Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
J Am Soc Cytopathol. 2023 May-Jun;12(3):216-228. doi: 10.1016/j.jasc.2023.01.005. Epub 2023 Feb 7.
Metastatic sarcomas to pleural effusion are extremely rare, accounting for <1% of all malignant pleural effusions. We aim to present our experience with pleural effusion specimens containing metastatic sarcomas over a 10-year period.
We performed a 10-year retrospective search of cytopathology archives to identify all pleural effusions that were involved by metastatic sarcoma. All available cytopathology and surgical pathology specimens were retrieved and reviewed.
Twenty-eight pleural fluids from 22 patients with metastatic sarcoma were identified in our search. The patients' ages ranged from 12 to 73 years. The pleural fluid volumes ranged from 10 to 1500 ml. Rhabdomyosarcoma was the most commonly encountered metastatic sarcoma to pleural effusion (n = 7). Other metastatic sarcomas were as follows: epithelioid angiosarcoma (n = 4), Ewing sarcoma (n = 3), clear cell sarcoma (n = 2), high grade conventional osteosarcoma (n = 2), undifferentiated pleomorphic sarcoma (n = 1), epithelioid sarcoma, proximal type (n = 1), dedifferentiated liposarcoma (n = 1), and conventional chondrosarcoma (n = 1). The time between initial diagnosis and effusion varied from 3 months to 25 years. Two patients are alive with disease at 6 and 21 months of follow-up. All other patients were dead of disease and the survival after a malignant pleural effusion ranged from <1 month to 18 months.
Metastatic bone and soft tissue sarcomas to pleural effusions are rare and their cytologic features can be mistaken for carcinoma, melanoma, or mesothelioma. Careful review of the patient's medical history, comparison of the previous pathology and the use of ancillary studies are crucial for the evaluation of pleural effusions involved by metastatic sarcomas.
胸膜转移肉瘤极为罕见,占所有恶性胸腔积液的<1%。我们旨在展示我们在过去 10 年中处理胸膜转移肉瘤胸腔积液标本的经验。
我们对细胞病理学档案进行了为期 10 年的回顾性搜索,以确定所有含有转移性肉瘤的胸腔积液。检索并回顾了所有可用的细胞病理学和外科病理学标本。
在我们的搜索中,从 22 名患有转移性肉瘤的患者中确定了 28 份胸腔积液。患者年龄从 12 岁至 73 岁不等。胸腔积液量从 10 至 1500 毫升不等。横纹肌肉瘤是最常见的胸膜转移肉瘤(n = 7)。其他转移性肉瘤包括上皮样血管肉瘤(n = 4)、尤因肉瘤(n = 3)、透明细胞肉瘤(n = 2)、高级别常规骨肉瘤(n = 2)、未分化多形性肉瘤(n = 1)、上皮样肉瘤,近端型(n = 1)、去分化脂肪肉瘤(n = 1)和常规软骨肉瘤(n = 1)。初始诊断和胸腔积液之间的时间从 3 个月到 25 年不等。2 名患者在随访 6 个月和 21 个月时仍患有疾病。所有其他患者均因疾病死亡,恶性胸腔积液后的生存时间从<1 个月到 18 个月不等。
胸膜转移骨和软组织肉瘤非常罕见,其细胞学特征可能与癌、黑色素瘤或间皮瘤混淆。仔细审查患者的病史、比较先前的病理学和使用辅助研究对于评估胸膜转移肉瘤的胸腔积液至关重要。