Makarov Marina R, Jo Chan-Hee, Liu Raymond W, Birch John G
Texas Scottish Rite Hospital for Children, Dallas, Texas.
Rainbow Babies Children's Hospital, Cleveland, Ohio.
JB JS Open Access. 2025 Aug 15;10(3). doi: 10.2106/JBJS.OA.25.00151. eCollection 2025 Jul-Sep.
We sought to determine the relationship between Greulich and Pyle (G-P) and modified Fels (mFels) skeletal age in infantile and adolescent Blount diseases, where skeletal age (SA) is often advanced relative to chronological age (CA). We also sought to determine whether there was a difference between affected and unaffected extremity mFels SA in unilateral cases.
We reviewed databases of patients treated for subjects meeting inclusion criteria of unilateral infantile or adolescent Blount disease and concurrent interpretable hand and knee films. SA using the G-P atlas and of both knees by mFels method was compared with each other and CA.
Twenty subjects with infantile Blount and 36 with adolescent Blount met inclusion criteria. Overall, there was no difference in mFels between affected and unaffected sides in either of these conditions (p = 0.6). SA was advanced by both methods in patients with both types of Blount disease, ranging from 5 to 18 months, depending on sex and diagnosis (p < 0.01). mFels was less advanced than G-P in both infantile and adolescent Blount diseases, but the differences were statistically significant only in boys with adolescent Blount disease (mean 10 months, p < 0.01).
Our study confirmed relatively advanced SA in patients with both forms of Blount disease. mFels SA was generally comparable in affected and unaffected extremities in these conditions. Given the epiphysial distortion typical of infantile Blount disease, comparability of affected/unaffected sides was an unexpected finding and should be validated by a larger cohort. Nevertheless, we recommend familiarization with and use of the mFels SA determination in these conditions.
Level III, controlled case series. See Instructions for Authors for a complete description of levels of evidence.
我们试图确定婴儿期和青少年期布朗特病中格吕利希和派尔(G-P)骨龄与改良费尔斯(mFels)骨龄之间的关系,在这些疾病中,骨龄(SA)通常相对于实际年龄(CA)提前。我们还试图确定在单侧病例中,患侧与未患侧肢体的mFels骨龄是否存在差异。
我们回顾了符合单侧婴儿期或青少年期布朗特病纳入标准且同时有可解读的手部和膝部X线片的患者数据库。将使用G-P图谱确定的骨龄和通过mFels方法确定的双侧膝部骨龄相互比较,并与实际年龄进行比较。
20例婴儿期布朗特病患者和36例青少年期布朗特病患者符合纳入标准。总体而言,在这两种情况下,患侧与未患侧的mFels骨龄均无差异(p = 0.6)。两种类型的布朗特病患者通过两种方法确定的骨龄均提前,提前时间为5至18个月,具体取决于性别和诊断(p < 0.01)。在婴儿期和青少年期布朗特病中,mFels骨龄的提前程度均低于G-P骨龄,但仅在青少年期布朗特病男孩中差异具有统计学意义(平均10个月,p < 0.01)。
我们的研究证实了两种形式的布朗特病患者的骨龄相对提前。在这些情况下,患侧与未患侧肢体的mFels骨龄通常具有可比性。鉴于婴儿期布朗特病典型的骨骺畸形,患侧/未患侧的可比性是一个意外发现,应由更大的队列进行验证。尽管如此,我们建议在这些情况下熟悉并使用mFels骨龄测定方法。
III级,对照病例系列。有关证据水平的完整描述,请参阅作者指南。