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[原发性肺隐球菌病的临床病理分析]

[Clinicopathological analysis of primary pulmonary cryptococcosis].

作者信息

Lu Shao-hua, Hou Ying-yong, Tan Yun-shan, Liu Tao, Wang Qun, Bai Chun-xue

机构信息

Department of Pathology, Zhongshan Hospital, Fudan University, Shanghai 200032, China.

出版信息

Zhonghua Jie He He Hu Xi Za Zhi. 2009 Jun;32(6):430-3.

Abstract

OBJECTIVE

To investigate the clinicopathological and CT features of primary pulmonary cryptococcosis (PC), and its underlying reasons for misdiagnosis.

METHODS

The clinical data and pathological features of 52 cases of PC in Zhongshan Hospital from 1998 to 2008 were retrospectively reviewed.

RESULTS

The 52 patients consisted of 36 males and 16 females aged from 17 to 80 years, with a median age of 48. The early symptoms were cough, phlegm and chest pain. Thirteen cases had a history of chronic diseases or malignant tumor or liver transplantation, including liver cancer and transplantation (n = 2), diabetes (n = 2), chronic hepatitis (n = 2), pituitary adenoma (n = 1), sarcoidosis (n = 1), diabetes concomitant with liver cancer and tuberculosis (n = 1), with tuberculous pleurisy (n = 1) and with hypertension (n = 1). Pulmonary nodules, either solitary or multiple, were the most common CT findings, present in 37 of the 45 cases. Cavitation was found in 4 cases, lobar consolidations in 3 cases, diffuse mixed pattern in 1 case. The CT diagnosis before surgery included malignant tumor (n = 27), pneumonia (n = 15) or tuberculosis (n = 3). Microscopically, cryptococcosis granuloma formation was found in 49 of the 52 cases, and the other 3 showed fibrosis with fungi. Cryptococcosis neoformans was detected in all the cases by mucicarmine and Grocott histopathological examination.

CONCLUSIONS

Chest CT findings of PC in immunocompetent patients show a predominant pattern of localized and mixed lesions. PC does not have any specific clinical manifestations and image findings, and it is difficult to be differentiated from lung cancer, tuberculosis or pneumonia. The correct diagnosis relies on histopathological examination. CT guided percutaneous biopsy is useful in confirming the diagnosis.

摘要

目的

探讨原发性肺隐球菌病(PC)的临床病理及CT特征,以及误诊的原因。

方法

回顾性分析1998年至2008年中山医院52例PC患者的临床资料及病理特征。

结果

52例患者中男性36例,女性16例,年龄17至80岁,中位年龄48岁。早期症状为咳嗽、咳痰和胸痛。13例有慢性疾病、恶性肿瘤或肝移植病史,包括肝癌及肝移植(n = 2)、糖尿病(n = 2)、慢性肝炎(n = 2)、垂体腺瘤(n = 1)、结节病(n = 1)、糖尿病合并肝癌及肺结核(n = 1)、合并结核性胸膜炎(n = 1)及合并高血压(n = 1)。肺结节,单发或多发,是最常见的CT表现,45例中有37例出现。4例有空洞形成,3例有肺叶实变,1例为弥漫性混合模式。术前CT诊断包括恶性肿瘤(n = 27)、肺炎(n = 15)或肺结核(n = 3)。显微镜下,52例中有49例发现隐球菌肉芽肿形成,另外3例显示真菌纤维化。所有病例经黏液卡红和Grocott组织病理学检查均检测到新型隐球菌。

结论

免疫功能正常患者PC的胸部CT表现以局限性和混合性病变为主。PC没有任何特异性临床表现和影像学表现,难以与肺癌、肺结核或肺炎相鉴别。正确诊断依赖于组织病理学检查。CT引导下经皮活检有助于确诊。

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