Tominaga M, Tanaka M, Fukuoka M, Kawashima M, Yatsunami J, Nakahara Y, Aoki Y, Hayashi S
Division of Internal Medicine, Department of Saga Medical School.
Nihon Kokyuki Gakkai Zasshi. 2001 May;39(5):347-50.
A 71-year-old woman with no history of asbestos exposure was referred to our hospital for evaluation of mediastinal soft tissue density. Six months prior to the admission, she had developed back pain and had been diagnosed as having intercostal neuralgia. Since the symptoms progressed, she was referred to another hospital. While chest radiography revealed no abnormality, chest computed tomography showed the prominence of mediastinal soft tissue, extending to the left hilum and partially destroying the nearby vertebrae. However, no pleural effusion was noted. After admission, a thoracoscopic examination was performed, and a whitish mass was found on the pleural surface partially adhering to the chest wall. Histological examination of the biopsied material showed dense areas of collagenous tissue with small foci of slightly atypical spindle cells. These findings led to the diagnosis of desmoplastic malignant pleural mesothelioma. The patient was treated with combined chemo-radiotherapy, but the response to this treatment was unclear. To date, reports for this subgroup of malignant mesothelioma are still rare.
一名71岁无石棉接触史的女性因纵隔软组织密度异常被转诊至我院。入院前6个月,她出现背痛,被诊断为肋间神经痛。由于症状进展,她被转诊至另一家医院。胸部X线检查未见异常,但胸部计算机断层扫描显示纵隔软组织突出,延伸至左肺门并部分破坏附近椎体。然而,未发现胸腔积液。入院后,进行了胸腔镜检查,发现胸膜表面有一个白色肿块,部分附着于胸壁。活检材料的组织学检查显示有致密的胶原组织区域,伴有少量轻度非典型梭形细胞灶。这些发现导致诊断为促纤维增生性恶性胸膜间皮瘤。患者接受了联合放化疗,但对该治疗的反应尚不清楚。迄今为止,关于这一亚组恶性间皮瘤的报道仍然很少。