Evidence map›Paper›PMID 41377270›Full record

ArticleAnnals of medicine and surgery (2012)2025

Veinguard: a rare case of an external jugular vein angioma.

Syeda Wila-E-Zehra, Mohammad Irshad Malik, Amna Rafique, Zirwa Javed, Anurag Jha, Ursula Abu Nahla

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Article in Annals of medicine and surgery (2012), 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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5 · Who and what money

Authors and funding

6 authors.

Syeda Wila-E-ZehraDepartment of Medicine, Fatima Jinnah Medical University, Lahore, Pakistan.
Mohammad Irshad MalikDepartment of Otorhinolaryngology Unit I, Sir Ganga Ram Hospital, Lahore, Pakistan.
Amna RafiqueDepartment of Otorhinolaryngology Unit I, Sir Ganga Ram Hospital, Lahore, Pakistan.
Zirwa JavedDepartment of Otorhinolaryngology Unit I, Sir Ganga Ram Hospital, Lahore, Pakistan.
Anurag JhaDepartment of Medicine, King Edward Medical University, Lahore, Pakistan.
Ursula Abu NahlaDepartment of Medicine, Hebron University, Hebron, Palestine.ORCID https://orcid.org/0009-0001-2356-0751

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction and Importance: Neck masses are common, but primary vascular tumors of the external jugular vein are exceptionally rare and often overlooked in differential diagnoses. This case is notable for its prolonged course, distinctive clinical presentation, and histological confirmation, underscoring the value of imaging, surgical excision, and attention to cosmetic outcomes. Case Presentation: We describe a 20-year-old female who presented with an 8-year history of a progressively enlarging right-sided neck swelling that became painful in the past 2 years. On examination, a 3 × 2 cm nonreducible mass with bluish discoloration was noted in the lower anterior triangle of the neck, which enlarged on coughing and during the Valsalva maneuver. Initial imaging with ultrasonography revealed a vascular lesion, further characterized by CT angiography as a 20 × 15 mm enhancing mass attached to the right external jugular vein. Surgical excision was performed under general anesthesia. Intraoperatively, a well-circumscribed vascular mass was found adjacent to the sternocleidomastoid muscle and excised completely. Histopathological analysis confirmed a benign venous angioma. Clinical Discussion: Vascular tumors of the external jugular vein are exceptionally uncommon and often absent from routine differential diagnoses. Their clinical presentation may mimic benign cysts or lymphadenopathy, contributing to diagnostic uncertainty. Imaging helps narrow the diagnosis but cannot confirm histology. Surgical excision is essential for both definitive diagnosis and symptom relief. In this case, the patient also had aesthetic concerns, which were addressed successfully with a concealed incision and uneventful recovery. Conclusion: Venous angioma of the external jugular vein is a rare differential for neck masses. Surgical excision remains the mainstay for diagnosis and management, with excellent long-term outcomes.

Indexed as

external jugular veinneck massrare case reportsurgical excisionvascular tumorvenous angioma

Identifiers

PMID41377270
PMCPMC12688754

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