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CASE REPORT
Year : 2019  |  Volume : 14  |  Issue : 4  |  Page : 1245-1248

Atypical symptomatic bilateral spontaneous cavernous carotid aneurysm with systemic vessel wall pathology in young female: A rare case report


1 Department of Neurosurgery, Banbutane Hotokukai Hospital, Fujita Health University, Nagoya, Aichi, Japan
2 Department of Neurosurgery, Asahikawa Red Cross Hospital, Asahikawa, Japan

Correspondence Address:
Dr. Paresh Korde
Flat No. 8, Meghdoot Building No. 3, JNMC Campus, Sawangi, Meghe, Wardha - 442 001, Maharashtra
Japan
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ajns.AJNS_210_19

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Bilateral cavernous carotid aneurysm (CCA) is a rare entity. Its association with connective tissue disorder makes the diagnosis and treatment of symptomatic patient an enigma. We present a case report of a 25-year-old female medical student presented to us with bilateral spontaneous atypically symptomatic CCA with incidentally diagnosed case of Ehlers–Danlos syndrome. Both surgical and endovascular options of treatment were weighed and were ultimately treated satisfactorily by high-flow bypass with carotid artery ligation with an insurance bypass.


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