Yuri Takashi, Kimura Ayako, Yoshizawa Katsuhiko, Emoto Yuko, Kinoshita Yuichi, Tsubura Airo
Department of Pathology II, Kansai Medical University, Hirakata, Osaka 573-1010, Japan.
Case Rep Pathol. 2013;2013:807197. doi: 10.1155/2013/807197. Epub 2013 Jul 10.
A case of autoimmune hepatitis complicated with pulmonary and meningeal cryptococcosis during long-term treatment with corticosteroid is reported. An 84-year-old woman who received long-term corticosteroid therapy (40 mg/day prednisolone for two years) for autoimmune hepatitis developed a headache, slight fever, and anorexia and was diagnosed with cryptococcal meningitis two months prior to hospital admission. Due to deterioration of her condition, the patient was transferred to our university hospital. After admission, a pulmonary nodule 1 cm in diameter was noticed in the patient's right lower lobe. Cryptococcal meningitis was diagnosed as positive for cryptococcal antigen from both serum and cerebrospinal fluid (CSF) as well as the growth of Cryptococcus neoformans (C. neoformans) in fungal culture. A combination therapy of amphotericin B and flucytosine was started, and the corticosteroid therapy was gradually reduced and finally discontinued. In addition to continuous cryptococcal infection, complications of Pseudomonas aeruginosa and methicillin-resistance Staphylococcus aureus infection caused death after a 2-month hospitalization. Autopsy disclosed encapsulated yeast in the lungs and subarachnoid space characteristic of Cryptococcus. The pulmonary nodule was found to be squamous cell carcinoma coexisting with C. neoformans within and around the cancer cell nests.
报告了1例自身免疫性肝炎患者在长期使用糖皮质激素治疗期间并发肺和脑膜隐球菌病的病例。一名84岁女性因自身免疫性肝炎接受长期糖皮质激素治疗(泼尼松龙40mg/天,持续两年),在入院前两个月出现头痛、低热和厌食,被诊断为隐球菌性脑膜炎。由于病情恶化,患者被转至我院。入院后,在患者右下叶发现一个直径1cm的肺结节。血清和脑脊液(CSF)隐球菌抗原检测均为阳性,真菌培养发现新型隐球菌生长,确诊为隐球菌性脑膜炎。开始使用两性霉素B和氟胞嘧啶联合治疗,糖皮质激素治疗逐渐减量并最终停用。除持续的隐球菌感染外,铜绿假单胞菌和耐甲氧西林金黄色葡萄球菌感染并发症导致患者在住院2个月后死亡。尸检发现肺部和蛛网膜下腔有隐球菌特有的包膜酵母。肺结节被发现为鳞状细胞癌,癌细胞巢内及周围并存新型隐球菌。