Buschke-Lö温斯坦肿瘤(BLT)/巨大尖锐湿疣(GCA):免疫发病机制的见解

P. Christopher, H. Kosim, R. Wijaya, Silvi Suhardi, L. J. Wijayadi
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引用次数: 1

摘要

Buschke Lö温斯坦瘤(BLT)/巨大尖锐湿疣是一种罕见的变异ofÂ由人乳头瘤病毒(HPV) 6型和11型引起的性传播感染。HPV有其病毒因子,通过1)仅感染上皮基底层,2)下调宿主免疫,3)抑制病毒清除所必需的促炎蛋白,从而避免免疫监视和控制。在一般人群中,BLT/GCA的发病率估计为0.1%,男性的风险比女性高2.7倍。 BLT/GCA表现为疣状肿瘤或可触及的菜花样肿块,外生生长,肉色,表面凹凸不平。BLT/GCA的最终诊断是典型的形态学以及组织病理学检查和/或病毒血清分型。BLT/GCA的治疗需要多学科的方法,根据年龄、病变程度、器官受累和器官位置来确定。
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Buschke-Löwenstein tumour (BLT)/giant condyloma acuminatum (GCA): An immunopathogenesis insight
Buschke Löwenstein tumor (BLT)/giant condyloma acuminatum is a rare variant of sexually transmitted infection caused by human papillomavirus (HPV) type 6 and 11. HPV has its viral factors that exist to avoid immune surveillance and control through 1) infecting only the basal layer of the epithelium, 2) downregulation of host immunity, 3) suppression of proinflammatory proteins essential for viral clearance. The incidence of BLT/GCA is estimated to be 0.1% in the general population, with males having 2.7 times increased risk than females. BLT/GCA is characterized by verrucous tumor or palpable cauliflower-likemass, exophytic growth, flesh-colored, and uneven surface. The definitive diagnosis of BLT/GCA is typical morphology along with histopathological examination, and/or viral serotyping. Treatment of BLT/GCA requires a multidisciplinary approach, determined based on age, the extent of the lesion, organ involvement, and organ location.
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