Journal of Dermatology and Dermatologic Surgery (Jan 2022)

CD1a-positive dendritic cell-enriched pigmented purpuric dermatosis in association with dyslipidemia

  • Tiffany Hinojosa,
  • Daniel J Lewis,
  • Madeleine Duvic,
  • Carlos A Torres-Cabala

DOI
https://doi.org/10.4103/jdds.jdds_85_20
Journal volume & issue
Vol. 26, no. 2
pp. 89 – 91

Abstract

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Indeterminate cells (ICs) are dendritic cells (DCs) that share the histologic features of Langerhans cells and macrophages but lack Birbeck granules. It remains unclear whether IC histiocytosis is a separate disease entity or a reactive process. We report the case of a male with an 8-year history of dyslipidemia who developed extensive pigmented purpuric papules. Laboratory studies revealed peripheral monocytosis (8.2%), and two skin biopsies showed a dermal lichenoid lymphohistiocytic infiltrate composed of CD4+ T cells and CD8+ T cells and CD68+CD163+CD1a+Langerin histiocytes. PD-1/PD-L1+T cells were present in the dermis. Our case may help in understanding the pathogenesis of IC histiocytosis, and we hypothesize that expression of CD1a+ dermal DCs and T-cell dysfunction is a reactive process to dyslipidemia.

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