de la Torre-Aláez Manuel, Iñarrairaegui Mercedes
Liver Unit, Clínica Universidad de Navarra, Madrid, Spain.
Liver Unit, Clínica Universidad de Navarra, Pamplona, Spain.
Eur J Case Rep Intern Med. 2020 Jan 3;7(1):001407. doi: 10.12890/2020_001407. eCollection 2020.
Autoimmune hepatitis (AIH) was the first liver disease for which an effective therapeutic intervention was carried out, using prednisolone; its usefulness was demonstrated in several clinical trials. Nevertheless, AIH still remains a difficult diagnosis in some cases, because it is necessary to dismiss other possible diagnoses, and perhaps due to it being a heterogeneous disease. The relationship between drug-induced liver injury (DILI) and AIH is complex and not fully understood. There are three possible scenarios: (1) DILI with a strong immunoallergic component mimicking AIH; (2) AIH mimicking a DILI due to drug exposure and (3) AIH triggered by exposure to an offending drug (drug-induced AIH). Drug-induced AIH is well described and documented for some drugs such as nitrofurantoin and minocycline. Histologically distinguishing DILI from AIH remains a challenge. We present an interesting case report which met serologic criteria and histological confirmation to establish AIH, but discontinuation of a suspected drug resolved hypertransaminasaemia.
Idiosyncratic drug-induced liver injury is one of the most challenging liver disorders.Diagnosis of drug-induced liver injury is a complex question; this can evolve to severe hepatotoxicity if it is not diagnosed promptly.Usually, olmesartan and similar anti-hypertensive drugs are not considered drugs with the potential to cause liver damage.
自身免疫性肝炎(AIH)是第一种采用泼尼松龙进行有效治疗干预的肝脏疾病;其有效性在多项临床试验中得到了证实。然而,AIH在某些情况下仍然难以诊断,因为有必要排除其他可能的诊断,也可能是由于它是一种异质性疾病。药物性肝损伤(DILI)与AIH之间的关系复杂且尚未完全明确。存在三种可能的情况:(1)具有强烈免疫过敏成分的DILI模仿AIH;(2)AIH因药物暴露而模仿DILI;(3)接触致病药物引发的AIH(药物性AIH)。对于某些药物,如呋喃妥因和米诺环素,药物性AIH已有充分的描述和记录。从组织学上区分DILI和AIH仍然是一项挑战。我们报告了一例有趣的病例,该病例符合血清学标准并经组织学证实为AIH,但停用可疑药物后高转氨酶血症得到缓解。
特异质性药物性肝损伤是最具挑战性的肝脏疾病之一。药物性肝损伤的诊断是一个复杂的问题;如果不及时诊断,可能会发展为严重的肝毒性。通常,奥美沙坦及类似的抗高血压药物不被认为是有潜在肝损伤风险的药物。