Clinician’s perspective on the diagnosis of primary cutaneous B-cell lymphoma


Submitted: 3 April 2023
Accepted: 27 May 2023
Published: 14 June 2023
Abstract Views: 412
PDF: 126
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Authors

Of all cutaneous lymphomas, 25% are primary cutaneous B-cell lymphomas (PCBCLs). Of these, primary cutaneous follicle center lymphoma (PCFCL), primary cutaneous marginal zone B-cell lymphoma (PCMZL), and primary cutaneous diffuse large B-cell lymphoma, leg type (PCDLBCL-LT) are the most common subtypes. For the diagnosis of PCBCLs, a biopsy combined with immunohistochemistry and histological examination is the gold standard. PCBCLs are categorized into indolent or intermediate to aggressive subtypes based on their clinical behavior in a clinically oriented approach. PCDLBCL-LT has an aggressive course that spreads to extracutaneous sites in about 45% of cases, whereas PCFCL and PCMZL are indolent diseases. As a result, instrumental staging is advised for PCDLBCL-LT but not for extracutaneous disease after a diagnosis of PCMZL or PCFCL. Lastly, dermatoscopy may offer a novel diagnostic tool to improve the clinical recognition of various PCBCL subtypes when used in conjunction with a strong clinical suspicion.


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Ciolfi, C., Tartaglia, J., Sernicola, A., & Alaibac, M. (2023). Clinician’s perspective on the diagnosis of primary cutaneous B-cell lymphoma. Dermatology Reports, 16(s2). https://doi.org/10.4081/dr.2023.9723

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