2015Dermatologic ClinicsOpen access

Practical Management of CD30+ Lymphoproliferative Disorders

Lauren C. Hughey

Open full text 21 citations

Abstract

Lymphomatoid papulosis Primary cutaneous anaplastic large cell cutaneous lymphoma Mycosis fungoides with large cell transformation CD30 1 cutaneous lymphoproliferative disorders KEY POINTSThe CD30 1 cutaneous lymphoproliferative disorders can look similar both clinically and histologically.Evaluation by a clinician and dermatopathologist with expertise in cutaneous lymphomas is invaluable in the correct classification of these disorders.Correct classification sets the stage for choosing an appropriate treatment regimen for each of these disorders.Lymphomatoid papulosis (LyP) rarely requires systemic therapy, whereas refractory or multifocal cutaneous anaplastic large cell lymphoma (cALCL) and mycosis fungoides (MF) with large cell transformation (LCT) may require systemic therapy in combination with skindirected therapy.Given the chronic nature and typical good prognosis of most CD30 1 lymphoproliferative disorders (LPDs), the clinician should take into account possible deleterious long-term side effects of treatment options.

Open-access reader

About this research paper

What this paper is about

Lymphomatoid papulosis Primary cutaneous anaplastic large cell cutaneous lymphoma Mycosis fungoides with large cell transformation CD30 1 cutaneous lymphoproliferative disorders KEY POINTSThe CD30 1 cutaneous lymphoproliferative disorders can look similar both clinically and histologically.Evaluation by a clinician and dermatopathologist with expertise in cutaneous lymphomas is invaluable in the correct classification of these disorders.Correct classification sets the stage for choosing an appropriate treatment regimen for each of these disorders.Lymphomatoid papulosis (LyP) rarely requires systemic therapy, whereas refractory or multifocal cutaneous anaplastic large cell lymphoma (cALCL) and mycosis fungoides (MF) with large cell transformation (LCT) may require systemic therapy in combination with skindirected therapy.Given the chronic nature and typical good prognosis of most CD30 1 lymphoproliferative disorders (LPDs), the clinician should take into account possible deleterious long-term side effects of treatment options.

Why it matters

OpenAlex reports 21 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Lymphomatoid papulosis Primary cutaneous anaplastic large cell cutaneous lymphoma Mycosis fungoides with large cell transformation CD30 1 cutaneous lymphoproliferative disorders KEY POINTSThe CD30 1 cutaneous lymphoproliferative disorders can look similar both clinically and histologically.Evaluation by a clinician and dermatopathologist with expertise in cutaneous lymphomas is invaluable in the correct classification of these disorders.Correct classification sets the stage for choosing an appropriate treatment regimen for each of these disorders.Lymphomatoid papulosis (LyP) rarely requires systemic therapy, whereas refractory or multifocal cutaneous anaplastic large cell lymphoma (cALCL) and mycosis fungoides (MF) with large cell transformation (LCT) may require systemic therapy in combination with skindirected therapy.Given the chronic nature and typical good prognosis of most CD30 1 lymphoproliferative disorders (LPDs), the clinician should take into account possible deleterious long-term side effects of treatment options.

Key concepts: Lymphomatoid papulosis, Medicine, Lymphoproliferative disorders, Mycosis fungoides, CD30, Brentuximab vedotin, Dermatology, Pathology

Related papers

Back to paper searchBrowse research topicsOriginal source
Practical Management of CD30+ Lymphoproliferative Disorders — Research Paper | ScholarLens