Rakotoson J L, Andrianasolo R, Rakotomizao J R, Rakotoharivelo H, Andrianarisoa A C F
Unité de soins de formations et de recherche (USFR) de pneumologie, CHU d'Antananarivo, Antananarivo, Madagascar.
Rev Pneumol Clin. 2012 Feb;68(1):40-4. doi: 10.1016/j.pneumo.2011.01.008. Epub 2011 Aug 5.
Thoracic actinomycosis, caused by bacteria of the Actinomyces genus, is a rare infection, with poor prognosis if untreated, whose clinical and radiological picture is misleading, which can simulate a tumoral or tuberculous disease.
This is a case of generalised pseudotumoral pulmonary actinomycosis in a non-smoking, non-drinking 48-year-old man, who for one month has been presenting a cough with haemoptoic sputum, dyspnoea associated with fever and a deterioration in general condition. The clinical examination discovered weight loss, diffuse crackling rales and multiple dental caries. Biologically, he presented an inflammatory syndrome. The radiological imaging and lung and liver CT-scans discovered a peripheral lung mass right side associated with multiple nodular cannon-ball opacities, multiple liver lesions of metastatic appearance. The bacteriological examination of the bronchoalveolar lavage fluid (Gram stain and culture) and the transparietal biopsy of the lung mass confirmed the presence of Actinomyces. Progress under treatment with 10 million international units of parenteral penicillin G daily over a period of six weeks substituted by three grams of amoxicillin/clavulanic acid daily over a period of 12 months and following an oral preparatory procedure was favourable. The thoraco-abdominal scan carried out three months after the treatment showed that the lesions had completely disappeared.
Our case illustrates the diagnostic difficulty of actinomycosis particularly faced with a picture of multiple lung and liver metastasis. Hence, the importance of a histological and bacteriological examination of samples. The prognosis of this complaint is generally good following well-managed, prolonged treatment; and the prognosis peculiar to disseminated forms is less certain.
由放线菌属细菌引起的胸段放线菌病是一种罕见的感染性疾病,若不治疗,预后较差,其临床和影像学表现具有误导性,可类似肿瘤性或结核性疾病。
这是一例48岁不吸烟、不饮酒男性的广泛性假瘤型肺放线菌病病例,患者咳嗽伴咯血痰1个月,伴有发热引起的呼吸困难及全身状况恶化。临床检查发现体重减轻、弥漫性湿啰音和多发龋齿。实验室检查显示存在炎症综合征。影像学检查及肺部和肝脏CT扫描发现右侧周边肺部肿块,伴有多个结节状“炮弹”样混浊影,肝脏有多个转移瘤样病变。支气管肺泡灌洗液的细菌学检查(革兰氏染色和培养)及肺部肿块的经皮活检证实存在放线菌。经6周每日静脉注射1000万国际单位青霉素G治疗,之后改为每日3克阿莫西林/克拉维酸治疗12个月,并在口服预处理后病情好转。治疗3个月后进行的胸腹扫描显示病变已完全消失。
我们的病例说明了放线菌病的诊断困难,尤其是面对多发肺和肝转移的情况。因此,对样本进行组织学和细菌学检查很重要。经过妥善管理的长期治疗,这种疾病的预后通常良好;而播散型的预后则不太确定。