Evidence map›Paper›PMID 41497044›Full record

ArticleAnnals of medicine and surgery (2012)2026

Cavernous hemangioma: a rare case report in the maxillary sinus.

Omed Shafiq Hamamin, Saman Wahid Abdulrahman, Jeza Muhamad Abdul Aziz, Muhammad Jabar Rashid, Mohammad Rashidul Hashan

Abstract readCase Reports
In one paragraph

Article in Annals of medicine and surgery (2012), 2026. 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Omed Shafiq HamaminBiomedical Science Department, Komar University of Science and Technology, Sulaymaniyah, Kurdistan Regional Government, Iraq.
Saman Wahid AbdulrahmanDepartment of Oral and Maxillofacial Surgery, Baxshin Hospital, Sulaymaniyah, Kurdistan Regional Government, Iraq.
Jeza Muhamad Abdul AzizBiomedical Science Department, Komar University of Science and Technology, Sulaymaniyah, Kurdistan Regional Government, Iraq.
Muhammad Jabar RashidBaxshin Research Center, Baxshin Hospital, Sulaymaniyah, Kurdistan Regional Government, Iraq.
Mohammad Rashidul HashanDirectorate General of Health Service, Ministry of Health and Family Welfare, Government of Bangladesh, Dhaka, Bangladesh.ORCID https://orcid.org/0000-0002-1627-4976

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction and Importance: Cavernous hemangiomas are rare vascular malformations of the maxillary sinus that present diagnostic and therapeutic dilemmas. Case Presentation: This case report presents a 52-year-old woman with a slowly enlarging, painless swelling over the right infra-nasal region, leading to gross facial deformation. Imaging studies revealed a large, diffuse radiopaque mass in the upper right posterior maxilla, with a differential diagnosis favoring fibrous dysplasia. The patient underwent surgical excision via hemimaxillectomy under general anesthesia. Histopathological examination revealed a cavernous hemangioma. No perceptible aesthetic sequelae or recurrence was observed at follow-up months after treatment. Clinical Discussion: In the maxillofacial area, it is a rare entity, with the intraosseous type being even rarer, accounting for less than 1% of all bony tumors. The mandible is the most commonly affected site, accounting for approximately two-third hemangiomas of the jaw. The clinical manifestations of maxillary cavernous hemangiomas are highly variable and often nonspecific, making diagnosis challenging. Conclusion: Cavernous hemangiomas should be included in the differential diagnosis of maxillary sinus lesions. Surgical excision is the treatment of choice and results in an excellent prognosis with low recurrence rates.

Indexed as

cavernous hemangiomafacial deformityintraosseous tumormaxillary sinusvascular malformation

Identifiers

PMID41497044
PMCPMC12768128

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