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Distinction between Mitochondrial Antibody-Positive and -Negative Primary Biliary Cholangitis
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 pa...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Author(s). Published by S. Karger AG
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9895762/ https://www.ncbi.nlm.nih.gov/pubmed/36742099 http://dx.doi.org/10.1159/000528437 |
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author | Matli, Venkata Vinod Kumar Dies, David F. Pandit, Sudha Wellman, Gregory Morris, James D. |
author_facet | Matli, Venkata Vinod Kumar Dies, David F. Pandit, Sudha Wellman, Gregory Morris, James D. |
author_sort | Matli, Venkata Vinod Kumar |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9895762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Author(s). Published by S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-98957622023-02-04 Distinction between Mitochondrial Antibody-Positive and -Negative Primary Biliary Cholangitis Matli, Venkata Vinod Kumar Dies, David F. Pandit, Sudha Wellman, Gregory Morris, James D. Case Rep Gastroenterol Case Report 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. The Author(s). Published by S. Karger AG 2023-01-06 /pmc/articles/PMC9895762/ /pubmed/36742099 http://dx.doi.org/10.1159/000528437 Text en © 2023 The Author(s). Published by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Case Report Matli, Venkata Vinod Kumar Dies, David F. Pandit, Sudha Wellman, Gregory Morris, James D. Distinction between Mitochondrial Antibody-Positive and -Negative Primary Biliary Cholangitis |
title | Distinction between Mitochondrial Antibody-Positive and -Negative Primary Biliary Cholangitis |
title_full | Distinction between Mitochondrial Antibody-Positive and -Negative Primary Biliary Cholangitis |
title_fullStr | Distinction between Mitochondrial Antibody-Positive and -Negative Primary Biliary Cholangitis |
title_full_unstemmed | Distinction between Mitochondrial Antibody-Positive and -Negative Primary Biliary Cholangitis |
title_short | Distinction between Mitochondrial Antibody-Positive and -Negative Primary Biliary Cholangitis |
title_sort | distinction between mitochondrial antibody-positive and -negative primary biliary cholangitis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9895762/ https://www.ncbi.nlm.nih.gov/pubmed/36742099 http://dx.doi.org/10.1159/000528437 |
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