Hyperpigmentation Therapy
Mostrando 1-7 de 7 artigos, teses e dissertações.
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1. Frontal fibrosing alopecia and lichen planus pigmentosus: diagnosis and therapeutic challenge
Abstract Frontal fibrosing alopecia is a variant of lichen planopilaris with marginal progressive hair loss on the scalp, eyebrows and axillae. We report a case of frontal fibrosing alopecia and lichen planus pigmentosus in a postmenopausal woman, that started with alopecia on the eyebrows and then on the frontoparietal region, with periocular and cervical h
An. Bras. Dermatol.. Publicado em: 2017
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2. Hyperpigmentation as a peculiar presentation of mycosis fungoides
Abstract Hyperpigmented mycosis fungoides is an extremely rare subtype of mycosis fungoides. It presents as multiple pigmented macules and patches without poikilodermatous changes and characterized by a CD8+ phenotype on immunohistochemistry. This report describes a typical case of hyperpigmented mycosis fungoides in a 62-year-old woman, who presented with a
An. Bras. Dermatol.. Publicado em: 2017
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3. Acquired hyperpigmentations
Cutaneous hyperpigmentations are frequent complaints, motivating around 8.5% of all dermatological consultations in our country. They can be congenital, with different patterns of inheritance, or acquired in consequence of skin problems, systemic diseases or secondary to environmental factors. The vast majority of them are linked to alterations on the pigmen
An. Bras. Dermatol.. Publicado em: 2014-01
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4. Avaliação dos achados clínicos e histopatológicos nas lesões de poiquilodermia de Civatte antes e após o tratamento com luz intensa pulsada / An evaluation of the clinical and histopathological findings of the lesions of poikiloderma of Civatte before and after treatment with intense pulsed light
A poiquilodermia de Civatte é uma condição caracterizada por hiperpigmentação, telangiectasia e atrofia que acomete predominantemente o pescoço e a face de forma simétrica, poupando a área encoberta pelo mento. A sua ocorrência é associada à predisposição genética, à exposição cumulativa ao sol, ao processo de envelhecimento, à hipersensibi
Publicado em: 2005
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5. Hipercromia cutânea idiopática da região orbital: avaliação clínica, histopatológica e imunohistoquímica antes e após tratamento com luz pulsada de alta energia / Cutaneous idiopathic hyperchromia of the orbital region: clinical, histopathological and immunohistochemestric evaluation before and after the treatment with intense pulsed light
Introdução: A hipercromia cutânea idiopática (HCIRO) não tem sua etiopatogenia bem esclarecida. Parecem estar envolvidos fatores genéticos (herança familiar autossômica dominante), aumento de melanina na derme, vasculatura proeminente e frouxidão da pele palpebral. Encontraram-se, na revisão da literatura, alguns artigos que contribuíram para o es
Publicado em: 2004
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6. Myopathy in Addison's disease.
Since the first description of primary adrenocortical insufficiency by Thomas Addison in 1855 several large series of patients with Addison's disease have been published. The common signs and symptoms include: weakness, hyperpigmentation, weight loss, gastrointestinal complaints, and hypotension. It is rare for patients with Addison's disease to present with
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7. Normal and abnormal regulation of β-MSH in man
The regulation of plasma β-melanocyte-stimulating hormone (β-MSH) in man has been studied utilizing a radioimmunoassay previously described (1). In normal subjects plasma β-MSH values ranged from 20 to 110 pg/ml. Metyrapone increased and dexamethasone decreased plasma β-MSH levels. Surgical stress stimulated β-MSH secretion. Plasma β-MSH levels were el