Lichen Myxedematosus Scholarly Articles

Although lichens growing on trees are particularly sensitive to this air pollutant, there are few studies of lichen recolonization following pollution episodes. A survey of 29 sites in the north and.

Localised lichen myxedematosus (LM) is a chronic idiopathic papular mucinosis that can be divided into five subtypes: a discrete papular (DPLM) form, acral persistent papular mucinosis (APPM), papular mucinosis of infancy, a nodular form and self-healing cutaneous mucinosis.1

Lichen myxedematosus is an idiopathic, cutaneous mucinosis with 2 clinicopathologic subsets. There is the generalised papular and sclerodermoid form, more properly termed scleromyxedema, and the localised papular form. We report the first case, to our knowledge, of lichen myxedematosus in association with rheumatoid arthritis as well as a case.

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Summary. A patient is described with typical skin lesions of lichen myxedematosus and IgG-type lambda paraproteinemia. Fibroblasts cultured from the skin of the patient and from the skin of control persons were used to study glycosaminoglycan and collagen synthesis; the cultures were labelled with 3 H-glucosamine and 3 H-proline, respectively. Fibroblasts from the patient grew to a cell.

Lichen myxedematosus (LM) is a rare, chronic disease characterized by infiltration of the skin with mucin-producing fibroblasts. Typical examination findings include shiny, flesh-colored to erythematous papules, nodules, and plaques. More extensive cutaneous disease can cause widespread thickening and hardening of the skin with large, raised folds.

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Objectives To assess the effectiveness and safety of any form of palliative therapy against placebo for the treatment of symptomatic oral lichen planus. Data sources Search strategy: Medline 1966–98,

The newly published research focuses on plants, moss, and lichen, but the results will probably apply to many other organism populations in the Arctic. Many of the Arctic species are threatened by.

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The discrete papular form of lichen myxedematosus (LM) is a rare idiopathic skin disorder. We present a case of this type in an 80-year-old African American woman. She was treated with pimecrolimus cream, which resulted in symptomatic relief. To our knowledge, this is the first report of the discrete papular form of LM occurring in an African American, as well as the first report on the.

Green flame moths: Scientists discover two new Limacodidae species from China and Taiwan. Below are relevant articles that may interest you. ScienceDaily shares links with scholarly publications in.

Mar 19, 2012  · Papular mucinosis is a rare skin disorder characterized by deposits of mucin in the skin. The terms "papular mucinosis" and "lichen myxoedematosus" are generally used interchangeably to describe the occurrence of this condition as a localized and less severe form, while the term scleromyxoedema refers to a generalized, more severe form.

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Lichen myxedematosus is an idiopathic, cutaneous mucinosis with 2 clinicopathologic subsets. There is the generalised papular and sclerodermoid form, more properly termed scleromyxedema, and the localised papular form. We report the first case, to our knowledge, of lichen myxedematosus in association with rheumatoid arthritis as well as a case in association with dermatomyositis.

A newly disovered yeast partner may explain the unusual compounds found in many lichens. PHOTOS: TIM WHEELER Lichen isn’t much to look at—often just a gray, yellow-green, or garish orange crust on.

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Scleromyxedema—the generalized form of lichen myxedematosus, a primary mucinosis—is a rare disease in human patients. It is characterized by dermal mucin deposits, increased numbers of fibroblasts, and variable fibrosis in the absence of thyroid disease. It is accompanied in 80% of cases by a monoclonal gammopathy. To date, scleromyxedema with systemic involvement has not been.

Most of the fossils represent extant lineages of the Lecanoromycetes, an almost exclusively lichen-symbiotic class of Ascomycota. The fossil lichens show a wide diversity of morphological adaptations.

Study selection Studies were included if they reported prevalence of hepatitis C virus (HCV) in people who have oral lichen planus (OLP), compared clinical and histological features of OLP in patients.

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Scleratrophic skin lesions like morphea, lichen sclerosus etatrophicus (LSA. Bentham Science Publishers. "Atrophosclerodermic manifestations of lyme borreliosis." ScienceDaily. ScienceDaily, 25.

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The common pale form of the moth is camouflaged against lichen growing on tree bark. During the Industrial Revolution — when pollution killed lichen and bark was darkened by soot — a darker-winged.

In return, the fungi and bacteria thrive on the carbohydrates that plants provide from photosynthesis. Lichen — the frilly white-green algae-fungus amalgamations that grow on rocks and trees — are.

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Atypical Lichen Myxedematosus is a skin condition that comprises of subtypes that may exhibit features from both the generalized form and localized forms of lichen myxedematosus, which is a rare skin abnormality characterised by mucin deposition in the skin.

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Abstract. Scleromyxedema or lichen myxedematosus is a rare papular mucinosis of chronic and progressive course and unknown etiology. It is commonly associated with monoclonal gammopathy and may show extracutaneous manifestations, affecting the heart, lung, kidney, and nerves.

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Some plants and lichen (lichen are like plants) can absorb water from dew. It’s a little bit like they are “drinking” the dew. I hope this helps.

We read with interest the article by Thomas et al., recently published in the Indian Journal of Dermatology.[1] In this article, the authors described a case of lichen myxedematosus (LM) and classified it as “an atypical scleromyxedema (SM)” based on the criteria proposed by Rongioletti and.

Localised lichen myxedematosus (LM) is a chronic idiopathic papular mucinosis that can be divided into five subtypes: a discrete papular (DPLM) form, acral persistent papular mucinosis (APPM), papular mucinosis of infancy, a nodular form and self-healing cutaneous mucinosis.1 DPLM presents as a chronic eruption of red or flesh-coloured 2–5 mm papules, symmetrically involving the limbs and trunk.

Academic researchers engaged in clinical trials. but her most challenging condition cropped up three years ago when she was diagnosed with oral lichen planus, which makes eating, sometimes even.

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Mar 19, 2012  · Papular mucinosis is a rare skin disorder characterized by deposits of mucin in the skin. The terms "papular mucinosis" and "lichen myxoedematosus" are generally used interchangeably to describe the occurrence of this condition as a localized and less severe form, while the term scleromyxoedema refers to a generalized, more severe form.