Almoqati Mehad, Althobaiti Renad, Zafer Dai, Alabbadi Asma S, Alluhaibi Razan, Al Hawsawi Khalid
General Medicine, King Abdulaziz Hospital, Makkah, SAU.
College of Medicine, Umm Al-Qura University, Makkah, SAU.
Cureus. 2025 Apr 3;17(4):e81641. doi: 10.7759/cureus.81641. eCollection 2025 Apr.
Lichen planus (LP) is a chronic inflammatory disorder that affects the skin, mucous membranes, nails, and hair. Cutaneous LP (CLP) is characterized by violaceous, polygonal, flat-topped papules and plaques that are intensely pruritic. Although it can develop on any part of the body, it most commonly affects the flexor surfaces of the wrists, lower back, and ankles. This report presents an atypical case of LP in a 33-year-old woman who initially exhibited poikilodermatous changes with bluish-gray patches, persisting for a decade. Due to the overlapping clinical and histopathological features, an extensive diagnostic workup including pan-computed tomography, lymph node biopsy, and immunohistochemistry was performed to exclude poikilodermatous mycosis fungoides. One year later, skin examination and histopathological evaluation revealed the classical features of LP, leading to a definitive diagnosis. This case highlights an unusual presentation in which poikiloderma preceded the classic clinical picture of LP. Our findings contribute to the existing knowledge of LP by emphasizing the importance of recognizing atypical presentations for accurate diagnosis and management.
扁平苔藓(LP)是一种慢性炎症性疾病,可累及皮肤、黏膜、指甲和毛发。皮肤扁平苔藓(CLP)的特征是紫红色、多边形、平顶丘疹和斑块,伴有剧烈瘙痒。虽然它可发生于身体的任何部位,但最常见于手腕屈侧、下背部和脚踝。本报告介绍了一例33岁女性的非典型扁平苔藓病例,该患者最初表现为斑驳状皮肤异色症伴蓝灰色斑块,持续了十年。由于临床和组织病理学特征重叠,进行了包括全计算机断层扫描、淋巴结活检和免疫组织化学在内的广泛诊断检查,以排除斑驳状蕈样肉芽肿。一年后,皮肤检查和组织病理学评估显示出扁平苔藓的典型特征,从而得出明确诊断。该病例突出了一种不寻常的表现,即斑驳状皮肤异色症先于扁平苔藓的经典临床表现出现。我们的发现通过强调认识非典型表现对于准确诊断和管理的重要性,为扁平苔藓的现有知识做出了贡献。