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Primary Cutaneous CD30+ Anaplastic Large Cell Lymphoma That Developed after Lymphomatoid Papulosis / 대한피부과학회지
Korean Journal of Dermatology ; : 1081-1085, 2010.
Article in Korean | WPRIM | ID: wpr-90083
ABSTRACT
Lymphomatoid papulosis (LyP) and primary cutaneous anaplastic large cell lymphoma (ALCL) are grouped under the category of cutaneous T-cell lymphomas as CD30+ lymphoproliferative disorders. Though LyP is clinically characterized by chronic recurrent papulonodular cutaneous lesions, it shows malignant features on the histologic findings. LyP is associated with lymphomas, including primary cutaneous ALCL, mycosis fungoides and other lymphoproliferative disorders. A few cases of LyP related to ALCL have been reported in Korea. We report here on an interesting case of primary cutaneous ALCL that developed in succession after LyP in a 38-year-old female.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Lymphoma, T-Cell, Cutaneous / Mycosis Fungoides / Lymphomatoid Papulosis / Lymphoma, Large-Cell, Anaplastic / Lymphoma, Primary Cutaneous Anaplastic Large Cell / Korea / Lymphoma / Lymphoproliferative Disorders Limits: Adult / Female / Humans Country/Region as subject: Asia Language: Korean Journal: Korean Journal of Dermatology Year: 2010 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Lymphoma, T-Cell, Cutaneous / Mycosis Fungoides / Lymphomatoid Papulosis / Lymphoma, Large-Cell, Anaplastic / Lymphoma, Primary Cutaneous Anaplastic Large Cell / Korea / Lymphoma / Lymphoproliferative Disorders Limits: Adult / Female / Humans Country/Region as subject: Asia Language: Korean Journal: Korean Journal of Dermatology Year: 2010 Type: Article