Yoshino A, Katayama Y, Watanabe T, Kurihara J, Kimura S
Department of Neurological Surgery, Nihon University School of Medicine, Tokyo, Japan.
J Neurosurg. 1998 Mar;88(3):581-5. doi: 10.3171/jns.1998.88.3.0581.
Except for villous hypertrophy of the choroid plexus that may not be true tumors, multiple choroid plexus papillomas are extremely rare. The authors report a case involving multiple choroid plexus papillomas that were distinct from villous hypertrophy. These lesions were localized, one in the atrium of the right lateral ventricle and the other in the inferior horn of the left lateral ventricle. A review of the literature revealed that this case represented the first reported case of true multiple choroid plexus papillomas documented by findings on magnetic resonance imaging.
除了脉络丛绒毛状肥大可能并非真正的肿瘤外,多发性脉络丛乳头状瘤极为罕见。作者报告了一例涉及多发性脉络丛乳头状瘤的病例,这些肿瘤与绒毛状肥大不同。这些病变局限于一处,一个位于右侧脑室的房部,另一个位于左侧脑室的下角。文献回顾显示,该病例是首例经磁共振成像检查结果证实的真正的多发性脉络丛乳头状瘤病例。