A case report of Gardner syndrome with hereditary widespread osteomatous jaw lesions
A case report of Gardner syndrome with hereditary widespread osteomatous jaw lesions
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DOI：
10.1016/j.tripleo.2008.10.018
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发表时间：
2009-03-01
期刊：
影响因子：
--
通讯作者：
Kim, Eun Cheol
中科院分区：
文献类型：
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作者：
Lee, Byung Do;Lee, Wan;Kim, Eun Cheol
加德纳综合征（GS）是一种家族性腺瘤性息肉病的异常，伴有特征性颌部病变。加德纳综合征肠息肉有100%发生恶变的风险；因此，疾病的早期识别和手术干预对于延长患者的生命非常重要。我们介绍了一名 55 岁女性的 GS 病例。家族性腺瘤性息肉病、骨瘤性颌骨和眼部病变、多种牙齿异常以及腹部硬纤维瘤是该病例的特征。该病例表明存在不寻常的、广泛的、遗传性的骨瘤性颌部病变，导致与家族性巨型牙骨质瘤的诊断混淆。 (Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2009;107:e68-e72)
Gardner syndrome (GS) is an abnormality of familial adenomatous polyposis accompanied by characteristic jaw lesions. Gardner syndrome intestinal polyps have a 100% risk of undergoing malignant transformation; consequently, early identification and surgical intervention of the disease are important to prolong the life of the patient. We present a case of GS in a 55-year-old woman. Familial adenomatous polyposis, osteomatous jaw and ocular lesions, several dental abnormalities, and an abdominal desmoid tumor are the characteristic features of this case. This case demonstrates the presence of unusual, widespread, hereditary, osteomatous jaw lesions that caused diagnostic confusion with familial gigantiform cementoma. (Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2009;107:e68-e72)