女性婴儿成熟胃畸胎瘤伴旋转不良1例报告

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL
Maja Zecevic, Z. Marjanovic, D. Živanović, M. Slavković
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引用次数: 0

摘要

胃畸胎瘤是一种极为罕见的肿瘤,占所有儿童畸胎瘤的不到1%,以男性为主。病例史:在此报告一例3个月大女婴的成熟胃畸胎瘤,并伴有旋转不良、张力低下、斜颈和小阴唇融合。由于腹胀,孩子被送进儿科外科。体格检查,可触及一个大肿块,实验室检查结果正常。计算机断层扫描(CT)显示右半腹部主要的不均匀实性形成,延伸到骨盆并穿过中线。婴儿接受手术并完全切除源自胃小弯的肿瘤。肿瘤重600克,大小为10 × 14 × 8厘米。组织病理学检查显示为成熟型胃畸胎瘤。术后过程及后续随访无事件发生。结论:一旦诊断,手术是至关重要的,特别是在未成熟畸胎瘤的情况下,恶性改变是可能的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mature gastric teratoma in a female infant associated with malrotation: A case report
Gastric teratoma is a extremely infrequent tumor and accounts for less than 1% of all teratomas among children population with male predominance. Case history: Herewith is described a case of mature gastric teratoma in a three months-old female infant associated with malrotation, hypotonia, torticollis and fusion of labia minoria. Due to the abdominal distension, the child was admitted to the Paediatric Surgery Department. On physical examination, a large lump was palpable, and laboratory findings were normal. Computed tomography (CT) showed a major heterogeneous solid formation within the right hemi-abdomen, extending to pelvis and crossing the midline. The infant underwent surgery and complete excision of tumor originating from lesser curvature of the stomach was made. Tumor was weighing 600 gr and was 10 x 14 x 8 cm large. The histopathological examination finding pointed to mature gastric teratoma. The post-operative course and further follow-up were eventless. Conclusion: As soon as the diagnosis is made, the surgery is of paramount importance, especially in cases of immature teratomas, where malignant alteration is possible.
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来源期刊
Acta Facultatis Medicae Naissensis
Acta Facultatis Medicae Naissensis MEDICINE, GENERAL & INTERNAL-
CiteScore
0.70
自引率
0.00%
发文量
13
审稿时长
12 weeks
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