Dados do Trabalho

Título

Fetal dural sinus thrombosis: case report and management review.

Apresentação do caso

The patient was the second child of healthy non-consanguineous parents. Her mother presented only with hypothyroidism during an otherwise uneventful pregnancy. Ultrasound at 30 weeks revealed bilateral ventriculomegaly, hypoplasia of corpus callosum and absent septum pellucidum. Further fetal MRI evidenced thrombosis of the torcular, both transverse sinuses, ⅓ of the straight and sagittal sinus, venous dilatation at parasagittal high convexity and signs of previous hemorrhage in both choroid plexus, symmetrical ventricular dilatation, intraventricular clots, absent septum pellucidum and thin corpus callosum. She was full-term, born in a cesarean birth due to non-reassuring fetal status. She was small for gestational age, normal head circumference and presented with mild global hypotonia. Neonatal brain MRI confirmed fetal findings. No maternal or neonatal coagulopathy or infection was found and baby was discharged with no complications at 17 days old.

Discussão

Fetal dural sinus thrombosis (DST) is a rare condition diagnosed antenatally through ultrasound by the identification of an echogenic posterior fossa mass, containing a focal hyperechoic area within. MRI fetal studies provide confirmation of the DST and insight into complications such as ventriculomegaly and local compression. Less than 100 cases are described in literature. To date, there is no evidence to support association with maternal or neonatal coagulopathy, infection or trauma. It has been hypothesized that anatomical malformations of the dural sinus may occur, leading to disturbance of blood circulation and damage of the vascular endothelium.
A minority of cases result in fetal or neonatal death and most cases results in decrease or complete resolution of thrombosis antenatally. In majority cases no intervention is needed. If there is hydrocephalus or parenchymal congestion, post-natal anticoagulation and embolization of arteriovenous fistulas should be considered, especially if rapid progression of thrombosis occurs.

Comentários finais

We report a rare case of DST. This unusual condition is usually suspected in fetal US and confirmed through MRI. There is no current consensus guideline for treatment, but anticoagulation and embolization should be considered if there are signs of worsening venous hypertension.

Referências (se houver)

1. Sacco, A., Pannu, D., Ushakov, F., Dyet, L., & Pandya, P. (2021). Fetal dural sinus thrombosis: A systematic review. Prenatal Diagnosis, 41(2), 248–257. https://doi.org/10.1002/pd.5869
2. Wierzbowski, K. A., Wing, S. E., Brown, B. P., Martinez, M. L., & Golomb, M. R. (2022). Fetal Cerebral Sinovenous Thrombosis and Dural Sinus Malformation. Pediatric Neurology, 126, 89–93. https://doi.org/10.1016/j.pediatrneurol.2021.10.010
3. Yang, edward, storey, armide, Olson, heather, soul, J., estroff, J., Trenor, cameron, cooper, B. K., smith, edward, & Orbach, D. B. (2018). Imaging features and prognostic factors in fetal and postnatal torcular dural sinus malformations, part II: synthesis of the literature and patient management Neuroimaging. J NeuroIntervent Surg, 10, 475–479. https://doi.org/10.1136/neurintsurg-2017-013343.

Palavras Chave

Fetal dural sinus thrombosis; dural venous sinus ectasia; torcula herophili;

Fonte de Fomento (se houver)

Declaração de conflito de interesses de TODOS os autores

The authors declare that they have no conflict of interest

Área

Neurologia neonatal