Qian Hai-rong, Meng Yu-hong, Gui Qiu-ping, Zheng Kui-hong, Yao Sheng, Qi Xiao-kun
Department of Neurology, Navy General Hospital of PLA, Beijing 100048, China.
Zhonghua Nei Ke Za Zhi. 2013 May;52(5):403-6.
To improve the diagnostic ability of leukoencephalopathy with cerebral calcifications and cysts (LCC), a rare central nervous system disease.
The clinical manifestations, neuroimages and neuropathological features of a 19-year-old male patient were analyzed. A total of 20 cases from 14 literatures were reviewed.
The patient was admitted with right limb weakness, cognitive decline, headache and blurred eyesight. Head CT scan showed multiple calcifications, cysts formation and leukoencephalopathy. Brain MRI showed several cysts in bilateral hemisphere, basal ganglia, thalamus and paraventricular areas. A mural nodule was noted inside one of the cyst, which was enhanced on the contrasted MRI. The wall of the cysts was partially enhanced, but not with the fluid inside the cysts. The corresponding CT calcifications foci showed on T1 and T2 with either both hyperintensity or both hypointensity, which was also partial enhanced. Extensive leukoencephalopathy was formed around the cysts and the ventricles. But neither Cho nor NAA changed a lot on MRS. Amplitude diagram of SWI series exhibited multiple round small dark signals all over the affected areas with mixed signals showed in the phase diagram, which indicated both calcifications and microbleeding at the lesions. Neuropathological examinations found no tumor cells in the operated cyst, and showed angiomatous small blood cells were dominant in the cyst wall. Hyaline degenerations, microcalcifications and hemosiderin deposition were observed. No obvious demyelination was discovered, while gliosis, numerous Rosenthal fibers and fibrinoid vascular necrosis were found around the lesions. The clinical, neuroimaging and pathological features of this patient were in accordance with the cases reported in the literatures.
Neuroimaging is the most important method for the diagnosis of LCC. As small vessel lesions are probably closely related to the pathophysiology of LCC, SWI could be recommended to further reveal the etiology of LCC.
提高对脑钙化和囊肿性白质脑病(LCC)这一罕见中枢神经系统疾病的诊断能力。
分析1例19岁男性患者的临床表现、神经影像及神经病理特征。回顾了14篇文献中的20例病例。
该患者因右下肢无力、认知功能减退、头痛及视力模糊入院。头颅CT扫描显示多发钙化、囊肿形成及白质脑病。脑部MRI显示双侧半球、基底节、丘脑及脑室周围区域有多个囊肿。其中一个囊肿内可见壁结节,增强MRI上有强化。囊肿壁部分强化,而囊肿内液体未强化。相应的CT钙化灶在T1和T2上均呈高信号或低信号,也有部分强化。囊肿及脑室周围形成广泛的白质脑病。但磁共振波谱分析中胆碱(Cho)和N-乙酰天门冬氨酸(NAA)均无明显变化。磁敏感加权成像(SWI)序列的幅度图显示病变区域布满多个圆形小暗信号,相位图显示混合信号,提示病变处既有钙化又有微出血。神经病理检查发现手术切除的囊肿内无肿瘤细胞,囊肿壁以血管瘤样小血细胞为主。可见透明变性、微钙化及含铁血黄素沉积。未发现明显脱髓鞘,病变周围有胶质增生、大量Rosenthal纤维及类纤维血管坏死。该患者的临床、神经影像及病理特征与文献报道的病例相符。
神经影像学是诊断LCC的最重要方法。由于小血管病变可能与LCC的病理生理密切相关,推荐使用SWI进一步揭示LCC的病因。