Distinction between Mitochondrial Antibody-Positive and -Negative Primary Biliary Cholangitis.

IF 0.5 Q4 GASTROENTEROLOGY & HEPATOLOGY
Venkata Vinod Kumar Matli, David F Dies, Sudha Pandit, Gregory Wellman, James D Morris
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引用次数: 1

Abstract

Antimitochondrial antibody-positive primary biliary cholangitis (AMA-pos PBC) is an autoimmune disorder in which monoclonal antibodies are produced against epitopes in the mitochondrial membranes of biliary epithelial cells, resulting in progressive nonsuppurative biliary cholangitis. Up to 5% of patients lack these autoantibodies, termed antimitochondrial antibody-negative (AMA-neg) PBC. Although a somewhat new variant of AMA-pos PBC, it is not an overlapping syndrome. Few studies to date have described this phenomenon. An 87-year-old woman was referred to our clinic with elevated serum alkaline phosphatase (714 U/L). She reported fatigue but no other symptoms. A physical examination revealed a benign lesion and bilateral lower extremity swelling secondary to lymphedema. The serological profile was significant for a high antinuclear antibody titer (>1:2,560) with a centromere pattern and negative for antimitochondrial antibody (AMA). The hepatitis panel was negative for viruses A, B, and C. Her serum immunoglobulin G level was 871 mg/dL (normal, <1,600 mg/dL). The rest of the serological tests, including anti-smooth muscle antibodies (ASMA) and anti-liver/kidney microsomal antibodies, were negative. Computed tomography of the abdomen and pelvis without contrast showed normal liver parenchyma and no acute intra-abdominal pathology. Histopathology indicated florid duct lesions. The background parenchyma showed no significant steatosis, and inflammatory changes were limited to the portal areas. Periodic acid-Schiff staining revealed intact hepatic parenchyma and architecture. The patient was diagnosed with AMA-neg PBC and responded well to ursodeoxycholic acid therapy. This case highlights the importance of recognizing AMA-neg PBC as a variant of AMA-pos PBC and differentiating between them. Autoimmune cholangitis is a vague and imprecise condition. All patients with AMA-negative PBC should be tested for other PBC-specific autoantibodies. Although the prognosis and bile duct damage and loss are worse in AMA-neg PBC for unknown reasons, treatment remains the same for both.

Abstract Image

Abstract Image

原发性胆道胆管炎线粒体抗体阳性与阴性的区别
抗线粒体抗体阳性的原发性胆道胆管炎(AMA-pos PBC)是一种自身免疫性疾病,其单克隆抗体针对胆道上皮细胞线粒体膜上的表位产生,导致进行性非化脓性胆道胆管炎。高达5%的患者缺乏这些自身抗体,称为抗线粒体抗体阴性(AMA-neg) PBC。虽然是AMA-pos PBC的一种新变体,但它不是一种重叠综合征。迄今为止,很少有研究描述过这种现象。一名87岁妇女因血清碱性磷酸酶升高(714 U/L)而转诊至本诊所。她报告疲劳,但没有其他症状。体格检查显示良性病变和双侧下肢继发淋巴水肿肿胀。血清抗核抗体滴度高(>1:2 560),具有着丝点模式,抗线粒体抗体(AMA)阴性。肝炎面板A、B、c病毒均阴性。血清免疫球蛋白G水平为871 mg/dL(正常,
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来源期刊
Case Reports in Gastroenterology
Case Reports in Gastroenterology Medicine-Gastroenterology
CiteScore
1.10
自引率
0.00%
发文量
99
审稿时长
7 weeks
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