Faculty of Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, Vietnam.
Department of Neurosurgery, Nguyen Tri Phuong Hospital, Ho Chi Minh City, Vietnam.
Am J Case Rep. 2024 Jun 24;25:e943718. doi: 10.12659/AJCR.943718.
BACKGROUND Monostotic fibrous dysplasia is a benign proliferation of fibrous and osseous tissues that expand medullary bone to cause symptoms due to compression of adjacent organs and anatomical structures. Focal seizures are rarely the first sign of this kind of lesion. This report describes a young female patient with left-sided focal motor seizures associated with fibrous dysplasia presenting as a mass in the right parietal bone. CASE REPORT An 18-year-old female student with left-sided focal motor seizures presented with a mass in the right parietal bone. Computed tomography revealed an expansile mixed-density lesion on the right parietal bone, a relatively homogeneous ground-glass appearance in the outer circumferential portion, and a lucent eccentric area with thinned but sclerotic borders. Magnetic resonance imaging revealed a homogeneously hypointense signal on T1WI, a small hyperintense signal on T2WI, and avid enhancement signal intensity on post-contrast T1. Electroencephalogram showed inter-ictal epileptiform activities derived from the right fronto-central lobe. Surgical en bloc resection with a margin of normal bone and cranioplasty were performed. Histopathology showed features indicative of fibrous dysplasia, including osteoid trabeculae arranged haphazardly in a dense fibroblastic stroma, irregular trabeculae lacking conspicuous osteoblastic rimming, and intervening fibrous stroma containing cytologically bland spindle cells. The patient achieved seizure control and has remained neurologically intact. CONCLUSIONS This report has highlighted the importance of early diagnosis of fibrous dysplasia of bone to exclude primary bone malignancy or bone metastasis, to ensure rapid management and symptom control.
单骨性纤维结构不良是一种纤维和骨组织的良性增生,它会扩张髓腔骨,导致由于邻近器官和解剖结构受压而产生症状。局灶性癫痫发作很少是这种病变的第一个迹象。本报告描述了一例年轻女性患者,其左侧局灶性运动性癫痫发作与纤维结构不良有关,表现为右顶骨肿块。
一名 18 岁女学生,因左侧局灶性运动性癫痫发作,右侧顶骨出现肿块。计算机断层扫描显示右顶骨有一个膨胀性混合密度病变,外周部分呈相对均匀的磨玻璃样外观,有透光偏心区,边界变薄但硬化。磁共振成像显示 T1WI 均匀低信号,T2WI 小高信号,增强后 T1 信号强度有明显增强。脑电图显示来自右额-中央叶的发作间期癫痫样活动。行整块切除带正常骨缘的肿瘤和颅骨成形术。组织病理学显示出纤维结构不良的特征性表现,包括排列杂乱的骨样小梁,密集的成纤维细胞基质,不规则的小梁缺乏明显的成骨细胞包绕,以及包含细胞学上温和的梭形细胞的纤维基质。患者实现了癫痫控制,神经功能完整。
本报告强调了早期诊断骨纤维结构不良的重要性,以排除原发性骨恶性肿瘤或骨转移,确保快速治疗和症状控制。