Moran C A, Suster S, Przygodzki R M, Koss M N
Department of Pulmonary and Mediastinal Pathology, Armed Forces Institute of Pathology, Washington, DC 20306-6000, USA.
Cancer. 1997 Aug 15;80(4):691-8. doi: 10.1002/(sici)1097-0142(19970815)80:4<691::aid-cncr7>3.0.co;2-q.
Primary seminomas of the mediastinum are unusual neoplasms that are morphologically indistinguishable from their gonadal counterparts but may have different biologic behavior because they arise at this particular location.
The clinical and pathologic features in 120 cases of primary mediastinal seminoma were reviewed, and the immunohistochemical staining patterns in 50 of these tumors were also analyzed.
The patients were all men between the ages of 14 and 79 years (mean age, 46.5 years). Their clinical symptoms included cough, chest pain, and dyspnea. In some patients, the lesions were asymptomatic and discovered incidentally on routine chest radiographs. None of the patients had a previous history of testicular neoplasm or tumor elsewhere. Macroscopically, the tumors were described as soft and tan, with a slightly lobulated cut surface, and measured up to 16 cm in greatest dimension. Histologically, the morphologic features were similar to those of tumors occurring in the gonads, namely, a neoplastic proliferation of round-to-polygonal cells with indistinct cell borders, clear-to-lightly-eosinophilic cytoplasm with round-to-oval nuclei and prominent nucleoli, associated with a prominent inflammatory background composed mainly of mature lymphocytes. Necrosis, hemorrhage, multinucleated giant cells, granulomatous reaction, and remnants of thymic tissue were observed in a variable number of cases; mitoses were rare. Immunohistochemical studies in 50 cases showed cytoplasmic staining with placental alkaline phosphatase in 80% of the tumors, focal dotlike positivity for CAM 5.2 low-molecular-weight keratins in 75%, focal cytoplasmic staining for wide-spectrum keratin in 70%, focal positive reaction with vimentin in 70%, and focal positivity with HCG in singly scattered cells in 5%. Immunostains for carcinoembryonic antigen, epithelial membrane antigen, and alpha-fetoprotein were negative in all the cases studied. Fifty patients were Stage I, 3 patients were Stage II, and 12 patients were Stage III. Clinical follow-up information was obtained for 65 cases (54%). Forty-nine patients were alive and disease free after a period ranging from 1 to 19 years (mean follow-up, 10 years). Sixteen patients died within the same period and were found to have metastases to distant organs. Of the 16 patients who died, 6 showed extension of the tumor outside of the mediastinal compartment at the time of initial diagnosis (Stage III lesions). Aside from clinical staging, the authors' findings also suggest that patients >37 years have worse outcomes than younger individuals. The authors were unable to find any correlation between histopathologic features and clinical behavior in any of these cases.
Clinical and pathologic staging of mediastinal seminomas are important parameters that can be useful in determining the clinical outcomes of patients with these tumors. Tumor invasion into adjacent organs represents a marker of increased morbidity and mortality. The authors' findings suggest that patients with mediastinal seminomas may have a very good prognosis when the diagnosis is made early; patients with more advanced lesions may require more aggressive therapy for improved local control and prevention of distant metastases.
纵隔原发性精原细胞瘤是一种罕见的肿瘤,其形态与性腺来源的精原细胞瘤无法区分,但因其起源于特定部位,可能具有不同的生物学行为。
回顾了120例纵隔原发性精原细胞瘤的临床和病理特征,并分析了其中50例肿瘤的免疫组化染色模式。
患者均为男性,年龄在14至79岁之间(平均年龄46.5岁)。临床症状包括咳嗽、胸痛和呼吸困难。部分患者无症状,在常规胸部X线检查时偶然发现。所有患者既往均无睾丸肿瘤或其他部位肿瘤病史。大体上,肿瘤质地柔软,呈黄褐色,切面略呈分叶状,最大直径达16 cm。组织学上,形态特征与性腺肿瘤相似,即圆形至多边形细胞的肿瘤性增生,细胞边界不清,胞质清亮至轻度嗜酸性,核圆形至椭圆形,核仁明显,伴有以成熟淋巴细胞为主的显著炎症背景。部分病例可见坏死、出血、多核巨细胞、肉芽肿反应及胸腺组织残留;有丝分裂少见。50例免疫组化研究显示,80%的肿瘤胎盘碱性磷酸酶呈胞质染色阳性,75%的肿瘤CAM 5.2低分子量角蛋白呈局灶点状阳性,70%的肿瘤广谱角蛋白呈局灶胞质染色阳性,70%的肿瘤波形蛋白呈局灶阳性反应,5%的肿瘤单个散在细胞HCG呈局灶阳性。所有研究病例中癌胚抗原、上皮膜抗原和甲胎蛋白免疫染色均为阴性。50例患者为Ⅰ期,3例为Ⅱ期,12例为Ⅲ期。65例(54%)获得临床随访信息。49例患者在1至19年(平均随访10年)后存活且无疾病复发。16例患者在同一时期死亡,尸检发现有远处器官转移。16例死亡患者中,6例在初诊时肿瘤已侵犯纵隔外区域(Ⅲ期病变)。除临床分期外,作者的研究结果还表明年龄>37岁的患者预后较年轻患者差。作者未发现这些病例中任何组织病理学特征与临床行为之间存在相关性。
纵隔精原细胞瘤的临床和病理分期是重要参数,有助于判断这些肿瘤患者的临床结局。肿瘤侵犯邻近器官是发病率和死亡率增加的标志。作者的研究结果表明,纵隔精原细胞瘤患者若早期诊断,预后可能很好;病变较晚期的患者可能需要更积极的治疗,以改善局部控制并预防远处转移。