Martin J J, Cras P
Acta Neuropathol. 1985;66(2):140-4. doi: 10.1007/BF00688689.
The neuropathologic study of a 7-month-old female patient affected by familial erythrophagocytic lymphohistiocytosis (FEL) reveals three main features: (1) a lymphohistiocytic leptomeningitis with erythrophagocytosis; (2) perivascular lymphohistiocytic cuffs in the cerebral and cerebellar white matter and, to a lesser extent, in the thalamus, the reticular formation of the brain stem and the griseum pontis; (3) perifocal gliosis and demyelination, especially in the cerebellar white matter. The lesions remind of the perivenous post-infectious encephalomyelitides. Perifocal demyelination has been reported in FEL very seldom. Although its pathogenesis is not known, immune mechanisms could play a role by analogy with perivenous encephalomyelitis.
对一名患有家族性噬血细胞性淋巴组织细胞增生症(FEL)的7个月大女性患者进行的神经病理学研究揭示了三个主要特征:(1)伴有噬红细胞现象的淋巴细胞性脑膜炎;(2)大脑和小脑白质中血管周围淋巴细胞性套袖状浸润,丘脑、脑干网状结构和脑桥灰质中程度较轻;(3)灶周胶质增生和脱髓鞘,尤其是在小脑白质中。这些病变使人联想到静脉周围感染后脑脊髓炎。FEL中很少报道灶周脱髓鞘。虽然其发病机制尚不清楚,但免疫机制可能通过与静脉周围脑脊髓炎类推而发挥作用。