Couto Joana, Sobrosa Patricia, Afonso Ana, Maia Rosana, Santos Luís P
Internal Medicine, Unidade Local de Saúde do Alto Minho, Viana do Castelo, PRT.
Cureus. 2021 Nov 21;13(11):e19784. doi: 10.7759/cureus.19784. eCollection 2021 Nov.
Langerhans cell histiocytosis is a rare hematologic neoplasm with a myeloid origin, which can affect numerous organs, the skin being the second most frequently affected by this disease. In this report, a case of a 44-year-old female, who was intermittently followed due to a suspected persistent cutaneous candidiasis in which a skin biopsy revealed Langerhans cell histiocytosis with immunohistochemistry positive for CD1a and S100 protein, is described. The management of Langerhans cell histiocytosis is difficult because these disorders respond inconsistently to immunosuppressive and chemotherapeutic strategies. The authors present this case to highlight a differential diagnosis of refractory cutaneous candidiasis and raise awareness of the importance of skin biopsy in these cases.
朗格汉斯细胞组织细胞增多症是一种起源于髓系的罕见血液肿瘤,可累及多个器官,皮肤是该疾病第二常见的受累部位。在本报告中,描述了一例44岁女性病例,该患者因疑似持续性皮肤念珠菌病而接受间歇性随访,皮肤活检显示为朗格汉斯细胞组织细胞增多症,免疫组化结果显示CD1a和S100蛋白呈阳性。朗格汉斯细胞组织细胞增多症的治疗具有挑战性,因为这些疾病对免疫抑制和化疗策略的反应不一致。作者展示该病例以强调难治性皮肤念珠菌病的鉴别诊断,并提高对这些病例中皮肤活检重要性的认识。