Results 51 to 60 of about 2,266 (189)

Solitary Fibrous Tumour of the Pleura and Paraneoplastic Symptoms:A Case Report and Literature Review [PDF]

open access: yes, 2017
Background: Solitary Fibrous Tumors of the Pleura (SFTP) are rare neoplasms deriving from mesenchymal cells. They are mostly benign and may be accompanied by paraneoplastic syndromes, particularly hypoglycaemia and hypertrophic pulmonary osteoarthropathy
Braathen, Alexander, Bødtger, Uffe
core   +1 more source

Solitary Fibrous Tumor of the Pleura Presenting as a Giant Thoracic Mass: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Solitary fibrous tumors of the pleura are rare and may present as large thoracic masses. Timely imaging and histopathological confirmation are essential for accurate diagnosis and effective surgical management.
Zahra Sadin   +8 more
wiley   +1 more source

Pachydermoperiostosis or primary hypertrophic osteoarthropathy: A rare clinicoradiologic case

open access: yesIndian Journal of Radiology and Imaging, 2009
Pachydermoperiostosis (PDP) or primary hypertrophic osteoarthropathy is a rare syndrome with diverse radiological and clinical features. Though the diagnosis can be made on the basis of the classic clinical and radiological features, it is often missed ...
Rajul Rastogi   +5 more
doaj   +1 more source

A case of finger clubbing associated with nasopharyngeal carcinoma in a young girl, and review of pathophysiology [PDF]

open access: yes, 2009
Hypertrophic osteoarthropathy is characterized by clubbing of the digital tips and periosteal reaction of long bones. Most of the cases are associated with malignancy or other conditions such as congenital heart disease, liver cirrhosis, pulmonary ...
Abbasi, Ahmed Nadeem   +5 more
core   +1 more source

Osteoartropatia hipertrófica associada a linfoepitelioma de nasofaringe: relato de caso [PDF]

open access: yes, 2012
Malignant neoplasms of the nasopharynx are very rare and has two peaks of incidence: below the age of 30, and between the 4th and 5th decade of life. It is, however, uncommon after the 60 years of age.
Cotrim, Deborah P.   +1 more
core   +2 more sources

Primary Hypertrophic Osteoarthropathy (Pachydermoperiostosis): Two Brothers Misdiagnosed As Inflammatory Arthritis

open access: yesTrends in Urology &Men's Health, Volume 16, Issue 4, August 2025.
ABSTRACT Primary hypertrophic osteoarthropathy (Pachydermoperiostosis) is a rare, inherited genetic disorder of the skeleton and the skin, characterised by clubbing of the fingers, thickening of the skin especially of the face and forehead (pachydermia) and periostosis. Patients often present with pain and swelling of the knees and ankles.
Ahmed AbdulBari   +3 more
wiley   +1 more source

Touraine-Solente-Gole Syndrome: A Rare Case Report

open access: yesDelhi Journal of Ophthalmology, 2017
Touraine-Solente-Gole Syndrome, also known as Pachydermoperiostosis (PDP) or Primary Hypertrophic Osteoarthropathy, is a rare hereditary disorder, which affects both bones and skin.
Dharmil Doshi   +2 more
doaj   +1 more source

Osteoartropatía hipertrófica pulmonar asociada a megaesófago en un perro [PDF]

open access: yes, 1995
La osteoartropatía hipertrófica pulmonar (OHP) es una enfermedad de escasa presentación en la clínica rutinaria canina, secundaria a patologías intratorácicas crónicas, con lesiones que ocupan un cierto volumen intratorácico (neoplasias, abscesos, etc.),
Mayoral, I.   +5 more
core  

A Case Study of a Female Infant With Primary Hypertrophic Osteoarthropathy Demonstrates That Early Initiation of Celecoxib Slows but Does Not Prevent Symptom Progression

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 5, May 2025.
ABSTRACT Primary Hypertrophic Osteoarthropathy (PHOAR1) is characterized by autosomal recessive loss of function variants in 15‐hydroxyprostaglandin dehydrogenase (HPGD) leading to digital clubbing, periostosis, pachydermia, and severe hyperhidrosis. HPGD catalyzes the first step of prostaglandin E2 (PGE2) degradation.
Kara Zehr   +6 more
wiley   +1 more source

Touraine–Solente–Gole syndrome: Clinical manifestation with bilateral true eyelid ptosis

open access: yesJPRAS Open, 2019
Touraine–Solente–Gole syndrome (pachydermoperiostosis [PDP] or primary idiopathic hypertrophic osteoarthropathy [HOA]) is a rare hereditary disorder that is characterized by a triad of manifestations that consists of skin changes (pachydermia), abnormal ...
Nutthawut Akaranuchat   +1 more
doaj   +1 more source

Home - About - Disclaimer - Privacy