Rico H, Fernandez-Miranda E, Sanz J, Gomez-Castresana F, Escriba A, Hernandez E R, Krsnik I
Bone. 1986;7(5):325-9. doi: 10.1016/8756-3282(86)90251-6.
A case of oncogenous osteomalacia secondary to a fibrous malignant histiocytoma in a 31-year-old male is described. The patient also demonstrated a lupuslike anticoagulant. Clinical signs of osteomalacia preceded by 9 years those of the tumor, a feature occurring in only 8% of these malignancies. Surgical resection of the tumor and surrounding tissues was followed by a clinical improvement and a return to normal of serum phosphorus and tubular reabsorption of phosphate, though the lupuslike anticoagulant persisted. This first description of a fibrous malignant histiocytoma with associated osteomalacia and lupuslike anticoagulant makes compulsory the inclusion of these syndromes among those already described that may appear with this tumor.
本文描述了一名31岁男性因纤维性恶性组织细胞瘤继发致癌性骨软化症的病例。该患者还表现出狼疮样抗凝物。骨软化症的临床症状比肿瘤症状早9年出现,这一特征仅在8%的此类恶性肿瘤中出现。肿瘤及周围组织手术切除后,临床症状改善,血清磷和肾小管磷酸盐重吸收恢复正常,尽管狼疮样抗凝物仍然存在。首次描述纤维性恶性组织细胞瘤伴发骨软化症和狼疮样抗凝物,使得必须将这些综合征纳入已描述的可能与此肿瘤相关的综合征之中。