ArticleAnais brasileiros de dermatologia
Primary cutaneous anaplastic large-cell lymphoma--case report.
Article in Anais brasileiros de dermatologia. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Primary cutaneous ALK-negative anaplastic large cell lymphoma.Oxford medical case reports · 2025Article
- Tiny Fighter, Fierce Disease: Coexistence of Anaplastic Large Cell Lymphoma with Situs Inversus Totalis.Indian journal of surgical oncology · 2025Article
- Primary cutaneous anaplastic large cell lymphoma arising from a long-standing erythema nodosum: A case report.Medicine · 2018Article
- Dermatological Complications After Solid Organ Transplantation.Clinical reviews in allergy & immunology · 2018Review
- Article
- Primary Cutaneous Anaplastic Large-Cell Lymphoma.Dermatopathology (Basel, Switzerland)Article
- CD30-positive cutaneous lymphoma: report of four cases with an emphasis on clinicopathological correlations.Anais brasileiros de dermatologiaArticle
- Anaplastic Large Cell Lymphoma Presenting as Ulcerative Facial Mass: A Case Report.Case reports in oncologyArticle
Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Primary cutaneous anaplastic large-cell lymphoma is part of the spectrum of CD30+ lymphoproliferative cutaneous processes, characterized by single or multifocal nodules that ulcerate, are autoregressive and recurrent. Extracutaneous dissemination may occur, especially to regional lymph nodes. Histology shows a diffuse, non-epidermotropic infiltrate , anaplastic large lymphoid cells of immunohistochemistry CD30+, CD4+, EMA-/+, ALK-, CD15- and TIA1-/+. Prognosis is good and does not depend on lymphatic invasion. Radiotherapy, removal of the lesion and/or low-dose methotrexate are the treatments of choice. The present study reports the case of a 57-year-old-woman presenting Primary cutaneous anaplastic large-cell lymphoma with multifocal lesions. The patient evolved with pulmonary involvement 7 years later. She showed a good response to the treatment with low-dose methotrexate prescribed weekly.
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Registered trials
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