Squier Waney, Cowan Frances M
Department of Neuropathology, Radcliffe Infirmary, Oxford OX2 6HE, UK.
Semin Neonatol. 2004 Aug;9(4):331-45. doi: 10.1016/j.siny.2004.01.003.
Autopsy is invaluable in identifying the causes of severe depression and very low Apgar score after birth and in assessing contributory conditions. Brain scans are increasingly used in the care of neonates who fail to respond to resuscitation at birth but their interpretation depends on the information gained from sound neuropathological studies. Asphyxia, both acute intrapartum asphyxia and chronic asphyxia, is an important cause of low Apgar scores. The gestational age and the nature of the asphyxial insult both have a profound influence on the ultimate pattern of injury. Asphyxia in the preterm brain tends to damage preferentially the white matter but some white matter damage is also seen in many infants who have an hypoxia-ischaemic insult at term though the predominant site of injury is to the central grey matter. The nature of the cellular damage and reactive change seen at autopsy is described. There is an association between low Apgar scores and intrauterine exposure to infection and maternal pyrexia. Detailed autopsy examination should include the search for infection. The placenta, cord and membranes should be examined in view of the mounting evidence of the association between intrauterine infection of the placenta and fetal membranes and prenatal brain damage. Additionally, the presence of placental thrombosis and infarction should be sought in relation to focal and global injury in the full term infant. Acquired prepartum lesions rarely cause the infant to present with a low Apgar score. The exception to this is severe damage to the brainstem and basal ganglia. Traumatic injury to the brain is now much less common than in previous decades. Subdural haemorrhage occurs more frequently than intraventricular or subarachnoid haemorrhage. Instrumental and assisted deliveries are associated with an increased incidence of subdural haemorrhage though these rarely cause significant long term damage. Careful autopsy, particularly of the neck and paravertebral tissues, spinal cord, brainstem and nerve roots is important where trauma is suspected. Tearing of nerve roots or fibre bundles in the spinal cord is readily demonstrated under the microscope using immunocytochemistry to beta-amyloid precursor protein. Disorders of the spinal cord, peripheral nerve and muscle as well as some metabolic diseases may cause a baby to be both floppy and weak. Metabolic disease, including peroxisomal disorders, non-ketotic hyperglycinaemia, lipid and glycogen storage disorders and mitochondrial diseases may cause profound hypotonia and respiratory failure at birth or shortly afterwards.
尸检对于确定严重抑郁症的病因、出生后极低的阿氏评分以及评估相关情况具有极高的价值。脑部扫描越来越多地用于护理出生时对复苏无反应的新生儿,但对其解读取决于从可靠的神经病理学研究中获得的信息。窒息,包括急性产时窒息和慢性窒息,是阿氏评分低的重要原因。胎龄和窒息损伤的性质对最终的损伤模式都有深远影响。早产脑的窒息往往优先损害白质,但许多足月时遭受缺氧缺血性损伤的婴儿也可见一些白质损伤,尽管主要损伤部位是中央灰质。描述了尸检时所见的细胞损伤和反应性变化的性质。阿氏评分低与宫内感染和母体发热有关。详细的尸检检查应包括寻找感染。鉴于越来越多的证据表明胎盘和胎膜的宫内感染与产前脑损伤之间存在关联,应检查胎盘、脐带和胎膜。此外,对于足月婴儿的局灶性和全身性损伤,应查找胎盘血栓形成和梗死。产前获得性病变很少导致婴儿出现低阿氏评分。脑干和基底节严重损伤是个例外。现在脑部创伤性损伤比过去几十年少见得多。硬膜下出血比脑室内或蛛网膜下腔出血更常见。器械助产和辅助分娩与硬膜下出血的发生率增加有关,不过这些很少造成严重的长期损害。在怀疑有创伤时,仔细的尸检,特别是对颈部和椎旁组织、脊髓、脑干和神经根的尸检很重要。使用针对β-淀粉样前体蛋白的免疫细胞化学方法,在显微镜下很容易显示脊髓神经根或纤维束的撕裂。脊髓、周围神经和肌肉疾病以及一些代谢性疾病可能导致婴儿既松软又无力。代谢性疾病,包括过氧化物酶体疾病、非酮症高甘氨酸血症、脂质和糖原储存疾病以及线粒体疾病,可能在出生时或出生后不久导致严重的肌张力低下和呼吸衰竭。