| Literature DB >> 227568 |
M T Hull, K A Warfel, J Muller, J T Higgins.
Abstract
Von Hippel-Lindau's Disease is an hereditary disorder characterized by the development of hemangioblastomas of the cerebellum and retina and a variety of cystic and neoplastic lesions of other organs such as renal cell carcinoma and pheochromocytoma. In a single generation of a family with Von Hippel-Lindau's disease, all four siblings developed lesions classically associated with the complex. Additionally, two of the four developed islet cell tumors of the pancreas, one in one patient and five in the other. While a familial incidence of islet cell tumors is known in multiple endocrine adenomatosis, type I and Zollinger-Ellison syndrome, such a familial occurrence has been heretofore unrecorded in the Von Hippel-Lindau complex.Entities:
Mesh:
Year: 1979 PMID: 227568 DOI: 10.1002/1097-0142(197910)44:4<1523::aid-cncr2820440452>3.0.co;2-0
Source DB: PubMed Journal: Cancer ISSN: 0008-543X Impact factor: 6.860