Isobe Kenichi, Shimizu Tominaga, Akahane Tsutomu, Kato Hiroyuki
Department of Orthopedic Surgery, Shinshu University, School of Medicine, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan.
AJR Am J Roentgenol. 2004 Aug;183(2):331-6. doi: 10.2214/ajr.183.2.1830331.
We surveyed the clinical symptoms and radiologic features of ancient schwannoma, a rare variant of schwannoma characterized by degenerative changes.
We present the clinical, radiologic, and pathologic features in seven patients with ancient schwannoma (mean age, 62 years; range, 45-80 years) treated at our department between 1998 and 2003.
The most characteristic clinical features were a sign like Tinel's sign and a long interval between the onset of symptoms and surgery (mean interval, 8.3 years). Ancient schwannomas can grow large; the biggest tumor seen in our study was 14 cm long. The highly accurate radiologic assessment made possible with contrast-enhanced MRI and CT scanning showed enhancement at a peridegenerative area and sometimes at a capsule. These findings differ from those of the typical schwannoma and neurofibroma patterns reported to date. Furthermore, bone scintigraphy showed uptake in the tumor, but no accumulation was seen on gallium-67 citrate scintigraphy.
The characteristic clinical and radiologic findings of ancient schwannoma should make it possible to differentiate it from malignant tumors.
我们调查了陈旧性神经鞘瘤的临床症状和放射学特征,这是一种以退行性改变为特征的罕见神经鞘瘤变体。
我们呈现了1998年至2003年间在我院接受治疗的7例陈旧性神经鞘瘤患者(平均年龄62岁;范围45 - 80岁)的临床、放射学和病理学特征。
最具特征性的临床特征是类似Tinel征的体征以及症状出现与手术之间的间隔时间长(平均间隔8.3年)。陈旧性神经鞘瘤可长得很大;我们研究中见到的最大肿瘤长14厘米。对比增强MRI和CT扫描所实现的高度准确的放射学评估显示在退变周边区域有时在包膜处有强化。这些发现与迄今报道的典型神经鞘瘤和神经纤维瘤模式不同。此外,骨闪烁显像显示肿瘤有摄取,但枸橼酸镓闪烁显像未见积聚。
陈旧性神经鞘瘤的特征性临床和放射学表现应使其能够与恶性肿瘤相鉴别。