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

Kyosuke Miyatani; Paresh Korde; Yasuhiro Yamada; Tsukasa Kawase; Katsumi Takizawa; Yoko Kato

doi:10.4103/ajns.AJNS_210_19

Asian Journal of Neurosurgery, Table of Contents

CC BY-NC-ND 4.0 · Asian J Neurosurg 2019; 14(04): 1245-1248
DOI: 10.4103/ajns.AJNS_210_19

Case Report

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

Kyosuke Miyatani

⁰Department of Neurosurgery, Banbutane Hotokukai Hospital, Fujita Health University, Nagoya, Aichi

,

Paresh Korde

⁰Department of Neurosurgery, Banbutane Hotokukai Hospital, Fujita Health University, Nagoya, Aichi

,

Yasuhiro Yamada

⁰Department of Neurosurgery, Banbutane Hotokukai Hospital, Fujita Health University, Nagoya, Aichi

,

Tsukasa Kawase

⁰Department of Neurosurgery, Banbutane Hotokukai Hospital, Fujita Health University, Nagoya, Aichi

,

Katsumi Takizawa

¹Department of Neurosurgery, Asahikawa Red Cross Hospital, Asahikawa

,

Yoko Kato

⁰Department of Neurosurgery, Banbutane Hotokukai Hospital, Fujita Health University, Nagoya, Aichi

› Author Affiliations

Abstract

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.

Key-words:

Bilateral cavernous carotid aneurysm - Ehlers–Danlos syndrome - high-flow bypass - insurance bypass

Full Text

References

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