A. S. Sumpono, Alva Sinung Anindita, J. Yunus, D. S. Heriyanto
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引用次数: 0
摘要
摘要胸膜肺母细胞瘤(PPB)是一种非常罕见的儿童肺部肿瘤,主要发生在肺实质、纵隔和胸膜。肿瘤进展迅速,因此预后非常差。我们报告了一名4岁女孩,她在过去的8周内抱怨高烧和呼吸急促。病人因肺部肿块从原来的医院转诊过来。胸部CT造影剂示左肺1、2、3段实性囊性肿块伴坏死,大小4.8 x 8.1 x 6.6 cm3。由于肿瘤不能手术,我们采用超声引导下的细针穿刺活检(FNAB)诊断肺部病变。基于FNAB细胞学和免疫细胞化学染色,我们认为肺肿瘤为PPB。PPB的组织病理学特征与胎儿肺组织相似。通过细针穿刺细胞学涂片和细胞块获得的细胞学特征,再加上免疫细胞化学分析,可以为不能手术的手术病理病例提供正确和准确的诊断。
Cytologic diagnostic approach of pleuropulmonary blastoma: a case report
Pleuropulmonary blastoma (PPB) is a very rare pediatric lung tumor that arises in the pulmonary parenchyma, mediastinum, and pleura. The tumor has rapid disease progression and therefore the prognosis is remarkably poor. We reported a 4-year-old girl who complained of high fever and shortness of breath for the past 8 weeks. The patient was referred from the previous hospital with a pulmonary mass. CT scan of the chest with contrast showed a solid cystic mass with necrotic areas in the 1st, 2nd, and 3rd segments of the left lung with sized 4.8 x 8.1 x 6.6 cm3. As the tumor mass was inoperable, an ultrasound-guided fine-needle aspiration biopsy (FNAB) was conducted to diagnose the pulmonary lesion. We concluded that the lung tumor was a PPB based on FNAB cytology and immunocytochemistry staining. The histopathology feature of PPB appeared similar to fetal lung tissue. Cytologic features obtained from fine-needle aspiration cytology smears and cell blocks followed by immunocytochemistry assay could provide a proper and accurate diagnosis in an inoperable surgical pathology case.