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dc.contributor.authorSu, O
dc.contributor.authorOnsun, N
dc.contributor.authorTuzuner, N
dc.contributor.authorEsckazan, AE
dc.contributor.authorSoysal, T
dc.contributor.authorDemirkesen, C
dc.date.accessioned2021-03-05T12:21:14Z
dc.date.available2021-03-05T12:21:14Z
dc.date.issued2004
dc.identifier.citationDemirkesen C., Tuzuner N., Su O., Esckazan A., Soysal T., Onsun N., "Primary cutaneous immunocytoma/marginal zone B-cell lymphoma: A case with unusual course", AMERICAN JOURNAL OF DERMATOPATHOLOGY, cilt.26, ss.119-122, 2004
dc.identifier.issn0193-1091
dc.identifier.otherav_acc515d5-e13b-44f3-a3f6-839df2b27d95
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/115282
dc.identifier.urihttps://doi.org/10.1097/00000372-200404000-00006
dc.description.abstractAlthough primary cutaneous immunocytoma/marginal zone B-cell lymphoma (PCI/MZBL) is considered as an indolent lymphoma with excellent prognosis, extracutaneous spread and even death due to disseminated disease have been reported. This is a case report of a PCI/MZBL showing dissemination to the regional lymph node and bone marrow, 22 months after the initial diagnosis. Furthermore, in the lymph node, there were focal areas of high-grade transformation. On the other hand, the bone marrow involvement displayed low-grade morphology. We suggest that it should be kept in mind that there is still a possibility of systemic involvement in PCI/MZBL.
dc.language.isoeng
dc.subjectDermatoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectDERMATOLOJİ
dc.titlePrimary cutaneous immunocytoma/marginal zone B-cell lymphoma: A case with unusual course
dc.typeMakale
dc.relation.journalAMERICAN JOURNAL OF DERMATOPATHOLOGY
dc.contributor.department, ,
dc.identifier.volume26
dc.identifier.issue2
dc.identifier.startpage119
dc.identifier.endpage122
dc.contributor.firstauthorID171373


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