Cairns A, McMahon R F
Department of Histopathology, Manchester Royal Infirmary.
J Clin Pathol. 1996 Feb;49(2):183-4. doi: 10.1136/jcp.49.2.183.
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 paraesthesia 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 paramyxoviruses 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.
巨大肝细胞常见于多种新生儿和婴儿肝脏疾病,但在成人肝脏疾病中很少见。一名42岁白人女性,有5个月的上肢和下肢感觉异常及麻木病史,伴有模糊的腹痛。常规筛查发现肝功能异常。腹部超声扫描显示有胆结石;钡灌肠、内镜逆行胰胆管造影(ERCP)和计算机断层扫描均正常。双链DNA的IgG抗体滴度为40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、丙型肝炎病毒及副粘病毒血清学检查均为阴性,嗜异性凝集试验也为阴性。临床诊断为系统性红斑狼疮(SLE)伴轴索性感觉多神经病,后者经腓肠神经活检证实。肝活检发现有巨细胞。该患者接受了皮质类固醇治疗;随访两年后肝功能有所改善。当肝活检发现广泛的巨细胞转化,尤其是当伴有神经病时,应考虑与SLE相关的可能性。