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  • 1
    ISSN: 1432-1920
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Résumé Les auteurs rapportent un cas d'hémangiome du rachis dorsal chez un adolescent de 11 ans, devenu paraparétique après un léger traumatisme. La myélographie montrait un arrêt complet du produit opaque au niveau de la vertèbre angiomateuse. L'angiographie médullaire sélective permettait d'opacifier l'hémangiome et ses pédicules vasseaux provenant des artères intercostales ge droite et gauche. — Après la visualisation de l'artère de Adamkiewicz, provenant de la 7eartère intercostale gauche, une embolisation pré-opératoire de l'hémangiome est réalisée. L'intervention chirurgicale de laminectomie s'est révélée simple et peu hémorragique. L'enfant marchait correctement 2 mois après l'operation.
    Abstract: Zusammenfassung Die Autoren berichten über einen Fall mit einem Hämangiom der Brustwirbelsäule bei einem elfjährigen Kind, das nach einem leichten Trauma paraparetisch geworden war. Eine Myelographie ergab einen kompletten Stop des Kontrastmittels in der Höhe des angiomatösen Wirbels. Mit einer selektiven Rückenmark-Angiographie wurden das Hämangiom und seine Versorgungsgefäße aus der linken und rechten 9. Interkostalarterie dargestellt. Darauf wurde nach Darstellung der Arterie von Adamkiewicz mit ihrem Ursprung aus der linken 7. Interkostalarterie die präoperative Embolisierung des Hämangioms durchgeführt. Der darauffolgende chirurgische Eingriff, eine Laminektomie, war einfach und ging ohne nennenswerten Blut verlust vor sich. Zwei Monate nach der Operation hatte sich das Kind gut erholt und begann normal zu gehen.
    Notes: Summary The authors report one case of dorsal haemangioma in an eleven year old boy who became paraparetic following slight trauma. Myelography revealed a complete block at the level of the angiomatous vertebra. — Selective medullary angiography gave complete visualization of the haemangioma and of its vascular peduncles which started from the right and left 9th inter costal arteries. After having visualized Adamkiewicz's artery, which started from Th7 on the left, the angioma was embolised with sponge fragments. This made decompressive laminectomy much easier since it reduced the risk of profuse bleeding. The child was walking normally two months after operation.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neurology 225 (1981), S. 67-72 
    ISSN: 1432-1459
    Keywords: Ewing sarcoma ; Epidural tumors ; Spinal cord compression ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Es wird ein Ewing-Sarcom, welches sich außerhalb des Skelettes bei einem Kind entwickelte, geschildert. Klinisch manifestierte es sich als epidurale Masse. Bei der chirurgischen Exploration zeigte sich ein brüchiges Gewebe, welches 2–3 cm lang war und nicht vom Knochen ausging. Lichtmikroskopisch und elektronenmikroskopisch ließ sich die Diagnose eines Ewing-Sarcoms stellen. Es werden morphologische Aspekte und differentialdiagnostische Überlegungen in Zusammenhang mit Tumoren des Epiduralraumes diskutiert.
    Notes: Summary The clinicopathological findings in a child with extraskeletal Ewing sarcoma are described. The patient complained of pain in the lower back and difficulty walking. An extraskeletal, epidural, friable tumor, 2–3 cm long was removed from the epidural space. It had no relationship with the bone structures. Light and electron microscopic examination of the tumor led to the diagnosis of Ewing sarcoma. The morphological aspects of this neoplasia and the problem of the differential diagnosis with other small cell tumors of the epidural space are discussed.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0942-0940
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0942-0940
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Bei Patienten mit akinetischem Mutismus als Folge von Schädelverletzungen wurden Untersuchungen der Schlafstrukturen durchgeführt. Ein vollständig physiologisches Schlafverhalten war bei 7 Patienten festzustellen. Bei 2 Fällen fand sich eine gute Schlaforganisation, aber mit Fehlen derjenigen Schlafphase, die durch eine Desynchronisation des EEG und durch rasche Augenbewegungen charakterisiert ist. Zweimal wurden atypische schlafähnliche EEG-Veränderungen registriert. Bei 3 Patienten schließlich konnten keine Zeichen von Schlaf gefunden werden. Es ließen sich gewisse Korrelationen zwischen dem Schlafverhalten und der Entwicklung des akinetischen Mutismus aufzeigen: Einem guten Grad von Schlaforganisation folgte häufig eine günstige Entwicklung des Krankheitsbildes und umgekehrt. Es wurde der Versuch unternommen, die Charakteristika des Hirnschadens bei den verschiedenen beobachteten Fällen unter Berücksichtigung der Arten der Schlaforganisation und der bisherigen Erkenntnisse der neurophysiologischen Mechanismen des Schlafes zu interpretieren.
    Abstract: Résumé On a étudié la structure électroencéphalographique du sommeil chez des patients présentant un mutisme akinétique à la suite d'un traumatisme crânio-cérébral. Sept patients présentaient des tracés typiques de sommeil. Chez deux patients, les tracés montraient une bonne organisation de sommeil; la phase de sommeil disparaissait avec les mouvements rapides des yeux, l'E.E.G. montrant alors une désynchronisation. Deux patients avaient des tracés atypiques de sommeil. Chez trois autres, il n'y avait aucune évidence électroencéphalographique de sommeil. Il semblait exister une certaine relation entre le tracé de sommeil obtenu et l'évolution du mutisme akinétique; chez les patients qui présentèrent un tracé de sommeil, l'évolution était favorable et vice-versa. A la lumière des connaissances actuelles des mécanismes neurophysiologiques du sommeil, et à l'analyse des tracés obtenus, les auteurs tentent d'interpréter les caractéristiques des lésions cérébrales.
    Notes: Summary Sleep patterns has been studied in patients in akinetic mutism due to head injury. Completely organized sleep patterns occurred in 7 patients. Well organized sleep patterns, which lacked only the sleep phase with “desynchronized” EEG and rapid eye movements, were observed in 2 cases. Some atypical sleep-like EEG manifestations were recorded twice. Finally, no sign of sleep could be found in 3 patients. Some correlation between sleep patterns and the clinical course of the akinetic mutism was apparent: well organized sleep patterns were frequently followed by favourable clinical progress and viceversa. An attempt has been made to interpret the characteristics of the brain damage in the different cases observed by relating the type of sleep organization with what is known of the neurophysiological mechanisms of sleep itself.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Acta neurochirurgica 85 (1987), S. 87-95 
    ISSN: 0942-0940
    Keywords: Head injury ; carotid angiography ; CT scan ; Glasgow Coma Scale ; prognosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary This is a study of the changes that have occurred in the field of severe head injury since the advent of CT scanning, comparing two homogeneous series of patients selected by clinical status (Glasgow Coma Scale ⩽ 8), namely a series of 1,000 cases admitted to our Department between 1973 and 1976, already published in this Journal31, and one of 385 cases cared for between 1979 and 1980, when CT scanning had become generally available. The two series of patients compare very closely in many respects, particularly in the incidence of surgical cases. In the more recent series the overall outcome was better both in surgical and in non-surgical cases. Among patients in the CT scan series the incidence of brain contusion associated with haematoma was greater than that of pure subdural haematomas. In non-surgical patients the CT scan, unlike cerebral angiography, afforded better identification of traumatic lesions and the grouping of patients into homogeneous categories correlating with a given outcome. On admission, cerebral angiography and CT scanning were equally effective in detecting lesions of surgical import; later in the course of the illness, however, CT scanning proved far more effective in detecting changes, with fully 15% of the patients being referred for surgery in the light of repeat CT scan findings as opposed to only 4% undergoing surgery on the indications of repeat angiography. Also, in the new series the mean interval from injury to surgery was shorter, with 64% of patients being operated on within 6 hours of the injury. The incidence of lucid intervals dropped from 30% in the first series to 16% in the second, both among surgical and non-surgical patients. That the systematic repetition of CT scans was instrumental in preventing the worsening of clinical status is demonstrated by the fact that 54 patients treated surgically for expanding lesions were excluded from the second series because they could be treated before they reached a GCS score of 8 or less, whereas such cases were quite exceptional in the older series. The CT scan approach resulted in a material increase of surgical interventions. Overall, the comparison of these two series of cases selected only by the criterion of clinical severity fails to provide a complete expression of the impact of CT scanning on our daily dealing with severe head injuries.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Acta neurochirurgica 138 (1996), S. 350-354 
    ISSN: 0942-0940
    Keywords: Cerebello-pontine angle ; CT scan ; epidermoid ; MRI
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The authors present the case of a patient accurately diagnosed and operated on for an epidermoid cyst in the CPA region, 30 years after the clinical onset with the initial symptom of hypoacusis. At the time of the operation, the patient presented with advanced CPA syndrome, and the tumour had grown to an enormous size. Complete capsule removal was not attempted due to its tenacious adherence to vital neurovascular structures. Thirteen years after surgery, the patient underwent a second operation due to tumour regrowth. The case provides supporting evidence that the clinical findings of a CPA epidermoid cyst may be minimal, and remain so for extended periods of time until the tumour has spread widely. Epidermoids tend to insinuate in the cisterns around cranial nerves, blood vessels, and the brainstem, rather than compressing these structures. The importance of early detection and radical removal, presently facilitated by Magnetic Resonance Imaging, is emphasized.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0942-0940
    Keywords: Carotid-cavernous sinus fistula ; pseudoaneurysm
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A case of a 17-year-old boy presenting with a traumatic carotid-cavernous sinus fistula (CCSF), associated with an intracavernous pseudo-aneurysm, is reported. On angiography, the CCSF proved to be a direct and low-flow shunt. Conservative management was chosen and definitive closure of the fistula was obtained in two months by daily self-compression of the common carotid artery.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Acta neurochirurgica 72 (1984), S. 167-195 
    ISSN: 0942-0940
    Keywords: Head injury ; carotid angiography ; clinical examination ; Glasgow Coma Scale ; prognosis ; multiple injuries ; regional planning
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary This is a review of 1,000 consecutive cases of severe head injury admitted to our Neurosurgical Department between January 1973 and August 1976, before the advent of CT scanning. All patients were comatose following head injury (GCS⩽8) and were treated homogeneously by the same neurosurgical team by a protocol that included immediate resuscitation on arrival, diagnosis of intracranial lesions by angiography, early surgery when needed, mechanical ventilation, steroids, and mannitol. Extracranial lesions, even if preponderant, were treated by various specialists in the Neurosurgical Department, which for all practical purposes operated as an Emergency Department. Admission criteria were very broad with no preadmission selection. The overall mortality for this series was 45%. A little less than half the patients made good recoveries or remained moderately disabled (47%); 6% were severely disabled, and 2% survived in a persistent vegetative state. More than two-thirds of the patients were brought to our Neurosurgical Department after a short stay at a general hospital; 72% were admitted within 6 hours of injury; 71% were traffic accident victims; and 34% had significant associated extracranial injuries. Carotid angiography was performed in 78% of the patients and indicated the presence of an intracranial haematoma requiring surgery in 36% of the whole series. Mortality was significantly higher in operated than in unoperated patients (56% versus 39%); those treated surgically, however, were older, in worse clinical condition, and showed a higher incidence of acute subdural haematomas associated with brain contusion. Carotid angiography proved very effective in revealing the presence of an expansive lesion but failed to reflect the severity of brain damage, since the group with “negative” angiograms showed a high mortality (52%). Patients with a lucid interval had a higher percentage of surgical lesions than those with immediate coma (58% versus 26%); but fully 42% of them did not require surgery, and 25% had negative angiograms. From the prognostic point of view the clinical data elicited after initial resuscitation were highly predictive of the outcome: some individual neurological signs, such as mydriasis, posturing and eye movements, were not inferior to the GCS score in that respect. Age also proved a strong predictor, since elderly patients are more likely to have severe subdural and parenchymal lesions and their clinical severity is accordingly greater. Our series amounts to a data bank of cases both contemporary to and in good agreement with that collected by Jennett and his associates in their 1977 multinational study; and it affords a useful reference in the assessment of epidemiological variations and alternative management in relation to outcome.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0942-0940
    Keywords: Keywords: Foramen magnum tumour; hypoglossal neurinoma; dorsolateral suboccipital transcondylar approach; neuro-imaging.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary  A case of dumbbell-shaped hypoglossal neurinoma with intra- and extracranial extension is reported. The tumour was surgically completely removed in a one-stage operation via a dorsolateral suboccipital transcondylar approach. Clinical presentation and the role of high-resolution CT-scan, MRI and angio-MRI in diagnosis and surgical planning are discussed. We include a review of the literature concerning these rare tumours of the foramen magnum region.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Child's nervous system 10 (1994), S. 392-395 
    ISSN: 1433-0350
    Keywords: Sturge-Weber angiomatosis ; Epilepsy ; Microgyria ; Corticogenesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A case is reported of an infant affected with Sturge-Weber disease who underwent left hemispherectomy due to untreatable seizures when 97 days old. Pathological analysis of the surgical specimens revealed the presence of four-layered microgyric cortex below the angiomatosis, intense gliosis, and the presence of calcifications of both the abnormal cortex and the underlying white matter. These findings suggest that the early infantile form of Sturge-Weber disease is associated with a developmental disorder of the cortical organization. Such abnormalities are consistent with the presence of an epileptogenic condition that is unresponsive to pharmacological treatment.
    Type of Medium: Electronic Resource
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