Results 41 to 50 of about 2,266 (189)
Reverse frontal lifting: alternative for the treatment of pachydermoperiostosis [PDF]
Introduction: Patient diagnosed with pachydermoperiostosis, presenting a strong cutaneous manifestation, making it impossible to correct the defect by the usual facial lifting techniques.
Ronaldo Pontes +4 more
doaj +1 more source
Pachydermodactyly is a rare and benign form of acquired digital fibromatosis characterized by the expansion of soft tissue around proximal phalanges and interphalangeal joints.
Camila Bueno Requena +3 more
doaj +1 more source
Pachydermoperiostosis as a Rare Cause of Blepharoptosis
A 37-year-old male patient diagnosed with pachydermoperiostosis at another center came to our clinic to rectify his blepharoptosis. The physical examination of the patient revealed skeleton and skin symptoms typical for pachydermoperiostosis.
Özlem Yalçın Tök +5 more
doaj +1 more source
Pachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy (PHO), also known as the Touraine–Solente–Gole syndrome, is an autosomal dominant genetic disorder that is rare and is identified by finger clubbing, skin thickening, and periosteal ...
Fatima Khurshid +3 more
doaj +9 more sources
Primary Hypertrophic Osteoarthropathy with Gastric Hypertrophy [PDF]
Primary hypertrophic osteoarthropathy (HOA) is a rare congenital disease that is not well recognized. Gastric hypertrophy will be infrequently involved; only 3 case reports describe this scarce manifestation in the English-language literature1,2,3. A 19-year-old Chinese male presented with a 4-year history of thickened skin and joint pain and swelling.
Sun, Xue-Feng +10 more
openaire +3 more sources
SECONDARY HYPERTROPHIC OSTEOARTHROPATHY (PIERRE MARIE–BAMBERGER SYNDROME)
This article describes a clinical case of a cancer patient with secondary hypertrophic osteoarthropathy (Pierre Marie–Bamberger syndrome). The patient underwent complex examination including bone scan, X-ray, computed tomography and magnetic resonance ...
A. S. Krylov +8 more
doaj +1 more source
Herbst’s Triad as a Manifestation of Gastroesophageal Reflux Disease [PDF]
The Herbst triad (HT) was described in 1976 by Herbst et al. (1) when detecting the association of iron deficiency anemia, hypoalbuminemia and clubbing in 3 children with hiatal hernia and severe esophagitis secondary to gastroesophageal reflux (GER ...
Blasco Alonso, Javier +6 more
core +1 more source
Pachydermoperiostosis-Like Disease In Captive Red Ruffled Lemurs (Varecia Variegatus Rubra) [PDF]
Pachydermatoperiostosis, a rare form of hypertrophic osteoarthropathy, is of unknown etiology and previously thought limited to humans. The only periosteal reaction previously reported in prosimians is related to renal disease.
Bruce Rothschild +2 more
core +1 more source
Lung carcinoma with hypertrophic osteoarthropathy in a teenager [PDF]
Hypertrophic osteoarthropathy (HOA) characterised by arthralgia, clubbing and periosteal proliferation of long bones, is rarely encountered in children and adolescents.
Al-Qahtani AR +22 more
core +3 more sources
Диференційна діагностика гіпертрофічної остеоартропатії (огляд літератури та власне спостереження) [PDF]
У статті узагальнено дані літератури щодо диференційної діа- гностики вторинної та первинної гіпертрофічної остеартропатії. Продемонстровано клінічний випадок запізнілої діагностики рідкісного варіанта гіпертрофічної остеоартропатії ...
Bushman, Svitlana Vasylivna +29 more
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