Mendes da Costa P, Heimann R
Acta Chir Belg. 1976 May;75(3):365-73.
This is a case of alveolar rhabdomyosarcoma with a rare clinical evolution. A first metastasis causes paraplegia; a second causes obstructive jaundice; a third subcutaneous metastasis is resected; the primitive tumor is discovered accidentally in the right calf, 8 weeks after the beginning of the disease. The literature is reviewed. Diagnosis of the alveolar rhabdomyosarcoma is often difficult because of confusion with a lymphoma, another type of sarcoma, a melanoma or even an epithelial tumor. The surgeon who removes a superficial node, obviously malignant, in a young subject, should think of this type of tumor. A multidisciplinary treatment associating radical resection, radio- and chemotherapy improves the very poor prognosis of this sarcoma.
这是一例具有罕见临床病程的肺泡横纹肌肉瘤病例。首次转移导致截瘫;第二次转移导致梗阻性黄疸;第三次皮下转移灶被切除;在疾病开始8周后,原始肿瘤在右小腿意外发现。对相关文献进行了综述。肺泡横纹肌肉瘤的诊断常常很困难,因为它容易与淋巴瘤、另一种肉瘤、黑色素瘤甚至上皮肿瘤相混淆。在年轻患者中切除一个明显为恶性的浅表淋巴结的外科医生,应考虑到这种类型的肿瘤。联合根治性切除、放疗和化疗的多学科治疗可改善这种肉瘤极差的预后。