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Coexistence of large cell transformed mycosis fungoides and diffuse large B-cell lymphoma in one patient.
Rohan, Thomas Z; Suriano, Jayson; Tekmen, Volkan; Bhatti, Safiyyah; Talasila, Sahithi; Joffe, Daniel; Holtmeyer, Caleb; Lee, Jason B; Alpdogan, Onder; Nikbakht, Neda.
Affiliation
  • Rohan TZ; Department of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
  • Suriano J; Department of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
  • Tekmen V; Department of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
  • Bhatti S; Department of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
  • Talasila S; Department of Medical Oncology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
  • Joffe D; Department of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
  • Holtmeyer C; Department of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
  • Lee JB; Department of Pathology and Genomic Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
  • Alpdogan O; Department of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
  • Nikbakht N; Department of Medical Oncology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
J Cutan Pathol ; 2024 Jul 05.
Article in En | MEDLINE | ID: mdl-38967043
ABSTRACT
Diffuse large B-cell lymphoma (DLBCL) is the most common and aggressive subtype of non-Hodgkin lymphoma. The overall risk of developing DLBCL is increased in patients with other lymphomas, such as mycosis fungoides (MF). In this report, we present an 81-year-old female with early-stage MF who simultaneously progressed to tumor stage, large-cell transformed (LCT) MF and developed a primary DLBCL in a lymph node (LN). She presented with a tumor on her leg and new lymphadenopathy in her right axilla. Skin biopsy of the tumor revealed infiltration of large atypical CD3+, CD4+, and CD30+ cells, and a smaller portion of CD8+ cells in the dermis, consistent with LCT MF. Biopsy of the axillary LN revealed diffuse sheets of CD20+, BCL-2+, c-MYC+, and CD10- cells, highly suggestive of double expressor DLBCL. High-throughput sequencing revealed monoclonal T cells in the skin tumor and a monoclonal B-cell population in the LN. The above findings led to simultaneous diagnoses of LCT MF and nodal double expressor DLBCL. Our case demonstrates the importance of performing a full pathological workup in cutaneous T-cell lymphoma patients presenting with lymphadenopathy.
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Full text: 1 Database: MEDLINE Language: En Journal: J Cutan Pathol Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Language: En Journal: J Cutan Pathol Year: 2024 Type: Article Affiliation country: United States