Afonso Catarina, Dias Tiago, Teixeira Carlos, Rodrigues David, Mira Marília
General Practice/Family Medicine, Unidade de Saúde Familiar Planície, Unidade Local de Saúde do Alentejo Central, Évora, PRT.
Nursing, Escola Superior de Enfermagem São João de Deus, Universidade de Évora, Évora, PRT.
Cureus. 2024 Sep 25;16(9):e70141. doi: 10.7759/cureus.70141. eCollection 2024 Sep.
Langerhans cell histiocytosis (LCH) is a rare histiocytic neoplastic disorder that mainly affects the skin and bones, with dermatological manifestations that can be easily confused with other dermatological conditions, such as seborrheic eczema, psoriasis, lesions of herpes simplex virus infection, fungal infection, lichen planus, and cutaneous lymphomas. This case report describes an eight-month-old infant who, at a child health appointment, presented with progressive erythematous papulovesicular lesions, initially treated with hygiene measures (skin hydration and hygiene) and mupirocin ointment, but which persisted and worsened, leading to a skin biopsy. The diagnosis of self-limiting congenital histiocytosis was confirmed, and the child was referred to the Portuguese Oncology Institute. The case highlights the importance of early recognition of LCH, the multidisciplinary approach, and the crucial role of the family doctor in the diagnosis and appropriate management of this rare condition.
朗格汉斯细胞组织细胞增多症(LCH)是一种罕见的组织细胞肿瘤性疾病,主要累及皮肤和骨骼,其皮肤表现很容易与其他皮肤病混淆,如脂溢性湿疹、银屑病、单纯疱疹病毒感染性皮损、真菌感染、扁平苔藓和皮肤淋巴瘤。本病例报告描述了一名8个月大的婴儿,在儿童健康检查时出现进行性红斑丘疹水疱性皮损,最初采用卫生措施(皮肤保湿和清洁)和莫匹罗星软膏治疗,但皮损持续且加重,最终进行了皮肤活检。确诊为自限性先天性组织细胞增多症,该患儿被转诊至葡萄牙肿瘤研究所。该病例强调了早期识别LCH的重要性、多学科方法以及家庭医生在这种罕见疾病的诊断和适当管理中的关键作用。