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Ulcerated eyelid lesion leading to a lymphomatoid papulosis diagnosis.
J Fr Ophtalmol
December 2024
Department of Ophthalmology, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Lymphomatoid papulosis associated with Hodgkin lymphoma: two case reports and a short review of literature.
J Dtsch Dermatol Ges
November 2024
Dermatology Clinic, Maggiore Hospital, University of Trieste, Trieste, Italy.
[Cutaneous T-cell lymphomas].
Bull Cancer
November 2024
Service de dermatologie et oncologie cutanée, centre hospitalier Estaing, CHU de Clermont-Ferrand, université Clermont-Auvergne, place Lucie-Aubrac, 63000 Clermont-Ferrand, France. Electronic address:
Article Synopsis
- Primitive cutaneous T-cell lymphomas are skin-specific lymphomas, distinct from systemic lymphomas affecting the skin.
- The most common types include mycosis fungoides, CD30+ lymphoproliferations, and erythrodermic T-cell lymphomas, with several rarer forms also identified.
- Diagnosis relies on clinical skin exams and biopsies, enhanced by molecular genetics, while treatments are categorized into five main types, including skin therapies and immunotherapies.
Clinical and Pathological Features of Primary Cutaneous Lymphomas in Nepal: A retrospective cohort study from a dermatology referral centre.
Kathmandu Univ Med J (KUMJ)
September 2024
Department of Dermatology and Venereology, Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Maharajgunj, Kathmandu, Nepal.
Article Synopsis
- In Nepal, a study looked at rare skin cancers called Primary cutaneous lymphomas to learn more about them.
- The researchers reviewed patient records from a dermatology center, finding 12 cases diagnosed between 2010 and 2020, mostly affecting older adults.
- They discovered that T-cell lymphomas were more common than B-cell lymphomas, and sadly, three patients died during the study period.
Lymphomatoid Papulosis Type D in a Mestizo-Ancestry Man.
Am J Dermatopathol
November 2024
Service of Dermatology, Hospital General de México "Dr. Eduardo Liceaga, " S.S./School of Medicine, Universidad Nacional Autónoma de México, Mexico City, Mexico; and.
Article Synopsis
- * Type D LyP is characterized by the presence of abnormal CD8+ and CD30+ lymphocytes, which presents diagnostic challenges due to similarities with more aggressive forms of skin lymphomas.
- * A clinical case of a 22-year-old man with type D LyP demonstrated a favorable prognosis, highlighting the need to share findings related to this condition, especially among mestizo or Latin-American patients, as there are few published cases in this demographic.*
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