Blauth W, Borisch N C
Orthopädische Universitätsklinik Kiel, Federal Republic of Germany.
Clin Orthop Relat Res. 1990 Sep(258):41-8.
The authors studied 45 cleft feet from among their patients and 128 from the literature with regard to their roentgenographic morphology. An increasing degree of malformation was found, from deepening of a central interdigital commissure to a monodactylous cleft foot. These observations resulted in a classification of six groups based on the number of metatarsal bones. Types I and II are cleft feet with minor deficiencies, both having five metatarsals. The metatarsals are all normal in Type I and partially hypoplastic in Type II. As the degree of malformation increases, only four metatarsals in Type III, three metatarsals in Type IV, and two metatarsals in Type V can be identified. Type VI represents the monodactylous cleft foot. Of the 173 feet studied, 166 could be assigned to one of these types. Two additional forms were also found: four cleft feet with central polydactyly are described as polydactylous type, and three monodactylous feet with lower-leg diastasis or tibial aplasia or both are described as diastatic type. According to the distribution of syndactylies, synostoses, and aplasias, it became evident that cleft formation begins at the second or third ray. It then proceeds in a longitudinal direction from distal to proximal as well as in a transverse direction from tibial to fibular, while the first ray remains intact. The first ray is only missing in the monodactylous cleft foot, which possesses only the fifth ray. The defects are always larger distally than proximally. Synostoses are found only at the margin of the cleft. Cross-bones are rare and usually occur in mild cases of the deformity. Another rare feature is polydactyly.(ABSTRACT TRUNCATED AT 250 WORDS)
作者研究了他们自己患者中的45例裂足以及文献中的128例裂足的X线形态。发现畸形程度不断增加,从中央趾间缝加深到单指裂足。这些观察结果基于跖骨数量将其分为六组。I型和II型是轻度缺陷的裂足,两者都有五根跖骨。I型跖骨全部正常,II型部分发育不全。随着畸形程度增加,III型可识别出四根跖骨,IV型三根跖骨,V型两根跖骨。VI型代表单指裂足。在研究的173只足中,166只可归入这些类型之一。还发现了另外两种形式:4例中央多指的裂足被描述为多指型,3例伴有小腿间隙或胫骨发育不全或两者皆有的单指足被描述为间隙型。根据并指、骨性连接和发育不全的分布情况,很明显裂足形成始于第二或第三跖骨。然后它从远端向近端纵向发展,同时从胫骨向腓骨横向发展,而第一跖骨保持完整。第一跖骨仅在单指裂足中缺失,单指裂足仅拥有第五跖骨。缺损总是远端比近端大。骨性连接仅见于裂足边缘。交叉骨罕见,通常发生在畸形较轻的病例中。另一个罕见特征是多指。(摘要截短至250字)