Results 221 to 230 of about 89,083 (252)

Primary hypertrophic osteoarthropathy: an update

Frontiers of Medicine, 2013
Digital clubbing, which has been recognized as a sign of systemic disease, is one of the most ancient diseases. However, the pathogenesis of clubbing and hypertrophic osteoarthropathy has hitherto been poorly understood. The study of a clinically indistinguishable idiopathic form (primary hypertrophic osteoarthropathy, PHO) provides an opportunity to ...
Zeng Zhang, Zhen-Lin Zhang, Changqing Zhang   +2 more
openaire   +3 more sources

Hypertrophic Osteoarthropathy in a Patient With Primary Hepatic Angiosarcoma.

Clinical Nuclear Medicine, 2019
Primary hepatic angiosarcoma was diagnosed in a 59-year-old woman who presented an arthralgia of limbs and dry cough for 6 weeks. Physical examination revealed digital clubbing.
Jun Zhang, Meng-jie Dong, Zhanxiong Yi, Congcong Yu   +3 more
semanticscholar   +1 more source

Clubbing and Hypertrophic Osteoarthropathy

New England Journal of Medicine, 1993
Figure 1. Clubbing and Hypertrophic Osteoarthropathy. On examination the hands of a 70-year-old woman with worsening cough and pretibial pain show digital clubbing (Panel A). The terminal phalanges are enlarged, and there is loss of the normal nail-to-cuticle angle.
Kim Eagle, Melvin D. Burton, John C. Wain   +2 more
openaire   +2 more sources

IDIOPATHIC CLUBBING AND HYPERTROPHIC OSTEOARTHROPATHY

Archives of Internal Medicine, 1956
To the Editor: —This letter is in explanation of an error in our paper "Idiopathic Clubbing and Hypertrophic Osteoarthropathy," which appeared in the March, 1956, issue of theArchives. Since publication of our paper our attention has been drawn to discrepancies in the data.
Delbert Buchman, Edward A. Hrowat
openaire   +3 more sources

Hypertrophic Osteoarthropathy Associated With Pancoast Tumor: Do Not Miss Secondary Hypertrophic Osteoarthropathy!

Journal of clinical rheumatology, 2023
Hirotaka Yamamoto, Y. Taniguchi
semanticscholar   +1 more source

Hypertrophic Osteoarthropathy

Musculoskeletal Imaging Volume 1, 2019
Chapter 69 discusses hypertrophic osteoarthropathy (HOA), which is a clinical triad of periostitis, digital clubbing, and swollen joints. When caused by an underlying pulmonary disease, it is termed hypertrophic pulmonary osteoarthropathy (HPOA). HPOA is
N. Belkind, A. Zoga
semanticscholar   +1 more source

Hypertrophe Osteoarthropathie

Zeitschrift für Rheumatologie, 2011
Hypertrophic osteoarthropathy (HOA) is the classical neoplastic disease in rheumatology characterized by a combination of digital clubbing, joint and bone pain, and proliferative periostitis. This combination of symptoms should initiate an intensive search for an underlying malignant disease usually of thoracic organs.
A. Lindner, Georg Schett, B. Manger, K. Manger, J. Wacker   +4 more
openaire   +5 more sources

The Features and Significance of Hypertrophic Osteoarthropathy

Archives of Internal Medicine, 1957
Introduction Hypertrophic osteoarthropathy is usually accompanied by clubbed fingers and commonly by arthralgia, bone pain, enlargement of the hands and feet, thickening of the wrists and ankles, and gynecomastia. Although it is relatively common, some physicians are not familiar with the syndrome. Cases are sometimes misdiagnosed as acromegaly, Paget'
James F. Hammarsten, John O'leary
openaire   +3 more sources

[Identification of a HPGD mutation in three families affected with primary hypertrophic osteoarthropathy].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 2018
OBJECTIVE To detect mutation of HPGD gene among three pedigrees affected with primary hypertrophic osteoarthropathy (PHO) by DNA sequencing and high-resolution melting (HRM) analysis.
Wanying Zhang, Tao Wang, Shuaiwu Huang, Xiuli Zhao   +3 more
semanticscholar   +1 more source

Cranio-osteoarthropathy: a rare variant of hypertrophic osteoarthropathy

Irish Journal of Medical Science, 2009
To highlight the clinical features and diagnosis of cranio-osteoarthropathy, an extremely rare disease.Case report and literature review.A 2.3-year-old child presented with mild swelling of his distal phalanges at the age of 5 months that became pronounced gradually. His parents were consanguineous and his 14-year-old sister had albinism.
Chao-chun Zou, Zhengyan Zhao, Xiaochun Chen, G P Dong, Li Liang   +4 more
openaire   +2 more sources