AI Article Synopsis

  • Primary cutaneous diffuse large B-cell lymphoma, leg type (PCDLBCL-LT) is a rare and serious skin cancer that can be difficult to diagnose due to its varied skin presentations.
  • A case study discusses a 66-year-old woman with a medical history who developed abscess-like lesions on her buttocks, which were ultimately diagnosed as PCDLBCL-LT after biopsies.
  • She underwent a successful treatment regimen (R-CHOP) followed by radiation therapy, leading to complete remission, and she remained in remission for several years after treatment.

Article Abstract

Primary cutaneous diffuse large B-cell lymphoma, leg type (PCDLBCL-LT) is one of the rarest forms of primary cutaneous lymphomas (PCLs) and it confers a poor prognosis. Diagnosis of PCDLBCL-LT can be challenging and complex as it can manifest with a myriad of dermatological presentations. However, early treatment with chemo-radiation leads to an appropriate response. We present the case of a 66-year-old female with a history of polymyositis and interstitial lung disease on immunosuppression who presented to our institution with recurrent abscess-like lesions localized to buttocks that were later biopsied and diagnosed as the leg-type variant of PCL. She received chemotherapy with the rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) regimen and subsequent involved-site radiation therapy (ISRT), which resulted in complete remission. The patient was later followed up and remained in remission for years.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494052PMC
http://dx.doi.org/10.7759/cureus.17766DOI Listing

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