Results 31 to 40 of about 35,257,949 (270)

Hypoxemia, high alveolar‐arterial gradient, and bubbles in both sides of heart: A case of hepatopulmonary syndrome in the setting of COVID‐19 pandemic

open access: yesClinical Case Reports, 2021
In presence of tachypnea, digital clubbing and cyanosis in a patient with the hallmarks of chronic liver disease, hepatopulmonary syndrome should be suspected and investigated.
Javier Torres‐Valencia   +2 more
doaj   +1 more source

Hypertrophic pulmonary osteoarthropathy secondary to pulmonary malignancy: A case report

open access: yesJournal of Orthopaedic Reports, 2022
Background: Hypertrophic pulmonary osteoarthropathy is a rare type of paraneoplastic rheumatic manifestation which classically presents with bilateral, symmetrical periostitis of long bones, digital clubbing, and non-inflammatory arthritic pain and ...
Steven R. Cooperman, Raffi Salibian
doaj   +1 more source

Etoricoxib as a treatment of choice for patients with SLCO2A1 mutation exhibiting autosomal recessive primary hypertrophic osteoarthropathy: A case report

open access: yesFrontiers in Genetics, 2022
We reported a 22-year-old Emirati male with autosomal recessive primary hypertrophic osteoarthropathy caused by a possibly pathogenic homozygous non-synonymous variant in the SLCO2A1 gene (NM_005630.3: c.289C>T, p.
Areej Albawa'neh   +6 more
doaj   +1 more source

Digital clubbing may be an indicator of systemic atherosclerosis even at microvascular level [PDF]

open access: yes, 2012
WOS: 000314345000014Background: Presence of any relationship between digital clubbing and microvascular atherosclerosis was tried to be understood. Methods: Cases with digital clubbing and controls were studied. Results: The study included 104 cases with
Aydın, Yusuf   +2 more
core   +3 more sources

Cor triatriatum dexter associated to Ebstein anomaly with tricuspid double lesion and atrial septal defect

open access: yesArchivos de Cardiología de México, 2021
Female 23-year-old patient with heart murmur diagnosed in the first year of life. She attended to our institute with progressive dyspnea and palpitations of 7-month evolution. Physical examination showed perioral and distal cyanosis with digital clubbing,
Ricardo Álvarez-Santana   +4 more
doaj   +1 more source

Complete form of pachydermoperiostosis, [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2020
Pachydermoperiostosis (PDP) or primary hypertrophic osteoarthropathy (PHO) is a rare hereditary disease characterized by digital clubbing, pachydermia, and periostosis. Its pathogenesis is uncertain and the diagnosis is based on clinical and radiological
Mônica Larissa Padilha Honório   +2 more
doaj   +1 more source

Surgically cured hypoglycemia secondary to pleural solitary fibrous tumour: case report and update review on the Doege-Potter syndrome

open access: yesJournal of Cardiothoracic Surgery, 2009
The association of paraneoplastic hypoglycemia [Doege-Potter syndrome] and finger clubbing [Pierre-Marie-Bamberg syndrome] with pleural solitary fibrous tumour is rare.
Kalebi Ahmed Y   +4 more
doaj   +1 more source

Pierre Marie-Bamberger Syndrome: A unique case report

open access: yesLiaquat Medical Research Journal, 2021
Hypertrophic osteoarthropathy (HOA) was described by Friedreich in 1868. It is a rare condition with variable presentations including clubbing of the toes and fingers, arthralgia with edema, bilateral ptosis, thickening of the skin and leonine facies ...
Syed A. Abbas   +3 more
doaj  

Lung Abscess

open access: yesSouth African Family Practice, 2007
Lung abscesses are most frequently caused by mouth anaerobes and may arise as a complication of aspiration pneumonia. Patients may present with a productive cough of foul smelling sputum with or without associated digital clubbing.
C. Koegelenberg
doaj   +1 more source

A patient with pachydermoperiostosis harboring SLCO2A1 variants with a history of differentiating from acromegaly

open access: yesBone Reports, 2023
Pachydermoperiostosis (PDP) is a rare hereditary disease characterized by digital clubbing, pachydermia, and periostosis. We describe a Japanese male patient with PDP who was differentially diagnosed with acromegaly by identification of compound ...
Yukako Nakano   +5 more
doaj   +1 more source

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