Abdelmalek Mark, Stanko Christine
Department of Dermatology, Drexel University College of Medicine, Philadelphia, Pennsylvania, USA.
Am J Clin Dermatol. 2008;9(1):61-5. doi: 10.2165/00128071-200809010-00008.
Maffucci syndrome is a rare, sporadic disease characterized by the development of multiple enchondromas and subcutaneous hemangiomas. Patients with Maffucci syndrome have a 23-37% risk of malignancy, with chondrosarcomas being the most common. Although the development of a chondrosarcoma in a patient with Maffucci syndrome may be expected, intracranial chondrosarcomas are rare. We present a patient with Maffucci syndrome who was diagnosed with an intracranial chondrosarcoma after presenting with hearing loss and vomiting. After three craniotomies and two recurrences of chondrosarcoma of the right skull base, the patient demonstrated a positive outcome to treatment with external radiation therapy.
马富西综合征是一种罕见的散发性疾病,其特征为多发性内生软骨瘤和皮下血管瘤的形成。马富西综合征患者发生恶性肿瘤的风险为23%至37%,其中软骨肉瘤最为常见。虽然马富西综合征患者发生软骨肉瘤在意料之中,但颅内软骨肉瘤却很罕见。我们报告一例马富西综合征患者,该患者在出现听力丧失和呕吐后被诊断为颅内软骨肉瘤。在进行了三次开颅手术以及右侧颅底软骨肉瘤两次复发后,患者接受外照射治疗取得了良好效果。