Wakhlu A, Wakhlu A K
Department of Paediatric Surgery, King George's Medical College, Lucknow, India.
Eur J Pediatr Surg. 2002 Dec;12(6):375-8. doi: 10.1055/s-2002-36851.
This paper reviews our experience with patients presenting with gastric teratoma treated over an eighteen-year period. This rare paediatric tumour has an excellent prognosis after curative resection.
There were seven patients, all males. Investigations included a haematological profile, plain radiography and ultrasound of the abdomen. All patients were operated and the specimens subjected to histopathological examination.
The age at presentation ranged from 1 month to 7 years. Two patients presented with melaena and the rest with progressively increasing abdominal mass. Our oldest patient had a massive tumour occupying nearly the whole abdomen. None of the children had metastases and none of the lesions had invaded adjacent structures. The tumours could be completely resected and all patients had an uneventful recovery. Histology of the tumours showed mature elements arising from the three germ layers in 6 children, one child had an immature teratoma. The average follow-up was 3 years (range 2 - 6 years). None of the patients has had a recurrence or any other problem.
Gastric teratoma is a rare tumour but amenable to curative resection with an excellent prognosis.
本文回顾了我们在18年期间治疗胃畸胎瘤患者的经验。这种罕见的儿科肿瘤在根治性切除后预后良好。
共有7例患者,均为男性。检查包括血液学检查、腹部平片和超声检查。所有患者均接受手术治疗,标本进行组织病理学检查。
就诊年龄为1个月至7岁。2例患者出现黑便,其余患者腹部肿块逐渐增大。我们年龄最大的患者有一个巨大肿瘤,几乎占据了整个腹部。所有儿童均无转移,所有病变均未侵犯相邻结构。肿瘤可完全切除,所有患者恢复顺利。肿瘤组织学检查显示,6例儿童肿瘤由三个胚层产生成熟成分,1例儿童为未成熟畸胎瘤。平均随访3年(范围2 - 6年)。所有患者均无复发或其他问题。
胃畸胎瘤是一种罕见肿瘤,但可通过根治性切除治愈,预后良好。