Results 161 to 170 of about 926 (179)
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Myelofibrosis in a patient with pachydermoperiostosis

Clinical and Experimental Dermatology, 2005
Pachydermoperiostosis (idiopathic or primary hypertrophic osteoarthropathy) is a rare condition of unknown origin involving the skin and the skeleton, with an autosomal dominant transmission. We report a case of anaemia in a patient with pachydermoperiostosis indicating myelofibrosis, and review the literature and the pathogenetic mechanisms.
C. Bachmeyer   +3 more
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PACHYDERMOPERIOSTOSIS

Acta Medica Scandinavica, 1970
Abstract. The report concerns pachydermoperiostosis in two women, mother and daughter, a relationship which has never before been noted. Another unusual aspect is that the characteristic features of the condition were noted already at the birth of the daughter. Moreover both have had symptoms of disturbed gonadal function.
openaire   +2 more sources

Pachydermoperiostosis-Clinical Spectrum

Archives of Internal Medicine, 1965
PACHYDERMOPERIOSTOSIS (idiopathic hypertrophic osteoarthropathy) is characterized by digital clubbing, periosteal bone changes, furrowing of the skin, and sebaceous gland overactivity.1The fully developed case is easily recognized if there is an awareness of this entity.
Murray Sachs   +3 more
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Ptosis Caused by Pachydermoperiostosis

Annals of Plastic Surgery, 2002
A 39-year-old man with pachydermoperiostosis is presented. He had enlarged, thickened upper eyelids that made it difficult for him to open his eyes. Eyelid correction was performed by resecting the excessive skin and orbicularis muscle in a fusiform shape and shortening the levator aponeurosis by plication. A wedge resection of the lateral third of the
M. Akif Karan   +4 more
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Eyelid Reconstruction in Pachydermoperiostosis

Plastic and Reconstructive Surgery, 1988
Our experience with an unusual case of pachydermoperiostosis is described. This case was accompanied by enlargement of the eyelids, excessive secretions, and difficulty in opening the eyes. Partial and serial excisions of the upper and lower eyelids were done to correct the thickened eyelids.
Morimasa Ohtsuka, Susumu Takayanagi
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A case of pachydermoperiostosis associated with arthritis

Modern Rheumatology, 2003
Abstract Pachydermoperiostosis (PDP) is characterized by clubbing fingers, furrowing of the facial skin, and perio-steal hypertrophy. We report a case of a patient with PDP associated with severe arthritis of the knee and ankle joints. His serum C-reactive protein (CRP) levels were increased, and an analysis of serum and synovial fluid showed high ...
Hiroyuki Shindo   +2 more
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Pachydermoperiostosis: The value of molecular diagnosis

Annales de Dermatologie et de Vénéréologie, 2017
Pachydermoperiostosis is a rare autosomal recessive genetic disorder characterized by the association of periostosis and pachydermia. To date, two genes involved in prostaglandin metabolism, HPGD and SLCO2A1, have been identified.A 7-year-old girl presented digital clubbing of the hands and feet, curved nails, hyperhidrosis, and pachydermia, as well as
V. Seta   +4 more
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Pachydermoperiostosis

Orbit, 2023
Md Shahid Alam, Shamayita Gupta
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Primary Pachydermoperiostosis: A Case Report

The Journal of Dermatology, 2000
AbstractPachydermoperiostosis (PDP), a rare genodermatosis, occurred in a 38‐year‐old Indian male. He presented with progressive thickening of the skin on the face and scalp of 15 years duration. Widening of his wrists and ankles and broadening of the fingers and toes had also developed since then.
G Sethuraman   +3 more
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Skeletal scintigraphy in pachydermoperiostosis

European Journal of Nuclear Medicine, 1981
Skeletal scintigraphic findings and radiographic correlation in a 39-year-old patient with pachydermoperiostosis are described. Although the literature suggests that pachydermoperiostosis is associated with decreased blood flow, enhanced activity was observed in the patient's bone scan. This apparent discrepancy is discussed.
openaire   +3 more sources

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