Primary cutaneous anaplastic large cell lymphoma initially clinically considered to be pyoderma gangrenosum
| dc.contributor.author | Şener, Serpil | |
| dc.contributor.author | Altunışık, Nihal | |
| dc.contributor.author | Saraç, Gülbahar | |
| dc.date.accessioned | 2024-08-04T19:53:22Z | |
| dc.date.available | 2024-08-04T19:53:22Z | |
| dc.date.issued | 2017 | |
| dc.department | İnönü Üniversitesi | en_US |
| dc.description.abstract | Primary CD30+ anaplastic large cell lymphoma, which is generally seen in adults, is the second most common cutaneous T-cell lymphoma after mycosis fungoides. The lesions are characterized by red-brown plaque or nodules often with ulceration. Although usually solitary, there may occasionally be multiple lesions. Here in this case report, a 44-year old male patient with multifocal primary cutaneous anaplastic large cell lymphoma is presented. Primary cutaneous anaplastic large cell lymphoma is a rare disease especially when it is multifocal and has no systemic involvement like in this case. Therefore this case is found valuable to share | en_US |
| dc.identifier.endpage | 773 | en_US |
| dc.identifier.issn | 2147-0634 | |
| dc.identifier.issue | 4 | en_US |
| dc.identifier.startpage | 771 | en_US |
| dc.identifier.trdizinid | 263989 | en_US |
| dc.identifier.uri | https://search.trdizin.gov.tr/yayin/detay/263989 | |
| dc.identifier.uri | https://hdl.handle.net/11616/89723 | |
| dc.identifier.volume | 6 | en_US |
| dc.indekslendigikaynak | TR-Dizin | en_US |
| dc.language.iso | en | en_US |
| dc.relation.ispartof | Medicine Science | en_US |
| dc.relation.publicationcategory | Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.title | Primary cutaneous anaplastic large cell lymphoma initially clinically considered to be pyoderma gangrenosum | en_US |
| dc.type | Article | en_US |
