Ippolito Ernesto, Bray Edward W, Corsi Alessandro, De Maio Fernando, Exner Ulrich G, Robey Pamela Gehron, Grill Franz, Lala Roberto, Massobrio Marco, Pinggera Oswald, Riminucci Mara, Snela Slawomir, Zambakidis Christos, Bianco Paolo
Department of Orthopedic Surgery, University of Rome Tor Vergata, Rome, Italy.
J Pediatr Orthop B. 2003 May;12(3):155-77. doi: 10.1097/01.bpb.0000064021.41829.94.
A multicenter study on fibrous dysplasia of bone (FD) was promoted by the European Pediatric Orthopaedic Society in 1999 in order to gain insight into the natural history of the disease and to evaluate current diagnostic and therapeutic approaches. We collected and reviewed clinical, radiographic, pathological, and molecular genetic data when possible, from a total of 64 cases diagnosed as either monostotic FD (MFD), polyostotic FD (PFD), or McCune-Albright syndrome (MAS), evaluated or treated in 11 participating centers. Results from the initial analysis of the series indicate five main points: (1) Significant diagnostic pitfalls affect the diagnosis of MFD and, to a lesser extent, PFD in orthopedic centers and allied radiology and pathology facilities, which may be circumvented by the adoption of stringent diagnostic criteria, and in some cases by the analysis of FD-associated GNAS1 mutations. (2) MFD carries a significant risk for fracture in the face of limited disease in the proximal femur, whereas its tendency to progress is restricted to a minority of cases, and long-term outcome is usually satisfactory, regardless of treatment, in non-progressive cases. (3) The profile of tibial disease, both in MFD and in PFD, is markedly different from that of femoral disease. (4) As expected, MAS patients have the most extensive disease and the most complicated course, regularly experience multiple fractures, and require adequate surgical treatment. It appears that conservative treatment of femoral fracture, or curettage and cancellous bone grafting, or fixation with screws and plates are not indicated for the treatment of femoral fractures in these patients and should all be discouraged. Internal fixation with intramedullary nails provides stabilization of extensively affected bones, and prevents further fractures and major deformities, and thus providing a better option both for acute and elective surgery in patients with extensive involvement of the femur or of other limb long bones. (5) Evaluation of patients with FD at orthopedic centers should include, but rarely does, a thorough evaluation of endocrine profile and phosphate metabolism, and proper pathological and radiographic assessment.
1999年,欧洲小儿骨科学会发起了一项关于骨纤维发育不良(FD)的多中心研究,旨在深入了解该疾病的自然史,并评估当前的诊断和治疗方法。我们尽可能收集并回顾了11个参与中心评估或治疗的64例诊断为单发性FD(MFD)、多发性FD(PFD)或McCune-Albright综合征(MAS)患者的临床、影像学、病理和分子遗传学数据。该系列的初步分析结果表明了五个要点:(1)在骨科中心以及相关放射学和病理学机构中,显著的诊断陷阱影响MFD的诊断,在较小程度上也影响PFD的诊断,采用严格的诊断标准以及在某些情况下分析与FD相关的GNAS1突变可避免这些陷阱。(2)MFD在股骨近端疾病有限的情况下存在骨折的重大风险,而其进展趋势仅限于少数病例,在非进展性病例中,无论治疗如何,长期结果通常令人满意。(3)MFD和PFD中胫骨疾病的特征与股骨疾病明显不同。(4)正如预期的那样,MAS患者的疾病最为广泛,病程最为复杂,经常发生多处骨折,需要进行充分手术治疗。对于这些患者股骨骨折的治疗,似乎不适合采用股骨骨折保守治疗、刮除和松质骨移植或螺钉和钢板固定,所有这些方法都应予以摒弃。髓内钉内固定可为广泛受累的骨骼提供稳定,防止进一步骨折和严重畸形,因此对于股骨或其他肢体长骨广泛受累的患者,无论是急诊手术还是择期手术,都是更好的选择。(5)在骨科中心对FD患者的评估应包括但很少包括对内分泌状况和磷酸盐代谢的全面评估以及适当的病理和影像学评估。