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題名 | Klippe1-Trénaunay-Weber Syndrome: Extradural Arachnoid Cyst, Nevus Flammeus, and Hemihypertrophy=Klippe1-Trénaunay-Weber症候群 |
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作者 | 黃佳雯; 施玲娜; 郭長豐; 林水龍; 王怡人; Huang, Chia-wen; Shih, Ling-na; Kuo, Charng-fong; Lin, Shoei-loong; Wang, I-jen; |
期刊 | 醫學與健康期刊 |
出版日期 | 20140300 |
卷期 | 3:1 2014.03[民103.03] |
頁次 | 頁97-102 |
分類號 | 417.509 |
語文 | eng |
關鍵詞 | Klippel-Trénaunay-Weber症候群; 蛛網膜囊腫; 葡萄酒色斑; 半邊肢體肥大; Klippel-Trénaunay-Weber syndrome; Arachnoid cyst; Port-wine stain; Hemihypertrophy; |
中文摘要 | 本文介紹一名Klippel-Trénaunay-Weber (KTW)症候群的案例,並建立後續追蹤之建議。 KTW症候群為一罕見先天性疾病,其特徵為葡萄酒紅IJI 、血管瘤、靜脈曲張及淋巴畸形,以及肢體半邊肥大o 神經學影像異常的病患可能同時合併神經學異常。本文介紹一名十一個月大男畫,合併有服體半邊肥大以及葡萄酒紅斑。我們為他安排了腦部磁振造影(MRI)檢查,發現後顱窩有一蜘蛛網膜囊腫,而病童並沒有神經學要常。我們建議當看到病童合併有肢體半邊肥大及葡萄酒紅斑,應安排腦部影像學檢查,且必須長期追蹤病重的神經學症狀及神經發育。 |
英文摘要 | Objectives: KTW syndrome is a rare congenital disorder with port-wine stain, hemangioma, venous and lymphatic malformation, and hemihypertrophy. Patients with abnormal neuroradiographic findings might present with neurological deficits. However, some cases may not be diagnosed until adulthood because of the obscure symptoms. More famililarity with Klippel-Trénaunay-Weber (KTW) syndrome is needed. Case report: Herein we report a case of KTW involving an 11-month-old boy with hemihypertrophy and port-wine stains. Based on recommendation by studies of neurocutaneous syndromes, we performed a brain magnetic resonance imaging (MRI) examination for the boy. A large arachnoid cyst in the posterior fossa was found incidentally, though no neurologic deficits were found at that time. Conclusions: We recommend brain image studies when encountering a child with hemihypertrophy and port-wine stain. Long-term follow-up for the neurodevelopment is warranted in these children. |
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