Sivathapandi Thangalakshmi, Amalachandran Jaykanth, Simon Shelley, Elangovan Indirani
Department of Nuclear Medicine and PET-CT, Apollo Hospitals, Chennai, Tamil Nadu, India.
Indian J Nucl Med. 2018 Apr-Jun;33(2):128-131. doi: 10.4103/ijnm.IJNM_134_17.
The primary hypertrophic osteoarthropathy (PHOA) (pachydermoperiostosis) is a rare genetic/hereditary disease characterized by skin changes (pachydermia), clubbing of fingers and periosteal thickening (periostitis) with sub-periosteal new bone formation. Here we describe a case of an adolescent male who presented with clubbing and polyarthralgia. On evaluation with scintigraphy and SPECT-CT, he was diagnosed to have incomplete form of PHOA(skeletal manifestations without skin changes). The identification of incomplete form of primary hypertrophic osteoarthropathy which can be easily misdiagnosed as rheumatoid arthritis is discussed here.
原发性肥厚性骨关节病(PHOA)(厚皮性骨膜病)是一种罕见的遗传/遗传性疾病,其特征为皮肤改变(厚皮症)、手指杵状指和骨膜增厚(骨膜炎)伴骨膜下新骨形成。在此,我们描述一例青少年男性病例,其表现为杵状指和多关节痛。经骨闪烁显像和SPECT-CT评估,他被诊断为不完全型PHOA(无皮肤改变的骨骼表现)。本文讨论了原发性肥厚性骨关节病不完全型的识别,其易被误诊为类风湿关节炎。