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Unveiling the uncommon: Giant internal jugular vein aneurysm in a neurofibromatosis patient: A case report.
Khan, Khalid; Kaya, Ahmet; Mahdi, Rawan A.
Affiliation
  • Khan K; Department of Radiology; Salmaniya Medical Complex, Building 929, Road 1015, Sanabis 410, P.O. Box: 12, Kingdom of Bahrain.
  • Kaya A; Department of Radiology; Salmaniya Medical Complex, Building 929, Road 1015, Sanabis 410, P.O. Box: 12, Kingdom of Bahrain.
  • Mahdi RA; Department of Radiology; Salmaniya Medical Complex, Building 929, Road 1015, Sanabis 410, P.O. Box: 12, Kingdom of Bahrain.
Radiol Case Rep ; 19(10): 4133-4137, 2024 Oct.
Article in En | MEDLINE | ID: mdl-39114860
ABSTRACT
Neurofibromatosis Type 1 (NF1) is a rare autosomal dominant disorder that has a wide array of clinical manifestations. NF1 Vasculopathies constitute 0.4% to 6.4% of the findings and they often develop in the arterial circulation while venous involvement is rare. We present a case of a 73-year-old male with NF1 with an incidental finding of right neck swelling for 2 months. Different radiological modalities were performed, identifying the lesion as an internal jugular vein aneurysm. The patient was managed conservatively as he was asymptomatic in relation to the swelling. NF1 venous vasculopathies are rare but they have detrimental consequences such as rupture and severe hemorrhage in view of the fragility of the aneurysmal wall and the infiltration of the neurofibroma into the vessel. Hence, high clinical suspicion and selective imaging and follow-up is advisable for physicians.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Radiol Case Rep Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Radiol Case Rep Year: 2024 Document type: Article