Goldfarb Charles A, Wall Lindley, Manske Paul R
Department of Orthopaedic Surgery, Washington University School of Medicine, Barnes-Jewish Hospital, St. Louis, MO 63110, USA.
J Hand Surg Am. 2006 Sep;31(7):1176-82. doi: 10.1016/j.jhsa.2006.05.012.
Radial longitudinal deficiency (RLD) is associated with certain syndromes and medical and musculoskeletal conditions. The purpose of this investigation was to evaluate the incidence of these conditions with RLD.
A comprehensive chart review identified patients with RLD and a complete medical record. These charts were evaluated for the presence of associated medical and musculoskeletal conditions and biographic information on gestation, delivery, and family history.
A total of 164 patients with 245 affected extremities were identified; 138 patients had radius abnormalities and 26 patients had isolated thumb hypoplasia. Twenty-five patients had thrombocytopenia absent radius syndrome; 22 patients had vertebral, anal, cardiac, tracheoesophageal, renal, and limb abnormalities association; 7 patients had Holt-Oram syndrome; and 1 patient had Fanconi anemia. There were 32 patients with cardiac abnormalities and 60 patients with spinal or lower-extremity musculoskeletal abnormalities. The percentage of patients with associated abnormalities increased with an increasing severity of RLD. One hundred two of the 138 patients with types I through V RLD had associated medical or musculoskeletal abnormalities. In contrast, only 9 of 26 patients with an isolated thumb hypoplasia (type 0 RLD) had associated abnormalities.
The high incidence of associated medical and musculoskeletal abnormalities in patients with RLD emphasizes the importance of a complete assessment including a complete musculoskeletal examination, cardiac auscultation, complete blood count, echocardiogram, renal ultrasound, and spinal radiographs. Although approximately one third of patients in this investigation had a syndrome commonly associated with RLD, most patients with RLD types I through V had an additional medical or musculoskeletal anomaly. Patients with type 0 RLD were less likely to have comorbidities.
桡骨纵列发育不全(RLD)与某些综合征以及医学和肌肉骨骼疾病相关。本研究的目的是评估这些疾病在RLD患者中的发生率。
通过全面查阅病历确定患有RLD且有完整医疗记录的患者。对这些病历进行评估,以确定是否存在相关的医学和肌肉骨骼疾病以及有关妊娠、分娩和家族史的传记信息。
共确定了164例患者,涉及245个受累肢体;138例患者有桡骨异常,26例患者有孤立性拇指发育不全。25例患者患有血小板减少症伴桡骨缺失综合征;22例患者患有脊柱、肛门、心脏、气管食管、肾脏和肢体异常综合征;7例患者患有 Holt-Oram 综合征;1例患者患有范可尼贫血。有32例患者存在心脏异常,60例患者存在脊柱或下肢肌肉骨骼异常。伴有异常的患者百分比随着RLD严重程度的增加而增加。138例I至V型RLD患者中有102例伴有相关的医学或肌肉骨骼异常。相比之下,26例孤立性拇指发育不全(0型RLD)患者中只有9例伴有异常。
RLD患者中相关医学和肌肉骨骼异常的高发生率强调了进行全面评估的重要性,包括完整的肌肉骨骼检查、心脏听诊、全血细胞计数、超声心动图、肾脏超声检查和脊柱X线片检查。尽管本研究中约三分之一的患者患有通常与RLD相关的综合征,但大多数I至V型RLD患者还有其他医学或肌肉骨骼异常。0型RLD患者合并症的可能性较小。