SciELO - Scientific Electronic Library Online

 
vol.21 número2Arteritis de Takayasu de evolución fulminante por enfermedad multivascular en adultoPolimiositis asociada a neumopatía intersticial en adulto mayor índice de autoresíndice de assuntospesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Journal

Artigo

Indicadores

Links relacionados

  • Não possue artigos similaresSimilares em SciELO

Compartilhar


Acta médica Grupo Ángeles

versão impressa ISSN 1870-7203

Resumo

DIAZ SANCHEZ, Mario de Jesús et al. Von Hippel-Lindau syndrome. Acta méd. Grupo Ángeles [online]. 2023, vol.21, n.2, pp.167-169.  Epub 20-Out-2023. ISSN 1870-7203.  https://doi.org/10.35366/110266.

Introduction:

Von Hippel-Lindau disease (VHL) is an inherited disorder that predisposes the development of various tumors that mainly affect the central nervous system, kidney, and pancreas. Due to its possibility of developing renal cell carcinoma and having clinical consequences in the pancreas, imaging surveillance is necessary to identify these manifestations promptly.

Clinical case:

a 23-year-old female patient, recently diagnosed with VHL disease and evidence of hemangioblastoma in the cerebellum that required surgical treatment, presented asymptomatically for an abdominal MRI as part of her screening studies.

Conclusion:

imaging studies are necessary for patients diagnosed with VHL to make a timely diagnosis of the possible affectations in the organs most frequently related to the disease.

Palavras-chave : Von Hippel-Lindau syndrome; magnetic resonance imaging; diagnostic imaging; neoplastic syndromes; renal cysts; pancreatic cysts.

        · resumo em Espanhol     · texto em Espanhol     · Espanhol ( pdf )