Emilie Doré Badje, MD, Trilok Tejasvi, MD, Alexandra Hristov, MD

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Presentation transcript:

γδ lymphomatoid papulosis type D: A histologic mimic of primary cutaneous γδ T-cell lymphoma Emilie Doré Badje, MD, Trilok Tejasvi, MD, Alexandra Hristov, MD JAAD Case Reports Volume 5, Issue 3, Pages 264-266 (March 2019) DOI: 10.1016/j.jdcr.2019.01.009 Copyright © 2019 American Academy of Dermatology, Inc. Terms and Conditions

Fig 1 Clinical presentation of a patient with γδ lymphomatoid papulosis type D. Small erythematous papules involving the extremities. The lesions are asymptomatic, last approximately 1 month and then self-resolve. JAAD Case Reports 2019 5, 264-266DOI: (10.1016/j.jdcr.2019.01.009) Copyright © 2019 American Academy of Dermatology, Inc. Terms and Conditions

Fig 2 Histopathologic findings in γδ lymphomatoid papulosis, type D. Biopsy reveals epidermotropic enlarged and atypical lymphoid cells (A, Hematoxylin-eosin stain; original magnification: ×200). These cells express TCR gamma (B, ×200) and TCR delta (C, ×200). JAAD Case Reports 2019 5, 264-266DOI: (10.1016/j.jdcr.2019.01.009) Copyright © 2019 American Academy of Dermatology, Inc. Terms and Conditions