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  • Articles: DFG German National Licenses  (3)
  • Hirschsprung's disease  (3)
  • Electron-microscopy  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric surgery international 3 (1988), S. 141-146 
    ISSN: 1437-9813
    Keywords: Hirschsprung's disease ; Enterocolitis ; Immunocytochemistry ; Mucins
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Mucosal defence mechanisms of the excluded bowel were studied in 12 patients with Hirschsprung's disease. The entire resected segment of colon obtained following Swenson's operation was cut at 0.5-cm intervals and serially examined by routine haematoxylin and eosin staining, immunocytochemistry, and mucin histochemistry. Seven patients who had clinical evidence of enterocolitis prior to defunctioning colostomy showed histological and immunological evidence of enterocolitis (crypt abscesses, ulceration, leucocyte aggregation, Paneth cell metaplasia, and marked immunocyte responses) in the excluded bowel even several months after diversion of the faecal stream. Mucin histochemistry showed marked depletion of neutral mucins and sulphomucins in the excluded bowel with inflammatory changes and reversal of the sialo- to sulphomucin ratio. These results indicate that patients with enterocolitis complicating Hirschsprung's disease have persistent inflammatory changes in the excluded large bowel after diversion of the faecal stream by colostomy. Environmental factors such as bacterial stimulation and proliferation probably cause inhibition of cell renewal, resulting in abnormalities of mucin fractions. Changes in mucin composition, which is an important mechanical and chemical factor of the mucosal defence mechanism, may lead to altered susceptibility to bacterial degradation and hence may be important in the pathogenesis of enterocolitis.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric surgery international 4 (1989), S. 326-331 
    ISSN: 1437-9813
    Keywords: Hirschsprung's disease ; Electron-microscopy ; Schwann cells ; Monoclonal antibodies
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The pathophysiology of Hirschsprung's disease is not fully understood. Using light microscopy we have previously demonstrated the absence of a unique Schwann-cell antigen in the circular muscle of aganglionic colon identified by D7 monoclonal antibody. In an attempt to characterise the morphological changes in neuronal cells at subcellular level, we studied innervation patterns in normal and aganglionic colon by electron microscopy. The most striking observation on ultrastructural serial examination of the entire resected specimen of colon from patients with Hirschsprung's disease was the presence of grossly swollen monoaxonal or oligoaxonal Schwann cell units with loss of cellular contents in the circular muscle of aganglionic colon. The extent of subcellular changes in Schwann cells and axons corresponded with a diminution of immunoreactivity with a panel of neuronal cell antibodies. These ultrastructural findings suggest that degenerative changes in Schwann cells and axons within the circular muscle coat of aganglionic segment may be a significant factor in the pathogenesis of Hirschsprung's disease.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric surgery international 7 (1992), S. 12-17 
    ISSN: 1437-9813
    Keywords: Internal anal sphincter ; Achalasia ; Neuropeptides ; Enzyme histochemistry ; Hirschsprung's disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The internal anal sphincter is morphologically derived from the circular muscle of the rectum, but marked differences have been observed in the motor activities of these two morphologically continuous structures. Immunocytochemical studies using anti-neurotransmitter antibodies (vasoactive intestinal peptide, substance P, metenkephalin, neuropeptide Y), enzyme histochemistry for acetylcholinesterase, and electron microscopy were carried out on internal sphincter specimens from 14 patients with internal sphincter achalasia, 5 normal controls, and on rectum from 4 patients with Hirschsprung's disease (HD). The various peptide-containing nerves were increased in internal sphincter achalasia compared to normal controls and patients with HD. The pathophysiology of internal sphincter achalasia appears to differ from that of HD. It is a distinct clinical entity and should be considered separate from the latter.
    Type of Medium: Electronic Resource
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