CASE REPORT |
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Year : 2020 | Volume
: 65
| Issue : 1 | Page : 57-60 |
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Mycosis fungoides, lymphomatoid papulosis and Hodgkin's lymphoma in the same patient: Apropos of a possible monoclonal origin
Montserrat Molgo1, Leonardo Espinoza-Benavides1, Patricio Rojas2, Sergio González3
1 Department of Dermatology, Pontificia Universidad Católica de Chile, Santiago de Chile, Chile 2 Department of Hematology, Pontificia Universidad Católica de Chile, Santiago de Chile, Chile 3 Department of Pathology, Pontificia Universidad Católica de Chile, Santiago de Chile, Chile
Correspondence Address:
Leonardo Espinoza-Benavides Vicuna Mackenna 4686, Macul, Santiago de Chile Chile
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/ijd.IJD_16_19
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A 59-year-old man with Hodgkin's lymphoma was referred by a hematologist for consultation for cutaneous issues. Physical examination revealed generalized scaling and erythematous scaly patches located in the groin, abdomen, and arms. The biopsy was compatible with mycosis fungoides (MF). At his next medical visit, painful nodules with erythematous halo and scabby surface were noted, and a subsequent biopsy was compatible with lymphomatoid papulosis (LyP). Mycosis fungoides, the most common primary cutaneous T-cell lymphoma, is usually defined in its classic form as a CD4+ non-Hodgkin lymphoma; LyP corresponds to a CD30+ lymphoproliferative disorder; and Hodgkin's lymphoma (HL) constitutes a lymphoid neoplasia characterized by the presence of Reed–Sternberg cells and its variants. Although these entities have been defined independently, evidence suggests the possibility of a common monoclonal origin. To our knowledge, this is the first case of MF, LyP, and HL in a single patient.
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