaie , Brandon Velazquez , Jill Menell , Colin Bethel
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引用次数: 0

Abstract

Introduction

Primary ovarian mucinous adenocarcinoma in the adolescent population is extremely rare, with limited cases reported in the literature.

Case presentation

A 14-year-old female presented with a two-week history of progressive abdominal pain, distension, bloating, early satiety, and fatigue. Physical examination revealed a significantly distended abdomen with diffuse tenderness. Contrast-enhanced CT imaging demonstrated a large multiloculated cystic adnexal mass measuring 36 × 32 × 21 cm, with displacement of bowel loops. Laboratory evaluation showed normal tumor markers except for a mildly elevated CA-125 of 47 U/mL (reference range: <35 U/mL). The patient initially underwent diagnostic laparoscopy, which was converted to open laparotomy due to the tumor's size and complexity. Replacing the left ovary, a unilateral, encapsulated mucinous tumor was entirely excised along with the associated incorporated left ovary and fallopian tube, with preservation of the uterus and contralateral adnexa. Histopathology demonstrated mucinous cystadenoma (70 %), borderline tumor (25 %), and a focal invasive mucinous adenocarcinoma component (<5 %), without lymphovascular or infiltrative invasion. The postoperative course was uneventful, and the patient was discharged on postoperative day 2. Upon follow up, she continued to have elevated CA-125 of 56 U/mL, and underwent staging laparoscopy, noted to be negative for any metastatic disease, repeat CA-125 normalized 13 U/mL. Long term planned follow up with routine ultrasounds and CA-125 levels.

Conclusion

Mucinous ovarian tumors can have borderline and malignant components and therefore require a thorough histopathologic analysis.
青春期卵巢粘液腺瘤伴恶性成分:1例报告
原发性卵巢粘液腺癌在青少年人群中极为罕见,文献中报道的病例有限。病例介绍一名14岁女性,有两周进行性腹痛、腹胀、早期饱腹感和疲劳病史。体格检查显示腹部明显膨胀并伴有弥漫性压痛。CT增强成像显示一个大的多室囊性附件肿块,尺寸为36 × 32 × 21 cm,伴肠袢移位。实验室检查显示肿瘤标志物正常,CA-125轻度升高47 U/mL(参考范围:35 U/mL)。患者最初接受了诊断性腹腔镜检查,由于肿瘤的大小和复杂性,转为开腹手术。替换左卵巢,切除单侧包膜黏液性肿瘤,同时切除合并的左卵巢和输卵管,保留子宫和对侧附件。组织病理学表现为粘液囊腺瘤(70%)、交界性肿瘤(25%)和局灶性浸润性粘液腺癌成分(5%),无淋巴血管或浸润性浸润。术后过程顺利,患者于术后第2天出院。在随访中,她的CA-125继续升高至56 U/mL,并进行了分期腹腔镜检查,注意到任何转移性疾病均为阴性,重复CA-125正常化13 U/mL。长期计划随访常规超声检查和CA-125水平。结论卵巢黏液性肿瘤可有交界性和恶性成分,因此需要进行彻底的组织病理学分析。
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
CiteScore
0.60
自引率
25.00%
发文量
348
审稿时长
15 days
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