Ehrenpreis S J, Kristt D A, Rigamonti D
Friedenwald Eye Institute, Maryland General Hospital, Baltimore 21201.
J Neuroophthalmol. 1994 Sep;14(3):183-7.
Intraventricular hemangioblastomas are exceptionally rare. Of the cases described in the literature, very few were associated with von Hippel-Lindau disease. We present a highly unusual case of a fourth ventricular hemangioblastoma associated with a pheochromocytoma and a renal medullary fibroma. This may represent a forme fruste of the von Hippel-Lindau complex. A workup for papilledema resulted in the discovery of this rare finding.
脑室内血管母细胞瘤极为罕见。在文献中描述的病例中,很少有与冯·希佩尔-林道病相关的。我们报告一例极为罕见的第四脑室血管母细胞瘤,同时伴有嗜铬细胞瘤和肾髓质纤维瘤。这可能代表冯·希佩尔-林道综合征的一种不完全型。对视乳头水肿的检查发现了这一罕见情况。