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Clinicopathological and Immunological Changes in Indian Post Kala-Azar Dermal Leishmaniasis (PKDL) Cases in relation to Treatment: A Retrospective Study

机译:印度Kala-Azar后皮肤利什曼病(PKDL)病例与治疗相关的临床病理和免疫学变化:回顾性研究

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摘要

Post-kala-azar dermal leishmaniasis (PKDL) is an important factor in kala-azar transmission; hence its early detection and assessment of effective treatment is very important for disease control. In present study on 60 PKDL cases presented with macular, mixed papulonodular, or erythematous lesions, Leishmania parasites were demonstrated microscopically in 91% of papulonodular and 40% of macular lesions. Cellular infiltrates in skin biopsy imprint smears from lesions were mononuclear cells, 25–300/OIF (oil immersion field), predominantly histiocytes with vacuolation, many lymphocytes, some plasma cells, and Leishmania amastigotes 0–20/OIF. Cases with no demonstrable parasites were diagnosed on the basis of past history of VL, lesion's distribution, cytopathological changes, and positive DAT (86.83%). Following antileishmanial treatment with SAG, papulonodular forms of PKDL lesions disappeared clinically but microscopically the mononuclear cells (20–200/OIF) persisted in the dermal lesions. Response observed in macular PKDL lesions was poor which persisted both clinically and cytopathologically. Follow-up of PKDL will assess the effectivity of treatment as either disappearance of lesions or any relapse. Studies on involvement of immunological factors, that is, certain cytokines (IL-10, TGF-β, etc.) and chemokines (macrophage inflammatory protein, MIP 1-α, etc.) in PKDL, may provide insight for any role in the treatment response.
机译:黑热病后皮肤利什曼病(PKDL)是黑热病传播的重要因素。因此,早期发现和评估有效治疗对控制疾病非常重要。在本研究中,对60例出现黄斑,混合性丘疹或红斑病变的PKDL病例进行了显微镜检查,在91%的丘疹和40%的黄斑病变中发现了利什曼原虫的寄生虫。病变处皮肤活检印迹涂片上的细胞浸润为单核细胞,25–300 / OIF(油浸视野),主要是组织细胞呈空泡状,许多淋巴细胞,某些浆细胞和利什曼原虫为0–20 / OIF。根据VL的既往病史,病变分布,细胞病理学变化和DAT阳性诊断出无明显寄生虫的病例(86.83%)。经过SAG的抗肛肠治疗后,乳头状形式的PKDL病变在临床上消失了,但在显微镜下,单核细胞(20–200 / OIF)仍然存在于真皮病变中。在黄斑PKDL病变中观察到的反应较差,其在临床和细胞病理学上均持续存在。 PKDL的随访将评估病灶消失或任何复发的治疗效果。有关免疫因素(即某些细胞因子(IL-10,TGF-β等)和趋化因子(巨噬细胞炎性蛋白,MIP1-α等))参与PKDL的研究,可能会为了解在DLDL中的任何作用提供线索。治疗反应。

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