Sequential teratoma in pediatric patients: causation or coincidence?

Q3 Medicine
M Velayos, J Serradilla, K Estefanía-Fernández, A J Muñoz-Serrano, C Ramírez Amorós, M C San Basilio Berenguer, A Vilanova-Sánchez, M V López-Santamaría, F Hernández-Oliveros
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引用次数: 0

Abstract

We describe the unusual case of a female patient with a history of two mature teratomas non-correlated in terms of location and occurrence. A 12-year-old girl presented at our consultation as a result of a growing tumor in the hypogastric region, with no further clinical signs. She had undergone surgery neonatally due to a mature cystic sacrococcygeal teratoma, which was fully removed. No clinical sequelae were noted and no additional treatment was required over a 10-year follow-up. Radiological examination showed a large 20 × 12 × 18 cm cystic mass extending from the pelvic region to the lower hemiabdomen, associated with two similar small formations adjacent to the right ovary. Tumor markers were negative, and a laparoscopic right salpingoophorectomy was carried out, with an excellent postoperative progression. Pathological examination revealed it was, again, a mature cystic teratoma. The genetic study ruled out causation in this respect.

小儿继发性畸胎瘤:原因还是巧合?
我们描述了一个不寻常的情况下,女性患者的历史,两个成熟畸胎瘤在位置和发生方面不相关。一名12岁女孩因下腹区域肿瘤生长而就诊,无其他临床症状。由于成熟的囊性骶尾畸胎瘤,她在出生时就接受了手术,并被完全切除了。在10年的随访中,没有发现临床后遗症,也不需要额外的治疗。x线检查显示一个20 × 12 × 18厘米的巨大囊性肿块,从骨盆区延伸到下半腹部,并伴有右侧卵巢附近的两个类似的小形成。肿瘤标志物呈阴性,行腹腔镜右侧输卵管卵巢切除术,术后进展良好。病理检查再次显示为成熟囊性畸胎瘤。基因研究排除了这方面的因果关系。
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来源期刊
CiteScore
1.40
自引率
0.00%
发文量
64
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