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
    ISSN: 1432-2307
    Keywords: Neuroectodermal bone tumours ; Immunochemistry ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Peripheral neuroectodermal tumours (PNET) of bone are rare and mimick those seen in soft tissue (peripheral neuroepithelioma of soft tissue). Their differential diagnosis from Ewing's sarcoma (Es) is extremely difficult by optical means. Here we report 14 new cases of PNET of bone (other than Askin's neoplasm) located primarily in the limbs, pelvic girdle and scapula. Clinically and radiologically they displayed Ewing's sarcoma-like features: mean age was 14.4 years, male/ female ratio being 3:11. Metastasis was present in 6 cases at diagnosis (5 with bone metastasis). Prognosis was poor; thirteen patients died; only one with a metatarsal located tumour is alive and free of disease. The mean survival rate was 25 months following diagnosis and treatment with radio- and multimodal chemotherapy. Histologically the 14 cases displayed Homer-Wright rosettes and pseudorosette-like structures, as well as a fibrillary background and lobular pattern. Immunohistochemistry revealed positivity in a number of neural markers when using paraffin-embedded material: NSE, B-2-microglobuline, HNK-1 (leu-7) and E-36 antibodies. At EM level the cell cytoplasms evidenced dense-core granules with neurosecretion, neurotubules and intermediate filaments like those seen in peripheral neuroepithelioma.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1569-8041
    Keywords: ABMT ; anaplastic large-cell lymphoma ; children ; relapse ; vinblastine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Purpose:to study response to chemotherapy and the outcome ofchildren treated for a relapsed anaplastic large-cell lymphoma (ALCL) and toevaluate the role of bone marrow transplantation (BMT) in these patients. Patients and methods:Clinical data concerning the 41 relapsesthat occurred in 119 patients with ALCL enrolled in 3 consecutive studiessince 1975 were analysed. First-line treatment consisted of intensivechemotherapy according to the COPAD protocol for the first series of 12patients treated between 1975 and 1989 and to the SFOP (French Society ofPediatric Oncology) HM protocols for the 30 patients treated between 1989 and1997. Twenty-eight patients were treated with CV(B)A (CCNU, vinblastine, ara-Cwith or without bleomycin), and the others with miscellaneous protocols forrecurrent disease. Fifteen patients underwent autologous BMT and 1 allogeneicBMT while in CR2. Results:Thirty-six of forty-one (88%) patients achievedCR2. With a median follow-up of 5 years, 12 patients died, 9 of their diseaseand 29 patients are alive in CR2 (20 patients), CR3 (5 patients), CR4 (2patients), CR5 (1 patient) or CR6 (1 patient). Overall and disease-freesurvival are respectively 69% (53%–82%) and44% (29%–61%) at three years. In univariateanalysis, patients treated with ABMT while in CR2 did not appear to have abetter outcome than the other. Remarkably, a long-lasting remission wasobtained in 8 of 13 patients treated with weekly vinblastine for a relapseincluding 6 relapses occurring after ABMT. Conclusions:Relapsed ALCL are highly chemosensitive but over40% of the patients experience several relapses. Prolonged conventionalchemotherapy based on vinblastine might, in some cases, be as efficient asshort intensive treatment with ABMT.
    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...