Strada M, Tesoro Tess J D, Cozzi G, Musumeci R
Radiol Med. 1983 May;69(5):296-303.
Fifty-two patients with histologically proven histiocytosis X and intrathoracic and/or bone lesions have been evaluated. In the group, bone lesions appear clearly prevalent (51/52 patients) mainly as localized monostotic disease (31/51). Flat bones were more frequently involved, with special evidence for skull and ribs. Short as well as long bones were only seldom compromised, almost only in polyostotic and generalized disease. On the basis of our experience the most suggestive radiological findings in bone to diagnose an histiocytosis X were the following: preferential involvement of a flat bone, osteolytic pattern, sharp borders (72.9%), rare evidence of pathological fracture (20%) and periostitis (10%). On the contrary, the involvement of the neighbouring soft tissues (38.8%) appears to be significant.
对52例经组织学证实为组织细胞增多症X且伴有胸内和/或骨病变的患者进行了评估。在该组中,骨病变明显更为常见(51/52例患者),主要表现为局限性单骨病变(31/51)。扁骨受累更为频繁,颅骨和肋骨尤为明显。短骨和长骨很少受累,几乎仅见于多骨病变和全身性疾病。根据我们的经验,骨组织细胞增多症X最具提示性的放射学表现如下:扁骨优先受累、溶骨型、边界清晰(72.9%)、病理性骨折罕见(20%)和骨膜炎少见(10%)。相反,邻近软组织受累(38.8%)似乎较为显著。