Lee Yujin, Kim Seong Ik, Kim Seung-Ki, Kim In One, Park Sung-Hye
Department of Pathology, Seoul National University College of Medicine, 103 Daehak-ro, Jongno-gu, Seoul, 110-799, Republic of Korea.
Department of Neurosurgery, Seoul National University Children's Hospital and College of Medicine, Seoul, Republic of Korea.
Brain Tumor Pathol. 2016 Apr;33(2):147-50. doi: 10.1007/s10014-015-0242-4. Epub 2015 Dec 15.
We report a novel case of a mixed choroid plexus papilloma (CPP) and ependymoma with cartilaginous differentiation. This kind of mixed tumor has not been previously reported in the English literature. The patient was a 5-year-old girl, who presented with a 1-week history of fever and numbness of the right lower limb. Magnetic resonance imaging of the brain with gadolinium revealed a heterogeneously enhancing mass in the occipital horn of the left lateral ventricle. Histologically, the tumor showed an intermixed CPP area and a low-grade papillary ependymoma-like area, which was studded with cartilage islands and psammoma bodies. In many foci, direct transition of CPP and ependymoma was observed, but there were no high-grade features. We report this novel case, describe the unique microscopic and immunohistochemical features, and speculate on the pathogenesis.
我们报告了一例伴有软骨分化的混合性脉络丛乳头状瘤(CPP)和室管膜瘤的新病例。这种混合性肿瘤此前在英文文献中未见报道。患者为一名5岁女孩,有1周发热及右下肢麻木病史。头颅钆增强磁共振成像显示左侧脑室枕角有一不均匀强化肿块。组织学上,肿瘤表现为CPP区域与低级别乳头状室管膜瘤样区域混合,其间散在软骨岛和砂粒体。在许多病灶中,观察到CPP与室管膜瘤的直接移行,但未见高级别特征。我们报告这一新病例,描述其独特的微观及免疫组化特征,并对其发病机制进行推测。