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

T. Hinojosa, D. Lewis, M. Duvic, C. Torres‐Cabala
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引用次数: 1

Abstract

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.
cd1a阳性树突状细胞富集的色素性紫癜性皮肤病与血脂异常相关
不确定细胞是树突状细胞,具有朗格汉斯细胞和巨噬细胞的组织学特征,但缺乏Birbeck颗粒。目前尚不清楚IC组织细胞增多症是一种单独的疾病实体还是一种反应性过程。我们报告的情况下,男性与8年的历史血脂异常谁发展广泛的色素紫癜丘疹。实验室检查显示外周单核细胞增多(8.2%),两次皮肤活检显示真皮地衣样淋巴组织细胞浸润,由CD4+ T细胞、CD8+ T细胞和CD68+CD163+CD1a+Langerin组织细胞组成。真皮中存在PD-1/PD-L1+T细胞。我们的病例可能有助于理解IC组织细胞增多症的发病机制,我们假设CD1a+真皮dc的表达和t细胞功能障碍是血脂异常的反应过程。
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