Tamayo GME, García RAD, Rodríguez CAA, Charli JY, Mazier AAG

Language: Spanish
References: 5
Page: 300-303
PDF size: 2727.17 Kb.

ABSTRACT

Primary cutaneous B-cell lymphomas (PCBCL) represent a rare type of non-Hodgkin lymphoma, characterized by a favorable prognosis but a challenging diagnostic approach. We present the case of a male patient previously diagnosed and treated for cutaneous lymphocytoma who presented with the development of new ipsilateral dermatoses in the temporal and parietal regions, with dermoscopic findings suggestive of PCBCL. The histopathological diagnosis was established by a dermatopathologist specialized in cutaneous lymphomas and subsequently confirmed with staging studies. Treatment consisted of surgical excision followed by radiotherapy. The patient is currently in remission. Reporting rare cutaneous neoplasms in the Mexican population contributes to their recognition and to the dissemination of diagnostic and management strategies.

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