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PACHYDERMOPÉRIOSTOSE:SYNDROME DE TOURAINE, SOLENTE ET GOLÉ Tomoe KATOH 1 1Department of Dermatology, Chiba University School of Medicine pp.275-283
Published Date 1969/3/1
DOI https://doi.org/10.11477/mf.1412200477
  • Abstract
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Only six cases of the complete form of this syndrome were reported in the literature in English until 1966.

A 21-year-old man with the complete form was reported. Past history: The patient suffered from pulmonary tuberculosis and received a medical treat-ment at 13 years of age. Since then he has had cholecystopathy and orthostatic albuminuria. Present history: In autumn, 1964 he noted thickening of the fingers and toes, and found furrows on the scalp and forehead in April, 1967.

At his first visit on May 31, 1967, he had typical cutis verticis gyrata and clubbed fingers. Laboratory tests: A chest roentgenogram showed nothing contributative, and BMR was -8%. The gonadotropin level in the urine, scrum mineral contents and results of liver function tests were within normal limits. A roentgenogram revealed a thickend skull but the size and figure of the sella trucica were normal. Thickening and elongation of the phalangeal bones of the fingers and toes, especially cauliflower-like proliferations of the distal part of the ungual phalanges were proved. A histologic specimen showed hypertrophy of the sebaceous glands. A mucinous substance which was obtained by biopsy showed negative PAS reaction but positive alcian blue reaction at pH 2.5.


Copyright © 1969, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1324 印刷版ISSN 0021-4973 医学書院

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