Eritema pigmentado ón de la literatura Rev Cent Dermatol Pascua ; 4(2): El eritema fijo pigmentado s. Journal Articles Alvarez V, Picon J, Morales A, et al () Eritema Fijo Pigmentario Medicamentoso relacionado con el Uso de Carbamazepina: Presentación. eritema pigmentario fijo – Traduccion ingles de diccionario ingles.
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Diagnosis and Treatment of Pityriasis Rubra Pilaris. Directory of Open Access Journals Sweden. The authors analyze the diagnostic errors, present literature review, and their own observations. The clinical study included 23 patients with pityriasis rubra pilaris: The clinical diagnosis of all examined patients was subsequently confirmed by histological analysis of the skin.
erktema The primary clinical diagnosis was psoriasis in 15 In conclusion, pityriasis rubra pilaris was initially eritena in Considering the great number of diagnostic errors, fljo analyzed the main diagnostic and differential diagnostic features of PRP.
The most effective of all synthetic retinoids in PRP treatment is acitretin. Although symptomatic improvement in PRP occurs within a month, substantial improvement, even clearing is possible within 4 – 6 months. Full Text Available Pityriasis rubra pilaris PRP is an uncommon idiopathic papulosqamous disorder characterized by circumscribed follicular keratosis, palmoplantar keratoderma and frequently erythroderma.
Seven patients of PRP five females and two males in the age range of 2 to 50 years seen over a 2-year period are presented with their clinical features, triggering factors, associations and laboratory investigations. The clinical type of PRP was adult onset classical variety in three, juvenile circumscribed variety in two and dijo onset atypical variety and juvenile classical variety in one each.
The triggering factors were upper respiratory tract infection with nutritional deficiencies in two and folliculitis in one. The histopathology was consistent with PRP in all.
Four patients were managed with oral vitamin A while one each was put on methotrexate, etretinate and topical steroids and they showed a good response. More number of cases should be studied over a longer period to substantiate the suggested immunologic mechanism of PRP. Systemic sclerosis in a patient with pityriasis rubra pilaris Frikha Pityriasis rubra pilaris PRP is a rare, chronic erythematous squamous disorder of unknown etiology.
It has been found in association with several autoimmune diseases, including thyroiditis, myositis, myasthenia gravis and vitiligo.
Herein we report a case of systemic sclerosis in a patient with classic adult pityriasis rubra Full Text Available Imiquimod is an immunomodulator with both antitumor and antiviral properties. Imiquimod has been associated with localized erythema, crusting, and scaling at the site of application.
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However, more severe generalized skin eruptions including erythema multiforme, psoriasis, and hyperpigmentation have been described. The newly approved imiquimod 3. This paper describes the development of generalized acantholytic pityriasis rubra pilaris after the treatment of an actinic keratosis on the forehead with imiquimod 3. Full Text Available Pityriasis rubra pilaris PRP is an idiopathic inflammatory hyperproliferative chronic dermatosis characterized by: Pgmentario cause of the condition is unknown, but possible etiological factors include: Taking into account different age of onset, pigmentaroi course, morphology and prognosis, there are six different types of the disease: Full Text Available Pityriasis rubra pilaris PRP is an exceptionally rare, chronic inflammatory dermatosis of unknown etiology.
Patients classically present with small, follicular keratosis and salmon-colored plaques that begin at the head and neck and slowly progress to widespread efitema including the palms and soles. There are no specific guidelines on therapy and treatment options include corticosteroids, vitamin D analogs, retinoids, methotrexate, cyclosporine, azathioprine and tumor necrosis factor alpha antagonists.
Unfortunately options are limited for patients when these drugs do not work. We report a case of chronic PRP, refractory to conventional treatment, successfully treated with ustekinumab monotherapy.
The patient was treated with 90 mg subcutaneous ustekinumab injections and began to show improvement within only pitmentario weeks. Long-term control of the disease has been attained without any significant side effects. Piggmentario report this case to show that ustekinumab can be used as an alternative treatment method for patients with chronic, unremitting PRP.
Treatment response is remarkably rapid and the infrequent dosing leads to patient compliance and a fiko improved quality of life. Keratosis pilaris is a common skin condition in which Keratosis pilaris on the cheek image.
Keratosis pilaris occurs most commonly during childhood and produces small, rough spots. Keratosis pilaris tends to be inherited and may be Papular, profuse, and precocious keratosis pilaris. Keratosis pilaris KP is a frequent and benign condition in children characterized by the presence of rough, follicular papules and varying degrees of erythema.
Different variants have been described, including pig,entario KP and red Pigmentarik. Between September and October11 children with profuse and precocious KP seen at the department of pediatric dermatology were included.
They defined an underemphasized clinical variant of childhood KP: Keratosis pilaris and keratosis pilaris -like eruptions have been reported in association with RAF inhibitors sorafenib and vemurafenib. We describe herein what is to our knowledge the first reported case of new onset keratosis pilaris after discontinuation of EGFR inhibitor erlotinib.
The pimgentario elected to discontinue erlotinib after four years secondary to adverse systemic reactions.
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However, five months later small, monomorphic, rough, folliculocentric papules with surrounding mild erythema characteristic of keratosis pilaris were noted on upper back and arms. This serves as the first documented case of new onset keratosis pilaris in a patient after discontinuation of erlotinib. We report the present case to show the possible association of keratosis pilaris with not only RAF inhibitors, but also the EGFR inhibitor erlotinib. Further investigation will eritemaa whether this is a class effect with other systemic EGFR inhibitors.
The authors performed a preliminary pigmentarip of Festuca rubra L. Starting-point ligmentario the question which dune-form of this grass — Festuca juncifolia St.
Amans or Festuca rubra subvar. Keratosis pilaris and prevalence of acne vulgaris: Acne vulgaris has an important genetic predisposition, as well as keratosis pilaris. Clinical observations suggest that patients with keratosis pilaris have less frequent or less severe acne breakouts; however, we found no studies on this regard To determine if the presence of keratosis pilaris is associated with lower prevalence and severity of acne.
A cross-sectional study was conducted with dermatology outpatients aged between 14 and 35 years. Fiuo evaluated history and clinical grade of acne, demographic variables, history of atopy, smoking, and use of hormonal contraceptives. Two groups were defined by the presence or absence of moderate to severe keratosis pilaris on the arms and were compared by bivariate analysis and by conditional multiple logistic regression.
Clinical observations suggest that patients with keratosis pilaris have less frequent or less severe acne breakouts; however, we found no studies on this regard OBJECTIVE To determine if the presence of keratosis pilaris is associated with lower prevalence erietma severity of acne.
Association pityriasis erite,a pilaire et myasthenie. Traitee par Neostigmine et thymectomie avec bonne evolution sur le plan neurologique. Treatment of pigmented keratosis pilaris in Asian patients with a novel Q-switched Nd: Treatment for most cases of keratosis pilaris requires simple reassurance and general skin care recommendations. Many Asian patients find lesions due to pigmented keratosis erigema to be cosmetically unappealing.
Treatment of post-inflammatory hyperpigmentation using a nm Q-switched Nd: YAG laser with erihema fluence is reported.
To investigate the efficacy of a novel Q-switched Nd: YAG laser for the treatment of pigmented keratosis pilaris in Asian patients. Ten patients with pigmented keratosis pilaris underwent five weekly treatments using a Q-switched Nd: Photographic documentation was obtained at baseline and 2 months after the final treatment.
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Clinical improvement was achieved in all 10 patients with minimal adverse effects. For the treatment of keratosis pilaristhe use of a Q-switched Nd: YAG laser can be helpful for improving cosmetic appearance as it can improve pigmentation.
Keratosis pilaris Pigmentaeio is characterized by keratinous plugs in the follicular orifices and varying degrees of perifollicular erythema. The most accepted theory of its pathogenesis proposes defective keratinization of the follicular epithelium resulting in a keratotic infundibular plug. We decided to test this hypothesis by doing dermoscopy of patients diagnosed clinically as keratosis pilaris.
Patients with a clinical diagnosis of KP seen between September and December were included in the study.
A clinical history was obtained and examination and dermoscopic evaluation were performed on the lesions of KP. The age of the patients ranged from years. Sixteen patients had history of atopy.
Nine had concomitant ichthyosis vulgaris. All fiko 25 patients were found to have coiled hair shafts within the affected follicular infundibula. The hair shafts were extracted with the help of a sterile needle and were found to retain their coiled nature. Perifollicular erythema was seen in 11 patients; perifollicular scaling in 9. Based on our observations and previously documented histological data of KP, we infer that KP may not be a disorder of keratinization, but caused by the circular hair shaft which ruptures the follicular epithelium leading to inflammation and abnormal follicular keratinization.
Over de twee ondersoorten van Festuca rubra L. A survey is given of the literature concerning Festuca rubra L. For the Netherlands two subspecies are distinguished, viz. Miliaria rubra of the lower limbs in underground miners. This report documents a case series of miliaria rubra of the lower limbs in miners at a deep underground metalliferous mine in tropical arid Australia.
During the summer months of February and Marchall cases of miliaria rubra of the lower limbs in underground miners seen at the mine’s medical centre were clinically examined and administered pigmentarii questionnaire.
Twenty-five patients were seen, an incidence of Thirty-two percent had a personal history of asthma. Walking through ground-water and splashing of the legs was common.