...
首页> 外文期刊>Journal of Pediatric Surgery Case Reports >Congenital infantile myofibromatosis
【24h】

Congenital infantile myofibromatosis

机译:先天性婴儿肌纤维瘤症

获取原文
   

获取外文期刊封面封底 >>

       

摘要

T2 and isointense in Tl with peripheral capsular enhancement with no central enhancement in the delayed phase. The largest lesion measured 5.1 x 2.6 x 4.4 cm insin- uated through the anterior and posterior right cervical triangular space, encasing the carotid sheath and also reaching to the retropha- ryngeal and paraspinal spaces in the same side. The other lesions were seen as following; internal surface of the left mid thoracic cage, right paratracheal area, the inner surface of the lower right ribs which abutting theanterior surface of the right hepatic lobe with no involve- ment of the liver, in the posterior paraspinous space at level of L2 to L5, the posterior aspect of the iliac bone bilaterally in the gluteus re- gion, in the medial aspect of the left femoral head, few lesions noted in the lower thighs bilaterally, mainly in the lateral aspect with some involvement of the adjacent femoral bone mainly noted in the left dis- tal metaphysic [Fig. 3A, B and C]. Surgical biopsy from the right par- avertebral mass carried out, histologic examination revealed a nodu- lar growth pattern on low power. There was vascular and spindle cell proliferation. The blood vessels were thin-walled and irregularly branching (hemangiopericytoma-like). The myofibroblasts at the cen- ter of the lesion are polygonal or round with large hyperchromatic nu- clei while the peripheral myofibroblasts are spindle shaped with elon- gated nuclei and vesicular chromatin. The mitotic activity was low and reaches 2/10 HPF at some foci [Fig. 4]. Patient remained stable during hospitalization, hypersalivation decreased gradually. At the age of 5-months patient was sent home on NGT feeding.
机译:T2和诸如TL中的诸如外围胶囊增强,延迟阶段没有中央增强。最大的病变测量通过前右颈部三角形空间内心的5.1×2.6×4.4cm,包裹着颈动脉护套,也可以在同一侧达到逆床和肩胛骨。其他病变被视为以下;左中间胸腔内表面,右平衡面积,右下肋骨的内表面,邻近肝叶的Theanteriorior,没有肝脏的涉及,在L2至L5水平的后复隙空间中。 ,髂骨后侧的后骨骨在臀部重膜中,在左股头的内侧方面,小大腿下方的几个病变双侧,主要是在横向方面,一些涉及相邻的股骨骨的涉及在左侧的形而上来[图。 3a,b和c]。来自正确的防疗性的手术活组织检查,组织学检查显示低功率的Nodu-Lar增长模式。血管和主轴细胞增殖。血管是薄壁和不规则的支化(血管泛卵瘤样)。损伤的延长的肌纤维细胞是多元或圆形的,而外周肌纤维素纤维素是用椭圆髓鞘的主轴形成。在一些焦点下,有丝分裂活性低,达到2/10hpf [图。 4]。患者在住院期间保持稳定,过度激活逐渐减少。 5个月的患者在NGT喂养时被送回家。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号