Khan Iqbal Shabir, Spiro Alexander S, Rueger J M, Priemel Matthias
Department of Orthopedics and Trauma, Fujairah Government Hospital, Fujairah, United Arab Emirates.
Department of Pediatric Orthopedics, Children's Hospital Altona, AKK, Hamburg, Germany.
J Orthop Case Rep. 2018 Mar-Apr;8(2):95-99. doi: 10.13107/jocr.2250-0685.1068.
Fibrous dysplasia (FD) is an uncommon benign tumor of bone. Although FD can affect flat bones, it is rare for the scapula to be involved. In addition, little is known about the management of FD when it involves the scapula. We present possibly the first comprehensive case report of the management of advanced unilateral FD of the scapular region.
A 47-year-old male presented to us with pain and swelling over the left shoulder. The swelling was 11 cm × 15 cm × 8 cm and was hard and tender with rough texture. Radiograph showed large homogenous lesion with irregular but well-defined margins and a ground glass appearance. Magnetic resonance imaging scans showed well-defined borders with the expansion of the bone, with intact overlying cortices and endosteal scalloping. Biopsy confirmed the lesion to be FD. An innovative application of an existing surgical technique to minimize the impact of the residual deformity and dead space left after curettage of the scapula was done. The patient had good clinical and functional outcome at 6-month follow-up.
Surgical exercise in FD is purely on symptomatic basis. In our case, the swelling was causing most discomfort, and we curettaged and compressed the bony swelling which resulted in excellent outcome in this patient.
骨纤维异常增殖症(FD)是一种罕见的骨良性肿瘤。虽然FD可累及扁骨,但肩胛骨受累较为罕见。此外,对于FD累及肩胛骨时的治疗方法知之甚少。我们可能首次全面报道了肩胛区晚期单侧FD的治疗情况。
一名47岁男性因左肩疼痛和肿胀前来就诊。肿胀大小为11厘米×15厘米×8厘米,质地硬且有压痛,表面粗糙。X线片显示为大的均匀性病变,边界不规则但清晰,呈磨玻璃样外观。磁共振成像扫描显示边界清晰,骨膨胀,皮质完整,骨内膜呈扇贝样改变。活检证实病变为FD。我们创新性地应用了一种现有手术技术,以尽量减少肩胛骨刮除术后残留畸形和死腔的影响。患者在6个月随访时临床和功能结果良好。
FD的手术治疗完全基于症状。在我们的病例中,肿胀引起了最大的不适,我们对骨肿胀进行了刮除和加压处理,该患者取得了极佳的效果。