Evidence map›Paper›PMID 41313742›Full record

ArticleThe American journal of case reports2025

Persistent Primitive Hypoglossal Artery in a 55-Year-Old Woman with Recurrent Dizziness, Identified on Ultrasound and Computed Tomography Imaging.

Weiwei Zhang, Zhenli Huang, Liya Wei, Yanrong Sun, Fei Sang

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In one paragraph

Article in The American journal of case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Weiwei ZhangDepartment of Ultrasound, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Zhenli HuangDepartment of Ultrasound, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Liya WeiDepartment of Ultrasound, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Yanrong SunDepartment of Ultrasound, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Fei SangDepartment of Radiology, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Persistent primitive hypoglossal artery (PPHA) is a rare congenital condition due to an embryological vascular remnant consisting of an artery that usually originates at the C1-C2 vertebral level from the internal carotid artery (ICA), which bypasses the usual vertebral artery (VA) supply to the basilar artery (BA), and passes through the hypoglossal canal to the posterior fossa to connect to the vertebrobasilar system. This report describes the case of a 55-year-old woman presenting with dizziness due to a PPHA identified on ultrasound (US) and computed tomography (CT) angiography (CTA). CASE REPORT A 55-year-old woman presented with recurrent dizziness. First, carotid Doppler ultrasound (CDU) revealed the dilated left ICA with an increased peak systolic velocity (PSV) and an anomalous branch vessel at its distal end, plus hypoplastic bilateral extracranial VAs with high-resistance flow. Next, transcranial color-coded sonography (TCCS) showed no intracranial VA flow and reduced bilateral posterior cerebral arteries (PCAs) PSV upon left common carotid artery (CCA) compression. The combined findings of CDU and TCCS were suggestive of PPHA (eg, dilated left ICA with anomalous branch, hypoplastic bilateral VAs, reduced bilateral PCAs PSV upon left CCA compression). Subsequent CTA confirmed left-sided PPHA (ICA-C1 origin, hypoglossal canal passage, BA connection) and absent bilateral posterior communicating arteries. Finally, the patient received conservative medication. CONCLUSIONS This report presents a rare congenital vascular anomaly, PPHA, and aims to raise awareness of this condition, highlighting the approach to diagnosis using US and CT imaging.

Indexed as

Carotid Artery, InternalDizzinessComputed Tomography AngiographyFemaleHumansMiddle AgedRecurrenceUltrasonography, Doppler, Transcranial

Identifiers

PMID41313742
PMCPMC12729222

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.