Results 151 to 160 of about 9,963 (189)
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British Journal of Dermatology, 1985
This paper describes five cases of an uncommon acral rash, acute palmoplantar pustulosis, which is precipitated by infection, and may represent a true pustular bacteria. Acute and chronic palmoplantar pustulosis are probably different forms of the same disease, but the prognosis in the acute form is good and aggressive therapy is not indicated.
S M, Burge, T J, Ryan
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This paper describes five cases of an uncommon acral rash, acute palmoplantar pustulosis, which is precipitated by infection, and may represent a true pustular bacteria. Acute and chronic palmoplantar pustulosis are probably different forms of the same disease, but the prognosis in the acute form is good and aggressive therapy is not indicated.
S M, Burge, T J, Ryan
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Palmoplantar Keratoderma with Amyotrophy
Dermatologica, 2009Four members of a South African Black family who have palmoplantar keratoderma with amyotrophy are reported. No neuromuscular defects have been found and the muscle thinning appears to result from disuse atrophy. Volar hyperhidrosis, nail abnormalities and in 2 cases knuckle pads, were additional features.
W K, Jacyk, P L, Bill
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Circumscribed Palmoplantar Keratoderma
Australasian Journal of Dermatology, 1970SUMMARYA case of focal tender thickening of the palms and soles, with associated abnormalities of the cornea, is described. It is believed to be an example of circumscribed palmo‐plantar keratoderma, of autosomal recessive inheritance. Possible mechanisms involved in the production of the lesions are considered, and an approach to treatment discussed.
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Cyclosporin for palmoplantar pustulosis
Journal of Autoimmunity, 1992Palmoplantar pustulosis (PPP) is a chronic skin disease characterized by persistent erythematous, scaly plaques incorporating sterile pustules on palms and soles, which is resistant to most treatments. Recently, two published uncontrolled studies suggested that cyclosporin (CsA) could be an effective treatment for PPP.
S, Reitamo, P, Erkko, A, Remitz
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Idiopathic Palmoplantar Hidradenitis
The American Journal of Dermatopathology, 1996Idiopathic plantar hidradenitis (IPH) is a recently described condition primarily affecting healthy children who develop tender lesions localized to the plantar or lateral aspects of the feet with histologic findings similar to those seen in neutrophilic eccrine hidradenitis (NEH), although with certain notable exceptions including the absence of ...
G F, Buezo +4 more
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Iontophoresis for palmoplantar hyperhidrosis
Journal of Cosmetic Dermatology, 2004SummaryThe pathogenesis of palmoplantar hyperhidrosis (HH) remains unknown. A causative therapy is therefore not possible yet. Step by step treatment for palmoplantar HH is advised. This includes: topical aluminium salts, tap water iontophoresis (TWI), botulinum toxin (BTX) injections and endoscopic thoracoscopic sympathectomy (ETS).The mechanism of ...
exaly +3 more sources
Acquired Palmoplantar Keratoderma
American Journal of Clinical Dermatology, 2007Palmoplantar keratodermas (PPKs) are a diverse entity of disorders that are characterized by abnormal thickening of the skin on the palms and soles. Traditionally they have been classified as either hereditary or acquired and are distinguished from each other on the basis of mode of inheritance, presence of transgrediens (defined as contiguous ...
Shaily, Patel +2 more
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Palmoplantar Psoriasis and Palmoplantar Pustulosis: Current Treatment and Future Prospects
American Journal of Clinical Dermatology, 2016Palmoplantar psoriasis and palmoplantar pustulosis are chronic skin diseases with a large impact on patient quality of life. They are frequently refractory to treatment, being generally described as a therapeutic challenge. This article aims to review the definitions of palmoplantar psoriasis and palmoplantar pustulosis, highlighting the similarities ...
Inês, Raposo, Tiago, Torres
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Hereditary Palmoplantar Keratodermas
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2009SummaryHereditary palmoplantar keratodermas (PPK) comprise a clinically and genetically heterogeneous group of genodermatoses, which share impaired epidermal differentiation resulting in prominent palmoplantar hyperkeratosis. Classically, keratodermas have been separated according to their clinical appearance into diffuse, focal, and as a feature of ...
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