Vuković Jelena, Plavec Goran, Aćimović Slobodan, Jović Milena, Stojsavljević Marko, Trimčev Jovana, Nikolajević Sanja, Skuletić Vesna, Lončarević Olivera, Živković Vladan, Zolotarevska Lidija, Cerović Snežana
Vojnosanit Pregl. 2016 Dec;73(12):1168-72. doi: 10.2298/VSP150811138V.
Pseudomesotheliomatous lung carcinoma is a special, rare entity characterized by large pleural growth and minor invasion of lung tissue. Clinically, radiologically, macroscopically and even histologically this tumor can be misdiagnosed as malignant pleural carcinoma.
We represent a 64-year-old male patient, former smoker. Due to difficulties in the form of dry cough, feeling of dis-comfort and pain in the right hemithorax, fatigue, heavy breathing, sweating, fever up to 39.6°C the patient was treated as with combined antibiotic therapy (macrolides, cephalosporins and penicillin), but without improving of his condition. Chest radiography showed a shadow of pleural effusion by the height of the front end of the third right rib. Chest MSCT showed the extremely thickened pleura apically and to the posterior along the upper right lobe in addition to existence of massive pleural effusion. Subpleural condensation of parenchyma ranging about 30 mm was described in the upper right lobe. Cytological analysis of the pleural effusion showed the presence of malignant cells impossible to differentiate whether they were metastasis of adenocarcinoma or malignant pleural mesothelioma. By histochemical and immunohistohemical analyses of a pleural sample, pseudomesotheliomataus lung adenocarcinoma was diagnosed.
Pseudomesotheliomataus carcinoma of the lungs can be a diagnostic problem. Its diagnosis is based on recognition of histopathological characteristics which enable its discernment from the epithelial variant of malignant pleural mesothelioma.
假间皮瘤样肺癌是一种特殊的罕见实体,其特征为胸膜大量生长且对肺组织侵犯较小。在临床、放射学、大体及组织学层面,该肿瘤都可能被误诊为恶性胸膜间皮瘤。
我们报告一例64岁男性患者,既往有吸烟史。因干咳、右半胸不适与疼痛、疲劳、呼吸急促、出汗、体温高达39.6°C等症状,患者接受了联合抗生素治疗(大环内酯类、头孢菌素类和青霉素),但病情未见改善。胸部X线显示右侧第三肋骨前端高度处有胸腔积液阴影。胸部MSCT显示右上叶顶端及后部胸膜极度增厚,此外还有大量胸腔积液。右上叶可见约30mm的胸膜下实质凝聚。胸腔积液的细胞学分析显示存在恶性细胞,无法区分其是腺癌转移还是恶性胸膜间皮瘤。通过对胸膜样本进行组织化学和免疫组织化学分析,诊断为假间皮瘤样肺腺癌。
肺假间皮瘤样癌可能是一个诊断难题。其诊断基于对组织病理学特征的识别,这些特征使其能够与恶性胸膜间皮瘤的上皮型相鉴别。