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  • 1
    ISSN: 0165-4608
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric surgery international 13 (1998), S. 197-199 
    ISSN: 1437-9813
    Keywords: Key words Renal tumor ; Cystic nephroma ; Multilocular renal cyst ; Child
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We report two boys aged 1 year and 2 years 2 months, respectively, with cystic nephromas. Both presented with a painless abdominal mass. Computed tomography showed a homogeneous, multicystic tumor of the lower pole of the kidney in both cases with thin septa without solid parts. Macroscopically, the surface of the tumor was smooth. Both patients underwent a renal-sparing procedure; histology confirmed the diagnosis of cystic nephroma.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European radiology 10 (2000), S. 1073-1075 
    ISSN: 1432-1084
    Keywords: Key words: Meningeal hemangiopericytoma – MR imaging – Single photon emission computed tomography – CT – Childhood
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. Meningeal hemangiopericytoma (MHP) is extremely rare in childhood. Mean age at diagnosis is between 38 and 43 years. We present an 8-year-old boy with MHP of the middle cranial fossa. Imaging findings were indistinguishable from an aggressive bone tumor such as Ewing's sarcoma. Imaging findings are presented and discussed. Our case indicates that MHP should be considered in the differential diagnosis of skull-base tumors despite the fact that MHP is extremely rare in childhood.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1569-8041
    Keywords: endocrine ; germ-cell tumour ; germinoma ; long-term sequelae ; neuropsychological ; ophthalmologic defects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background:Information on long-term follow-up of children andadolescents treated for intracerebral germ-cell tumour is scant. We report onthe results of a small series of patients treated at a single institution. Patients and methods:Hospital records from 15 patients treatedbetween 1980 and 1998 were reviewed. An attempt was made to correlate sequelaeto tumour location and treatment modalities. Results:This cohort constitutes 5.5% of all brain tumoursdiagnosed at our institution. Histology: 10 germinomas, 2 benign teratomas,2 malignant teratomas, and one mixed germ-cell tumour. Overall survival was87%, with a mean follow-up time of 7 years and 8 months. The majorityof patients have long-term sequelae involving one or several organ systems.In 66% endocrine, in 47% ophthalmologic, in 60%neuropsychological defects were observed. Endocrine and ophthalmologicsequelae show a correlation to tumour location. Neuropsychological long-termabnormalities are frequent and are associated with cranial irradiation inparticular at young age, but less with tumour location, irradiation dose orsurgery. Conclusions:Our preliminary data suggest that today intracerebralgerminomas and mature teratomas have a good prognosis even when a relapseoccurs. The outcome for mixed germ-cell tumours and malignant teratomas isless favourable. Although long-term sequelae are present in the majority ofpatients, there is some evidence that patients treated after 1990 suffer fewersevere long-term defects, thereby indicating that recent treatment protocolsmay result in a reduction of sequelae.
    Type of Medium: Electronic Resource
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