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

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

摘要

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