Pachydermoperiostosis in childhood

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منابع مشابه

Pseudoacromegaly in pachydermoperiostosis.

To cite: Chakraborty PP, Bhattacharjee R, Mukhopadhyay S, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2016214624 DESCRIPTION A 19-year-old male patient presented with a yearlong history of progressive painful enlargement of his hands and feet associated with excessive sweating and greasiness of the face, palms and soles. He also noticed pain over his wr...

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[Pachydermoperiostosis (idiopathic hypertrophic osteoarthropathy)].

Introduction Pachydermoperiostosis is a syndrome characterized by finger clubbing, periosteal new bone formation especially over the distal ends of long bones, and coarsening of the facial features, with thickening, furrowing and oiliness of the skin of the face and forehead. The first reported cases were the Hagner brothers, who had typical features of this syndrome. They were first described ...

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Pachydermoperiostosis Masquerading as Acromegaly

Context Acromegaly usually is suspected on clinical grounds. Biochemical confirmation is required to optimize therapy, but there are other differential diagnoses. Case Description We describe a 24-year-old Uzbek man who presented with many clinical symptoms and signs of apparent acromegaly. On examination, the patient showed a rugose folding of his scalp, with the formation of tender, painful...

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[Pachydermoperiostosis (Touraine-Solente-Gole syndrome)].

We report on a 38-year-old male patient suffering from pachydermoperiostosis (Touraine-Solente-Golé Syndrome), who underwent a cosmetic operation without success.

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Pachydermoperiostosis: Three case reports.

Three patients with pachydermoperiostosis are reported. All patients presented with moderate pain and swelling in multiple joints unresponsive to treatment, characteristic facial features which were marked in two cases, clubbing of nails and enlargement of distal parts of the extremities. One patient had spondylolisthesis of L5-S1 vertebrae, an association not previously described in this syndr...

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ژورنال

عنوان ژورنال: Rheumatology

سال: 1997

ISSN: 1462-0324,1462-0332

DOI: 10.1093/rheumatology/36.11.1224