Department of Dermatology, Chang Gung Memorial Hospital, Linkou, Taoyuan, Taiwan.
College of Medicine, Chang Gung University, Taiwan.
J Musculoskelet Neuronal Interact. 2022 Jun 1;22(2):292-295.
Buschke-Ollendorff syndrome (BOS) is a rare, usually benign, autosomal dominant genetic disease affecting about 0.005% globally. BOS commonly manifests with asymptomatic connective tissue nevi, sometimes with sclerotic bone lesions like osteopoikilosis or melorheostosis. However, BOS may develop severe, symptomatic complications that require surgical intervention. Here we report a 9-year-8-month girl presenting with multiple nonpruritic, nonpainful skin plaques scattered around the trunk, buttocks, and bilateral legs. She had a history of right varus foot with inadequate plantar flexion. Upon visiting, obvious leg length discrepancy (LLD) was noted. Lesional biopsy revealed increased fibroblasts within dermal collagen bundles. Verhoeff-van Gieson stain revealed scattered foci of thickened elastic fibers between collagen fibers, especially in the mid-dermis. Radiographic examination of the lower extremities showed multiple small, round-to-oval shaped, radiopaque spots on the pelvic bones, femurs, tibiae, and both feet. Hyperostosis along the long axis with "dripping candle wax" appearance was characteristic of osteopoikilosis and melorheostosis. Genetic analysis showed heterozygous point mutation in exon 1 of LEMD3 gene (c.1323C>A, p.Y441X), confirming diagnosis of BOS. Sequential and epiphyseodesis were performed to correct LLD with a favorable outcome at 2-year follow-up. BOS associated with severe bone abnormalities is rare, but orthopedic surgical intervention can provide satisfactory outcome.
布希科-奥尔伦多夫综合征(BOS)是一种罕见的、通常良性的常染色体显性遗传疾病,全球发病率约为 0.005%。BOS 常表现为无症状的结缔组织痣,有时伴有硬化性骨病变,如骨斑点症或硬化性骨髓炎。然而,BOS 可能会发展出严重的、有症状的并发症,需要手术干预。我们在此报告一例 9 岁 8 个月的女孩,其躯干、臀部和双侧腿部散在多发性无瘙痒、无痛性皮肤斑块。她曾有右侧足内翻伴足底屈肌功能不足的病史。就诊时,明显存在下肢不等长。皮损活检显示真皮胶原束内纤维母细胞增多。Verhoeff-van Gieson 染色显示胶原纤维间有散在的增粗弹性纤维灶,尤以中真皮层为著。下肢的影像学检查显示骨盆、股骨、胫骨和双脚上有多个小的、圆形至椭圆形的不透射线斑点。沿长轴的骨质增生呈“蜡烛滴蜡”样外观,具有骨斑点症和硬化性骨髓炎的特征。基因分析显示 LEMD3 基因外显子 1 存在杂合点突变(c.1323C>A,p.Y441X),确诊为 BOS。行序贯和骺融合术矫正下肢不等长,2 年随访时取得了良好的结果。BOS 合并严重的骨骼异常较为罕见,但矫形外科手术干预可获得满意的结果。