Skin biopsy in adult-onset Still's disease: A specific, rapid, and widely available diagnostic test.

Journal of human immunity Pub Date : 2026-11-02 Epub Date: 2026-09-18 DOI:10.70962/jhi.20260088
Derrick H Y Chong, Caroline Spaner, Ibrahim Elsharawi, Mark Trinder, Haya Al Bitar, Mariam Goubran, Amelia Perrotta, Rachael Horner, Dilys Chen, Jennifer Corpuz, Kun Huang, Trudy Taylor, Ian Marie Lano, Kerri Purdy, Jan P Dutz, Sylvia Pasternak, Richard I Crawford, Luke Y C Chen
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Abstract

Adult-onset Still's disease (AOSD) is a diagnostic challenge, as its features overlap with many inflammatory syndromes and no single finding is diagnostic. Skin biopsies showing dyskeratotic keratinocytes (DKs) in the superficial epidermis, including the horny layer, are thought to be highly specific for AOSD but are not included in current diagnostic or classification criteria. We conducted a retrospective clinicopathological study of 16 adults with confirmed AOSD and skin biopsies from a Canadian rare diseases program, and developed a differential diagnosis for superficial DKs using expert consensus and literature review. Clinical morphology varied, but histopathology was similar: 12 of 16 patients had DKs or necrotic keratinocytes in the upper epidermis. Superficial DKs have been reported in conditions distinct from AOSD, but not in its major mimics. Skin biopsy is low-cost, minimally invasive, and widely available and should be performed early in suspected AOSD; superficial DKs should be added to future diagnostic and classification criteria.

成人发病斯蒂尔氏病的皮肤活检:一种特异、快速、广泛可用的诊断试验。
成人发病斯蒂尔氏病(AOSD)是一个诊断挑战,因为它的特征与许多炎症综合征重叠,没有单一的发现是诊断。皮肤活检显示浅表皮(包括角质层)的角化异常角质细胞(dk)被认为是AOSD的高度特异性,但不包括在当前的诊断或分类标准中。我们对来自加拿大罕见病项目的16例确诊AOSD和皮肤活检的成年人进行了回顾性临床病理研究,并根据专家共识和文献综述制定了浅表DKs的鉴别诊断。临床形态各不相同,但组织病理学相似:16例患者中有12例在上表皮有ks或坏死的角化细胞。据报道,浅表性DKs与AOSD的情况不同,但在其主要模拟中没有。皮肤活检成本低、微创且可广泛获得,应在疑似AOSD的早期进行;未来的诊断和分类标准中应增加浅表性DKs。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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