Keratoderma Climactericum (Haxthausen) Treated with Œstrone
نویسندگان
چکیده
منابع مشابه
Spiny keratoderma of the palms successfully treated with topical tacalcitol.
Sir, Spiny keratoderma is a rare disease characterized by keratotic spicules resembling a “music box spine” located on the palms and soles (1). This entity has been reported under several different names, such as punctate keratoderma (2), punctate porokeratotic keratoderma (3), palmar filiform hyperkeratosis (4), and spiny keratoderma of the palms and soles (1). We present here a case of spiny ...
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Clouston syndrome (hidrotic ectodermal dysplasia) is characterized by the clinical triad of nail dystrophy, alopecia and palmoplantar hyperkeratosis. Clouston syndrome is transmitted as an autosomal dominant trait and caused by mutations in the GJB6 gene (13q12), encoding the gap junction protein connexin 30 (C × 30). At present, there is no treatment for the disease and management is purely su...
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A man aged 43 years, who was admitted to this hospital on Aug. 23, 1947, said that he had been quite well until 1938 when he was taken ill and treated in Coventry Hospital for acute rheumatism. Questioning, however, disclosed that the illness had consisted of conjunctivitis, -polyarthritis, and fever; there was no history of urethritis. After a year or so in hospital he was discharged with a co...
متن کاملKeratoderma blennorrhagica.
Coelho I, et al. BMJ Case Rep 2017. doi:10.1136/bcr-2017-222475 Description A 26-year-old woman, previously healthy, that a month ago started complaining of pain in the soles of both feet, which followed, additionally, to the right knee, the left knee, left elbow and right shoulder. She reported morning stiffness exceeding 1 hour that decreased with physical activity, worsened with rest, but im...
متن کاملSpiny keratoderma.
We present a case of a 48-year-old man with an approximately 30-year history of spiny projections on the palms, which were histopathologically consistent with spiny keratoderma. Spiny keratoderma is a rare entity of unknown etiology that has been described with both hereditary and acquired variants. The hereditary form, which is most likely the diagnosis in our patient, manifests at a younger a...
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1937
ISSN: 0035-9157
DOI: 10.1177/003591573703000627