Necrotic papulovesicular lesions mainly on sun‐exposed areas.

Autor:	Liu, Y., Liu, Z. Q., Gu, C. Y., Chen, L. J., Xiang, L. H.
Předmět:	CUTANEOUS T-cell lymphoma T-cell receptor genes LYMPHOPROLIFERATIVE disorders BLOOD cell count EPSTEIN-Barr virus diseases CHINESE women SKIN diseases
Zdroj:	Clinical & Experimental Dermatology; Jun2020, Vol. 45 Issue 4, p485-489, 5p, 1 Color Photograph, 2 Illustrations
Abstrakt:	A 21-year-old Chinese woman presented with a 1-year history of recurrent necrotic papulovesicular lesions distributed on her face, chest and extremities. EBER positivity of the atypical lymphocytes can be detected in all three subtypes of HV-LPD with the percentage of positive cells as the diseases progress, which is essential for differentiating HV-LPD from other lymphoproliferative diseases, such as subcutaneous panniculitis-like T-cell lymphoma and primary cutaneous peripheral T-cell lymphoma. Learning points HV-LPD is a progressive EBV-associated lymphoproliferative disease, including the spectrum from classic HV to severe HV and HVLL. [Extracted from the article]
Databáze:	Complementary Index
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