Terpstra Leonieke, Rauch Frank, Plotkin Horacio, Travers Rose, Glorieux Francis H
Genetics Unit, Shriners Hospital for Children and McGill University, Montréal, Québec, Canada.
J Bone Miner Res. 2002 Nov;17(11):1949-53. doi: 10.1359/jbmr.2002.17.11.1949.
Fibrous dysplasia (FD) of bone can be complicated by renal phosphate wasting. The effect of hypophosphatemia on normal and dysplastic bone of FD patients has not been well characterized. In this study, we compared serum phosphorus (sPi) levels to histomorphometric findings in 27 iliac bone samples from 23 children and adolescents (aged 4.2-16.4 years) with polyostotic FD. The samples were separated into two groups, based on the presence (n = 10) or absence (n = 17) of a dysplastic lesion within the specimen. Histomorphometric results were compared with those from 18 age-matched control subjects without metabolic bone disease. In dysplastic lesions, trabeculae were clearly thinner and increased in number. Osteoid indices, osteoblast surface per bone surface, and mineralization lag time were elevated in dysplastic areas, but there was no detectable effect of sPi concentrations on these indices. In nondysplastic bone tissue, low sPi levels were associated with mildly increased osteoid thickness and prolonged mineralization lag time. None of the 13 patients in whom hand X-rays were available at the time of biopsy had radiological signs of rickets. In conclusion, low sPi can cause a mild systemic mineralization defect in FD, but the more severe mineralization defect seen in dysplastic lesions is independent of sPi levels. It is debatable whether the mild systemic mineralization defect warrants treatment with oral phosphorus supplementation if signs of rickets are absent.
骨纤维发育不良(FD)可并发肾性磷酸盐消耗。低磷血症对FD患者正常骨和发育异常骨的影响尚未得到充分描述。在本研究中,我们比较了23例儿童和青少年(4.2 - 16.4岁)多骨型FD患者的27份髂骨样本中的血清磷(sPi)水平与组织形态计量学结果。根据样本中是否存在发育异常病变,将样本分为两组(存在组n = 10,不存在组n = 17)。将组织形态计量学结果与18名无代谢性骨病的年龄匹配对照受试者的结果进行比较。在发育异常病变中,小梁明显更薄且数量增加。发育异常区域的类骨质指数、每骨表面的成骨细胞表面和矿化延迟时间升高,但sPi浓度对这些指数没有可检测到的影响。在无发育异常的骨组织中,低sPi水平与类骨质厚度轻度增加和矿化延迟时间延长有关。活检时可获得手部X线片的13例患者中,均无佝偻病的放射学征象。总之,低sPi可在FD中引起轻度全身矿化缺陷,但在发育异常病变中所见的更严重矿化缺陷与sPi水平无关。如果没有佝偻病征象,这种轻度全身矿化缺陷是否需要口服磷补充剂治疗仍存在争议。