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1.
Br J Neurosurg ; : 1-4, 2022 May 05.
Article in English | MEDLINE | ID: mdl-35510560

ABSTRACT

BACKGROUND: Brain arteriovenous malformations (bAVMs) are vascular lesions that commonly present with intracranial haemorrhage. Pregnancy has been associated with an increased risk of bAVM rupture. However, their natural history in pregnant women is uncertain. CASE DESCRIPTION: A 27-year-old female at 28 weeks of gestation presented with a compromised neurological status secondary to a ruptured left frontal Spetzler-Martin scale (SM) III + bAVM. An emergent caesarean section was performed due to the high risk of foetal distress. Endovascular treatment successfully controlled the bleeding site, and stereotactic radiosurgery was offered as a subsequent treatment option. CONCLUSION: bAVMs should be considered in pregnant women with intracranial haemorrhage. The management of these lesions during pregnancy is controversial. Surgical risk and foetal development should be considered when selecting a management strategy.

2.
Surg Neurol Int ; 12: 312, 2021.
Article in English | MEDLINE | ID: mdl-34345453

ABSTRACT

BACKGROUND: Schwannomas of the cauda equina are rare intradural primary spinal tumors. Many of these patients initially present with cauda equina syndromes, and only 2.2% demonstrate clinical recurrence. Gross total excision is the procedure of choice. CASE DESCRIPTION: A 62-year-old female had undergone resection of a cauda equina schwannoma 5 years previously. She newly presented with cauda equina symptoms attributed to a recurrent schwannoma. Following gross total secondary tumor resection, the patient's preoperative deficits fully resolved, and the tumor never recurred. CONCLUSION: Secondary gross total excision of schwannomas of the cauda equina is critical to avoid further tumor recurrence.

3.
J Neurol Surg A Cent Eur Neurosurg ; 82(5): 490-493, 2021 Sep.
Article in English | MEDLINE | ID: mdl-33845513

ABSTRACT

BACKGROUND: Scalp arteriovenous fistulas (AVFs) are a rare vascular disease usually presenting as a progressively increasing pulsating mass in the scalp. These lesions can be associated with mild to severe complications, including congestive heart failure. If ruptures, this pathology constitutes a life-threatening medical emergency because of its potential to cause severe bleeding and acute anemia. METHODS: We describe the case of a young woman with a ruptured Yokouchi type C scalp AVF with eyelid involvement. RESULTS: The patient presented with hypovolemic shock and acute anemia due to severe bleeding from the lesion. Emergent treatment through a combined endovascular and open surgical approach was required to stop bleeding and stabilize the patient. CONCLUSIONS: Emergent and effective treatment is required to stop bleeding when a scalp AVF ruptures. A combination of endovascular embolization and microsurgical excision of the shunt is a treatment option.


Subject(s)
Arteriovenous Fistula , Embolization, Therapeutic , Arteriovenous Fistula/diagnostic imaging , Arteriovenous Fistula/surgery , Eyelids , Female , Humans , Scalp/surgery , Treatment Outcome , Young Adult
4.
J Clin Neurosci ; 80: 232-237, 2020 Oct.
Article in English | MEDLINE | ID: mdl-33099352

ABSTRACT

Intracranial high-grade dural arteriovenous fistulas (DAVFs) have higher bleeding rates compared to other intracranial vascular malformations. Endovascular treatment is usually recommended for high-grade lesions, aiming at a complete fistula obliteration. However, some patients have vascular abnormalities that limit endovascular access to the precise location of the shunt. Alternative techniques may be considered in this scenario. A middle-aged man presented with intracranial hypertension secondary to a high-grade DAVF. Because of vascular abnormalities precluding transvenous access to the intracranial venous circulation, the patient required treatment by a direct transcranial coil and Onyx embolization of the shunt. Direct transcranial cannulation of a dural sinus is an alternative and effective route for transvenous embolization of DAVFs, especially if abnormal venous anatomy precluding venous access to the required cranial venous system is identified.


Subject(s)
Central Nervous System Vascular Malformations/diagnostic imaging , Central Nervous System Vascular Malformations/therapy , Dimethyl Sulfoxide/administration & dosage , Embolization, Therapeutic/methods , Polyvinyls/administration & dosage , Adult , Cerebral Veins/diagnostic imaging , Cranial Sinuses/diagnostic imaging , Humans , Male , Treatment Outcome
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