Zisis Vasileios, Theodoridou Athina, Anagnostou Eleftherios, Poulopoulos Athanasios, Andreadis Dimitrios
Oral Medicine/Pathology, Aristotle University of Thessaloniki, Thessaloniki, GRC.
Rheumatology, Aristotle University of Thessaloniki, Thessaloniki, GRC.
Cureus. 2024 Jun 29;16(6):e63439. doi: 10.7759/cureus.63439. eCollection 2024 Jun.
Psoriatic arthritis (PsA) is a chronic inflammatory condition that impacts a significant proportion of individuals diagnosed with psoriasis. This report presents a rare case of a patient diagnosed with PsA who never had active psoriatic skin lesions but only a family history of psoriasis, with secondary lingual lesions, resembling geographic tongue (GT). A male patient, 24 years old, was referred with two painless erythematous areas resembling (without whitish borders, as in GT) rounded atrophic lesions on the dorsal surface of the tongue, resistant to any kind of antimicrobial/antifungal treatment for more than six months. The patient was diagnosed with PsA two years ago fulfilling the CASPAR (ClASsification for Psoriatic ARthritis) criteria. The patient never had active psoriatic skin lesions, but his father had psoriasis. The biopsy of lingual lesions showed moderate hyperkeratosis, spongiosis, and diffuse inflammatory infiltration of lymphocytes and neutrophils in the lamina propria as well as in the stratified squamous epithelium forming Munro's microabscesses at the superficial layers. The manifestation of the atypical psoriasiform, GT-like lingual lesions was considered as part of psoriasis manifestations and the patient was advised to follow regular checkups so that any major exacerbation of the systematic symptoms could be preemptively avoided. Not only GT but also atypical lingual GT-like reddish oral lesions may be considered as transient forms of psoriasis supporting an early diagnosis and monitoring of psoriasis/PsA.
银屑病关节炎(PsA)是一种慢性炎症性疾病,影响着很大一部分被诊断为银屑病的患者。本报告介绍了一例罕见病例,该患者被诊断为PsA,从未出现过活动性银屑病皮肤病变,仅有银屑病家族史,伴有继发性舌部病变,类似地图舌(GT)。一名24岁男性患者因舌背出现两个无痛性红斑区域前来就诊,这些区域类似圆形萎缩性病变(不像GT那样有白色边界),接受任何抗菌/抗真菌治疗超过六个月均无效。该患者两年前被诊断为PsA,符合CASPAR(银屑病关节炎分类标准)标准。患者从未有过活动性银屑病皮肤病变,但其父亲患有银屑病。舌部病变活检显示中度角化过度、海绵形成,固有层以及形成浅层Munro微脓肿的复层鳞状上皮中有淋巴细胞和中性粒细胞的弥漫性炎症浸润。非典型银屑病样、类似GT的舌部病变表现被认为是银屑病表现的一部分,建议患者定期进行检查,以便能预先避免系统性症状的任何重大加重。不仅GT,而且非典型的类似GT的舌部红色口腔病变也可能被视为银屑病的短暂形式,这有助于早期诊断和监测银屑病/PsA。