Kim Yeong Dae, Lee Chang Hun, Lee Min Ki, Jeong Yeon Joo, Kim Jee Yeon, Park Do Youn, Sol Mee Young
Department of Thoracic & Cardiovascular Surgery, College of Medicine, Pusan National University, Busan, Korea.
J Korean Med Sci. 2007 Apr;22(2):369-72. doi: 10.3346/jkms.2007.22.2.369.
Alveolar soft part sarcoma (ASPS) is a rare epithelial-like soft tissue sarcoma. The two main sites of its occurrence are the lower extremities in adults and the head and neck in children. Primary pulmonary involvement of this sarcoma, without evidence of soft tissue tumor elsewhere, is very exceptional. We present a case of primary ASPS of the lung in a 42-yr-old woman. A computed tomographic scan of the thorax demonstrated a well-circumscribed, solid tumor located in the right upper lobe. The mass was resected by right upper lobectomy. After 5 months, three metastatic lesions, involving lumbar vertebrae and occipital scalp, were found. Histologically, the tumor consisted of alveolar nests of large polygonal tumor cells, the cytoplasm of which frequently revealed periodic acid-Schiff-positive, diastase-resistant intracytoplasmic rod-like structures. On immunohistochemical staining, the tumor cells were positive only for vimentin and alpha-smooth muscle actin. Ultrastructural study using electron microscopy revealed characteristic electron-dense, rhomboid intracytoplasmic crystals.
肺泡软组织肉瘤(ASPS)是一种罕见的上皮样软组织肉瘤。其主要发生部位在成人是下肢,在儿童是头颈部。这种肉瘤原发性肺受累,且无其他部位软组织肿瘤证据的情况非常罕见。我们报告一例42岁女性原发性肺ASPS病例。胸部计算机断层扫描显示右肺上叶有一个边界清晰的实性肿瘤。通过右上叶切除术切除了肿块。5个月后,发现了三个转移病灶,累及腰椎和枕部头皮。组织学上,肿瘤由大的多边形肿瘤细胞的肺泡巢组成,其细胞质经常显示过碘酸希夫阳性、抗淀粉酶的胞浆内棒状结构。免疫组化染色显示,肿瘤细胞仅波形蛋白和α-平滑肌肌动蛋白呈阳性。使用电子显微镜的超微结构研究显示有特征性的电子致密、菱形胞浆内晶体。