Bilateral pheochromocytoma as first manifestation of von Hippel-Lindau disease: a case report

Catli G., ABACI A., Neumann H. C. H., Altincik A., DEMİR K., BÖBER E.

TURKISH JOURNAL OF PEDIATRICS, cilt.54, sa.5, ss.532-535, 2012 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 54 Sayı: 5
  • Basım Tarihi: 2012
  • Dergi Adı: TURKISH JOURNAL OF PEDIATRICS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.532-535
  • Anahtar Kelimeler: von Hippel-Lindau syndrome, pheochromocytoma, retinal hemangioblastoma
  • Dokuz Eylül Üniversitesi Adresli: Evet

Özet

Von Hippel-Lindau syndrome is an autosomal dominant disorder that includes susceptibility to hemangioblastomas of the eyes and central nervous system, renal clear cell carcinoma, multiple pancreatic cysts, serous cystadenomas and pancreatic neuroendocrine tumors, pheochromocytoma, endolymphatic sac tumors, and cystadenomas of the epididymis and broad ligament.