Yang Xing-Xiang, Lin Jian-Mei, Xu Kai-Ju, Wang Shu-Qiang, Luo Ting-Ting, Geng Xiao-Xia, Huang Ren-Gang, Jiang Nan
Xing-Xiang Yang, Jian-Mei Lin, Kai-Ju Xu, Shu-Qiang Wang, Ting-Ting Luo, Xiao-Xia Geng, Ren-Gang Huang, Nan Jiang, Department of Infectious Disease, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu 610072, Sichuan Province, China.
World J Gastroenterol. 2014 Nov 21;20(43):16372-6. doi: 10.3748/wjg.v20.i43.16372.
Hepatic actinomycosis is rare, with few published cases. There are no characteristic clinical manifestations, and computed tomography (CT) shows mainly low-density images, making clinical diagnosis difficult, and leading to frequent misdiagnosis as primary liver cancer, metastatic liver cancer or liver abscess. Diagnosis normally requires examination of both the aetiology and pathology. This article reports one male patient aged 55 who was hospitalized because of repeated upper abdominal pain for more than 2 mo. He exhibited no chills, fever or yellow staining of the skin and sclera, and examination revealed no positive signs. The routine blood results were: haemoglobin 110 g/L, normal numbers of leukocytes and neutral leukocytes, serum albumin 32 g/L, negative serum hepatitis B markers and hepatitis C antibodies, normal tumour markers (alpha-fetoprotein and carcinoembryonic antigen). An abdominal CT scan revealed an 11.2 cm × 5.8 cm × 7.4 cm mass with an unclear edge in the left liver lobe. The patient was diagnosed as having primary liver cancer, and left lobe resection was performed. The postoperative pathological examination found multifocal actinomycetes in the hepatic parenchyma, which was accompanied by chronic suppurative inflammation. A focal abscess had formed, and large doses of sodium penicillin were administered postoperatively as anti-infective therapy. This article also reviews 32 cases reported in the English literature, with the aim of determining the clinical features and treatment characteristics of this disease, and providing a reference for its diagnosis and treatment.
肝放线菌病较为罕见,发表的病例很少。其没有特征性临床表现,计算机断层扫描(CT)主要显示低密度影像,导致临床诊断困难,常被误诊为原发性肝癌、转移性肝癌或肝脓肿。通常需要对病因和病理进行检查才能确诊。本文报告1例55岁男性患者,因反复上腹部疼痛2个多月入院。患者无寒战、发热,皮肤及巩膜无黄染,检查未发现阳性体征。血常规结果为:血红蛋白110g/L,白细胞及中性粒细胞计数正常,血清白蛋白32g/L,血清乙肝标志物及丙肝抗体均为阴性,肿瘤标志物(甲胎蛋白和癌胚抗原)正常。腹部CT扫描显示左肝叶有一大小为11.2cm×5.8cm×7.4cm的肿块,边界不清。患者被诊断为原发性肝癌,行左叶切除术。术后病理检查发现肝实质内有多灶性放线菌,伴有慢性化脓性炎症,形成了一个局灶性脓肿,术后给予大剂量青霉素钠进行抗感染治疗。本文还回顾了英文文献报道的32例病例,旨在明确该病的临床特征和治疗特点,为其诊断和治疗提供参考。