#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Von Hippel-Lindau Disease. Case-report


Authors: M. Ludvíková 1;  P. Toufarová 2
Authors‘ workplace: Patologicko-anatomický ústav LF a FN, Plzeň, přednosta prof. MUDr. F. Fakan, CSc. 2Urologická klinika LF a FN, Plzeň, přednosta doc. MUDr. Z. Ouda, CSc. 1
Published in: Prakt. Lék. 2001; (3): 138-140
Category:

Overview

Von Hippel-Lindau disease (VHL) is an autosomally dominant inherited syndrome characterized by variable nevertheless typical manifestations of pathological lesions, the most common being haemangioblastomas of the central nervous system and renal cysts and neoplasms. The authors present clinical and morphological results of a 8-year observation of a patient suffering von Hippel-Lindau disease with gradual manifestation of different pathological tumorous and nontumorous lesions. The authors discuss the pathogenetic consequences, common and unusual VHL pathological changes and stress the diagnostic pitfalls as well as the necessity of regular examination of the patient.

Key words:
von Hippel-Lindau disease - pathological changes

Full text is not available online.
If interested in a scan of this journal, contact NTO ČLS JEP.

Labels
General practitioner for children and adolescents General practitioner for adults
Topics Journals
Login
Forgotten password

Enter the email address that you registered with. We will send you instructions on how to set a new password.

Login

Don‘t have an account?  Create new account

#ADS_BOTTOM_SCRIPTS#