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Fatal Progression of Gorham-Stout Disease with Skull Base Osteomyelitis and Lateral Medullary Syndrome

机译:颅底骨髓炎和外侧延髓综合征的高汉姆-斯托特病的致命进展

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摘要

Gorham-Stout disease (GSD) is a rare condition in which spontaneous, progressive resorption of bone occurs. There are no previous reports of patients with fatal progression of GSD with skull base osteomyelitis (SBO) and lateral medullary syndrome (LMS). We present the case of a 27-year-old man diagnosed with GSD with involvement of the maxillofacial bones and skull base. The patient developed SBO; LMS resulted from progressive osteolysis, and the patient died of associated brainstem stroke. Careful follow-up with special emphasis on the early detection of intracranial complications is critical in patients presenting with progressive GSD with involvement of the skull base.
机译:Gorham-Stout病(GSD)是一种罕见的疾病,其中会发生骨骼的自发性进行性吸收。先前没有报道患有GSD并伴有颅底骨髓炎(SBO)和外侧髓样综合征(LMS)的致命进展的患者。我们介绍了一名27岁的男性,被诊断患有GSD并涉及颌面部骨骼和颅底。患者发展为SBO; LMS是由进行性骨溶解引起的,患者死于相关的脑干中风。对于表现为进展性GSD并伴有颅底的患者,进行认真的随访特别是早期发现颅内并发症至关重要。

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