Bissenas Ashley, Bourne Mitchell, Samia Arthur M, Motaparthi Kiran
Department of Dermatology, University of Florida College of Medicine, Gainesville, USA.
Department of Internal Medicine, University of Florida College of Medicine, Gainesville, USA.
Cureus. 2025 May 30;17(5):e85097. doi: 10.7759/cureus.85097. eCollection 2025 May.
Rowell syndrome (RS) is a rare clinical entity characterized by erythema multiforme (EM)-like lesions and lupus erythematosus (LE). Immunologic findings associated with RS include a speckled antinuclear antibody (ANA) pattern, positive rheumatoid factor (RF), and anti-Ro (SS-A)/anti-La (SS-B) antibodies. While direct immunofluorescence (DIF) positivity is a hallmark of cutaneous LE (CLE), recent diagnostic criteria for RS suggest DIF should be negative, raising debate over whether RS is a distinct disease or a CLE variant. We present the case of a 42-year-old woman with systemic lupus erythematosus (SLE) who developed a diffuse, blistering rash consistent with RS. DIF of lesional skin demonstrated immunoreactivity for IgG, complement C3, and IgM along the basement membrane zone, contradicting the proposed RS criteria. This case reinforces the argument that RS is best classified as a CLE subtype rather than a distinct disease. The patient's clinical, serologic, and histopathologic findings, including DIF positivity, support this classification.
罗威尔综合征(RS)是一种罕见的临床病症,其特征为多形红斑(EM)样皮损和红斑狼疮(LE)。与RS相关的免疫学表现包括斑点状抗核抗体(ANA)模式、类风湿因子(RF)阳性以及抗Ro(SS - A)/抗La(SS - B)抗体。虽然直接免疫荧光(DIF)阳性是皮肤型红斑狼疮(CLE)的一个标志,但RS的最新诊断标准表明DIF应为阴性,这引发了关于RS是一种独特疾病还是CLE变体的争论。我们报告一例42岁系统性红斑狼疮(SLE)女性患者,其出现了符合RS的弥漫性水疱性皮疹。皮损皮肤的DIF显示沿基底膜带IgG、补体C3和IgM呈免疫反应性,这与RS的既定标准相矛盾。该病例强化了RS最好归类为CLE亚型而非独特疾病的观点。患者的临床、血清学和组织病理学表现,包括DIF阳性,均支持这一分类。