Ninomiya H, Hato T, Yamada T, Takada K, Miyamoto K, Yasukawa M, Fujita S
First Department of Internal Medicine, School of Medicine, Ehime University.
Intern Med. 1998 May;37(5):480-3. doi: 10.2169/internalmedicine.37.480.
We report a case of multiple diffuse fibrosarcoma of bone. The patient, a 38-year-old man, was referred to our hospital with knee pain, anemia and thrombocytopenia. No solid mass was seen on radiographic examination of the kneejoint, but magnetic resonance imaging showed hypointensity of the distal femur. Femoral biopsy revealed proliferation of long spindle-shaped fibrosarcoma cells, while a bone marrow biopsy of iliac bone (which appeared normal on radiographic examinations) showed replacement of hematopoietic cells by fibroblast-like spindle cells. A diagnosis of multiple diffuse fibrosarcoma of bone was therefore made. Autopsy revealed tumor invasion into multiple bones and several visceral organs and extramedullary hematopoiesis in the liver, spleen and lymph nodes. As this patient had leukoerythroblastic anemia with poikilocytosis, splenomegaly exhibiting extramedullary hematopoiesis, and apparent fibrotic change in his bone marrow, we suggest that this extremely rare disease should be considered in the differential diagnosis of myelofibrosis.
我们报告一例多发性骨弥漫性纤维肉瘤病例。患者为一名38岁男性,因膝关节疼痛、贫血和血小板减少症转诊至我院。膝关节X线检查未见实体肿块,但磁共振成像显示股骨远端低信号。股骨活检显示长梭形纤维肉瘤细胞增殖,而髂骨骨髓活检(X线检查显示正常)显示造血细胞被成纤维细胞样梭形细胞取代。因此诊断为多发性骨弥漫性纤维肉瘤。尸检发现肿瘤侵犯多个骨骼和几个内脏器官,肝脏、脾脏和淋巴结出现髓外造血。由于该患者有异形红细胞增多的幼粒-幼红细胞性贫血、表现为髓外造血的脾肿大以及骨髓明显的纤维化改变,我们建议在骨髓纤维化的鉴别诊断中应考虑这种极其罕见的疾病。