Von Hippel-Lindau syndrome from the urologist and oncologist perspective - literature review

被引:0
|
作者
Kowalik, Krzysztof [1 ]
Naroznicki, Pawel [2 ]
Hetman, Katarzyna [3 ]
Kolaczyk, Katarzyna [4 ]
Smogor, Artur [5 ]
Kasperowicz, Krystian [6 ]
Dutkiewicz, Grazyna [7 ]
Gruszczynska, Anna [8 ]
Modrzejewski, Andrzej [1 ]
机构
[1] Pomeranian Med Univ, Clin Dept Gen Surg, Ul Piotra Skargi 7?11, PL-70965 Szczecin, Poland
[2] Med Univ Lodz, Med Fac, Coll Mil Med, Fac Med, Lodz, Poland
[3] West Pomeranian Oncol Ctr, Dept Clin Oncol, Szczecin, Poland
[4] Pomeranian Med Univ, Univ Clin Hosp 1, Dept Imaging Diagnost & Intervent Radiol, Szczecin, Poland
[5] Med Off ARTIMED, Szczecin, Poland
[6] Northumbria Univ, Fac Hlth & Life Sci, Newcastle Upon Tyne, England
[7] Pomeranian Med Univ, Univ Clin Hosp 2, Dept Nephrol Transplantol & Internal Med, Szczecin, Poland
[8] Pomeranian Med Univ, Dept Forens Med, Szczecin, Poland
来源
ONCOLOGY IN CLINICAL PRACTICE | 2024年
关键词
von Hippel-Lindau syndrome; familiar angiomatosis of the retina and cerebellum; clear cell renal cell carcinoma; polycystic kidney disease; RENAL-CELL CARCINOMA; MALIGNANT PHEOCHROMOCYTOMAS; PRACTICE GUIDELINE; DISEASE; HEMANGIOBLASTOMAS; PARAGANGLIOMAS; CABOZANTINIB; MUTATION; FEATURES; THERAPY;
D O I
10.5603/ocp.101438
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Von Hippel-Lindau (VHL) syndrome is a rare genetic disorder characterized by multiple retinal and cerebellar hemangioblastomas that tend to occur in a familial setting. The pattern of inheritance is autosomal dominant. Patients with VHL syndrome have an increased risk of clear cell renal cell carcinoma (ccRCC) as well as pancreatic and testicular cysts and cystadenomas. Tumors associated with VHL syndrome manifest at a young age. This article presents diagnostic methods and discusses the treatment approaches for this syndrome based on a global literature review.
引用
收藏
页数:8
相关论文
共 50 条
  • [41] Progression of hemangioblastomas in pregnancy in von Hippel-Lindau syndrome
    Stokova, M.
    Musilova, B.
    Grubhoffer, M.
    Fiedler, J.
    CESKA A SLOVENSKA NEUROLOGIE A NEUROCHIRURGIE, 2023, 86 (05) : 333 - 335
  • [42] Von Hippel-Lindau Syndrome: Implications for Nursing Care
    Mahon, Suzanne M.
    Waldman, Laura
    ONCOLOGY NURSING FORUM, 2012, 39 (06) : 533 - 535
  • [43] Von Hippel-Lindau syndrome: molecular mechanisms of the disease
    María J. Calzada
    Clinical and Translational Oncology, 2010, 12 : 160 - 165
  • [44] von Hippel-Lindau disease
    Singh, AD
    Shields, CL
    Shields, JA
    SURVEY OF OPHTHALMOLOGY, 2001, 46 (02) : 117 - 142
  • [45] Postpartum cerebellar herniation in von Hippel-Lindau syndrome
    Othmane, IS
    Shields, C
    Singh, A
    Shields, J
    Goldman, W
    AMERICAN JOURNAL OF OPHTHALMOLOGY, 1999, 128 (03) : 387 - 389
  • [46] Von Hippel-Lindau syndrome presenting as pancreatic cysts
    Scolari, F
    Viola, BF
    Grazioli, L
    Maiorca, R
    RARE KIDNEY DISEASES, 2001, 136 : 325 - 330
  • [47] How 'eye' helped in von Hippel-Lindau syndrome
    Tyagi, Swati
    Kumar, Kritika Chopra
    Saluja, Komal
    EUROPEAN JOURNAL OF OPHTHALMOLOGY, 2023, 33 (01) : NP5 - NP9
  • [48] Von Hippel-Lindau's disease (VHL syndrome)
    Stenkula, S
    Crafoord, S
    ACTA OPHTHALMOLOGICA SCANDINAVICA, 1999, 77 (01): : 122 - 122
  • [49] VON HIPPEL-LINDAU DISEASE
    RICHARD, S
    OLSCHWANG, S
    CHAUVEAU, D
    RESCHE, F
    M S-MEDECINE SCIENCES, 1995, 11 (01): : 43 - 51
  • [50] VON HIPPEL-LINDAU DISEASE
    JOE, S
    SPENCER, WH
    ARCHIVES OF OPHTHALMOLOGY, 1964, 71 (04) : 508 - &