Results 1 to 10 of about 82,917 (137)

Primary hypertrophic osteoarthropathy – a rare cause of pain and arthritis in children. Description of 5 cases [PDF]

open access: yesCentral European Journal of Immunology, 2022
Primary hypertrophic osteoarthropathy (PHOA) is a very rare disease. The typical triad of symptoms, i.e. digital clubbing, periosteal bone formation with bone and joint deformities and skin hypertrophy, may be accompanied by other specific conditions. In
Joanna Wójtowicz   +3 more
doaj   +3 more sources

Hypertrophic osteoarthropathy associated with lung cancer: Possible links among hypoxia‐inducible factor‐1α, vascular endothelial growth factor, and hypervascularization [PDF]

open access: yesThoracic Cancer, 2023
Hypertrophic osteoarthropathy (HOA) is a paraneoplastic syndrome, the exact pathogenesis of which remains to be elucidated. The case of a 69‐year‐old man who developed intractably painful HOA secondary to lung cancer is presented.
Ryuta Tagawa   +12 more
doaj   +3 more sources

Hypertrophic Osteoarthropathy: A Secondary Manifestation of Malignant Melanoma

open access: yesCase Reports in Rheumatology, 2021
Background. Hypertrophic osteoarthropathy (HOA) is a rare finding in the setting of metastatic melanoma. A majority of cases of secondary HOA involve lung malignancies.
Shiva Malaty, Aditya Gupta
doaj   +2 more sources

Hypertrophic Osteoarthropathy: A Case of an Undifferentiated Polyarthritis. [PDF]

open access: yesCureus, 2023
Hypertrophic osteoarthropathy is a paraneoplastic syndrome and is considered an important secondary cause of rheumatic disease. It typically manifests as tibial and femoral bone pain, with arthralgia or synovitis of adjacent joints also being common ...
Carvalho MM, Raimundo S.
europepmc   +2 more sources

HYPERTROPHIC OSTEOARTHROPATHY IN A PATIENT WITH HETEROZYGOUS MUTATION IN THE SLCO2A1 GENE: A CASE REPORT

open access: yesCentral Asian Journal of Medical Hypotheses and Ethics, 2023
Hypertrophic osteoarthropathy (HOA) is a condition characterized by aberrant skin and osseous tissue proliferation in the distal extremities. Mutations in the 15-hydroxyprostaglandin dehydrogenase gene (HPGD) and the soluble carrier organic anion carrier
Ilke Coskun Benlidayi   +2 more
doaj   +2 more sources

Hypertrophic Osteoarthropathy Mimicking Rheumatoid Arthritis. [PDF]

open access: yesCureus
Paraneoplastic rheumatologic syndromes encompass a range of clinical conditions that mimic primary rheumatic diseases and occur in the context of malignancy. Hypertrophic osteoarthropathy (HOA) is a notable example of such a syndrome, which is frequently
Abid A, Nawaz U, Sunmboye KO.
europepmc   +2 more sources

Case report: Schizophrenia and hypertrophic osteoarthropathy, a rare syndrome hiding a life‐threatening condition

open access: yesClinical Case Reports, 2022
Schizophrenia is associated to somatic disorders especially cardio‐vascular and auto‐immune. Through this case report, we describe an association with hypertrophic osteoarthropathy (HPO).
Emna Baklouti   +3 more
doaj   +2 more sources

Case of Hypertrophic Osteoarthropathy (HOA) in a Female Burial from the Cathedral Hill Necropolis in Vyazma (Late XIII c. AD)

open access: yesНижневолжский археологический вестник, 2023
The necropolis at the Cathedral Hill in Vyazma is mainly dated to the late 13th c. AD, and likely contains burials of the citizens of a high social status.
Andrey A. Evteev, Anna A. Tarasova
doaj   +2 more sources

Possible Causes of Hypertrophic Osteoarthropathy in the La Ferrassie 1 Neanderthal. [PDF]

open access: yesCureus, 2023
For over a century, researchers have been perplexed by the unique osteological findings on La Ferrassie 1 (LF1), one of the most complete Neanderthal remains ever found.
Turner MD.
europepmc   +2 more sources

Touraine-Solente-Gole syndrome: pathogenic variant in SLCO2A1 presented with polyarthralgia and digital clubbing [PDF]

open access: yesPediatric Rheumatology Online Journal, 2023
Background Primary Hypertrophic Osteoarthropathy (PHO), also known as Touraine-Solente-Gole Syndrome, is a rare, multisystemic autosomal recessive disorder caused by pathogenic variants in the 15-hydroxyprostaglandin dehydrogenase (HPGD) or Solute ...
Rafaela Nicolau   +7 more
doaj   +2 more sources

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