Inflammatory pathogenesis of cortical polymicrogyria:: An autopsy study

被引:29
作者
Toti, P
De Felice, C
Palmeri, MLD
Villanova, M
Martín, JJ
Buonocore, G
机构
[1] Univ Siena, Inst Pathol, Nuovo Policlin, I-53100 Siena, Italy
[2] Univ Siena, Inst Prevent Pediat & Neonatol, I-53100 Siena, Italy
[3] Univ Siena, Inst Neurolog Sci, I-53100 Siena, Italy
[4] Univ Antwerp, Born Bunge Fdn, Neuropathol Lab, Wilrijk, Belgium
关键词
D O I
10.1203/00006450-199809000-00005
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Polymicrogyria, a cortical abnormality usually classified among neuron migration disorders, is characterized by different etiologies and pathogeneses. Recently, it has been proposed that polymicrogyria could be acquired as a consequence of a lasting damage to the developing brain. In this study, we test the hypothesis that an infection in the fetal adnexa may give rise to distant brain defects and eventually polymicrogyria. Thirty-two fetuses spontaneously aborted for extensive ascending chorioamnionitis at 15-26 wk of gestation were evaluated. Control subjects were represented by 8 fetuses aborted at 15-24 wk of gestation. A complete autopsy was carried out between 4 and 12 h after fetal expulsion. We found different histologic alterations in the primitive cortical architecture, both isolated and combined (undulation of the cortical ribbon, untimely cortical folding/molecular layer fusion, and neuronal loss). A total of 25 cases presented one or more of the above-described morphologic alterations in the brain (78%). On the contrary, similar alterations were never observed in any of the control brains (p = 0.019). Our findings indicate that chorioamnionitis significantly impairs brain cortex morphogenesis. Such neuron damage may be caused by an unspecific, indirect mechanism of injury to the developing cortex involving hypoxia and free radical generation. The reported brain abnormalities may even evolve into polymicrogyria in surviving fetuses.
引用
收藏
页码:291 / 296
页数:6
相关论文
共 36 条
[21]   EFFECT OF IBOTENATE ON BRAIN-DEVELOPMENT - AN EXCITOTOXIC MOUSE MODEL OF MICROGYRIA AND POSTHYPOXIC-LIKE LESIONS [J].
MARRET, S ;
MUKENDI, R ;
GADISSEUX, JF ;
GRESSENS, P ;
EVRARD, P .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1995, 54 (03) :358-370
[22]   CEREBRAL CORTICAL DYSPLASIA ASSOCIATED WITH PEDIATRIC EPILEPSY - REVIEW OF NEUROPATHOLOGIC FEATURES AND PROPOSAL FOR A GRADING SYSTEM [J].
MISCHEL, PS ;
NGUYEN, LP ;
VINTERS, HV .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1995, 54 (02) :137-153
[23]   Malformations of the brain [J].
Norman, MG .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1996, 55 (02) :133-143
[24]  
NORMAN MG, 1986, J NEUROPATH EXP NEUR, V45, P222
[25]  
RETZIUS G, 1895, HDB CLIN NEUROLOGY, P479
[26]   CEREBRAL MICROGYRIA IN A 27-WEEK FETUS - ARCHITECTONIC AND TOPOGRAPHIC ANALYSIS [J].
RICHMAN, DP ;
STEWART, RM ;
CAVINESS, VS .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1974, 33 (03) :374-384
[27]   A PERSPECTIVE - THE ROLE OF DISORDERED GENETIC-CONTROL OF NEUROGENESIS IN THE PATHOGENESIS OF MIGRATION DISORDERS [J].
RORKE, LB .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1994, 53 (02) :105-117
[28]   Increased levels of lipid peroxidation products malondialdehyde and 4-hydroxynonenal after perinatal hypoxia [J].
Schmidt, H ;
Grune, T ;
Muller, R ;
Siems, WG ;
Wauer, RR .
PEDIATRIC RESEARCH, 1996, 40 (01) :15-20
[29]  
SHAFRIR Y, 1996, ANN NEUROL, V40, P296
[30]  
STALLMACH T, 1995, LAB INVEST, V73, P384