A ruptured aneurysm arising from the total duplication of the posterior communicating artery

•The authors report a ruptured aneurysm arising from the total duplication of the posterior communicating artery (PcomA) and the ophthalmic artery originated from cavernous portion anomalously.•An aneurysm arising from the duplication of the PcomA is extremely rare.•The PcomA duplication-in addition...

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Published inInterdisciplinary neurosurgery : Advanced techniques and case management Vol. 24; p. 101021
Main Authors Suzuki, Yuhei, Kaku, Yasuyuki, Tokuda, Takaho, Takashima, Ryo, Morikawa, Yusuke, Amadatsu, Toshihiro, Uekawa, Ken, Mukasa, Akitake, Yamashiro, Shigeo
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.06.2021
Elsevier
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Summary:•The authors report a ruptured aneurysm arising from the total duplication of the posterior communicating artery (PcomA) and the ophthalmic artery originated from cavernous portion anomalously.•An aneurysm arising from the duplication of the PcomA is extremely rare.•The PcomA duplication-in addition to the ophthalmic artery’s anomalous origin-was speculated to be an anomaly related to the developmental processes of cerebral arteries. A 36-year-old male suffered from a sudden headache. Computed tomography (CT) showed a subarachnoid hemorrhage (SAH). CT angiography demonstrated an aneurysm arising from the duplicate origin of the right posterior communicating artery (PcomA). The aneurysm was at the junction of the internal carotid artery and the distal branch of the PcomA duplication. Frontotemporal craniotomy and neck clipping were performed for the ruptured aneurysm. The patient’s post-operative course was uneventful and without symptomatic vasospasm. Post-operative angiography revealed the total duplication of the PcomA. The ophthalmic artery originating from cavernous portion anomalously. Although the relationship between the frequency of aneurysms and PcomA duplication is unclear, the PcomA duplication-in addition to the ophthalmic artery's anomalous origin-was speculated to be an anomaly related to the developmental processes of cerebral arteries.
ISSN:2214-7519
2214-7519
DOI:10.1016/j.inat.2020.101021