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dc.contributor.author Kertész, Gabriella
dc.contributor.author Hauser, Péter
dc.contributor.author Varga P
dc.contributor.author Dabasi, Gabriella
dc.contributor.author Schuler, Dezső
dc.contributor.author Garami, Miklós
dc.date.accessioned 2018-10-13T08:50:33Z
dc.date.available 2018-10-13T08:50:33Z
dc.date.issued 2007
dc.identifier 35948939340
dc.identifier.citation pagination=774-775; journalVolume=29; journalIssueNumber=11; journalTitle=JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/4949
dc.identifier.uri doi:10.1097/MPH.0b013e318159a535
dc.description.abstract Although there has been considerable advancement in treatment techniques but still there are some illnesses that continue to exhibit a rather poor curability, such as thymoma. This report highlights the benefit of octreotide and prednisolone therapy in a 15-year-old girl, who was diagnosed with inoperable thymus carcinoma, with chemotherapy and radiotherapy being the last resort. The detection of type 2 somatostatin receptors on the surface of the tumor justified the introduction of treatment with somatostatin analog and prednisolone. Fortunately, after 6 months of this treatment, the tumor showed partial regression. However, 2 months later, somatostatin receptor negative metastases appeared; therefore, a switch over to imatinib became essential, because the tumor was CD-117 positive. Despite the therapy change, the patient's condition deteriorated owing to tumor progression.
dc.relation.ispartof urn:issn:1077-4114
dc.title Advanced Pediatric Inoperable Thymus Carcinoma (Type C Thymoma)
dc.type Journal Article
dc.date.updated 2018-02-21T13:14:17Z
dc.language.rfc3066 en
dc.identifier.mtmt 1091447
dc.identifier.wos 000251077300011
dc.identifier.pubmed 17984697
dc.contributor.department SE/AOK/K/II. Sz. Gyermekgyógyászati Klinika
dc.contributor.department SE/AOK/K/Transzplantációs és Sebészeti Klinika
dc.contributor.institution Semmelweis Egyetem


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