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Primary hypertrophic osteoarthropathy

Rheumatology International, 2010
Pachydermoperiostosis PDP (idiopathic or primary hypertrophic osteoarthropathy) is a rare congenital disease that inherited in an autosomal fashion. The disease is more common in males and develops gradually from adulthood. The disease is characterized by coarse facial features, clubbing of the fingers and radiographic periostitis of the distal long ...
Hadi, Poormoghim   +2 more
exaly   +3 more sources

Primary hypertrophic osteoarthropathy with myelofibrosis

Rheumatology International, 2007
Primary hypertrophic osteoarthropathy or pachydermoperiostosis is a rare congenital disease characterized by clubbing of the fingers, periostitis of the distal long bones, and hypertrophic skin changes (pachydermia) including thick folds in the skin of the face, forehead, scalp and extremities, and also joint pain.
Massoud Saghafi
exaly   +3 more sources

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   +2 more
exaly   +3 more sources

Hypertrophic osteoarthropathy and primary intestinal lymphoma

Gastrointestinal Radiology, 1986
Hypertrophic osteoarthropathy (HOA) in association with primary bowel disease is rare, but is usually seen in patients with chronic diarrheal states, such as Crohn's disease and ulcerative colitis. We record the first case of HOA associated with primary intestinal lymphoma in a patient who presented with chronic diarrhea.
R A, Bloom   +3 more
openaire   +2 more sources

Hypertrophic osteoarthropathy in primary liver rhabdomyosarcoma

Pediatric Radiology, 2004
Hypertrophic osteoarthropathy is a well-documented paraneoplastic phenomenon in adults. It is a rare, but important finding in children with malignant disease as it can indicate prognosis. We present a case of hypertrophic osteoarthropathy associated with primary liver rhabdomyosarcoma in a 14-year-old boy.
Timothy R, Geary   +2 more
openaire   +2 more sources

Cutaneous Fibrinolytic Activity in Primary Hypertrophic Osteoarthropathy

Scandinavian Journal of Rheumatology, 1987
Cutaneous fibrinolytic activity was investigated in 13 patients affected with Primary Hypertrophic Osteoarthropathy in the advanced phase. Biopsies were taken from periungueal skin of the ippocratic finger and from the dorsum of the first phalanx: cutaneous fibrinolytic activity was investigated with Todd's autohistographic method as modified by Lotti ...
MATUCCI CERINIC, MARCO   +5 more
openaire   +3 more sources

Primary Hypertrophic Osteoarthropathy

New England Journal of Medicine, 2022
Naveen Yadav, Uday Yanamandra
openaire   +2 more sources

Primary hypertrophic osteoarthropathy (pachydermoperiostosis): a case report

Rheumatology International, 2006
Hypertrophic osteoarthropathy is characterized by digital clubbing and periosteal reaction of long bones. Most cases are associated with malignancy or other conditions such as congenital heart disease, liver cirrhosis, pulmonary fibrosis, biliary atresia, and gastrointestinal polyps.
Murat, Karkucak   +5 more
openaire   +2 more sources

Primary hypertrophic osteoarthropathy: ultrasound and MRI findings

Pediatric Radiology, 2016
Primary hypertrophic osteoarthropathy is a rare genetic disorder related to failures in prostaglandin metabolism. Patients present with joint pain, limb enlargement, skin thickening and finger clubbing. Radiographs show characteristic periosteal reaction and thickening along the long bones.
Brook, Adams   +4 more
openaire   +2 more sources

[Primary hypertrophic osteoarthropathy].

Zeitschrift fur Orthopadie und ihre Grenzgebiete, 1995
A case of the very rare primary-hypertrophic-osteoarthropathy (Touraine-Solente-Golé-Syndrome) is reported. A middle-aged women was suffering from chronic joint- and limb-pain for more than twenty years. All diagnostical experiences only showed a cortical thickening mainly of the tubular bones and a craniosclerosis but no link for the possible origin ...
A, Eckardt, K F, Kreitner
openaire   +1 more source

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