Martínez-Varea Alicia, Vila-Vives Jose María, Hidalgo-Mora Juan José, Abad-Carrascosa Antonio, Llorens-Salvador Roberto, Perales-Marín Alfredo
Department of Obstetrics and Gynecology, La Fe University Hospital, 46026 Valencia, Spain.
Case Rep Obstet Gynecol. 2012;2012:954241. doi: 10.1155/2012/954241. Epub 2012 Dec 5.
We present a case of a twin pregnancy in which one fetus developed a rapidly growing unilateral intrathoracic tumor. While a cystic adenomatoid malformation was suspected in the ultrasound scan, the magnetic resonance scan suggested a pulmonary blastoma or a bronchioalveolar carcinoma. Postnatal chest radiography and contrast-enhanced computed tomography of the affected newborn were performed, and it was ruled out the possibility of malignant origin. Finally, the anatomopathologic exam revealed the presence of a mesenchymal hamartoma in the chest wall. Nevertheless, parents refused any treatment for the newborn.
我们报告一例双胎妊娠病例,其中一个胎儿发生了一个快速生长的单侧胸腔内肿瘤。超声扫描怀疑为囊性腺瘤样畸形,而磁共振扫描提示为肺母细胞瘤或细支气管肺泡癌。对受影响的新生儿进行了产后胸部X线摄影和增强计算机断层扫描,排除了恶性起源的可能性。最后,解剖病理学检查显示胸壁存在间叶性错构瘤。然而,父母拒绝为新生儿进行任何治疗。