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[冯雷克林霍增氏病与肝脏神经纤维瘤病]

[Von Recklinghausen disease and hepatic neurofibromatosis].

作者信息

Guzman Toro F, Hinestroza D, Colmenares D

机构信息

Cirugía de Postgrado, Hospital Universitario de Maracaibo.

出版信息

G E N. 1995 Oct-Dec;49(4):303-6.

PMID:8762661
Abstract

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.

摘要

冯雷克林霍增氏神经纤维瘤病是最常见的常染色体显性疾病之一,估计发病率为每3000例活产中有1例。特征性损害包括牛奶咖啡斑和沿周围神经走行的神经纤维瘤。神经纤维瘤病累及肝脏较为罕见,仅有少数病例报道。我们报告1例患有冯雷克林霍增氏病和肝脏神经纤维瘤病的青年男性病例,该患者有多处牛奶咖啡斑、皮肤神经纤维瘤、身材矮小和骨损害,并将其临床、放射学、手术及解剖病理学表现与先前文献中描述的其他病例进行比较。

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