Lymphomatoid papulosis (LyP) is a rare lymphoproliferative disorder, characterized by the development of self-regressing crops of papular, papulo-necrotic and/or nodular erythematous skin lesions with histologic features of a cutaneous CD30+ T-cell lymphoma. LyP shows an estimated world-wide incidence of 1.2 – 1.9 cases per million and has an excellent prognosis, with a 5-year diseasespecific survival rate close to 100%. However, in 20% –50% of cases, LyP may be associated with another type of cutaneous or systemic lymphoma, most commonly mycosis fungoides (MF), primary cutaneous anaplastic large-cell lymphoma (pcALCL), and more rarely Hodgkin lymphoma (HL).1,2 In this paper, we report two cases of HL-associated LyP along with a brief literature review.
Lymphomatoid papulosis associated with Hodgkin lymphoma: two case reports and a short review of literature / Zelin, Enrico; Corio, Andrea; Mazzoletti, Vanessa; Caposiena Caro, Raffaele Dante; Sonego, Benedetta; Bertuzzi, Clara; Albertini, Elisa; Sabattini, Elena; Zalaudek, Iris; Meo, Nicola Di. - In: JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT. - ISSN 1610-0379. - 23:2(2025), pp. 221-226. [10.1111/ddg.15616]
Lymphomatoid papulosis associated with Hodgkin lymphoma: two case reports and a short review of literature
Zelin, Enrico
Co-primo
;Corio, AndreaCo-primo
;Sonego, Benedetta;Sabattini, Elena;Zalaudek, IrisPenultimo
;Meo, Nicola DiUltimo
2025-01-01
Abstract
Lymphomatoid papulosis (LyP) is a rare lymphoproliferative disorder, characterized by the development of self-regressing crops of papular, papulo-necrotic and/or nodular erythematous skin lesions with histologic features of a cutaneous CD30+ T-cell lymphoma. LyP shows an estimated world-wide incidence of 1.2 – 1.9 cases per million and has an excellent prognosis, with a 5-year diseasespecific survival rate close to 100%. However, in 20% –50% of cases, LyP may be associated with another type of cutaneous or systemic lymphoma, most commonly mycosis fungoides (MF), primary cutaneous anaplastic large-cell lymphoma (pcALCL), and more rarely Hodgkin lymphoma (HL).1,2 In this paper, we report two cases of HL-associated LyP along with a brief literature review.| File | Dimensione | Formato | |
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