When the bronchoalveolar lavage makes the diagnosis of interstitial pneumonia

M. Mlika, Meriem Triki, H. Kwas, E. Braham, H. Ghédira, F. Mezni
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引用次数: 1

Abstract

A 30-year-old non-smoker woman without a particular past medical history consulted for dyspnoea and non-productive cough. Chest CT scan revealed mediastinal and hilar adenopathies associated with bilateral ground glass opacities with thickened interlobular septa. Bronchoalveolar lavage was performed (Fig. 1). The fluid was opaque with a milky turbid gross appearance. On microscopic examination, finely granular amorphous material was apparent in the background along with numerous lymphocytes and fragmented macrophages. Zhiel stain was performed but was negative. The diagnosis of pulmonary alveolar proteinosis (PAP) was suspected but the association of mediastinal adenomegalies was not concordant with the diagnosis. Surgical biopsy of the lung and the mediastinal lymph nodes was performed. Histological examination revealed granulomatous inflammation with caseous necrosis in the lymph nodes and an amorphous PAS positif lipoprotein material filling the alveolar spaces in the lung (Fig. 2). The final diagnosis of associated PAP with tuberculosis infection was established. The patient was put on anti-tuberculosis drugs and presented an improvement of her general state.
支气管肺泡灌洗可诊断为间质性肺炎
30岁非吸烟女性,既往无特殊病史,因呼吸困难和非生产性咳嗽就诊。胸部CT扫描显示纵隔及肺门腺病变伴双侧磨玻璃影及小叶间隔增厚。行支气管肺泡灌洗(图1)。液体不透明,大体呈乳状混浊。镜下背景可见细颗粒状无定形物质,伴大量淋巴细胞和碎片状巨噬细胞。进行Zhiel染色,结果为阴性。怀疑诊断为肺泡蛋白沉积症(PAP),但与纵隔腺肿大的关系与诊断不一致。手术活检肺和纵隔淋巴结进行。组织学检查显示肉芽肿性炎症伴淋巴结干酪样坏死,无定形PAS阳性脂蛋白物质填充肺肺泡间隙(图2)。最终诊断为PAP与结核感染相关。病人服用抗结核药物后,一般情况有所改善。
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