A case of pachydermoperiostosis with Bartter's syndrome.

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[Pachydermoperiostosis (Touraine-Solente-Golé syndrome). Case report].

Pachydermoperiostosis or primary hypertrophic osteoarthropathy, also known as Touraine-Solente-Golé syndrome, is a rare process, frequently inherited. In its complete form it is characterized by pachydermia (thickening of the skin), skeletal changes (periostosis) and acropachia (digital clubbing). We report a patient that consulted for skeletal symptoms, as the acropachia and cutaneous manifest...

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INTRODUCTION Pachydermoperiostosis is a rare, hereditary disease commonly presenting with digital clubbing, pachydermia and periosteal hypertrophy. Therapeutic options for pachydermoperiostosis are few because of the unknown pathogenesis. Here, we report the complicated case of a patient with pachydermoperiostosis combined with spondyloarthritides, who was refractory to steroids and tumor necro...

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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: Nihon Naika Gakkai Zasshi

سال: 1988

ISSN: 0021-5384,1883-2083

DOI: 10.2169/naika.77.63