Results 291 to 300 of about 50,269 (341)
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Palmar filiform hyperkeratosis
International Journal of Dermatology, 2012Filiform hyperkeratosis (FH) is a rare entity of unknown etiology clinically characterized by keratotic digitations located peripherally on palms and soles or centrally on the trunk. In our patient, cutaneous lesions were regarded as a clinical sign of the tumor, as she went into complete remission after surgery to treat liver metastases. Therefore, we
ROSINA, Paolo, PAPAGRIGORAKI, Anastasia
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Hyperkeratosis of the nipple and areola
Plastic and Reconstructive Surgery, 1985Usually hyperkeratosis of the nipple and areola is associated with ichthyosis and epidermal nevus. The patient's lesions will resemble acanthosis nigricans but histologically suggest a completely different entity. Presented is a case of hyperkeratosis of the nipples and areolae with no association with ichthyosis or epidermal nevus.
Steven J. Hodge +2 more
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JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2011
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Gulia, A, Di Cesare, A, Peris, Ketty
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Gulia, A, Di Cesare, A, Peris, Ketty
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Dermabrasion for Hyperkeratosis [PDF]
Although dermabrasion has its greatest usefulness in the treatment of acne scarring,1there are other areas in which the dermabrasion technique is of value. In our experience we have found the high-speed diamond fraise2valuable in the treatment of large hyperkeratotic plaques of the palms and soles.
Joseph M. Lehman, Walter B. Shelley
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British Journal of Dermatology, 1983
We report fifteen cases showing focal acral hyperkeratosis. They were clinically identical to acrokeratoelastoidosis (AKE) but lacked the elastorrhexis which is a feature of AKE. The name focal acral hyperkeratosis is proposed for this condition which differs histologically from AKE.
Pauline M. Dowd +2 more
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We report fifteen cases showing focal acral hyperkeratosis. They were clinically identical to acrokeratoelastoidosis (AKE) but lacked the elastorrhexis which is a feature of AKE. The name focal acral hyperkeratosis is proposed for this condition which differs histologically from AKE.
Pauline M. Dowd +2 more
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Uraemic follicular hyperkeratosis
Clinical and Experimental Dermatology, 1985Summary Cutaneous manifestations of Chronic Renal Failure (CRF) include pruritus, diffuse hyperpig-mentation xerosis, follicular hyperkeratosis, ‘uremic frost’, bullous dermatosis similar tn hepato-cutaneous porphyria, skin calcifications and half-and-half nails.
B. Garcia-Bravo +2 more
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Archives of Otolaryngology - Head and Neck Surgery, 1959
Hyperkeratosis of the larynx is a very important and perplexing subject to the laryngologist. It is considered a precancerous lesion, and in many cases such growths actually do metamorphose into true cancers. However, many of the lesions are benign, and so we feel that radical treatment is frequently unnecessary. The problem is, how do we differentiate
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Hyperkeratosis of the larynx is a very important and perplexing subject to the laryngologist. It is considered a precancerous lesion, and in many cases such growths actually do metamorphose into true cancers. However, many of the lesions are benign, and so we feel that radical treatment is frequently unnecessary. The problem is, how do we differentiate
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Hyperkeratosis Lenticularis Perstans
Archives of Dermatology, 1969Hyperkeratosis lenticularis perstans was first described by Flegel 1 in 1958. We describe here the clinical and histological features of two female patients with widespread keratoses affecting the limbs, features which closely resemble those of the patient reported by Flegel.
J. Rogers, E. J. Raffle
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The management and treatment of hyperkeratosis
Nurse Prescribing, 2017Rebecca Elwell, Macmillan lymphoedema advanced nurse practitioner, Royal Stoke University Hospital, discusses recommendations on management of this skin problem, which may co-occur with chronic oedema
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Disseminated Spiked Hyperkeratosis
International Journal of Dermatology, 1987ABSTRACT: Multiple small hyperkeratoses were observed in a 42–year‐old woman. They had first appeared in early adult life. There was 3 history of an apparently identical disorder affecting her father, her brother, and her brother's son. A similar condition has been described in four previous reports in which seven individual cases have been documented,
John J. Sullivan, Judith A. Nedwich
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