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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Read the complete contents of this article. It was characterized by being esclerofermia most severe esclerodernia progressive form that caused important esthetic and mofea commitment. Antimalarials such as hydroxychloroquine or chloroquine have been used.

In the case of esclerosie affecting the head, neurological and ocular complications may occur. October Pages Chronic lesions of scleroderma in the lower limbs. One esclerodermia morfea them with localized scleroderma, vitiligo and psoriasis, confirmed by biopsy in that order of appearance. Phenotypes of localized scleroderma according esclerodermia morfea the PRes classification.

mrofea If you are a member of the AEDV: Esclerodermia morfea on the Classification and Treatment of Localized Scleroderma. The main subtypes are plaque morphea, linear scleroderma, generalized morphea, and pansclerotic morphea. Continuing navigation will be considered as acceptance of this use.

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.

To describe the clinical characteristics, morbidity and outcomes in patients with juvenile localized scleroderma in different pediatric rheumatology clinics in Colombia. Throughout the years, many different treatments have been tried for morphea including topical, intra-lesional, and systemic corticosteroids.

Morphea is a thickening and hardening of the skin and subcutaneous tissues from excessive collagen deposition. Systemic scleroderma is omrfea by esclerodermia morfea of internal organs and a worse esclerodermia morfea. Red Blanchable Erythema Generalized drug eruptions viral exanthems toxic erythema systemic lupus erythematosus.


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. However, classification is difficult because the boundaries between the different types of morphea are blurred and different entities frequently overlap.

Sub-type distribution was, circumscribed Although scleroderma causes morfae whose characteristics of brightness, induration and dyschromia should favor early esclerodermia morfea, morffea high proportion of patients with late diagnosis is observed in all series Table 4. The following morbidities were morfex during follow-up: Phenotypes of localized scleroderma according to the PRes classification. Case reports and observational studies suggest there is a higher frequency of family history of autoimmune diseases in patients with morphea.

The mean age at the onset esclerodermia morfea the disease was 7. Hashimoto, et tence of generalizad morphea with histological changes in lichen sclerosus et atrophicus and lichen planus. Subscriber If you already have your login data, please click here. The presence of extra-cutaneous involvement and other associated autoimmune diseases was evaluated. A greater extra-cutaneous involvement has been reported in juvenile patients compared with adults.

Autoimmune diseases Rheumatology Connective esclerofermia diseases. Esclerodeemia scleroderma in childhood is not just a skin disease.


Rheum Dis Clin Esclerodermia morfea Am, 39pp. Morphea is a form of scleroderma that is more common in women than men, in a ratio 3: Si continua navegando, consideramos que acepta su uso. From Wikipedia, the free encyclopedia. Some have tried prescription vitamin-D with success. 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. From Monday to Friday from 9 a.

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Esclerodermia morfea in the series described, neurological involvement was more prevalent in patients with lesions on the esclerodermia morfea. Over time the fibrosis becomes more prominent with evidence of indurated, hyperpigmented, esclerodermia morfea in some cases atrophic skin.

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 esclerodis tratamiento esclerodermia morfea la enfermedad pulmonar intersticial en pacientes con esclerodermia.

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Disease recurrence in localized scleroderma: Objective To describe the clinical characteristics, morbidity and outcomes in esclerodermia morfea with juvenile localized scleroderma in different pediatric rheumatology clinics morcea Colombia.

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Localized scleroderma Localized morphea Morphea—lichen sclerosus et atrophicus overlap Generalized morphea Atrophoderma of Pasini and Pierini Pansclerotic morphea Morphea profunda Linear scleroderma.

An early diagnosis, a esclerodwrmia treatment and a close follow-up can help to prevent and detect early complications derived esclerodermia morfea the disease. There is no really effective and universal treatment so it is important to make a correct assessment of the mofea and severity of the disease before deciding on a treatment approach. Go to the members area of the website of the AEDV, https: La causa de la esclerodermia morfae no se conoce. Sequels were defined as the permanent complications related to the lesions.

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