A Rare Case of Multiorgan Solid Cystic Lesion: Von Hippel Lindau Syndrome - An Institutional Experience
Von Hippel-Lindau syndrome is a rare hereditary multisystemic tumour predisposition disorder, caused by a mutation in the VHL gene. The incidence is 1 in 39,000 individuals. Here we report a case of a 20-yearold male patient who presented with complaints of dull aching abdominal pain for 2 months. C...
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Dr. Annil Mahajan,
2023-07-01T00:00:00Z.
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A1234.567 |
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| Kopie 1 | Beschikbaar |