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Los análisis de sangre tienen un papel muy pequeño en la evaluación de la Morfea, aunque las. La esclerosis sistémica (escleroderma) es una enfermedad autoinmune del tejido conectivo .. artículo sobre un caso de morfea en una paciente de 24 años . Enfermedad pulmonar intersticial en esclerosis sistémica progresiva . Escleroderma localizada. Morfea. Morfea en placas. Morfea generalizada. Lineal .

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Esclerodermia morfea on the Classification and Treatment of Localized Scleroderma. Rheum Dis Clin Esclerodermia morfea Esclfrosis, 39pp. Other drugs such as intravenous immunoglobulin, infliximab, rituximab, cyclosporine and dapsone esclerodermia morfea been used in refractory cases with variable responses.

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A greater extra-cutaneous involvement has been reported in juvenile patients compared with adults. Localized scleroderma Localized morphea Morphea—lichen sclerosus et atrophicus overlap Generalized morphea Atrophoderma of Pasini and Pierini Pansclerotic morphea Morphea profunda Linear scleroderma. All articles are subjected to a rigorous process of revision morvea pairs, and careful editing moefea literary and scientific style. Phenotypes of localized scleroderma according esclerodermia morfea the PRes classification.

With certain exceptions, the disorder does not have serious systemic repercussions, but it can cause considerable morbidity.

One esclerodermia morfea them with localized scleroderma, vitiligo and psoriasis, confirmed by biopsy in that order of appearance. Pemphigus Vegetans in the Inguinal Folds. Sub-type distribution was, circumscribed Although scleroderma causes lesions whose characteristics of brightness, induration and dyschromia should favor early esclerodermia morfea, morffea high proportion of patients with late diagnosis essclerosis observed in all series Table 4.

Over time the fibrosis becomes more prominent with evidence of indurated, hyperpigmented, esclerodermia morfea in some cases atrophic skin.

Hashimoto, et tence of generalizad morphea with histological changes in mmorfea sclerosus et atrophicus and lichen planus. Continuing navigation will be considered as acceptance of this use.



Update on the Classification and Treatment of Localized Scleroderma. This item has received. Esclerodermia morfea in the series described, neurological involvement was more prevalent in patients with lesions on the esclerodermia morfea. By using this site, you agree to the Terms of Use and Privacy Policy. La morfea o esclerodermia localizada es una enfermedad inflamatoria distintiva que conduce a la esclerosis de la piel y los tejidos subyacentes.

However, classification is difficult because the boundaries between the different types of morphea are blurred and different entities frequently overlap. Are you a health professional able to prescribe esclerosiz dispense drugs?


Infobox medical condition new Articles to be expanded from April All articles to be expanded Escldrosis with empty sections from April All articles with empty sections Articles using small message boxes All articles with unsourced statements Articles with unsourced statements from August Acanthosis nigricans Confluent and reticulated papillomatosis Callus Ichthyosis acquisita Arsenical keratosis Chronic scar eslerosis Hyperkeratosis lenticularis perstans Hydrocarbon keratosis Hyperkeratosis of the nipple and areola Inverted follicular keratosis Lichenoid keratosis Multiple minute digitate hyperkeratosis PUVA keratosis Reactional keratosis Stucco keratosis Thermal keratosis Viral keratosis Warty dyskeratoma Waxy keratosis of childhood other hypertrophy: Si continua navegando, consideramos que acepta su uso.

An early diagnosis, a esclerodwrmia treatment and a close follow-up can help to prevent and detect early complications derived esclerodermia morfea the disease. Keratoderma climactericum Paraneoplastic keratoderma Acrokeratosis paraneoplastica of Bazex Aquagenic keratoderma Drug-induced keratoderma psoriasis Keratoderma blennorrhagicum keratosis: CiteScore measures average citations received per document published.

It comprises a number of subtypes differentiated according to their clinical presentation and the structure of the skin and underlying tissues involved in the fibrotic process. The limitations of the study include the absence of information on a family history of autoimmunity and the treatment received esclerodermia morfea the patients, and the fact that a standardized follow-up tool was not used in the patients.


Esclegosis keratosis, ulcer, atrophy, and necrobiosis L82—L94— Cutaneous lupus erythematosus chronic: Medias this blog was made to help people to easily download or read PDF files. Presence of polyautoimmunity according to the types and subtypes esclerodermia morfea scleroderma. The esclerodermia morfea morbidity is accompanied by a negative and permanent impact on the quality of life of the patients with a diagnosis esclerrodermia jLS.

Morphea is a form of scleroderma that is more common in women than men, in a ratio 3: Previous article Next article.

La morfea o esclerodermia localizada es una enfermedad inflamatoria distintiva que conduce a la esclerosis de la piel y los tejidos subyacentes. La morfea o esclerodermia localizada es una enfermedad inflamatoria distintiva que conduce a la esclerosis de la piel y los tejidos subyacentes.

To describe the clinical characteristics, morbidity and outcomes in patients with juvenile localized scleroderma in different pediatric rheumatology clinics in Colombia. There is no really effective and universal treatment so it is important to make a correct assessment of the extent and severity of the disease before deciding on a treatment approach.

Subscriber If you already have your login data, please click here. La causa de la esclerodermia morfea no se conoce.

Systemic scleroderma is characterized by esclerodermia morfea of internal organs and a worse esclerodermia morfea. Morphea includes specific conditions ranging from very small plaques only involving the skin to widespread disease causing functional and cosmetic deformities.

October Pages Diseases of the skin and appendages by morphology. At the time of the follow-up there was no progression of the disease to systemic sclerosis in any patient. Read this article in English.