Rawal Yeshwant B, Chandra Srinivasa R, Hall James M
Department of Oral and Maxillofacial Surgery, School of Dentistry, University of Washington, B-204 Magnuson Health Sciences Center, 1959 NE Pacific Street, Box 357133, Seattle, WA, 98195, USA.
Oral Maxillofacial - Head and Neck Oncologic and Reconstructive Microvascular Surgery, Harborview Medical Center, Seattle, WA, USA.
Head Neck Pathol. 2017 Jun;11(2):192-202. doi: 10.1007/s12105-016-0764-z. Epub 2016 Oct 22.
Extragnathic xanthomas are seen in the bones or as soft tissue masses. They are often associated with hyperlipidemia and are considered as reactive or metabolic lesions. Only 19 cases of xanthomas of the jaws have been reported so far in the English literature. A total of ten cases of central xanthoma of the jaw bones were identified from the Oral and Maxillofacial Pathology biopsy services of the University of Washington and the Tufts University School of Dental Medicine, between the years 2000-2016. The demographic and clinical information on these cases was tabulated logically on the basis of age, gender, location and presence or absence of symptoms, extragnathic lesions and serum hyperlipidemia. Radiographic and histopathological features were also examined. The findings in these cases were correlated with those available from the previously reported cases. Majority of cases are seen in the second and third decades of life. There is no gender predilection. Jaw lesions presented as solitary radiolucencies with a predilection for the posterior mandible. Unlike maxillary lesions, pain and expansion are inconsistent findings in mandibular lesions. Jaw lesions are not associated with extragnathic bone or soft tissue involvement or a hyperlipidemia. The central xanthoma of the jaws is a unique benign tumor. Histopathologically, many other jaw lesions contain variable numbers of foamy histiocytes. Therefore, a diagnosis of a central xanthoma of the jaws must be made after excluding all other such histiocyte containing lesions. This requires correlation of histopathological findings with clinical and radiographic features.
颌骨外黄色瘤可见于骨骼或表现为软组织肿块。它们常与高脂血症相关,被认为是反应性或代谢性病变。迄今为止,英文文献中仅报道了19例颌骨黄色瘤。2000年至2016年间,从华盛顿大学和塔夫茨大学牙医学院的口腔颌面病理活检服务中,共鉴定出10例颌骨中央性黄色瘤。根据年龄、性别、部位以及有无症状、颌骨外病变和血清高脂血症等情况,对这些病例的人口统计学和临床信息进行了合理列表。还检查了影像学和组织病理学特征。将这些病例的结果与先前报道病例的结果进行了对比。大多数病例见于第二和第三个十年。无性别倾向。颌骨病变表现为孤立的透射影,以后下颌骨为好发部位。与上颌病变不同,疼痛和膨隆在下颌病变中并非一致的表现。颌骨病变与颌骨外骨骼或软组织受累或高脂血症无关。颌骨中央性黄色瘤是一种独特的良性肿瘤。组织病理学上,许多其他颌骨病变含有数量不等的泡沫状组织细胞。因此,必须在排除所有其他含组织细胞的病变后,才能诊断颌骨中央性黄色瘤。这需要将组织病理学结果与临床和影像学特征相结合。