Triantafyllou George, Papadopoulos-Manolarakis Panagiotis, Tsanis George, Papanagiotou Panagiotis, Tsakotos George, Piagkou Maria
Department of Anatomy, School of Medicine, Faculty of Health Sciences, National and Kapodistrian University of Athens, 75 Mikras Asias Str., Goudi, 11527, Athens, Greece.
Department of Neurosurgery, General Hospital of Nikaia-Piraeus, Athens, Greece.
Anat Sci Int. 2025 Jun;100(3):370-374. doi: 10.1007/s12565-024-00818-x. Epub 2024 Dec 23.
The cerebral arterial circle morphologic variability has been extensively studied. The posterior cerebral artery (PCA) variants are rarely identified, except from the first segment (P1) hypoplasia or absence. Due to its unique morphology, the computed tomography angiography (CTA) of a 34-year-old female patient was further investigated. On the right side, the typical PCA originated as the terminal branch of the basilar artery. An accessory PCA was also identified originating from the right internal carotid artery (ICA), while the right posterior communicating artery was absent. This variant corresponds to the "complete" duplication of the PCA. The left-sided PCA originated from the ICA, while the P1 was hypoplastic, representing the "partial fetal-type PCA." The rest of the cerebral arterial circle was typical. The present case of PCA "complete" duplication corresponds to a scarce variant, with a reported prevalence of 0.04%, while the fetal-type PCA is the most commonly observed variant.
大脑动脉环的形态变异已得到广泛研究。除了第一段(P1)发育不全或缺失外,大脑后动脉(PCA)变异很少被发现。由于其独特的形态,对一名34岁女性患者的计算机断层血管造影(CTA)进行了进一步研究。右侧,典型的PCA起源于基底动脉的终末分支。还发现一条副PCA起源于右侧颈内动脉(ICA),而右侧后交通动脉缺失。这种变异对应于PCA的“完全”重复。左侧PCA起源于ICA,而P1发育不全,代表“部分胎儿型PCA”。大脑动脉环的其余部分是典型的。本病例中PCA的“完全”重复是一种罕见的变异,报道的患病率为0.04%,而胎儿型PCA是最常见的变异。