Prayson R A, Farver C F
Department of Anatomic Pathology, Cleveland Clinic Foundation, Ohio 44195, USA.
Am J Surg Pathol. 1999 Jun;23(6):722-6. doi: 10.1097/00000478-199906000-00013.
Fewer than 20 cases of primary pulmonary meningioma have been reported. Most of these cases have been histologically and clinically benign. We report an unusual case of primary pulmonary malignant meningioma with atypical histologic features and malignant behavior. A computed tomography scan of the head did not show evidence of tumor. The right upper lobe mass was resected and showed features of an atypical meningioma with loss of architectural pattern, mild nuclear pleomorphism, increased mitotic counts (up to 15 mitotic figures per 10 high power fields), and focally prominent nucleoli. Focally, cells with rhabdoid features were identified. The tumor's immunohistochemical and ultrastructural profiles were consistent with a meningioma. The tumor stained negative for estrogen and focally positive for progesterone receptors and had a MIB-1 labeling index (marker of cell proliferation) of 9.2%. Approximately 5 months after the initial resection, the patient experienced a tumor recurrence with multiple lymph node metastases, spread to the middle and lower lobes of the right lung, and metastasis to the diaphragm. Rarely, primary pulmonary meningiomas may present as high-grade malignant lesions.
原发性肺脑膜瘤的报道病例不足20例。其中大多数病例在组织学和临床上为良性。我们报告一例原发性肺恶性脑膜瘤的罕见病例,其具有非典型组织学特征和恶性行为。头部计算机断层扫描未显示肿瘤迹象。右上叶肿块被切除,显示为非典型脑膜瘤特征,包括结构模式消失、轻度核异形性、有丝分裂计数增加(每10个高倍视野多达15个有丝分裂象)以及局灶性明显核仁。局部可见具有横纹肌样特征的细胞。肿瘤的免疫组化和超微结构特征与脑膜瘤一致。肿瘤雌激素染色阴性,孕激素受体局灶性阳性,MIB - 1标记指数(细胞增殖标志物)为9.2%。初次切除后约5个月,患者出现肿瘤复发,伴有多处淋巴结转移,扩散至右肺中叶和下叶,并转移至膈肌。原发性肺脑膜瘤很少表现为高级别恶性病变。