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Infant pleuropulmonary blastoma: report of a rare case and review of literature

机译:婴儿胸膜肺母细胞瘤:一例罕见病例报告及文献复习

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摘要

In infants, pleuropulmonary blastoma is a rare but aggressive tumor. The typical histopathological presentation includes the aggregation of malignant primitive small cells, usually observed in sheets. So as to provide proper and timely treatment, the differential diagnosis includes pulmonary blastoma, sarcomatoid mesothelioma, fetal rhabdomyoma, synovial sarcoma, and primitive neuroectodermal tumor. Herein, we will present one male pediatric patient with pleuropulmonary blastoma. The patient was a 4-month-old male infant, who had a prolonged cough and dyspnea for 4 months that was complicated by cyanosis for 3 days. A physical examination revealed a solid mass in the right lung that was sized 9.0 × 6.0 × 4.0 cm and had a grayish-white cross section. The boundary between the mass and lung tissue was clear; the mass already occupied a great portion of the lung. A microscopic examination suggested that the tumor was composed of round or orbicular-ovate primitive fetal cells. The cells were medium sized, having little cytoplasm, but had a clearly visualized nucleolus and active karyokinesis. The tumor mass was biphasic, namely, fasciculated sarcoma (composed of spindle-shaped cells and short spindle-shaped cells) and malignant fibrous histiocytoma containing well-differentiated cartilage islands or cartilaginous nodes. Immunohistochemistry was performed for further detection: vimentin (+), S-100 protein (+), CK (AE1/AE3), EMA and TTF-1 in residual epithelial components (+), NSE (focal +), SMA (mesenchymal cells, focal +), CD99 (weak +), Bcl-2 (weak +), desmin (-), myoglobin (-), calretinin (-), calponin (-), FLI (-), MyoD-1 (-), and CD34 (-). Pleuropulmonary blastoma is extremely rare but highly aggressive neoplasm in children. Its typical histopathological presentation is the aggregation of primitive malignant small cells. Combining imaging and histopathological examinations and clinical data should help in determining the diagnosis of pleural pulmonary blastoma.
机译:在婴儿中,胸膜肺母细胞瘤是一种罕见但具有侵袭性的肿瘤。典型的组织病理学表现包括通常在薄片中观察到的恶性原始小细胞的聚集。为了提供适当和及时的治疗,鉴别诊断包括肺母细胞瘤,肉瘤样间皮瘤,胎儿横纹肌瘤,滑膜肉瘤和原始神经外胚层肿瘤。在这里,我们将介绍一名男性小儿胸膜肺母细胞瘤患者。该患者是一个4个月大的男婴,他有长时间的咳嗽和呼吸困难4个月,并伴有发osis 3天。体格检查发现右肺有一个固体肿块,大小为9.0×6.0×4.0 cm,横截面为灰白色。肿块与肺组织之间的界限很清晰;肿块已经占据了肺的很大一部分。显微镜检查表明该肿瘤由圆形或圆形卵形原始胎儿细胞组成。细胞中等大小,几乎没有细胞质,但具有清晰可见的核仁和活跃的核运动。肿瘤块是双相的,即束状肉瘤(由纺锤形细胞和短纺锤形细胞组成)和恶性纤维组织细胞瘤,其中软骨岛或软骨结节高度分化。进行了免疫组织化学以进一步检测:波形蛋白(+),S-100蛋白(+),残留上皮成分(+),NSE(局灶+),SMA(间质细胞)中的CK(AE1 / AE3),EMA和TTF-1 ,聚焦+),CD99(弱+),Bcl-2(弱+),结蛋白(-),肌红蛋白(-),钙黄蛋白(-),钙蛋白(-),FLI(-),MyoD-1(-)和CD34(-)。胸膜肺母细胞瘤在儿童中极为罕见,但具有高度侵袭性。其典型的组织病理学表现是原始恶性小细胞的聚集。影像学和组织病理学检查以及临床数据的结合应有助于确定胸膜肺母细胞瘤的诊断。

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