Tirelli Fernanda, Vernal Sebastian, Roselino Ana Maria
Division of Dermatology, Department of Medical Clinics, Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo (FMRP-USP) - Ribeirão Preto (SP), Brazil.
Medical Clinics Pos graduated Area, Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo (FMRP-USP) - Ribeirão Preto (SP), Brazil.
An Bras Dermatol. 2017 Sep-Oct;92(5):642-648. doi: 10.1590/abd1806-4841.20175794.
BACKGROUND: Cutaneous leishmaniasis is distributed worldwide, including Brazil. Its several clinical forms need to be distinguished from other dermatoses. Clinical similarities and lack of a gold standard diagnostic tool make leishmaniasis-like lesions a challenging diagnosis. OBJECTIVES.: To report the final diagnosis of patients primarily suspected of having American tegumentary leishmaniasis (ATL). METHODS.: A retrospective cross-sectional study was conducted on the basis of medical records of 437 patients with clinical suspicion of ATL, registered in electronic hospital system between 1980 and 2013. Demographic, clinical, and laboratory data were compiled. RESULTS.: Analysis of 86 cases (19.7%) registered as ATL in one of the hypothesis revealed a different final diagnosis; 55 (63.9%) and 31 cases (36.1%) had skin and mucosal lesions, respectively. In 58 cases (67.4%), the requested PCR did not identify Leishmania sp. In 28 cases (32.5%), biopsies established the diagnosis and confirmed tumors, mycobacteriosis, and subcutaneous or systemic mycosis. Overall, 27% of the cases had inflammatory etiology, mainly nasal nonspecific inflammatory processes; 27% had infectious etiology, especially paracoccidioidomycosis and leprosy; 20% had neoplastic etiology, mainly basal and squamous cell carcinoma; 15% had miscellaneous etiology, including neuropathic ulcer, traumatic ulcers, idiopathic ulcer; 11% missed the follow-up. STUDY LIMITATIONS: Some cases had no final diagnosis due to loss of follow-up. CONCLUSION.: ATL can be confused with several differential diagnoses, especially inflammatory and infectious granulomatous diseases as well as non-melanoma skin cancers. Clinicians working in tropical areas should be aware of the main differential diagnosis of leishmaniasis-like lesions.
背景:皮肤利什曼病在全球范围内均有分布,包括巴西。其多种临床形式需要与其他皮肤病相鉴别。临床症状的相似性以及缺乏金标准诊断工具使得利什曼病样病变的诊断颇具挑战性。 目的:报告主要疑似美洲皮肤利什曼病(ATL)患者的最终诊断结果。 方法:基于1980年至2013年间在电子医院系统中登记的437例临床疑似ATL患者的病历进行回顾性横断面研究。收集了人口统计学、临床和实验室数据。 结果:对86例(19.7%)在其中一种假设中登记为ATL的病例进行分析后发现最终诊断不同;分别有55例(63.9%)和31例(36.1%)出现皮肤和黏膜病变。在58例(67.4%)病例中,所要求的聚合酶链反应(PCR)未检测到利什曼原虫属。在28例(32.5%)病例中,活检确诊了肿瘤、分枝杆菌病以及皮下或系统性真菌病。总体而言,27%的病例病因是炎症性的,主要是鼻腔非特异性炎症过程;27%的病例病因是感染性的,尤其是副球孢子菌病和麻风病;20%的病例病因是肿瘤性的,主要是基底细胞癌和鳞状细胞癌;15%的病例病因多样,包括神经性溃疡、创伤性溃疡、特发性溃疡;11%的病例失访。 研究局限性:部分病例因失访而未得出最终诊断。 结论:ATL可能与多种鉴别诊断相混淆,尤其是炎症性和感染性肉芽肿性疾病以及非黑色素瘤皮肤癌。在热带地区工作的临床医生应了解利什曼病样病变的主要鉴别诊断。
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