Key result
Complete surgical excision of a rare intravascular papillary endothelial hyperplasia in the superficial temporal artery resulted in excellent healing with no recurrence during a 24-month follow-up.
Why the study?
Intravascular papillary endothelial hyperplasia is a rare benign vascular lesion that typically occurs in veins or vascular tumors, making its presentation within arterial vessels uncommon.
Case Report (n=1)
No
This report details a rare case of intravascular papillary endothelial hyperplasia in the superficial temporal artery, emphasizing the utility of ultrasound in identifying characteristic vascular penetration for preoperative diagnosis.
Rare arterial IPEH in superficial temporal artery warrants inclusion in pulsatile mass differentials; leaves open optimal management and pathogenesis.
Intravascular papillary endothelial hyperplasia is a rare benign vascular lesion that typically occurs in thrombosed dilated veins or vascular tumors, with its occurrence within arterial blood vessels being uncommon. In this report, we present a case of intravascular papillary endothelial hyperplasia within superficial temporal artery in a 35-year-old Chinese male patient. The patient initially noticed a non-tender pulsatile mass in his left temple three years ago, which has gradually increased in size over time. Ultrasound examination revealed a well-defined, hypoechoic oval lesion in the left temporal region, with a blood vessel traversing through it and connecting to the superficial temporal artery. Complete excision of the mass was performed, and histological examination confirmed intravascular papillary endothelial hyperplasia. We provide an extensive literature review on intravascular papillary endothelial hyperplasia tumor along with a discussion on ultrasound findings.
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Cong et al. (2025) conducted a case report in Intravascular papillary endothelial hyperplasia (IPEH) (n=1). Surgical excision was evaluated on Surgical outcome and recurrence. Complete surgical excision of a rare intravascular papillary endothelial hyperplasia in the superficial temporal artery resulted in excellent healing with no recurrence during a 24-month follow-up.
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