Staged embolisation of a giant torcular dural sinus malformation in a neonate.
Evan M LutherAria JamshidiHunter KingRobert StarkePublished in: BMJ case reports (2021)
Torcular dural sinus malformations (tDSMs) represent a rare subset of paediatric cerebrovascular malformations and are often diagnosed antenatally via ultrasound. The management of these in utero lesions remains controversial as previous studies suggested elective termination of the pregnancy because of their presumably high mortality and severe long-term morbidity. However, more recent evaluations have suggested that the overall prognosis for infants harbouring these lesions may be much better than previously believed. As such, we present the case of a neonate with a giant tDSM, diagnosed in utero, who was treated postnatally via staged transarterial and transvenous embolisation to alleviate worsening obstructive hydrocephalus and brainstem compression. We provide details regarding the surgical approach and long-term neurological outcomes for this patient. To the best of our knowledge, this is one of the largest reported tDSM presented in the literature.
Keyphrases
- magnetic resonance imaging
- systematic review
- healthcare
- emergency department
- patients undergoing
- case report
- cardiovascular events
- rare case
- early onset
- type diabetes
- risk factors
- metabolic syndrome
- subarachnoid hemorrhage
- computed tomography
- insulin resistance
- newly diagnosed
- cardiovascular disease
- weight loss
- skeletal muscle
- glycemic control
- brain injury