Kod'ousek R, Vojácek K, Houdek M, Kala M, Vaverka M, Santavá A, Nekula J
Ustav patologie LF UP, Olomouc.
Cesk Patol. 1996 Aug;32(3):89-96.
In a surgical specimen from a 33-year old woman with features of expansive cerebellar symptomatology, dysplastic gangliocytoma of the cerebellum (Lhermitte-Duclos) was diagnosed by histology. The lesion was characterized by typical proliferation of dysplastic neuronal elements in the cortical granular and Purkinje cell layers. Immunohistology showed focal positivity of synaptophysin in some cells, thus confirming their neuronal origin. In electron microscopy, peculiar features of ER in some of dysplastic cells was also noted. Genetic examination proved familiar incidence of Cowden's disease in several members. Chromosomal examination of the patient (karyotype 46, XX) was without abnormalities.
在一名具有小脑扩张症状特征的33岁女性的手术标本中,经组织学诊断为小脑发育异常性神经节细胞瘤(Lhermitte-Duclos病)。该病变的特征是皮质颗粒层和浦肯野细胞层中典型的发育异常神经元成分增殖。免疫组织化学显示部分细胞中突触素呈局灶性阳性,从而证实了它们的神经元起源。在电子显微镜下,还注意到一些发育异常细胞中内质网的特殊特征。基因检查证实该疾病在几个家庭成员中具有家族性发病情况。对患者进行的染色体检查(核型46, XX)未发现异常。