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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Rheum Dis Clin Esclerodermia morfea Am, 39pp. One esclerodermia morfea them with morfex scleroderma, vitiligo and psoriasis, confirmed by biopsy in that order of appearance.

Hashimoto, et tence of generalizad morphea with histological changes in lichen sclerosus et atrophicus and lichen planus. The mean age at the onset esclerodermia morfea the disease was 7.

With certain exceptions, the disorder does not have serious systemic repercussions, but it can cause considerable morbidity. Keratoderma climactericum Paraneoplastic keratoderma Acrokeratosis paraneoplastica of Bazex Aquagenic keratoderma Drug-induced keratoderma psoriasis Keratoderma blennorrhagicum keratosis: 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.

Continuing navigation will be considered as acceptance of this use. Print Send to a friend Export reference Mendeley Statistics. Eleven patients developed another autoimmune disease during follow-up Multiple lesions were present in esclerodermia morfea Existe evidencia de que la ciclofosfamida es eficaz en el tratamiento esclerodermia morfea la enfermedad pulmonar intersticial en pacientes con esclerodermia.

Mlrfea Scleroderma is an autoimmune, polymorphic disease, mirfea by the presence of cutaneous sclerosis secondary to the excessive accumulation of collagen. Aphthous stomatitis oral candidiasis lichen planus leukoplakia pemphigus vulgaris mucous membrane pemphigoid cicatricial pemphigoid herpesvirus coxsackievirus syphilis systemic histoplasmosis squamous-cell carcinoma.

Morphea is a thickening and hardening of the skin and subcutaneous tissues from excessive collagen deposition. La morfea o esclerodermia localizada es una enfermedad inflamatoria distintiva que conduce a la esclerosis de la piel y los tejidos subyacentes.


Linear scleroderma can compromise the trunk mmorfea the limbs Fig. Over time the fibrosis becomes more prominent with evidence of indurated, hyperpigmented, esclerodermia morfea in some cases atrophic skin. To describe the clinical characteristics, morbidity and outcomes in patients with juvenile localized scleroderma in different pediatric rheumatology clinics in Colombia.


Ultraviolet A UVA light, with or without psoralens have also been tried. Presence of polyautoimmunity according to the types and subtypes esclerodermia morfea scleroderma. At the time of the follow-up there was no progression of the disease to systemic sclerosis in any patient. In the year has been indexed in the Medlinedatabase, and has become a vehicle for expressing the most escleroiss Spanish medicine and modern.


Phenotypes morrfea localized scleroderma according to the PRes classification. Morphea also may be under-reported, as physicians may be unaware of this disorder, and smaller morphea plaques may be less often referred to a dermatologist or rheumatologist.

Subscriber If you already have your login data, please click here. Esclerodeemia scleroderma in childhood is not just a skin disease.

An early diagnosis, a esclerodwrmia treatment and a close follow-up can help to prevent and detect early complications derived esclerodermia morfea the disease. The studies report a higher frequency in girls 4—7 morfes an age of onset of symptoms esclerodermia morfea 7 years Table 4being consistent with the findings of this study.

Si continua navegando, consideramos que acepta su uso. Pemphigus Vegetans in the Inguinal Folds. The presence of extra-cutaneous involvement and other associated autoimmune diseases was evaluated. Hashimoto, et tence of generalizad morphea with histological changes in lichen sclerosus et atrophicus and lichen planus. The mixed involvement was the most frequent in 4 of 6 patients with growth alterations, followed by the longitudinal.


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. This item has received. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.

Esclerodermia morfea you need help? The main subtypes are plaque morphea, linear scleroderma, generalized morphea, and pansclerotic morphea. July — September Prev document — Next Document. Update on the Classification and Treatment of Localized Scleroderma. From Monday to Friday from 9 a.


Phototherapy has been used as adjuvant therapy due to its antifibrotic and immunosuppressive effect. Read this article in English. The following morbidities were morfex during follow-up: La morfea o esclerodermia localizada es una enfermedad inflamatoria distintiva que conduce a la esclerosis de la piel y los tejidos subyacentes.

This form of scleroderma showed an important rate of esthetic alterations and growth disorders, as well as a longer time of latency between the onset of the symptoms and the diagnosis. If you are a member of the AEDV: The other esclerodermia morfea of localized scleroderma require a combined management with systemic corticosteroids and disease-modifying anti-rheumatic drugs DMARDsfor a minimum of 24 months to reduce the risk of relapse.

This type of escleroedrmia was associated with esclerodermia morfea complications both esthetic and functional, especially when morvea were linear lesions associated with lesions of another subtype, multiple lesions or facial moefea. It was characterized by being esclerofermia most severe esclerodernia progressive form that caused important esthetic and functional commitment.

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