Primary Biliary Cholangitis with Normal Alkaline Phosphatase Level: Clinical Case and Literature Review

E.A. Sokolova, E. Vinnitskaya, S.N. Batskih, S. G. Khomeriki, T. Khaymenova
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Abstract

Antimitochondrial autoantibodies of the M2 subclass (AMA-M2) in primary biliary cholangitis (PBCh) under conditions of cholestasis are considered as one of the main criteria for diagnosis that does not require morphological confirmation. However, the detection of AMA-M2 in asymptomatic patients causes ambiguity of interpretation. Along with the assumption that such patients may have preclinical stage of PBCh, there is an opinion about the "healthy carrier" of AMA-M2. The article presents the clinical observation of a patient with the high AMA-M2 titer without significant clinical manifestations, the normal level of alkaline phosphatase, with changes in liver tissue characteristic of PBCh, revealed by the results of histological examination. Clinical observation demonstrates the need for liver biopsy for early detection of PBCh in AMA-M2-positive patients belonging to the risk group
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碱性磷酸酶水平正常的原发性胆管炎:临床病例与文献综述
在胆汁淤积的情况下,原发性胆汁性胆管炎(PBCh)中的 M2 亚类抗线粒体自身抗体(AMA-M2)被认为是无需形态学确认的主要诊断标准之一。然而,在无症状患者中检测到 AMA-M2,会造成解释上的歧义。在认为这类患者可能处于胆汁淤积症临床前期的同时,还有一种关于 AMA-M2 "健康携带者 "的观点。文章介绍了对一名 AMA-M2 滴度较高但无明显临床表现、碱性磷酸酶水平正常、组织学检查结果显示肝组织发生 PBCh 特征性变化的患者的临床观察。临床观察表明,需要对属于高危人群的 AMA-M2 阳性患者进行肝活检,以早期发现 PBCh。
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