Krugh Marissa, Vaidya Prabhakar N.
Campbell University
Campbell University School of OM
Hypertrophic osteoarthropathy (HOA) consists of digital clubbing, increased periosteal activity of the tubular bones, arthralgias, and joint effusion. It is characterized by abnormal proliferation of the skin, soft tissues, and osseous tissues in the distal parts of extremities. There are 2 forms of the disease, primary and secondary. Primary HOA (PHO), also called pachydermoperiostosis, comprises digital clubbing, periostosis, and pachydermia and is a rare genetic disease. At the same time, secondary hypertrophic osteoarthropathy is associated with a variety of pulmonary, cardiac, and other conditions. Clubbing is among the oldest signs in clinical medicine, first described in a man with curved fingernails and empyema by Hippocrates (460 BC-370 BC). Friedreich was the first to scientifically describe primary hypertrophic osteoarthropathy in 1868 as "hyperostosis of the entire skeleton" in 2 affected brothers. In 1935, Touraine, Solente, and Gole distinguished PHO as the primary form of HOA and distinct from HOA associated with an underlying disease like pulmonary or cardiac disease.
肥厚性骨关节病(HOA)包括杵状指、管状骨骨膜活动增加、关节痛和关节积液。其特征是四肢远端皮肤、软组织和骨组织异常增殖。该病有两种形式,原发性和继发性。原发性HOA(PHO),也称为厚皮性骨膜病,包括杵状指、骨膜增生和厚皮症,是一种罕见的遗传病。同时,继发性肥厚性骨关节病与多种肺部、心脏和其他疾病有关。杵状指是临床医学中最古老的体征之一,最早由希波克拉底(公元前460年 - 公元前370年)在一名患有弯曲指甲和脓胸的男子中描述。1868年,弗里德赖希首次科学地将原发性肥厚性骨关节病描述为两名患病兄弟中的“全身骨骼骨质增生”。1935年,图赖讷、索伦特和戈尔将PHO区分出来,作为HOA的主要形式,并与与肺部或心脏疾病等潜在疾病相关的HOA区分开来。