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dc.contributor.authorGulcan, P
dc.contributor.authorBaykal, Can
dc.contributor.authorBuyukbabani, N
dc.contributor.authorKavak, A
dc.date.accessioned2021-03-03T20:56:04Z
dc.date.available2021-03-03T20:56:04Z
dc.date.issued2003
dc.identifier.citationBaykal C., Kavak A., Gulcan P., Buyukbabani N., "Dyskeratosis congenita associated with three malignancies", JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, cilt.17, sa.2, ss.216-218, 2003
dc.identifier.issn0926-9959
dc.identifier.othervv_1032021
dc.identifier.otherav_5c8688d2-d04b-419f-89e2-819550b492b8
dc.identifier.urihttp://hdl.handle.net/20.500.12627/64868
dc.identifier.urihttps://doi.org/10.1046/j.1468-3083.2003.00585.x
dc.description.abstractDyskeratosis congenita is a rare inheritable disorder characterized by abnormalities of the skin, nails and oral mucosa. Aplastic anaemia resulting from bone marrow hypoplasia is a frequent cause of death. Squamous cell carcinoma developing from leukoplakia and visceral malignancies are other complications of the disease. We report here a case of dyskeratosis congenita in a man who developed three neoplasias of different systems over a period of many years. Squamous cell carcinoma and gastric adenocarcinoma manifested 17 years after the man was diagnosed with Hodgkin's disease.
dc.language.isoeng
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.subjectDermatoloji
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectDERMATOLOJİ
dc.titleDyskeratosis congenita associated with three malignancies
dc.typeMakale
dc.relation.journalJOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
dc.contributor.department, ,
dc.identifier.volume17
dc.identifier.issue2
dc.identifier.startpage216
dc.identifier.endpage218
dc.contributor.firstauthorID167868


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