Bertelsen C A, Eilber F R
J Surg Oncol. 1983 Nov;24(3):170-2. doi: 10.1002/jso.2930240304.
Paraneoplastic syndromes secondary to mesodermal tumors are relatively uncommon. In this report, we describe two unusual cases associated with soft-tissue sarcoma: a 69-year-old male who had a normochromic anemia, without apparent etiology, that resolved promptly after surgical resection of the primary tumor; and a 22-year-old female with hypercalcemia without evidence of bony destruction.
中胚层肿瘤继发的副肿瘤综合征相对少见。在本报告中，我们描述了两例与软组织肉瘤相关的不寻常病例：一名69岁男性，患有正色素性贫血，无明显病因，在原发肿瘤手术切除后迅速缓解；以及一名22岁女性，患有高钙血症，无骨破坏证据。
