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  • 1
    Electronic Resource
    Electronic Resource
    Neurofibroma: an unusual presentation (1993)
    Springer
    Neuroradiology 35 (1993), S. 614-615 
    Details
    ISSN: 1432-1920
    Keywords: Neurofibroma-Parotid gland-Computed tomography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We report neurofibroma discovered incidentally in a woman who suffered trauma to her cheek. The lesion was manifest on CT as a haematoma within a parotid tumour.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00588408
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Computed tomography of spontaneous intracranial haemorrhage due to haemostatic disorders in children (1993)
    Springer
    Neuroradiology 35 (1993), S. 619-621 
    Details
    ISSN: 1432-1920
    Keywords: CT ; Intracranial haemorrhage ; Hypoprothrombinaemia ; Thrombocytopenia ; Haemophilia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Intracranial haemorrhage is a serious problem in haemostatic disorders in children. Intracranial bleeding is sometimes more marked than suspected clinically. Computed tomography (CT) permits accurate, sensitive diagnosis of intracranial haemorrhage. We report 13 patients; 3 patients with hypoprothrombinaemia, 4 patients with thrombocytopenia or platelet dysfunction and 6 with haemophilia A, B or Von-Willebrand's disease. One patient with hypoprothrombinaemia had a subarachnoid hemorrhage (SAH), one a subdural haematoma (SDH) and the third a combination of SAH, SDH and intracerebral haematoma (ICH). One patient with thrombocytopenia or platelet dysfunction had a SDH, while the others had ICH. In the six patients with haemophilia A, B or Von-Willebrand's disease, there were four examples of ICH, five of SAH and six of SDH. A neurosurgical procedure was performed in only one patient. Three children died of serious intracranial complications with uncal herniation.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00588410
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Gastro-intestinal bleeding caused by leiomyoma of the small intestine in a child with neurofibromatosis (1999)
    Springer
    European journal of pediatrics 158 (1999), S. 460-462 
    Details
    ISSN: 1432-1076
    Keywords: Key words Gastro-intestinal bleeding ; Children ; Jejunal leiomyoma ; Neurofibromatosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Gastro-intestinal bleeding is an uncommon presentation in children with neurofibromatosis. Gastro-intestinal involvement caused by jejunal leiomyoma has only been described in adults. To the best of our knowledge, this is the first paediatric case of jejunal leiomyoma associated with neurofibromatosis. We present a 10-year-old girl with a 9-month history of anaemia and low gastro-intestinal bleeding. Abdominal sonography and small bowel series showed a submucosal mass in the proximal jejunum. On surgery, a submucosal tumour was excised and histological examination suggested a diagnosis of “smooth muscle tumour of undetermined malignant potential”. There were no recurrence of symptoms for 4 years after the operation. Conclusion Jejunal leiomyoma should be considered in a child with neurofibromatosis presenting with gastro-intestinal bleeding.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s004310051120
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    Paper (German National Licenses)
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  • 4
    Electronic Resource
    Electronic Resource
    Unusual causes of obstructive jaundice in children: diagnosis on CT (1992)
    Springer
    Pediatric radiology 22 (1992), S. 512-514 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Three cases are presented with unusual causes of obstructive jaundice diagnosed on abdominal CT in children under the age of 15 years. All the cases were initially examined by ultrasound which was inconclusive. CT studies were subsequently performed were diagnostic. These cases included hepatocellular carcinoma, a common bile duct web and duodenal hematoma. The first two cases were surgically confirmed, while the third case was proved by clinical follow-up.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02012997
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    Paper (German National Licenses)
    Fulltext
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