Abstract
The visceral manifestations of von Hippel-Lindau syndrome rarely are clinically significant until late in the disease process. Pancreatic endocrine insufficiency in the syndrome is extremely uncommon. We report a case of a 32-year-old woman with von Hippel-Lindau syndrome whose initial diagnosis came to light because of a clinical presentation with complications related to pancreatic endocrine insufficiency.
Original language | English (US) |
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Pages (from-to) | 598-604 |
Number of pages | 7 |
Journal | Surgery |
Volume | 105 |
Issue number | 5 |
State | Published - May 1989 |
ASJC Scopus subject areas
- Surgery