2006
DOI: 10.1007/s10620-006-3083-5
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Occurrence of Autoimmune Hepatitis During the Course of Primary Biliary Cirrhosis: Report of Two Cases

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Cited by 9 publications
(7 citation statements)
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“…We previously reported that corticosteroids are effective for AIH with acute presentation [2] and that they are also effective for overlap syndrome having AIH and PBC features with acute transaminase elevation [10]. Ichai et al [12] indicated that there is a point beyond which AIH cannot be salvaged by drug therapy, and this point can be defined only by assessing the immediate response to corticosteroid treatment [4].…”
Section: Discussionmentioning
confidence: 99%
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“…We previously reported that corticosteroids are effective for AIH with acute presentation [2] and that they are also effective for overlap syndrome having AIH and PBC features with acute transaminase elevation [10]. Ichai et al [12] indicated that there is a point beyond which AIH cannot be salvaged by drug therapy, and this point can be defined only by assessing the immediate response to corticosteroid treatment [4].…”
Section: Discussionmentioning
confidence: 99%
“…Some patients within the spectrum of autoimmune liver disease present with characteristics of both PBC and AIH and are commonly classified as having an ‘overlap syndrome’ [5, 10]. In AIH patients, AMA is occasionally seen at low titers, but an AMA anti-pyruvate dehydrogenase complex-E2 (AMA-M2) pattern, which is specific to PBC, is rarely detected [5].…”
Section: Introductionmentioning
confidence: 99%
“…Other cases are more sequential in nature. One recent study described two cases of AIH during the course of PBC (3). In each of these cases, the patient had a diagnosis of PBC for 1–2 years before the diagnosis of AIH.…”
Section: Discussionmentioning
confidence: 99%
“…Very little research has been carried out on this population. A recent paper (3) described two such cases. Each involved a patient diagnosed with PBC only to develop AIH 1–2 years later.…”
mentioning
confidence: 99%
“…AIH can occasionally have clinical, laboratory, histological, and genetic characteristics identical to those of PBC [10]. Some cases of AIH are difficult to diagnose [10][11][12][13][14]. The incidence of AIH differs in various geographic regions.…”
Section: Introductionmentioning
confidence: 99%