Background: The authors present a rare case of a ruptured aneurysm at the choroidal branch of the posterior inferior cerebellar artery (PICA).
Case Description: A 77-year-old female was admitted to our institute because of sudden onset of severe headache and vomiting. Radiologic examination revealed intraventricular hemorrhage caused by rupture of the aneurysm at the choroidal branch of the PICA. The fusiform aneurysm was resected after ligation via a midline suboccipital approach.
Conclusions: The conclusions drawn from this experience and a review of the literature include the following: (1) the aneurysm at the branch of the PICA is frequently associated with anomalies of the vascular structure, particularly in hypoplasty of the contralateral PICA; (2) hemodynamic stress is speculated to be a causative factor of these lesions; (3) cases with hypoplasty of the contralateral PICA have the possibility of developing nonmycotic peripheral aneurysms at the branch of the PICA; (4) these aneurysms should be managed immediately because of the high risk of rebleeding.
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http://dx.doi.org/10.1016/s0090-3019(03)00153-8 | DOI Listing |
Neurosurg Rev
December 2024
Neurosurgical Service, Beth Israel Deaconess Medical Center, Harvard Medical School, 110 Francis Street, Boston, MA, 02215, USA.
Anterior choroidal artery (AChA) aneurysms represent 2-5% of intracranial aneurysms. The proximity of the origin of the AChA to the aneurysm neck poses a risk of thromboembolic complications following treatment. AChA occlusion can result in significant neurological deficits.
View Article and Find Full Text PDFNeurol Sci
December 2024
Department of Neurosurgery, The Second Clinical Medical College, Nanchong Central Hospital, North Sichuan Medical College, No. 97 Renmin South Road, Nanchong, Sichuan, 637000, China.
Spontaneous disappearance of aneurysms, undetectable by conventional angiography, has been reported. This case report presents a patient with ventricular hemorrhage secondary to a ruptured lateral posterior choroidal artery aneurysm, confirmed by digital subtraction angiography (DSA). Without any intervention, follow-up DSA 11 months later showed an apparent "disappearance" of the aneurysm.
View Article and Find Full Text PDFAnn Med
December 2025
Department of Neurosurgery, The Third Bethune Hospital of Jilin University (China-Japan Union Hospital of Jilin University), Changchun, China.
Objective: Ruptured peripheral cerebral aneurysm (PPCA) associated with moyamoya disease (MMD) is rarely reported, and its optimal treatment remains controversial. This study aims to present the clinical characteristics, treatment strategies, and outcome predictors of this rare clinical entity.
Methods: A retrospective review of patients with hemorrhagic MMD from January 2013 to December 2020 was performed.
Asian J Neurosurg
December 2024
Department of Neurosurgery, Matsuyama Shimin Hospital, Matsuyama-city, Ehime, Japan.
Cureus
October 2024
Neurological Surgery, Tokuda Neurosurgical Hospital, Kanoya, JPN.
A 24-year-old obese female (height = 162 cm, weight = 84 kg, and BMI = 32.0) developed transient dysarthria and left hemiparesis, which was diagnosed as moyamoya disease (MMD) after imaging studies. Cerebral angiography and single photon emission computed tomography studies revealed that the above symptoms were caused by hemodynamic insufficiency in the bilateral hemispheres with right-sided predominance, and a right-sided superficial temporal artery-middle cerebral artery bypass was performed.
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