Abstract
Primary cutaneous CD30-positive (anaplastic) large T-cell lymphoma and lymphomatoid papulosis have many overlapping clinical, histologic, and immunophenotypic features. These entities are currently considered as parts of a spectrum of primary cutaneous CD30-positive lymphoproliferative disorders. We provide the clinician with practical guidelines for the diagnosis, management, and treatment of patients within this spectrum of primary cutaneous CD30-positive lymphoproliferative disorders. Most patients within this spectrum of disease have an excellent prognosis. Multi-agent chemotherapy should be reserved for patients who have extracutaneous disease.
MeSH terms
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Adolescent
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Adult
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Aged
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Aged, 80 and over
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Cell Transformation, Neoplastic
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Child
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Child, Preschool
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Diagnosis, Differential
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Female
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Humans
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Infant
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Lymphoma, Large-Cell, Anaplastic* / diagnosis
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Lymphoma, Large-Cell, Anaplastic* / epidemiology
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Lymphoma, Large-Cell, Anaplastic* / etiology
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Lymphoma, Large-Cell, Anaplastic* / pathology
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Lymphoma, Large-Cell, Anaplastic* / therapy
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Lymphomatoid Papulosis / etiology
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Lymphomatoid Papulosis / pathology
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Male
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Middle Aged
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Remission, Spontaneous
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Skin Neoplasms* / diagnosis
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Skin Neoplasms* / epidemiology
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Skin Neoplasms* / etiology
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Skin Neoplasms* / pathology
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Skin Neoplasms* / therapy
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Virus Diseases / complications