[小儿脑干胶质瘤2例临床病理分析]。

K Harada, J Yoshida, T Wakabayashi, K Sugita
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引用次数: 0

摘要

从1976年到1991年的16年间,33名患有脑干胶质瘤的儿童在名古屋大学神经外科接受了治疗。小儿脑干胶质瘤非常罕见,在所有33例病例中只有2例(6.1%)。本文报道了小儿脑干胶质瘤的临床病理研究。病例1:患者1在妊娠38周后出生,无智力和身体发育迟缓。他的父母在他4个月大的时候发现了他的斜颈。MRI显示延髓后外生性异常肿块增强。经颅切除术切除部分肿块,病理显示为II级星形细胞瘤。术后3个月,斜颈逐渐好转,6个月后完全消失。病例2:孕41周出生的患者2,腹部皮肤见咖啡色斑点2个,左肩及股骨区见血管瘤。对于最初的症状,左动眼肌麻痹在2个月大时被发现。CT表现为中脑及脑桥内固有增强异常肿块,不久后侵犯右额叶。病理检查为星形细胞瘤III级。IAR治疗后(干扰素- β 140 × 10(4), ACNU 20 mg × 2。辐射;全脑40.8 Gy,局灶9 Gy),左侧动眼性麻痹虽有暂时改善,但肿瘤侵袭性增大,患者11个月时死亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Clinico-pathological investigation for infantile brain stem glioma: report of two cases].

Thirty-three children harboring brain stem glioma were treated at Nagoya University, Department of Neurosurgery during in the 16-year period from 1976 to 1991. Infantile brain stem glioma is so rare and we have only two cases (6.1%) of all 33 cases. This paper reported clinico-pathological investigation of infantile brain stem glioma. Case 1: Patient 1 was born after 38 weeks gestation, and he showed no mental nor physical retardation. His parents noticed his torticollis at 4 months of age. MRI showed exophytic abnormal enhanced mass behind the medulla oblongata. The mass was partially removed by craniectomy, and its pathological study revealed astrocytoma grade II. Since 3 months after the operation, torticollis had been gradually improved and disappeared completely 6 months later. Case 2: Patient 2 born after 41 weeks gestation, two cafe-au-lait spots were seen on the abdominal skin and hemangiomas were seen on the left shoulder and femoral area. For the initial symptoms, left oculomotor palsy was recognized at 2 months old. CT showed intrinsic enhanced abnormal mass in the mid brain up to the pons and then it invaded into right frontal lobe soon. Open biopsy was performed and the pathological examination revealed astrocytoma grade III. After IAR therapy (Interferon-beta 140 x 10(4), ACNU 20 mg x 2. Radiation; whole brain 40.8 Gy, focal 9 Gy), although left oculomotor palsy was improved temporarily, the tumor enlarged invasively and the patient died at 11 months old.

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