Paediatric Lymphomatoid Papulosis: Diagnostic Challenges and Follow-up

  • Katarína Kieselová Interna de Dermatologia e Venereologia/Resident of Dermatology and Venereology, Centro Hospitalar de Leiria, Leiria, Portugal
  • Felicidade Santiago Assistente Hospitalar de Dermatologia e Venereologia/Consultant of Dermatology and Venereology, Centro Hospitalar de Leiria, Leiria, Portugal
  • Victória Guiote Assistente Hospitalar de Dermatologia e Venereologia/Consultant of Dermatology and Venereology, Centro Hospitalar de Leiria, Leiria, Portugal
  • Martinha Henrique Chefe de Serviço, Diretora do Serviço de Dermatologia/Consultant Chief, Head of Department of Dermatology, Centro Hospitalar de Leiria, Leiria, Portugal
  • Cristina Amado Assistente Hospitalar de Anatomia Patológica/Consultant of Pathology, Centro Hospitalar de Leiria, Leiria, Portugal
Keywords: Child, Lymphomatoid Papulosis, Skin Neoplasms

Abstract

Lymphomatoid papulosis is a rare primary T-cell lymphoproliferative cutaneous disorder, mostly affecting adults. Although histopathology suggests a malignant disease, in most cases, lymphomatoid papulosis is a self-limited condition with a good prognosis. We describe the case of an 8-year-old boy, otherwise healthy, who presented with a 4-6 week history of polymorphic cutaneous lesions disseminated over the whole body. Histology and immunohistochemistry confirmed the diagnosis of lymphomatoid papulosis type A. The authors discuss the main challenges in follow-up, treatment and the risk of progression of lymphomatoid papulosis to secondary lymphomas in this age group.

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Published
2017-04-17
How to Cite
Kieselová, K., Santiago, F., Guiote, V., Henrique, M., & Amado, C. (2017). Paediatric Lymphomatoid Papulosis: Diagnostic Challenges and Follow-up. Journal of the Portuguese Society of Dermatology and Venereology, 75(1), 87-91. https://doi.org/10.29021/spdv.75.1.724
Section
Case Reports