Arumugam Vasugi Gramani, Joseph Leena Dennis, Thangavel Periyasamy, Swaminathan Rajendiran, Sunderaj Ramya Rathinam
Demonstrator, Department of Pathology, Sri Ramachandra Medical College , Chennai, Tamil Nadu, India .
Professor, Department of Pathology, Sri Ramachandra Medical College , Chennai, Tamil Nadu, India .
J Clin Diagn Res. 2017 Feb;11(2):ED12-ED14. doi: 10.7860/JCDR/2017/22279.9271. Epub 2017 Feb 1.
Pulmonary Sclerosing Pneumocytoma (PSP) is a rare tumour of the lung and is always benign. Diagnosis is made incidentally following chest X-ray or chest CT scan performed for other clinical conditions. We report a case of PSP in a seven-year-old girl who got admitted for evaluation of an anterior mediastinal mass. Clinically, thought of teratoma or other germ cell tumour the mass was excised and sent for histopathological examination. Grossly, we received a pneumonectomy specimen measuring 13x11x8 cm with a nodular firm grey white lesion in the medial aspect of lower and middle lobe measuring 7.5x5.5x5 cm. Macroscopically, pleura was involved and adherent to the lung. Microscopy showed, an ill-defined lesion in the lung with extensive fibrosis and lymphoplasmacytic infiltrate. The lesion was composed of round to oval cells with ill defined cell border, moderate eosinophilic cytoplasm and bland nuclei. A panel of Immunohistochemical (IHC) markers was performed and the lesional cells were positive for Epithelial Membrane Antigen (EMA) and Thyroid Transcription Factor-1 (TTF-1). The prognosis after surgical resection is good and the patient is doing well.
肺硬化性肺细胞瘤(PSP)是一种罕见的肺部肿瘤,通常为良性。诊断通常是在因其他临床情况进行胸部X线或胸部CT扫描时偶然发现的。我们报告一例7岁女孩的PSP病例,该女孩因前纵隔肿块入院评估。临床上,考虑为畸胎瘤或其他生殖细胞肿瘤,遂将肿块切除并送去做组织病理学检查。大体上,我们收到一个肺切除标本,大小为13×11×8 cm,在中下叶内侧有一个结节状坚实灰白色病变,大小为7.5×5.5×5 cm。肉眼可见,胸膜受累并与肺粘连。显微镜检查显示,肺内有一个边界不清的病变,伴有广泛纤维化和淋巴浆细胞浸润。病变由圆形至椭圆形细胞组成,细胞边界不清,胞质中度嗜酸性,核淡染。进行了一组免疫组织化学(IHC)标记物检测,病变细胞上皮膜抗原(EMA)和甲状腺转录因子-1(TTF-1)呈阳性。手术切除后的预后良好,患者情况良好。