Freyschmidt J, Kasperczyk A
Z Rheumatol. 1997 May-Jun;56(3):136-43. doi: 10.1007/s003930050029.
27 patients with sternocostoclavicular hyperostosis (SCC) and/or pustulotic arthroosteitis (PAO) were examined with whole body scintigraphy, conventional radiography, and other imaging modalities, such as CT, MRI. 25 of 27 patients with SCCH showed a characteristic high bullhorn-like uptake of the sternocostoclavicular region with the manubrium sterni representing the skull and the inflamed sternocostoclavicular joints corresponding to the horns (= bullhorn-sign). Scintigraphy revealed additional skeletal manifestations (spondylitis, sacroilitis, osteitis, periostitis) in 19 of the 27 patients with SCCH and/ or PAO. In combination with PPP or psoriasis pustulosa, the typical scintigraphic bullhorn pattern enables the diagnosis of PAO (19 patients) with high confidence. Patients with SCCH but without skin disease at the time of presentation (8 of 27 patients) may develop PPP later and, therefore, it is justified to classify them as incomplete PAO with high risk to develop other skeletal manifestations later in the course of the disease.
对27例胸锁关节骨质增生(SCC)和/或脓疱性关节骨炎(PAO)患者进行了全身骨闪烁显像、传统X线摄影以及CT、MRI等其他影像学检查。27例SCC患者中有25例在胸锁关节区域显示出特征性的高牛角样摄取,其中胸骨柄代表头部,发炎的胸锁关节对应牛角(即牛角征)。骨闪烁显像显示,27例SCC和/或PAO患者中有19例存在其他骨骼表现(脊柱炎、骶髂关节炎、骨炎、骨膜炎)。结合掌跖脓疱病(PPP)或脓疱性银屑病,典型的骨闪烁显像牛角样表现有助于高度准确地诊断PAO(19例患者)。就诊时患有SCC但无皮肤病的患者(27例患者中的8例)可能随后会发展为PPP,因此,将他们归类为不完全PAO是合理的,因为他们在疾病后期有发生其他骨骼表现的高风险。