Department of Pathology, Hospital Universitario de Fuenlabrada, Madrid, Spain.
Department of Dermatology, Hospital Universitario de Fuenlabrada, Madrid, Spain.
J Cutan Pathol. 2020 Nov;47(11):1018-1025. doi: 10.1111/cup.13785. Epub 2020 Sep 8.
Traditional methods for the diagnosis of leishmaniasis yield poor sensitivity, which limits its effectiveness in lesions with a low parasite burden.
Retrospective pathologic study of 360 cases of cutaneous leishmaniasis and analysis of the different diagnostic methods used.
In 93% of the lesions, histopathology showed a dense and diffuse inflammatory infiltrate, consisting of lymphocytes, histiocytes and plasma cells, which occupied the superficial and mid dermis and variably extended to deep dermis and superficial subcutis (standard pattern). The remaining cases exhibited atypical features, such as perivascular, interstitial or perifollicular inflammatory patterns, folliculitis or panniculitis. Granulomas were identified in 84% of biopsies, most of them as small, poorly formed, non-necrotizing histiocytic aggregates. Amastigotes were visualized by routine histopathologic exam in 36% of biopsies. Immunohistochemistry stained 17 of 26 lesions (65%) negative by conventional stains. PCR provided the correct diagnosis in 218 cases (58% of the series) negative for Leishmania by other techniques.
Biopsies negative for Leishmania by traditional diagnostic methods that show the histopathologic standard pattern, those with atypical features from patients with clinical suspicion of cutaneous leishmaniasis in endemic areas, should be studied by immunohistochemistry and/or PCR for Leishmania in order to reach the definitive diagnosis.
传统的利什曼病诊断方法的灵敏度较差,这限制了其在寄生虫负荷低的病变中的有效性。
对 360 例皮肤利什曼病的回顾性病理研究,并分析了使用的不同诊断方法。
在 93%的病变中,组织病理学显示密集而弥漫的炎症浸润,由淋巴细胞、组织细胞和浆细胞组成,占据浅部和中部真皮,并不同程度地延伸至深部真皮和浅部皮下组织(标准模式)。其余病例表现出非典型特征,如血管周围、间质或滤泡周围炎症模式、滤泡炎或脂膜炎。肉芽肿在 84%的活检中被识别,其中大多数是小的、形态不规则、非坏死性组织细胞聚集。在 36%的活检中通过常规组织病理学检查观察到无鞭毛体。免疫组织化学染色在常规染色阴性的 26 个病变中的 17 个(65%)呈阳性。PCR 在其他技术检测为利什曼阴性的 218 例(该系列的 58%)中提供了正确的诊断。
对于通过传统诊断方法显示组织病理学标准模式且利什曼阴性、但来自临床疑似皮肤利什曼病的患者的具有非典型特征的活检,应通过免疫组织化学和/或 PCR 检测利什曼进行研究,以做出明确诊断。