Library

X
feed icon rss

Your email was sent successfully. Check your inbox.

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

Proceed reservation?

Export
Filter
  • Electronic Resource  (2)
  • CT-investigation  (1)
  • Chromosomal abnormalitis  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Diagnostic criteria in pituitary tumour recurrence—Combined modality of surgery and radiotherapy (1986)
    Springer
    Acta neurochirurgica 80 (1986), S. 73-78 
    Details
    ISSN: 0942-0940
    Keywords: Pituitary tumour recurrence ; clinical symptoms ; CT-investigation ; recurrence rate ; prolactin level examination ; combined modality of surgical and radiotherapy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The tumour recurrence rate of 210 patients with operated hypophysomas were investigated. Depending on the surgicaal approach, total or subtotal extirpation of the adenomas, the recurrence rates varied from 10,4 to 35%. 33 patients with pituitary tumour recurrences were followed up over a period of 20 years. Clinical symptoms CT-results at relapse are represented. Serum prolactin level (PRL) was determined before and after surgical and radiotherapy of PRL-producing adenomas. In these cases PRL can be accepted as a tumour marker. 13 patients with relapsed hypophysomas received local irradiation (5.7 MeV linear accelerator) after recurrence operation. An individual comparison in the same patient between surgical therapy alone and combined surgical and radiotherapy was possible. Based on the obtained experience with this combined treatment a therapy scheme using combined surgery and radiotherapy in pituitary tumours is suggested.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01812277
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Malignant progression of angioimmunoblastic lymphadenopathy (1979)
    Springer
    Journal of cancer research and clinical oncology 93 (1979), S. 255-263 
    Details
    ISSN: 1432-1335
    Keywords: Angio immunoblastic lymphadenopathy ; Chromosomal abnormalitis ; Non Hodgkins lymphoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In a 79-year-old woman, the progression of angioimmunoblastic lymphadenopathy with dysproteinemia (AILD) to malignant lymphoma was observed within one year after diagnosis. Three biopsy specimens from lymph nodes and one tonsil, obtained at intervals of several months, showed an increasing destruction of the tissue architecture and the development of histological criteria for a lymphoid neoplasm, which at autopsy was confirmed as a malignant non-Hodgkin's lymphoma. The demonstration of a chromosomally abnormal clone in lymph node derived and the laboratory findings were in agreement with the histological changes and the sequential clinical deterioation. Initially, a symptom-free interval of eight months was achieved with prednisone therapy. However, this treatment failed after the malignant transformation had become evident.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00964581
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...