Takahashi Hidenobu, Harada Masahiko, Maehara Sachio, Kato Harubumi
Department of Surgery, Tokyo Metropolitan Health and Medical Treatment Corporation Ebara Hospital, Tokyo, Japan.
Ann Thorac Cardiovasc Surg. 2007 Aug;13(4):262-6.
Because malignant mesothelioma is commonly seen as a diffuse neoplasm, a localized tumor is an extremely rare form of presentation. Only 45 cases have been reported, and little is known about their behavior. We report a new case of localized malignant mesothelioma with the microscopic appearance of diffuse malignant mesothelioma, but without any evidence of diffuse spread. A 54-year-old man, a former smoker, with a brief history of asbestos exposure for 3 months, presented with a severe right chest pain and a swelling in the same area. Chest-computed tomography (CT) showed a 4.5 cm extra pleural tumor with a smooth surface, located in the right anterior chest wall, and destruction of the 5th rib. A CT-guided needle biopsy revealed malignant mesothelioma. Detailed examinations revealed a resectable solitary localized mass with no distant metastasis. The patient underwent operation, a tumorectomy, plus a combined resection of the chest wall and part of the right middle lobe. A complete en bloc resection was achieved. Pathology revealed localized malignant mesothelioma, biphasic type. Immunohistochemical findings confirmed the mesothelial feature. Localized malignant mesothelioma should be distinguished from diffuse malignant mesothelioma because of its different biological behavior, and in the former complete resection it is associated with a good prognosis.
由于恶性间皮瘤通常被视为弥漫性肿瘤,局限性肿瘤是一种极其罕见的表现形式。仅报告了45例,对其行为了解甚少。我们报告一例局限性恶性间皮瘤新病例,其显微镜下表现为弥漫性恶性间皮瘤,但无任何弥漫性扩散的证据。一名54岁男性,既往吸烟,有3个月的石棉接触史,出现严重的右胸痛和同一部位肿胀。胸部计算机断层扫描(CT)显示右前胸壁有一个4.5厘米的胸膜外肿瘤,表面光滑,第5肋骨破坏。CT引导下针吸活检显示为恶性间皮瘤。详细检查发现一个可切除的孤立局限性肿块,无远处转移。患者接受了手术,即肿瘤切除术,外加胸壁和右中叶部分的联合切除术。实现了完整的整块切除。病理显示为局限性恶性间皮瘤,双相型。免疫组化结果证实了间皮特征。局限性恶性间皮瘤因其不同的生物学行为应与弥漫性恶性间皮瘤相区分,对于前者,完整切除与良好预后相关。