Pediatric puzzle: Large ovarian dermoid cyst and markedly elevated CA 19-9 in an 8-year-old.

Q3 Medicine Qatar Medical Journal Pub Date : 2024-09-16 eCollection Date: 2024-01-01 DOI:10.5339/qmj.2024.47
Muhamed Ahmed Abdelmoaty, Wael Soliman Taha
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引用次数: 0

Abstract

Background: Mature cystic teratomas, also known as dermoid cysts, are the most prevalent form of ovarian germ cell tumors. While they typically manifest in women of reproductive age, they can also occur in pediatric patients. These tumors are generally benign and comprise a diverse array of tissue types. However, large lesions, particularly those exceeding 10 cm in diameter, are infrequent and can present diagnostic and therapeutic challenges. Notably, elevated tumor markers, such as cancer antigen 19-9 (CA 19-9), are not commonly associated with mature cystic teratomas, rendering this case particularly unusual.

Case presentation: The clinical case involved an 8-year-old female patient who presented with an exceptionally large ovarian teratoma, measuring 13 × 12 cm. While the prepubertal presentation of such tumors is not uncommon, the remarkable size of the lesion was an extraordinary occurrence. Preoperative evaluation revealed markedly elevated levels of CA 19-9, a tumor marker, at 297 U/mL-an atypical finding for mature cystic teratomas. Imaging studies identified a complex cystic adnexal mass, indicative of a teratoma. Consequently, a laparotomy was performed, revealing an intact, benign lesion that was successfully resected via cystectomy, with preservation of the ovary. Histopathological examination confirmed the diagnosis of a mature cystic teratoma, without any evidence of malignant transformation. Notably, following the surgical intervention, the elevated CA 19-9 levels normalized, suggesting a potential association between the teratoma and the abnormal tumor marker levels.

Discussion: This report delineates the surgical management and clinical course of an exceptionally large ovarian teratoma in a pediatric patient with abnormal preoperative tumor markers. Despite atypical features, the excellent prognosis following fertility-sparing resection underscores the significance of conservative treatment in young females.

Conclusion: This case highlights the occurrence of a large mature cystic teratoma with elevated CA-19-9 in a pediatric patient with no complications such as torsion, rupture, or malignancy. The elevation in CA-19-9 likely relates directly to the teratoma itself. A conservative, fertility-sparing surgical approach proved effective, emphasizing the importance of careful preoperative evaluation and management in similar cases.

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儿科难题:8 岁儿童卵巢巨大皮样囊肿和明显升高的 CA 19-9。
背景:成熟囊性畸胎瘤又称皮样囊肿,是卵巢生殖细胞瘤中最常见的一种。虽然它们通常发生在育龄妇女身上,但也可能发生在儿童患者身上。这些肿瘤通常是良性的,由多种组织类型组成。然而,大的病变,尤其是直径超过 10 厘米的病变并不常见,会给诊断和治疗带来挑战。值得注意的是,肿瘤标志物(如癌抗原 19-9(CA 19-9))升高并不常见于成熟囊性畸胎瘤,因此本病例尤为罕见:该临床病例涉及一名 8 岁女性患者,其卵巢畸胎瘤异常巨大,大小为 13 × 12 厘米。虽然青春期前出现此类肿瘤的情况并不少见,但病灶的巨大尺寸却非同寻常。术前评估发现,肿瘤标志物 CA 19-9 水平明显升高,达到 297 U/mL,这在成熟囊性畸胎瘤中并不常见。影像学检查发现了一个复杂的囊性附件肿块,表明这是一个畸胎瘤。因此,医生对其进行了开腹手术,发现了一个完整的良性病灶,并通过囊肿切除术成功将其切除,同时保留了卵巢。组织病理学检查确诊为成熟的囊性畸胎瘤,没有任何恶变迹象。值得注意的是,手术干预后,CA 19-9水平升高趋于正常,这表明畸胎瘤与肿瘤标志物水平异常之间可能存在关联:本报告描述了一名术前肿瘤标志物异常的儿科患者卵巢特大畸胎瘤的手术治疗和临床过程。尽管特征不典型,但保全生育切除术后的良好预后强调了保守治疗对年轻女性的重要性:本病例强调了在一名儿童患者身上发生的CA-19-9升高的巨大成熟囊性畸胎瘤,且未出现扭转、破裂或恶性肿瘤等并发症。CA-19-9的升高可能与畸胎瘤本身直接相关。事实证明,保守、保胎的手术方法是有效的,这也强调了对类似病例进行仔细的术前评估和管理的重要性。
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来源期刊
Qatar Medical Journal
Qatar Medical Journal Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
77
审稿时长
6 weeks
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