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Review Article
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Lymphomatoid papulosis: a practical review for pathologists
Mario L. Marques-Piubelli, Carlos A. Torres-Cabala, Roberto N. Miranda
J Pathol Transl Med. 2026;60(4):388-397.   Published online July 15, 2026
DOI: https://doi.org/10.4132/jptm.2026.06.09
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AbstractAbstract PDF
Lymphomatoid papulosis (LyP) is a primary cutaneous CD30+ lymphoproliferative disorder characterized by a chronic and self-healing recurrent cluster of erythematous papules or nodules on the skin of the trunk and/or extremities. The disease has an indolent clinical course with spontaneous regression or waxing and waning clinical evolution. The histopathologic spectrum of LyP is vast and may show few to numerous atypical cells immersed in a mild to intense inflammatory background. The backbone for the diagnosis is the positivity for CD30, which is one of the criteria to define this group of lymphoproliferative disorders. The association of these different histological and immunophenotypical findings is used to subclassify this disease in different subtypes from A to E, associated with DUSP22/IRF4 rearrangement, and other rare forms. Although this differentiation is important to raise awareness of different differential diagnosis, it does not impact the prognosis or change the treatment, which is usually centered in symptom relief and faster regression. In this review, we aim to summarize the most updated information of the clinical, histopathological, and molecular characteristics of LyP and provide a practical assessment for the diagnostic features that could help with the main differential diagnosis.
Newsletter
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What’s new in hematopathology 2023: updates on mature T-cell neoplasms in the 5th edition of the WHO classification
Mario L. Marques-Piubelli, Roberto N. Miranda
J Pathol Transl Med. 2023;57(4):246-249.   Published online June 27, 2023
DOI: https://doi.org/10.4132/jptm.2023.06.15
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  • 2 Crossref
AbstractAbstract PDF
The overview of the upcoming Blue Book of the 5th edition of the World Health Organization Classification of Hematolymphoid Tumors was published in Leukemia in June 2022. The updates on mature T-/NK-cell lymphomas and leukemias are organized in nine groups based on cell of origin, morphology, clinical scenario, and localization, and are highlighted in this newsletter.

Citations

Citations to this article as recorded by  
  • Primary intestinal T-cell lymphoma discovered upon surgical resection: report of a monocentric Moroccan case series with diagnostic challenges
    Sabrine Derqaoui, Siham Mesmoudi, Taha Yassine Aaboudech, Soukaina Haidouri, Yahya Khedid, Hamza Sekkat, Ahmad Jahid, Kaoutar Znati, Zoubida Tazi Mezalek, Zakia Bernoussi, Gilbert Sterling Octavius
    Research Connections.2026;[Epub]     CrossRef
  • The Significance of the Microenvironment in T/Nk-Cell Neoplasms
    Ivan Petković, Michele Ritucci, Ana Stojković, Slavica Stojnev, Aleksandar Popović, Irena Conić, Milica Radić, Miljana Džunić, Miljan Krstić
    International Journal of Molecular Sciences.2025; 26(22): 11225.     CrossRef

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