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一名儿科患者的卵巢碰撞瘤:成熟畸胎瘤合并含有黏液性囊腺癌成分的复合肿瘤

Ovarian Collision Tumor in a Pediatric Patient: A Mature Teratoma Associated with a Combined Tumor Containing a Mucinous Cystadenocarcinoma Component.

作者信息

Keretić Dorotea, Petračić Ivan, Mašić Binder Silvija, Ulamec Monika, Plavec Živko Andrea, Stepan Giljević Jasminka, Bonevski Aleksandra, Habek Dubravko, Bašković Marko

机构信息

Department of Pediatric Surgery, Children's Hospital Zagreb, Ulica Vjekoslava Klaića 16, 10000 Zagreb, Croatia.

School of Medicine, University of Zagreb, Šalata 3, 10000 Zagreb, Croatia.

出版信息

J Clin Med. 2025 Sep 10;14(18):6387. doi: 10.3390/jcm14186387.

Abstract

: Collision tumors, especially in the ovary, are a rare phenomenon where two distinct types of tumors develop adjacent to each other within the same organ but remain separate histologically. We present a case of the first collision ovarian tumor in a 14-year-old girl consisting of a combined tumor and a mature teratoma. : A 14-year-old girl presented with abdominal swelling for the past three months, without other symptoms. Ultrasound (US) examination of the abdomen revealed a large cystic mass with multiple septa, filling the entire abdomen from the diaphragm to the pelvis. Magnetic resonance imaging (MRI) showed an intraperitoneal mass, inseparable from the right ovary, measuring 22 cm × 13 cm × 30 cm. Serum tumor markers were within normal limits. The tumor mass was completely extirpated along with the fallopian tube. Histological and immunohistochemical analysis determined that it was a mucinous cystadenocarcinoma, characterized by a transition pattern from benign and borderline components to an adenocarcinoma component with a smaller mature teratoma. Six-month follow-up revealed no recurrence or postoperative complications. : As the first documented case, this case provides valuable insights into pediatric ovarian neoplasms, guiding future diagnostic and therapeutic approaches.

摘要

碰撞瘤,尤其是卵巢碰撞瘤,是一种罕见的现象,即在同一器官内两种不同类型的肿瘤彼此相邻生长,但在组织学上保持分离。我们报告一例14岁女孩的首例卵巢碰撞瘤,该肿瘤由混合性肿瘤和成熟畸胎瘤组成。一名14岁女孩在过去三个月出现腹部肿胀,无其他症状。腹部超声(US)检查发现一个有多个分隔的大囊性肿块,从膈肌到盆腔充满整个腹部。磁共振成像(MRI)显示一个与右侧卵巢无法分离的腹腔肿块,大小为22 cm×13 cm×30 cm。血清肿瘤标志物在正常范围内。肿瘤肿块连同输卵管被完整切除。组织学和免疫组化分析确定其为黏液性囊腺癌,其特征是从良性和交界性成分向腺癌成分转变,并伴有较小的成熟畸胎瘤。六个月的随访显示无复发或术后并发症。作为首例有记录的病例,该病例为儿童卵巢肿瘤提供了有价值的见解,指导未来的诊断和治疗方法。

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