Non-Caseating Granulomatous Reaction to Red Tattoo Pigment in a Patient Receiving Immune Checkpoint Inhibitor Therapy.

IF 1.2 4区 医学 Q3 DERMATOLOGY
Ashley Gochoco, Sushila A Toulmin, Christopher Iriarte, Joshua F Goldsmith
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引用次数: 0

Abstract

Cutaneous adverse reactions associated with tattoos exhibit various histopathologic patterns, ranging from allergic or interface dermatitis to sarcoid-like granulomatous inflammation. Immune checkpoint inhibitors (ICIs) are also well known to induce granulomatous cutaneous eruptions, usually with sarcoid-like features. Interestingly, ICIs can enhance immune responses at previous antigen exposure sites, including tattoos. Herein, we report a case of a non-caseating granulomatous tattoo reaction associated with red pigment in the context of ICI therapy. Histopathologically, the granulomas exhibited a tuberculoid architecture characterized by prominent peripheral lymphoplasmacytic inflammation rather than the relatively "naked" granulomas more typical of sarcoidal reactions. This case highlights the morphologic heterogeneity of granulomatous reactions arising within tattoos during ICI therapy and underscores the complex interaction between host immunity, tattoo pigment, and immunotherapy. Awareness of this pattern may help prevent misclassification as cutaneous sarcoidosis or infection and guide clinical care for patients on ICIs who develop such granulomatous reactions.

接受免疫检查点抑制剂治疗的患者对红色纹身色素的非干酪化肉芽肿反应
与纹身相关的皮肤不良反应表现出各种组织病理学模式,从过敏性或界面皮炎到结节样肉芽肿炎症。众所周知,免疫检查点抑制剂(ICIs)也可诱发肉芽肿性皮肤疹,通常具有结节样特征。有趣的是,ICIs可以增强以前抗原暴露部位的免疫反应,包括纹身。在此,我们报告一个非干酪化肉芽肿纹身反应与红色素在ICI治疗的背景下。组织病理学上,肉芽肿表现为结核样结构,其特征是明显的外周淋巴浆细胞性炎症,而不是相对“赤裸裸”的肉芽肿,更典型的是结节样反应。该病例强调了ICI治疗期间纹身内肉芽肿反应的形态学异质性,并强调了宿主免疫、纹身色素和免疫治疗之间复杂的相互作用。意识到这种模式可能有助于防止误诊为皮肤结节病或感染,并指导临床护理发生此类肉芽肿反应的ICIs患者。
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来源期刊
CiteScore
3.20
自引率
5.90%
发文量
174
审稿时长
3-8 weeks
期刊介绍: Journal of Cutaneous Pathology publishes manuscripts broadly relevant to diseases of the skin and mucosae, with the aims of advancing scientific knowledge regarding dermatopathology and enhancing the communication between clinical practitioners and research scientists. Original scientific manuscripts on diagnostic and experimental cutaneous pathology are especially desirable. Timely, pertinent review articles also will be given high priority. Manuscripts based on light, fluorescence, and electron microscopy, histochemistry, immunology, molecular biology, and genetics, as well as allied sciences, are all welcome, provided their principal focus is on cutaneous pathology. Publication time will be kept as short as possible, ensuring that articles will be quickly available to all interested in this speciality.
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