[冯雷克林豪森病和肝神经纤维瘤病]。

G.E.N Pub Date : 1995-10-01
F Guzman Toro, D Hinestroza, D Colmenares
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引用次数: 0

摘要

Von Recklinghausen神经纤维瘤病是最常见的常染色体显性遗传病之一,估计发病率为1:30 000活产。特征性病变包括咖啡渍斑和沿周围神经路径的神经纤维瘤。神经纤维瘤病累及肝脏是罕见的,很少有病例被报道。我们报告一例年轻男性Von Recklinhausen病和肝脏神经纤维瘤病,伴有多个caf-au-lait斑点,皮肤神经纤维瘤,身材矮小和骨性病变,并将临床,放射学,外科和解剖学病理结果与先前文献中描述的其他结果进行比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Von Recklinghausen disease and hepatic neurofibromatosis].

Von Recklinghausen's neurofibromatosis is one of the most common autosomal dominant disease with an estimated frecuency of 1:3000 live births. Characteristic lesions include cafe-au-lait spots and neurofibromas following the path of peripheral nerves. Liver involvement by neurofibromatosis is rare and very few cases have been reported. We present a case of a young man with Von Recklinhausen's disease and hepatic neurofibromatosis with multiple caf-au-lait spots, cutaneous neurofibromas, short stature and osseous lesions and compare the clinical, radiological, surgical and anatomopathological findings with others describe previously in the literature.

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