Scopus
YÖKSİS Eşleşti
All-in-One Case: Comprehensive Detection of VHL Syndrome With 68 Ga-DOTATATE PET/CT
Clinical Nuclear Medicine · Nisan 2026
YÖKSİS Kayıtları
All-in-One Case: Comprehensive Detection of VHL Syndrome With 68Ga-DOTATATE PET/CT
Clinical Nuclear Medicine · 2025 SCI-Expanded
DOÇENT HASAN ÖNNER →
Makale Bilgileri
DergiClinical Nuclear Medicine
Yayın TarihiNisan 2026
Cilt / Sayfa51 · e262-e263
Scopus ID2-s2.0-105031820700
Özet
Von Hippel-Lindau (VHL) disease is a rare, autosomal dominant, multisystem cancer syndrome. A variety of benign and malignant tumors can develop in VHL, including cranial and spinal hemangioblastomas, retinoblastoma, endolymphatic sac tumor, pheochromocytoma, renal cell carcinoma, pancreatic neuroendocrine tumors, and renal, pancreatic, and genital cysts. Here we present a 57-year-old woman who was diagnosed with VHL and, in the same 68 Ga-DOTATATE PET/CT, exhibits all these components of the syndrome: pheochromocytoma, pancreatic neuroendocrine tumor, pancreatic cysts, renal cysts, liver hemangioma, and hemangioblastoma in the medulla oblongata.
Yazarlar (3)
1
M. N. Calderon Tobar
2
H. Önner
ORCID: 0000-0003-1002-2097
3
Ahmet Gorgel
Anahtar Kelimeler
DOTATATE
hemangioblastoma
pheochromocytoma
Von Hippel Lindau
Kurumlar
Selçuk Tip Fakültesi
Konya Turkey