Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of the European Academy of Dermatology and Venereology 7 (1996), S. 0 
    ISSN: 1468-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background In chronic graft-versus-host disease (cGvHD) cytotoxic and suppressor T lymphocytes probably play a decisive pathogenetic role. The efficacy of conventional immunosuppressive therapy is often insufficient, and drug side effects may produce further complications. Photochemotherapy with orally administered photosensitizer 8-methoxypsoralen (8-MOP) followed by UV-A irradiation of the skin (PUVA) has been reported as an advantage. Extracorporeal photochemotherapy (ECP) was introduced as an improved method of photochemotherapy compared with PUVA. ECP selectively affects autoreactive as well as malignant T lymphocytes and implies repeated ex vivo UV-A irradiation of chemically photosensitized leukocytes, followed by reinfusion. The treatment efficacy depends essentially on sufficient plasma levels of 8-MOP. In cases of considerable gastrointestinal malabsorption, however, therapeutic levels of 8-MOP are rarely achieved when the drug is administered orally. Objective In a case of severe cGvHD, ECP was used because of disease progression, despite massive conventional immunosuppressive therapy. Patient and method After bone marrow transplantation a 13-year-old girl developed acute GvHD, which turned later to severe cGvHD with massive involvement of the skin, oral mucosa, liver and gastrointestinal tract. The treatment with prednisolone, cyclosporin A (CsA), azathioprine and thalidomide was without success. When the patient was 15 we started ECP with individually adapted modifications. Especially because of severe gastrointestinal malabsorption, a liquid preparation of 8-MOP was administered directly into the leukocyte (buffy coat) fraction, received by leukapheresis. Results After 15 treatment cycles within 12 months immunosuppressive drugs were omitted because of noticeable improvement in cutaneous changes, liver function parameters and general condition (Karnofsky score 85–90% compared with 30–40% at the beginning). Conclusion It seems to us that this modification of ECP is a very effective and safe treatment modality for cGvHD without any side effects.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary High-resolution chromosome analysis of a 19-year-old female proband with syndromic intrahepatic ductular hypoplasia (Alagille syndrome, AWS) revealed an interstitial deletion of chromosome 20p with breakpoints provisionally located in or close to p11.22 and p12.2. Southern blots from digests of DNA of the proband and her chromosomally normal parents were hybridized with the human DNA probes pR12.21, HuPrPcDNA2, and pDS6-SgI, which have been mapped to the region 20 (p12-pter), and rehybridized with the F IX probe for calibration. Comparing the hybridization signals of the normally sized DNA fragments of the familiy, we found no evidence for loss of any of the three tested distal chromosome 20p loci in our proband. Furthermore, in situ hybridization with HuPrPcDNA2 revealed a specific accumulation of grains at or around the faint distal G band suspected to represent all or most of band p12.3 of the proband's deleted 20p and at p12 of the normal chromosome 20. Thus the AWS of our proband is associated with an interstitial deletion that preserved the three tested distal loci on 20p. Since nine further reported cases of 20p deletion are clinically similar, we propose AWS as a further “contiguous gene syndrome” and assign it to an approximately 8-Mb-large chromosome 20p segment (provisionally, p11.23–p12.1).
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...