Maeda Ryo, Isowa Noritaka, Miura Hiroshi, Tokuyasu Hirokazu, Kawasaki Yuji, Yamamoto Kazumichi
Matsue Red Cross Hospital, Horomachi, Shimane, Japan.
Gen Thorac Cardiovasc Surg. 2009 Dec;57(12):667-70. doi: 10.1007/s11748-009-0452-y.
This report presents a case of bilateral multiple sclerosing hemangiomas of the lung in a 73-year-old woman. A computed tomography (CT) scan of the chest showed a total of three well-defined small nodules in the right and left lower lobes of the lung. Because malignant metastatic lung tumors were highly suspected, a wedge resection of the left lower lobe was performed to obtain a definitive diagnosis. Histopathologically, two tumors of the left lower lobe were composed of epithelial-like cuboidal cells covering the surface of papillary protrusions and sheets of round to polygonal cells underneath the epithelial-like cells. The final diagnosis was that both tumors were sclerosing hemangiomas. After surgery the residual lesion of the right lower lobe was carefully followed by chest CT. The size of the right lung nodule did not change over the course of 9 years, and no new lesion has emerged.
本报告介绍了一名73岁女性双侧多发性肺硬化性血管瘤的病例。胸部计算机断层扫描(CT)显示,在左右下肺叶共有三个边界清晰的小结节。由于高度怀疑为恶性转移性肺肿瘤,因此对左下叶进行了楔形切除术以明确诊断。组织病理学检查显示,左下叶的两个肿瘤由覆盖乳头状突起表面的上皮样立方细胞和上皮样细胞下方的圆形至多边形细胞片组成。最终诊断为两个肿瘤均为硬化性血管瘤。手术后,通过胸部CT对右下叶的残留病变进行了仔细随访。右肺结节的大小在9年的时间里没有变化,也没有出现新的病变。