Umeda Chizuru, Ueda Koichi, Hirota Yuka
From the Department of Plastic and Reconstructive Surgery, Osaka Medical and Pharmaceutical University.
Plast Reconstr Surg Glob Open. 2024 Apr 5;12(4):e5717. doi: 10.1097/GOX.0000000000005717. eCollection 2024 Apr.
Postaxial polydactyly is a common congenital foot anomaly. However, the severity of the anomaly varies from simple cases with only soft tissue duplication to complex cases with bone and joint disorders. In our clinical practice, we found a new morphological anomaly of postaxial polydactyly. We encountered several cases of postaxial polydactyly with bone fragments located between the fourth and fifth toes. The bone fragments were independent of the joint cavity. The mechanisms underlying its development remain unknown because it is a novel disorder. In the present study, we investigated the characteristics of the excess bone to formulate an embryological hypothesis.
We examined the frequency and trends in the occurrence of excess bone using data from photographs and radiographs of these cases. An example of a disorder similar to excess bone is mosaic-like alignment, as reported by Iba et al. We also compared the characteristics of the mosaic-like alignment with those of the excess bone. Based on these data and existing embryological knowledge, we hypothesized the origin of the excess bone.
Excess bone and mosaic-like alignments showed different characteristics. Therefore, both were considered completely different disorders. We hypothesized that excess bone was caused by damage to the interdigital ectoderm immediately before interdigital programmed cell death.
We encountered a new form of postaxial polydactyly. This can be a factor influencing the treatment strategy because it can affect alignment and stability.
轴后多指畸形是一种常见的先天性足部异常。然而,该异常的严重程度各不相同,从仅伴有软组织重复的简单病例到伴有骨骼和关节疾病的复杂病例。在我们的临床实践中,我们发现了轴后多指畸形的一种新的形态学异常。我们遇到了几例轴后多指畸形病例,其第四和第五趾之间存在骨碎片。这些骨碎片与关节腔无关。由于这是一种新型疾病,其发育的潜在机制仍然未知。在本研究中,我们调查了多余骨骼的特征,以形成一个胚胎学假说。
我们使用这些病例的照片和X线片数据检查了多余骨骼出现的频率和趋势。Iba等人报道的一种与多余骨骼相似的疾病示例是镶嵌样排列。我们还将镶嵌样排列的特征与多余骨骼的特征进行了比较。基于这些数据和现有的胚胎学知识,我们推测了多余骨骼的起源。
多余骨骼和镶嵌样排列表现出不同的特征。因此,两者被认为是完全不同的疾病。我们推测多余骨骼是由指间程序性细胞死亡前指间外胚层受损引起的。
我们遇到了一种新形式的轴后多指畸形。这可能是影响治疗策略的一个因素,因为它会影响对线和稳定性。