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A case series of intraosseous hemangioma of the jaws: Various presentations of a rare entity.

作者信息

Chandra Srinivasa R, Chen Eleanor, Cousin Timothee, Oda Dolphine

机构信息

MD, DDS, Clinical Assistant Professor, 1959 NE Pacific St, Department of Oral & Maxillofacial Surgery, University of Washington School of Dentistry, Seattle, Washington 98195-7133, USA.

MD, PhD, Assistant Professor, Department of Pathology, University of Washington Medical Center , 1959 NE Pacific St Box 357705.

出版信息

J Clin Exp Dent. 2017 Nov 1;9(11):e1366-e1370. doi: 10.4317/jced.54285. eCollection 2017 Nov.

DOI:10.4317/jced.54285
PMID:29302291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5741852/
Abstract

BACKGROUND

Hemangiomas of the soft tissue are common in the head and neck area, especially in the tongue and in children under ten years of age. Intraosseous hemangiomas of the mandible and maxilla (IHM), on the other hand, are exceedingly rare and are not well characterized. This study presents six IHM cases focusing on the clinical, radiographic, and histologic characteristics.

MATERIAL AND METHODS

Six cases of IHM were retrieved from the archives of the Biopsy Services at the University of Washington. Clinical, radiologic, and histologic findings are described.

RESULTS

A total of six cases of IHM were reviewed. The patient age range was 16 to 65; the group comprised three females and three males. All six cases presented as swellings, two caused tooth resorption, and one was associated with pain and numbness. Three of the six IHM were present in the body of the mandible, two in the area of the extracted right mandibular third molar, and one in the anterior maxilla between the right canine and lateral incisor. Radiographically, five were radiolucent and one was radiopaque. Of the five radiolucent, two were unilocular and three multilocular. The one radiopaque case was exophytic, simulating a large osteoma. Histologic features ranged from cavernous to a mix of venous and arterial types. Follow-up is available for all six cases ranging between one to seven years; only one case recurred within the first year post-surgery.

CONCLUSIONS

IHM are exceedingly rare; IHM do not present in a consistent manner both clinically and radiographically. It is therefore important to recognize the wide spectrum of IHM's clinical, radiographic, and histological presentations. Hemangioma, Vascular Malformation, mandible, maxilla.

摘要

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Primary intraosseous cavernous hemangioma of the zygoma: a case report and literature review.颧骨原发性骨内海绵状血管瘤:一例报告及文献复习
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Hemangiomas and vascular malformations: current theory and management.血管瘤与血管畸形:当前理论与治疗
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Intraosseous venous malformation of the mandible: a review on interdisciplinary differences in diagnostic nomenclature for vascular anomalies in bone and report of a case.
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