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一名10日龄新生儿的高级别未成熟胃畸胎瘤:诊断挑战与治愈性手术治疗

High-Grade Immature Gastric Teratoma in a 10-Day-Old Neonate: Diagnostic Challenges and Curative Surgical Management.

作者信息

Uddin Wajeeh, Aylan Alshamsi Mariam, Alblooshi Mohammed, Ahmad Munir, Abdul Kader Masih

机构信息

Pediatric Surgery, Al Jalila Children's Specialty Hospital, Dubai, ARE.

Medicine, Dubai Health, Dubai, ARE.

出版信息

Cureus. 2025 May 6;17(5):e83613. doi: 10.7759/cureus.83613. eCollection 2025 May.

DOI:10.7759/cureus.83613
PMID:40336679
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12056341/
Abstract

Neonatal gastric teratomas are exceptionally rare germ cell tumors (<1% of pediatric teratomas) posing significant diagnostic and surgical challenges. Immature variants, particularly high‑grade tumors, can be locally aggressive yet typically have a favorable prognosis if completely resected. We report a 10‑day‑old male neonate (born at 36+1 weeks to a mother with gestational diabetes and pregnancy‑induced hypertension) presenting with a firm epigastric and left hypochondriac mass detected 24 hours after birth. Imaging revealed a mixed echogenic lesion containing fat and calcifications from the stomach's lesser curvature, and serum alpha‑fetoprotein was markedly elevated for age. On day 12, an exploratory laparotomy achieved en bloc resection via partial gastrectomy with clear margins, despite dense adhesions to the left hepatic lobe and an intragastric component. Postoperatively, the patient experienced a right femoral artery thrombosis managed with anticoagulation and wound dehiscence addressed by local care and antibiotics. Histopathology confirmed a Grade III immature gastric teratoma without malignant germ cell elements; a splenule was also identified. An upper gastrointestinal contrast study on postoperative day 11 showed an intact repair, and feeds were successfully advanced. This case underscores the importance of suspecting gastric teratoma in neonates, interpreting age‑adjusted tumor markers carefully, and ensuring complete surgical excision. Vigilant perioperative management and long‑term surveillance with serial imaging and alpha‑fetoprotein monitoring remain paramount, particularly for high‑grade immature lesions.

摘要

新生儿胃畸胎瘤是极其罕见的生殖细胞肿瘤(占儿童畸胎瘤的比例不到1%),带来了重大的诊断和手术挑战。不成熟的变体,尤其是高级别肿瘤,可能具有局部侵袭性,但如果完全切除,通常预后良好。我们报告了一名10天大的男婴(孕36 + 1周出生,母亲患有妊娠期糖尿病和妊娠高血压),出生后24小时发现上腹部和左季肋部有一实性肿块。影像学检查显示一个混合回声病变,包含来自胃小弯的脂肪和钙化,血清甲胎蛋白在该年龄时显著升高。在第12天,尽管与左肝叶有致密粘连且肿瘤有胃内成分,但通过部分胃切除术进行了剖腹探查并整块切除,切缘清晰。术后,患者出现右股动脉血栓形成,通过抗凝治疗,伤口裂开通过局部护理和使用抗生素处理。组织病理学证实为III级不成熟胃畸胎瘤,无恶性生殖细胞成分;还发现了一个副脾。术后第11天的上消化道造影显示修复完整,喂养顺利推进。该病例强调了怀疑新生儿胃畸胎瘤、仔细解读年龄校正后的肿瘤标志物以及确保完整手术切除的重要性。警惕的围手术期管理以及通过系列影像学检查和甲胎蛋白监测进行长期监测仍然至关重要,特别是对于高级别不成熟病变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/bd87b6036c08/cureus-0017-00000083613-i09.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/2daf7bf2d160/cureus-0017-00000083613-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/b86a347c2725/cureus-0017-00000083613-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/f3d0173008f1/cureus-0017-00000083613-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/9759bb9ad590/cureus-0017-00000083613-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/7c1d57942bb9/cureus-0017-00000083613-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/1274c7b9656a/cureus-0017-00000083613-i06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/fcd333a33c4b/cureus-0017-00000083613-i07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/e0770b1676c3/cureus-0017-00000083613-i08.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/bd87b6036c08/cureus-0017-00000083613-i09.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/2daf7bf2d160/cureus-0017-00000083613-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/b86a347c2725/cureus-0017-00000083613-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/f3d0173008f1/cureus-0017-00000083613-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/9759bb9ad590/cureus-0017-00000083613-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/7c1d57942bb9/cureus-0017-00000083613-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/1274c7b9656a/cureus-0017-00000083613-i06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/fcd333a33c4b/cureus-0017-00000083613-i07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/e0770b1676c3/cureus-0017-00000083613-i08.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/12056341/bd87b6036c08/cureus-0017-00000083613-i09.jpg

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A case of neonatal gastric teratoma complicated with occult gastrointestinal hemorrhage misdiagnosed as lymphangioma.一例新生儿胃畸胎瘤合并隐匿性胃肠道出血被误诊为淋巴管瘤。
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