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首页> 外文期刊>Journal of Pediatric Surgery Case Reports >Gastric plexiform fibromyxoma tumor in a child – Case report and?review of the literature
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Gastric plexiform fibromyxoma tumor in a child – Case report and?review of the literature

机译:儿童胃部丛状纤维肌瘤的病例报道及文献复习

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Plexiform fibromyxoma tumor (PFT) is an exceedingly rare tumor, particularly in children where only four cases have been reported to date. The patient reported herein presented with abdominal pain and vomiting related to gastric outlet obstruction caused by a large, polypoid PFT. We describe the clinical features, diagnostic evaluation, and surgical treatment of this rare tumor in our patient. Further, we review the literature of FPT to bring attention to this rare gastric tumor to the Pediatric Surgeon. Highlights ? Plexiform fibromyxoma is an exceedingly rare tumor in pediatric patients. ? Symptoms and signs are non-specific, ranging from an incidental finding to gastric perforation. ? The vast majority of these tumors are transmural tumors located in the distal stomach. ? Diagnosis rests on immunohistochemistry staining showing evidence of myofibroblastic differentiation.
机译:Plexiform纤维肌瘤瘤(PFT)是一种极为罕见的肿瘤,尤其是对于迄今仅报道四例的儿童而言。本文报道的患者表现出与大的息肉状PFT引起的胃出口阻塞有关的腹痛和呕吐。我们描述了该患者中这种罕见肿瘤的临床特征,诊断评估和外科治疗。此外,我们回顾了FPT的文献,以引起对这种罕见的胃肿瘤的重视,引起了小儿外科医生的注意。强调 ?在儿童患者中,Plexiform纤维粘液瘤是一种极为罕见的肿瘤。 ?症状和体征是非特异性的,范围从偶然发现到胃穿孔。 ?这些肿瘤中的绝大多数是位于胃远端的透壁肿瘤。 ?诊断取决于免疫组织化学染色,显示肌成纤维细胞分化的证据。

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