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Monstrous skull osteomas in a probable Gardner's syndrome: case report.

机译:Gardner综合征可能引起的巨大颅骨骨瘤:病例报告。

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BACKGROUND: Gardner's syndrome includes a clinical triad of familial polyposis coli, osteomas, and soft tissue tumors. METHODS: We present a very unusual case of probable isolated Gardner's syndrome characterized by extremely voluminous osteomas in the occipital and frontal areas associated with diffuse subcutaneous lipomas and without colic abnormality. RESULTS: The neurosurgical management included resection of the osteomas for cosmetic reasons. After a follow-up period of 5 years, the patient remains free of digestive complaints and the resected osteomas did not recur. CONCLUSIONS: The special clinical presentation of our case of possible Gardner's syndrome is discussed.
机译:背景:加德纳综合症包括家族性息肉病大肠杆菌,骨瘤和软组织肿瘤的临床三联征。方法:我们介绍了一个非常罕见的病例,可能是孤立的加德纳综合症,其特征是枕骨和额叶区域大量骨瘤伴发弥漫性皮下脂肪瘤,而无绞痛。结果:出于美容原因,神经外科治疗包括切除骨瘤。经过5年的随访,患者仍然没有消化道不适,并且切除的骨瘤没有复发。结论:讨论了我们可能的加德纳综合症病例的特殊临床表现。

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