颅骨缺损伴脑积水同期手术19例临床总结

探讨同期手术治疗颅骨缺损伴脑积水的临床疗效.同期手术治疗颅骨缺损伴脑积水可增加手术的协同性,减少术后并发症,缩短住院时间,减轻患者经济负担.     

Direct and CT measurements of canals and foramina of the skull base.

This investigation is based on measurements of 60 macerated adult European skulls from the Alexander-Ecker Collection at the Anatomy Department of the University of Freiburg. Computer tomographical (CT) and anatomical measurements were compared to assess the accuracy of the CT representation of osseous structures. Nine structures were examined: the optic canal; the superior orbital fissure; the foramen rotundum; the foramen ovale; the foramen spinosum; the foramen Vesalii (venosum); the carotid canal; the internal auditory canal, and the hypoglossal canal. The results show a good and even excellent correlation if the cranial opening is approximately at a right angle to the scanline. For this reason, the results of the coronal examination of the internal auditory canal are less satisfactory, and the coronal and axial measurements of the hypoglossal canal show only a moderately good correlation.     

Evaluation of pediatric hydrocephalus by computed tomography.

Computed tomography (CT) is a safe and reliable technique for the study of children with increased head circumference. Hydrocephalic children requiring drainage of cerebrospinal fluid may be shunted on the basis of the CT scan alone and their postsurgical course followed by serial CT scans thereafter. Any additional pneumographic studies required may be performed via the existing shunt tube, eliminating transcerebral catheterization and its attendant complications.     

自体颅骨修复颅骨缺损68例体会

总结68例自体颅骨修复颅骨缺损的手术方法及体会,认为自体颅骨修复颅骨缺损不失为一种经济、简便易行的好方法.     

颅骨缺损合并脑积水的同期手术治疗

目的总结颅骨缺损合并脑积水的同期行分流与颅骨修补手术治疗的临床经验。方法 13例颅骨缺损患者(10例外伤性,2例高血压脑出血术后,1例大面积脑梗死术后)合并慢性脑积水,同期行脑室腹腔分流与颅骨缺损修补。结果术后无颅内感染,术后近期观察9例患者意识及神经功能障碍不同程度改善。远期随访,所有患者神经功能均有不同程度改善。结论颅骨缺损合并脑积水的同期手术可有效改善神经功能,降低分期手术费用。     

Skull fractures through parietal foramina: report of two cases

Enlarged parietal foramina are related to a condition in which defective intramembranous ossification of the parietal bones results in enlargement of the normal foramina. Although generally believed to be a benign variant, scalp defects, seizures, and structural brain abnormalities have been reported in a small percentage of affected patients. These 2 cases now present evidence that parietal foramina constitute structural weak spots in the calvarium that may potentially increase risk of skull fracture after trauma.     

Radiographic manifestations of congenital anomalies of the skull

Congenital anomalies of the pediatric skull are caused by a diverse group of disorders. For the purposes of this discussion, these entities can be classified according to the radiographic appearance of the skull, which may be similar in a variety of different diseases. Enlarged parietal foramina, sinus pericranii, aplasia cutis congenita, anterior fontanelle dermoid, cephaloceles, and craniolacunia are all examples of loceles, and craniolacunia are all examples of calvarial defects. Although there are numerous causes for wormian bones (Table 1), OI, cleidocranial dysplasia, congenital hypothyroidism, and hypophosphatasia are disorders that are commonly associated with defective ossification and the appearance of wormian bones. Osteopetrosis is an important example of rare bony dysplasias that cause sclerosis and hyperostosis of the skull. A partial list of other disorders causing similar radiographic findings is found in Table 2. Craniosynostosis results in an abnormality of skull shape. The suture(s) involved may be predicted by the deformed calvarial configuration. Knowledge of the growth and development of the skull and an understanding of the varied causes of congenital skull anomalies can enable the radiologist to provide the diagnosis or an informed differential diagnosis when confronted with a specific radiographic finding.     

外伤性脑积水75例诊治分析

分析75例外伤性脑积水病例的临床特点,认为脑室-腹腔分流术是主要的治疗方法,大部分病人可恢复良好。     

Comparison of skull circumference and linear measurements with CSF volume MR measurements in hydrocephalus.

In children with hydrocephalus, accurate and reproducible estimation of the presence, severity, and course of the condition is of paramount importance for both clinical and scientific purposes. In this study, 30 hydrocephalic patients were assessed with a number of commonly used methods, such as occipitofrontal skull circumference (SC) measurements, Evans ratio (ER), and bicaudate index (BCI), as well as, for comparison, another ratio of linear measurements [ventricle-skull ratio (VSR)] and MR measurements of total intracranial CSF volume. In repeated CSF volume measurements in healthy volunteers, the MR method appeared to be accurate and reproducible. This technique was simpler and easier in application, requiring less interaction than comparable MR techniques described by others. The variation coefficients were within the same range. In increased CSF volumes, our technique can be recommended; in very small CSF volumes, another technique is more adequate. Direct assessment of CSF volume as a measure of hydrocephalus was preferable over derived estimations for scientific purposes and may function as a gold standard against which to evaluate other techniques that are easier to apply clinically. In comparison, SC measurements were poor; CSF volume changes were not reflected in SC changes. VSR was preferable over ER and BCI, because it correlated more closely with CSF volume.     

Clinical course of fetal hydrocephalus: 40 cases

The clinical course and outcome of hydrocephalus diagnosed in utero is not well understood. To approach this problem 40 cases were reviewed of intrauterine fetal hydrocephalus diagnosed with sonography, and follow-up information was obtained regarding them. Sonograms were evaluated for cerebral dimensions, biparietal diameter, brain mantle size, ventricular ratio, amount of amniotic fluid, and associated abnormalities. Neonatal brain sonograms and computed tomographic (CT) scans were reviewed also. Clinical charts were reviewed for maternal age and parity, referral source, family history, fetal age at diagnosis and delivery, mode of delivery, physical examination and/or autopsy findings, karyotype, amniotic alpha 1 fetoprotein level, cause of death, shunt placement after birth, and status of live infants. The observations indicate that the prognosis for fetal hydrocephalus is poor. Only six infants (15%) were alive after an average follow-up of 13 months. Three children were normal and the other three had neurologic abnormalities ranging from severe (paralysis and incontinence) to minimal (2-3 months delayed motor development). Thirty-four fetuses or neonates died. Nine families elected to terminate pregnancy. Ten opted for decompression at delivery for progressive hydrocephalus. Neural tube defects were present in 12 of 23 infants at delivery. Fourteen other infants had additional significant congenital abnormalities. Other abnormal sonographic findings included polyhydramnios (13 of 38), oligohydramnios or decreased fluid (nine of 38), neural tube defect (nine of 40), and other congenital abnormalities (nine of 40). These findings indicate that hydrocephalus diagnosed in utero by sonography is caused by a heterogeneous group of disorders. In general, the prognosis for normal development is poor. Individual prognoses, however, depend on the specific malformations and the interventions used.