首页> 外文期刊>The American Journal of Tropical Medicine and Hygiene >Appropriately Selected Nerve in Suspected Leprous Neuropathy Yields High Positive Results for Mycobacterium leprae DNA by Polymerase Chain Reaction Method
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Appropriately Selected Nerve in Suspected Leprous Neuropathy Yields High Positive Results for Mycobacterium leprae DNA by Polymerase Chain Reaction Method

机译:Appropriately Selected Nerve in Suspected Leprous Neuropathy Yields High Positive Results for Mycobacterium leprae DNA by Polymerase Chain Reaction Method

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Identification of Mycobacterium leprae DNA by polymerase chain reaction (PCR) is a reliable and an affordable method to confirm leprosy. DNA from 87 nerve samples (61 from paraffin blocks and 26 fresh samples) was extracted. Mycobacterium leprae DNA was amplified by PCR from 80/87 (92%) specimens. Patients were seen over a period of 11 years (2007-2019), and leprosy was diagnosed based on clinical and characteristic histopathology findings. The clinical diagnostic possibilities were as follows: leprous neuropathy in 73/80 (91.3%), mononeuritis multiplex of unknown etiology in four (5.0%), vasculitic neuropathy in two (2.5%), and distal symmetric sensory motor neuropathy in one (1.3%). The biopsied nerves were as follows: superficial radial = 34 (42.6%), dorsal cutaneous branch of ulnar = 19 (23.8%), sural =18 (22.5%), and superficial peroneal = 9 (11.3%), and corresponding neurological deficits were recorded in 77 (96.3%) cases. The histopathological diagnoses in total group were as follows: (borderline tuberculoid (BT) = 52, tuberculoid (TT) = 8, borderline lepromatous (BL) = 8, borderline borderline (BB) = 3, nonspecific inflammation = 3, healed/ fibrosed = 4, and axonopathy = 2). Acid fast bacilli (AFB) was demonstrated in 11 (13.7%) samples. For comparison, 31 clinically and histopathologically defined non-leprous disease control nerves (inherited neuropathy = 20, vasculitis = 8, and nutritional neuropathy = 3) subjected to PCR were negative for M. leprae DNA. In most instances, there are multiple thickened peripheral nerves in suspected cases of leprosy, but neurological deficits pertaining to the thickened nerve are not as widespread. The current findings emphasize the importance of selecting the most appropriate nerve for biopsy to obtain a positive PCR result. We infer that clinical, histopathological, and PCR tests complement each other to help achieve a definitive diagnosis of leprosy particularly in pure neuritic leprosy and in leprous neuropathy with negative skin smears/biopsy.
机译:通过聚合酶链式反应(PCR)鉴定分枝杆菌DNA是可靠的和实惠的方法以确认麻风病。提取来自87个神经样品的DNA(来自石蜡块的61和26个新鲜样品)。通过80/87(92%)样品通过PCR扩增菌杆菌DNA。患者在11年(2007-2019)中被观察到,并且基于临床和特征组织病理学发现诊断出麻风病。临床诊断可能性如下:73/80(91.3%)的麻醉神经病变,在两个(2.5%)的四(5.0%),血管神经病变中未知病因的单一炎多重,一个(2.5%),远端对称感觉运动神经病变(1.3 %)。活检神经如下:浅表径向= 34(42.6%),Ulnar = 19(23.8%),Sural = 18(22.5%),呈肤色腓骨= 9(11.3%),以及相应的神经缺陷记录在77例(96.3%)案件中。总组中的组织病理学诊断如下:(边缘结核(BT)= 52,结核抑制(TT)= 8,边缘Lepromatous(BL)= 8,边界边缘线(BB)= 3,非特异性炎症= 3,愈合/纤维= 4,轴突疗法= 2)。在11(13.7%)样品中证实了酸快杆菌(AFB)。对于比较,31种临床和组织病理学定义的非麻醉疾病控制神经(遗传性神经病变= 20,血管炎= 8,营养神经病变= 3)对PCR进行PCR对于M.Leprae DNA负阴性。在大多数情况下,在麻风病病例中存在多种增稠的外周神经,但与增稠神经有关的神经学缺陷并不像普及。目前的研究结果强调了选择最合适的神经以获得阳性PCR结果的重要性。我们推断临床,组织病理学和PCR测试彼此相互补充,以帮助实现麻风病的明确诊断,特别是在纯神经炎麻风病和阴性皮肤涂片/活组织检查的麻醉菌中。

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