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[一名接受皮质类固醇治疗的患者发生由乔治西里亚星诺卡菌引起的伴有巨大孤立性空洞结节的肺诺卡菌病]

[Pulmonary nocardiosis with a large solitary cavitary nodule caused by Nocardia cyriacigeorgica in a patient receiving corticosteroid therapy].

作者信息

Dervişoğlu Erkan, Willke Ayşe, Kalender Betül, Dişci Erdoğan Ayla, Irvem Arzu, Gündeş Sibel

机构信息

Kocaeli Universitesi Tip Fakültesi, Nefroloji Bilim Dali, Kocaeli.

出版信息

Mikrobiyol Bul. 2008 Jul;42(3):489-96.

Abstract

Nocardiosis is a rare disease generally caused by members of Nocardia asteroides complex, particularly in immunosupressed patients. Nocardia cyriacigeorgica is a newly described member of this complex. In this article, a case of pulmonary nocardiosis with a large solitary cavitary nodule caused by N. cyriacigeorgica, in a patient receiving corticosteroid therapy was presented. A 29 years old male patient receiving prednisolone for 5 months was admitted to our hospital with fever, cough, right thoracic pain and night sweats. Computed tomography scan of chest demonstrated a large solitary cavitary nodule in the right lower lobe. Gram stained smear of the sputum revealed gram-positive, beaded, branched filamentous bacilli. On the third day of his admission, a catalase positive, oxidase negative and immotile bacilli, compatible with Nocardia spp., were isolated from the sputum sample taken at the day of admission. The isolated bacterium was identified as N. cyriacigeorgica by reference laboratory (Lyon, France). Oral trimethoprim (320 mg/day) and sulfamethoxazole (1600 mg/day) therapy given for three months, resulted in complete cure of the lesion without any sequela. This was the fourth case of pulmonary nocardiosis caused by N. cyriacigeorgica reported from Turkey. Microbiological examination of sputum is the most important tool for the diagnosis. Treatment with appropriate antibiotics may achieve complete cure even in large cavitary lesions. In conclusion, pulmonary nocardiosis should be considered in differential diagnosis of solitary cavitary nodules, especially in immunocompromised patients.

摘要

诺卡菌病是一种罕见疾病,通常由星形诺卡菌复合体的成员引起,尤其是在免疫抑制患者中。西里亚基乔治诺卡菌是该复合体新描述的一个成员。本文报告了1例接受皮质类固醇治疗的患者发生的由西里亚基乔治诺卡菌引起的伴有大的孤立性空洞结节的肺诺卡菌病病例。一名接受泼尼松龙治疗5个月的29岁男性患者因发热、咳嗽、右胸痛和盗汗入院。胸部计算机断层扫描显示右下叶有一个大的孤立性空洞结节。痰涂片革兰染色显示革兰阳性、念珠状、分支丝状杆菌。入院第三天,从入院当天采集的痰样本中分离出一种过氧化氢酶阳性、氧化酶阴性且不运动的杆菌,与诺卡菌属相符。参考实验室(法国里昂)将分离出的细菌鉴定为西里亚基乔治诺卡菌。给予口服甲氧苄啶(320毫克/天)和磺胺甲恶唑(1600毫克/天)治疗三个月,病变完全治愈,无任何后遗症。这是土耳其报道的第四例由西里亚基乔治诺卡菌引起的肺诺卡菌病病例。痰的微生物学检查是诊断的最重要工具。即使是大的空洞性病变,使用适当的抗生素治疗也可能实现完全治愈。总之,在孤立性空洞结节的鉴别诊断中应考虑肺诺卡菌病,尤其是在免疫功能低下的患者中。

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