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Giant cell hepatitis associated with systemic lupus erythematosus

机译:巨细胞性肝炎伴系统性红斑狼疮

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Giant hepatocytes are commonly found in several neonatal and infantile liver diseases, but are rarely found in adult liver disease. A 42 year old white woman presented with a five month history of par-aesthesia and numbness of both the upper and lower limbs and with vague abdominal pain. Abnormal liver function was noted on routine screening. Ultrasound scan of the abdomen showed gallstones; barium enema, ERCP and computed tomography scan were all normal. IgG antibodies to double stranded DNA were present at a titre of 40 units. Anti-cardiolipin antibodies, anti-mitochondrial antibodies and rheumatoid factor were not detected. Serology for hepatitis A, B, C, and para-myxoviruses was negative, as was the Paul Bunnell test. A clinical diagnosis of systemic lupus erythematosus (SLE) with an axonal sensory polyneuropathy was made, the latter confirmed on biopsy of the sural nerve. Giant cells were noted on liver biopsy. The patient was treated with corticosteroids; liver function had improved after two years of follow up. When extensive giant cell transformation is noted on liver biopsy, particularly when neuropathy is also a feature, the possibility of an association with SLE should be considered.
机译:巨型肝细胞通常在几种新生儿和婴儿肝病中发现,但在成人肝病中很少发现。一名42岁的白人妇女表现出五个月的上肢和下肢麻木感和麻木感,并伴有模糊的腹痛。常规筛查发现肝功能异常。腹部超声检查显示胆结石。钡剂灌肠,ERCP和计算机断层扫描均正常。针对双链DNA的IgG抗体的滴度为40个单位。未检测到抗心磷脂抗体,抗线粒体抗体和类风湿因子。甲型,乙型,丙型肝炎和副粘病毒的血清学检查均为阴性,Paul Bunnell检验也为阴性。进行了系统性红斑狼疮(SLE)的轴索感觉性多发性神经病的临床诊断,后者在腓肠神经活检中得到证实。肝活检发现巨细胞。患者接受了皮质类固醇激素治疗;经过两年的随访,肝功能有所改善。当在肝活检中发现广泛的巨细胞转化时,特别是当神经病变也是一个特征时,应考虑与SLE相关的可能性。

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