Showing posts with label discoloration. Show all posts
Showing posts with label discoloration. Show all posts

Monday, October 28

Skin discoloration

Skin discoloration
Skin discoloration is the most common dermal condition experienced by us. Though skin discoloration usually may not pose as a problem, in some cases serious diseases may be associated with it.

Normally skin coloration and skin pigmentation are dependent on the ethnicity of an individual. On many instances the normal human skin color gets changed in patches or in great areas due to many factors including environment, hormones, foods, immune responses and diseases. The following pages discuss individual skin discolorations and their causes.

Types of skin discoloration

Changes in skin color usually appear as small irregular patches. However sometimes a greater area may show change in color. These skin discolorations can take up different hues. Changes in melanin pigment, pregnancy, hormonal imbalances and immune diseases can cause hypopigmentation or hyperpigmentation leading to pale, white, dark or brown color change.

Hypervascularization, inflammation or infections can cause red or pinkish color change in the affected area. Cyanosis, diet, hypercarotenemia, mineral overload, medicines and jaundice can also cause skin discolorations.

For more information read 'Types of skin discoloration'.


Skin discoloration pictures

The pictures of dermal color changes gives us a clear comparative idea about the medical conditions and help us in diagnosis and treatment of diseases. Addison's disease is a disorder of adrenal gland insufficiency. Addison disease primarily manifests as hyperpigmentation showing symptoms of patchy tanning.

Patients affected by type 2 diabetes develop scleroderma diabeticorum, a rare disorder of epidermis causing its thickening with excess black or dark brown melanin deposits. Mostly the skin on the upper back and the back of the neck is affected.

For more information read 'Skin discoloration pictures'.


White discoloration on skin

Though the human color is hereditary, pale or white patchy color changes can occur due to hypopigmentation or hypomelanosis. The reduced pigmentation may occur due to avitaminosis, certain congenital disorders, injuries or infections. Genetic disorders as in albinism and defective embryonic development as in leucism can cause complete or high level of whitening.

Color changes due to vitiligo are mostly brought about by autoimmune diseases causing death of melanin pigment producing cells (melanocytes). These hypopigmentation patches occur usually on the extremities like fingers. Color changes also occur around body orifices like umbilicus, mouth, genitalia, nostrils and eyes.

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Dark brown or black discoloration of skin

Excess production and deposition of melanin pigment (hyperpigmentation) on the epidermis gives rise to black or dark brown color changes. The appearance of dark brown or black patches may be due excess sun exposure, sun damage, excess tanning, diseases, hormones or injuries. It is found that persons of Mediterranean, African or Asian origin are more prone to excess pigmentation.

Melanocytic nevus, commonly known as birthmark, is a common dark brown or black growth of the epidermis. Melanocytic nevus may form subdermally or form as a pigmented growth on the skin. Birthmarks are congenital being present at the time of birth and melanocytic nevi may appear in the later stages of life. Moles and birthmarks which change color, shape or size and those which are painful may have to be medically investigated as some can turn into melanoma (a type of cancer).

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Reddish skin discoloration

Reddish color change is due to increased blood flow to dermis (hyperemia), bleeding underneath epidermis or formation of carboxyhemoglobin in the blood. The hyperemia of dermis is also known as erythema wherein there is increased blood flow in capillaries. Inflammations, injuries, cellulitis or infections can cause increased blood flow in the affected area. These color changes usually disappear with the resolution of the medical problem.

When there is bleeding underneath the dermis purple or reddish discoloration change occurs which is known as purpura. Purpura does not blanch on applying finger pressure while erythema disappears. Inhalation of carbon monoxide can form carboxyhemoglobin in the blood giving reddish coloration. Carbon monoxide inhalation causes debilitating effects at low levels and is fatal in high levels.

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Bluish discoloration of skin

Bluish coloration is usually due to oxygen depleted blood as in cyanosis, Raynaud's Syndrome and methemoglobinemia. Oxygen depleted blood appears dark red in color and generates shift in optical effects leading to bluish appearance. Mongolian spots appear as bluish patches with irregular shape and wavy borders.

Mongolian spots are due to melanocytes being entrapped and embedded deep in the dermis during their embryonic development and accumulation of melanin. Argyria is the bluish coloration due to accumulation of silver on the dermis caused by ingesting silver compounds as health potions.

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Yellow discoloration of skin

Yellow coloration can be due to the buildup of bilirubin in the blood and the onset of jaundice. Many diseases and conditions lead to buildup of bilirubin in the blood. Yellow coloration requires medical evaluation as it may be due to very serious life threatening diseases.

Increased rate of breakdown of red blood cells can cause pre-hepatic jaundice. Hepatocellular jaundice is caused when the bile does not flow to duodenum. Post-hepatic jaundice is usually due to interruption to the flow of bile inside liver as well as to duodenum.

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Reddened skin

Reddened skin can be due to thin epidermal layer and/or lack of pigment as in the case of lips. It can be also due to benign growths, swellings or tumors caused by endothelial cells involution as in the case of hemangioma. Hemangioma are benign infancy tumors and they usually resolve by the age of ten years.

Nevus flammeus, a birthmark, produces reddened coloration due to dilation of superficial and deeper capillaries. Nevus flammeus usually persists throughout the life. Salmon patches (nevus simplex) are again highly prevalent birthmarks appearing on the forehead, eyelids, knees, on lips or back of neck. Salmon patches are due to dilation of superficial blood vessels and resolve as the child grows.

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Orange skin discoloration

β-Carotene, a carotenoid antioxidant, imparts yellow-orange coloration to fruits and vegetables. When excess of fruits and vegetables, especially carrots, are consumed the carotenoids are deposited in the intercellular lipids of the stratum corneum imparting yellow-orange color (carotenemia).

The coloration is more pronounced where the stratum corneum is thicker as in palms, soles and nasolabial folds. Secondary carotenemia occurs when there is decreased metabolism or excretion of carotenoids requiring medical treatment. Normally orange coloration resolves over a few days when excess consumption of carrots is stopped.

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Carotene in carrots - Orange skin discoloration

Orange skin discoloration - Carotene in carrots
Excess consumption of carotene in carrots causes orange yellow skin discoloration. The β-carotene in carrots contributes to its orange color.
Though cosmetically displeasing to some, there is no apparent health impact of orange skin discoloration (carotenemia). However possible health effects of this condition have to be well researched.

Carotene in carrots

Carrots ((Daucus carota subsp. sativus) belong to Apiaceae family and are cultivated throughout the world. In a research study done in Netherlands it was found that regular consumption of carrots lowered the risk of cardiovascular disease (CVD). It was found to be due to the antioxidant activities of the carotenoids and polyacetylenes (falcarinol and falcarindiol) present in carrots.

Carotenes are a type carotenoids (tetraterpenoid organic pigments) which lack oxygen in their structure and are pure hydrocarbons. These fat-soluble carotenoids occur in the chloroplasts and chromoplasts of plants and occur in higher concentrations in some plants as in carrots giving them orange color.

Professor Heinrich Wilhelm Ferdinand Wackenroder (8 March 1798 – 4 September 1854), a German chemist and a professor at the University of Jena, isolated carotin (carotene) from carrots. Its structure was determined by Professor Paul Karrer (April 21, 1889 - June 18, 1971, a Nobel laureate, in early 1930s. Alpha-carotene present in carrots is found to be protective against the proliferation of human cancer cells.

β-carotene (C40H56) is the most studied of about fifty carotenoids identified in the human diet. Carrots are high in the (all-E)-beta-carotene isomer. It is an isomer form having higher bioavailability, provitamin A activity, and antioxidant activity when compared to Z (cis) isomer form of this carotenoid. The levels of all three Z isomers in raw carrots are low and are about 1.8% of the total isomers. Storage at low temperatures in fact increases the (all-E)-beta isomers.

There is thermal isomerization during cooking of carrots causing generation of all the three Z isomers. To get the maximum benefits, carrots should be stored at low temperatures. Carrots should be consumed raw or boiled for less than fifteen minutes to limit Z isomerization.

β-Carotene in fruits and vegetables

The β-carotene in many fruits and vegetables contributes to orange color. Orange and yellow fruits like mangoes, cantaloupe and papayas and orange roots like yam and carrots are rich sources of this carotenoid.

Though the Vietnamese gac fruit (Momordica cochinchinensis) and crude palm oil contain the highest amount of β-carotene, nearly ten times higher than carrots, gac fruit is less known outside Southeast Asia and the crude palm oil loses the β-carotene while processing and refining.

Carrots and yellow/orange skin discoloration

Excessive consumption of fruits and vegetables containing β-carotene causes carotenosis (carotenodermia, carotenemia or hypercarotenemia), a harmless condition giving a yellow-orange tint to the epidermis. This is due to deposition of these carotenoids in the outermost epidermal layer of skin.

This yellow-orange discoloration differs from that caused by the jaundice disease. In jaundice apart from yellowish pigmentation of the epidermis, the conjunctival membranes over the sclerae (whites of the eyes) also turn yellow whereas in carotenodermia sclerae remain white.

Carotenes have vitamin A activity and get partially converted into vitamin A (retinol) within the intestinal mucosa by a dioxygenase enzyme. If the vitamin A status of the individual is high, the conversion decreases and the excess carotenoids are stored/deposited in the fat tissues and epidermal layers. These carotenoids are deposited in the intercellular lipids of the stratum corneum of the skin.

Though the orange coloration can be generalised, it is more prominent in areas where stratum corneum is thicker and also in areas where there is profuse sweating. Palms, soles, nasolabial folds and behind ears are more prone to discoloration. The orange discoloration of epidermis reverses on cessation of consumption of carrots and other foods containing this carotenoid.

Some underlying health disorders may cause secondary carotenemia wherein increased serum lipids and decreased metabolism of carotenoids are the causes. In such cases treating the disease condition will resolve carotenemia.

If the orange skin discoloration is due to excess consumption of carrots, fruits or other vegetables, cessation of excess intake will reverse the skin condition without any blemishes, spots and marks.


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1.Imsic M, Winkler S, Tomkins B, Jones R. Effect of storage and cooking on beta-carotene isomers in carrots ( Daucus carota L. cv. 'Stefano'). J Agric Food Chem. 2010 Apr 28;58(8):5109-13.
Current Natural Skin Care topic: Carrots - Carotene - Orange skin discoloration

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Wednesday, December 15

Yellow skin discoloration - Causes of yellow skin color

Skin discoloration - Yellow skin color
There are many causes for yellow skin color and discoloration and the condition has to be evaluated immediately as some are harmless changes, whereas some are due to serious disorders which can be life threatening, requiring immediate treatment.

Causes of yellow skin color

Certain pigments in the food like carotene get deposited in the epidermal layers when in excess and their presence causes yellow skin color change which is harmless. However, certain disorders of the body systems can interfere with the metabolism of carotene.

These disorders induce carotene deposition and discoloration even though serum levels of carotene are normal, requiring investigation. The excretion of certain medicines through epidermal layers shows up as yellow skin color. The buildup of bilirubin in the blood and the onset of jaundice is due to many diseases and disorders leading to yellow coloration.

Jaundice caused yellow skin discoloration

Jaundice (aka icterus) is yellow pigmentation of the dermal and epidermal layers, sclerae (white of eyes) and mucous membranes. The increased levels of bilirubin in blood plasma (1.5 mg/dL), also known as hyperbilirubinemia, causes jaundice. Hyperbilirubinemia can be due to various factors and categorized into pre-hepatic, hepatocellular and post-hepatic types.

Any of the causes of increased rate of breakdown of red blood cells (hemolysis) leads to pre-hepatic jaundice. Tropical diseases like malaria, genetic diseases like thalassemia, organ disorders like hemolytic uremic syndrome affecting kidney, bilirubin metabolism disorders and high fevers as in leptospirosis (rat fever) causes jaundice and dermal color change.

In hepatocellular jaundice there is usually cholestasis (bile not flowing to duodenum) and the causes are hepatitis of any origin, liver toxicity, genetic disorders like Gilbert's syndrome, alcoholic liver disease and Crigler-Najjar syndrome. Post-hepatic jaundice is usually due to interruption to the flow of bile inside liver as well as to duodenum.

The causes can be gallstones in the bile duct, cancer of pancreas, obstruction by liver flukes, biliary atresia (passage closed or absent), ductal carcinoma (tumor in the duct), pancreatitis (inflammation of the pancreas) and pancreatic pseudocysts (circumscribed collection of fluid rich in pancreatic enzymes, blood, and necrotic tissue). Jaundice discoloration conditions require a combination of liver function tests to arrive at the exact causes and diagnosis.

Newborn and yellow skin color

Mild jaundice is observed in many newborns and this neonatal jaundice is usually harmless. This condition may be seen from second day to eighth day in normal birth and for about two weeks in premature births. It is presumed that apart from higher turnover of red blood cells, physiological and metabolic adjustments after birth, causes this increase in serum bilirubin in newborn.

This increased levels of bilirubin gets lowered with regular urination and bowel movement; hence regular and proper feeding of the baby are very important. However in a few rare cases, neonatal hyperbilirubinemia causes kernicterus, a brain-damaging condition, resulting in lifelong disability.

To avoid this risk it is better to treat the neonatal jaundice by exposing the baby to intense photo-therapy. Inadequate feed, infections, internal bleeding or liver disorder or malfunction or incompatible Rh blood factors of mother and child can also lead to skin discoloration requiring proper treatment.

Primary carotenoderma

Ingesting food containing high levels of carotenoids leads increased serum levels of carotene and its deposit in the skin. Carotenoids are deposited in the intercellular lipid containing spaces in stratum corneum.

Thick epidermal layers and regions of increased sweating like nasolabial folds, palms, knees and soles bear increased deposits and show greater color change. Carotenoderma differs from yellow color due to bilirubin in not showing coloration of white of eyes. Primary carotenoderma yellow color usually disappears after the reduction in intake of carotenoids.

Secondary carotenoderma

Usually a underlying disease condition causes increase in serum levels of carotene and secondary carotenoderma discoloration, though the carotene intake is normal. Kidney malfunction or dysfunction is usually associated with decreased excretion of carotenoids and hypercarotenemia and color change.

Impaired conversion of carotenoids to retinol is seen in diabetes mellitus and hypothyroidism. The associated increase in serum lipids as seen in diabetes mellitus, nephrotic syndrome and hypothyroidism causes yellow skin color and secondary carotenoderma. In Anorexia nervosa, a self-imposed starvation, diets may be rich in carotene. Liver disease also leads to yellow color change due to poor utilization and breakdown of carotene resulting in its increased serum levels.

Yellow skin color due to medicines

The use of certain medicines in the treatment of diseases causes yellow coloration. Tyrosine kinase inhibitors (TKIs) are used in the treatment of various cancers. Sunitinib (a TKI) used in the cancer therapy is associated with many adverse events and yellow color changes of the epidermal layers. Color changes start after a week of treatment and with the continuation of the treatment, color intensification has been noticed.

The sclerae and mucous membranes are spared of the color change and on the discontinuation of medicine resolves the coloration. Probably the excretion of the chemical via the epidermis causes this coloration. Another TKI, sorafenib also causes a diffuse yellow discoloration of the skin.

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Tuesday, December 7

Bluish discoloration of skin

Bluish skin discoloration
Bluish discoloration of skin can be due to cyanosis, Raynaud's Syndrome, methemoglobinemia, Mongolian spot or argyria. The skin color is determined by epidermal pigments and the colors of blood and pigments carried by the blood.
Oxygen saturated blood is bright red in color and oxygen depleted blood appears dark red. The optical properties of epidermal skin distort the color of the oxygen-depleted blood to appear bluish.

Bluish skin discoloration and cyanosis

Deoxygenated hemoglobin equal to 2.5 g/dL or greater in blood causes bluish coloration called cyanosis. Though the deoxygenated blood appears dark red, there are certain optical principles involved in its giving of different coloration. Tissues are low in oxygen in cyanosis and are filled up with dark red deoxygenated blood in place of oxygenated bright red blood.

Darker blood generates shift in optical effects leading to bluish skin discoloration. Cyanosis can be due to many health problems and notable among them are all types of blood circulatory problems, all types of ventilatory problems and extreme cold. Toxins such as cyanide interfere with oxygenation of blood and cause cyanosis.

In cyanosis two types of conditions are observed namely central and peripheral cyanosis. Circulatory or breathing problems cause reduced oxygenation of blood in the lungs and slowing down the oxygen circulation and the skin turns bluish. This is a serious situation can lead to lung or heart failure. In the peripheral cyanosis only the extremities become bluish due to inadequate blood oxygen supply. This can be corrected by increasing the oxygenated blood supply.

Raynaud's Phenomenon

Raynaud's Phenomenon is a vasospastic disorder in which blood vessels in fingers and toes spasm, leading to vasoconstriction. Raynaud's Phenomenon causes bluish color changes in the toes and fingers and their necrosis if unattended. Raynaud's Phenomenon occurs in sensitized persons as an exaggeration of vasomotor response to emotion or cold leading to bluish discoloration of skin.

In Raynaud's Phenomenon the sympathetic nervous system is hyperactivated affecting the peripheral blood vessels and their extreme vasoconstriction leading to tissue hypoxia. Recurrent attacks can cause tissue damage, ulceration, gangrene and necrosis. Shifting to a warm room and keeping fingers in warm water may relieve the symptoms and restore blood circulation. Persons prone to attacks of Raynaud's Phenomenon are advised to keep themselves warm and if necessary use vasodilatory drugs under the advice of physician.

Methemoglobinemia

Methemoglobinemia is a blood disorder wherein, methemoglobin, an oxidised form of hemoglobin is present in levels above normal condition. In methemoglobinemia, due to oxidative stress the oxygen carrying ferrous ion of hemoglobin molecule is oxidized to ferric state. This is results in conversion of hemoglobin to methemoglobin which does not bind oxygen. If the levels of methemoglobin are high in blood bluish chocolate-brown color is imparted to blood.

Methemoglobinemia impedes normal oxygen transport resulting in tissue hypoxia and bluish skin. Methemoglobinemia may be congenital with autosomal recessive inheritance pattern. Since congenital methemoglobinemia is recessive, there is a chance of inheritance in the offspring only if both the parents carry the gene. Patients with impaired production of NADH (the essential cofactor for diaphorase I) with the resultant pyruvate kinase deficiency have risk of getting methemoglobinemia and bluish skin.

Methemoglobinemia is acquired in people exposed to exogenous oxidizing drugs and chemicals. Antibiotics like dapsone, sulphonamides and trimethoprim can give rise to increased methemoglobin levels and methemoglobinemia. Certain local anaesthetics (prilocaine and articaine), chlorates, bromates, metoclopramide, nitrates and aniline dyes can also cause methemoglobinemia. Methemoglobinemia disorder can be treated with oxygen supplementation and administration of intravenous methylene blue 1% solution.

Mongolian spot

Mongolian spot is a congenital birthmark, which is flat, benign and harmless; it is sometimes mistaken as an injury or bruise during childbirth. Mongolian spot exclusively involves skin and is due to melanocytes (melanin producing cells) embedded deep in the dermis. Mongolian spot results from melanocytes entrapment in the dermis during their embryonic development.

Mongolian spot is usually a bluish skin and with irregular shape and wavy borders. Mongolian spot can appear as multiple skin discoloration spots usually on the shoulders, flanks, lower back and the buttocks. Mongolian spot is highly prevalent in East Asians, East Africans, Polynesians and Turkic people. As the child with Mongolian spot grows, the spot fades and disappears by puberty.

Argyria

Argyria is condition wherein irreversible bluish or bluish-grey skin discoloration is caused by exposure to silver dust, silver compound and elemental silver. Silver gets accumulated in the body and the dermis on chronic exposure. On exposure to sunlight these particles in the skin darken giving a dark discoloration. Generalized argyria occurs when silver containing compounds are ingested and the whole body gives bluish discoloration.

Localized argyria occurs due to continuous contact with silver and its compounds. Argyria is a harmless cosmetic problem which can be socially debilitating and mildly disfiguring. Though generally believed to be irreversible, avoidance of sun exposure and laser therapy appears to give good results.

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Sunday, December 5

Reddish skin discoloration

Reddish skin discoloration
Reddish skin discoloration (Erythema) is the result of increased blood flow (hyperemia) of the capillaries in the lower dermal layers.
Bruises, certain infections and injuries can give rise to purpura, a reddish coloration due to bleeding underneath the epidermis.

Erythema - reddish skin discoloration

Erythema is hyperaemia of the dermis, wherein there is increased blood flow in capillaries in the lower layers. Erythema usually has medical implications and occurs with any inflammation, injury or infection.

Erythema can be caused by dermatitis and rash, dermal and body infections, toxic insect bites, massage and friction, acne and acne medication, physical exercises, UV radiation and sunburn, radiation therapy, allergic reactions and hypersensitivity and dermabrasion. Dermatitis can result due to a wide varieties of conditions like fungal infections, eczema, psoriasis, parasitic infections, measles, Lyme disease, rubella, acne, meningitis, drug abuse, stress and anxiety.

The cause of erythema in 30-50% of incidences can be unclear and unknown. There is usually temperature elevation at the site of erythema due to engorgement of blood vessels with oxygenated blood. On finger pressure, erythema disappears whereas in purpura the reddish color persists. Fall in atmospheric pressure can also induce erythema.

Purpura and purple or reddish discoloration

Purpura is the appearance of purple or reddish color caused by bleeding underneath. Purpura does not blanch on applying finger pressure while erythema disappears. Purpura can result due to injuries and bruises, infections, cutaneous small-vessel vasculitis, foods, hereditary disorders and drug reactions. In bruise the capillaries and sometimes venules are damaged due to injury allowing blood to seep beneath the dermis and into surrounding interstitial tissues.

Disseminated intravascular coagulation is a pathological activation of blood clotting (coagulation) induced by certain infections. In typhus infection dull reddish rash appears on the middle of body and spreads. Meningitis caused by meningococcal bacteria may be accompanied by a characteristic rash. Inflammation of small blood vessels (cutaneous small-vessel vasculitis) is clinically characterized by purpura. Food-induced purpura may result from ingestion of food containing Escherichia coli, benzoates or tartrazine dye.

Allergic reactions to certain drugs can cause extensive purpura. Purpura can occur due to hereditary blood coagulation disorders as in the case of hemophilia or von Willebrand's disease. In most cases of purpura there is initially crimson coloration, which turns purple and then blue due to breakdown of blood cells.

Reddish skin coloration and carbon monoxide poisoning

Carbon monoxide is a poisonous gas formed by burning of carbon materials under low oxygen conditions when there is not sufficient oxygen to produce carbon dioxide. This gas may get produced in running car engine in a closed garage or by burning wood or operating stove in a small closed room. When this gas is inhaled in larger quantities carbon monoxide poisoning occurs which is highly visible on the victims as Reddish coloration.

Carbon monoxide is highly reactive with blood hemoglobin and forms carboxyhemoglobin. Carboxyhemoglobin at concentrations above 30% appears bright crimson and the color intensifies with increase in concentrations. Though at these concentrations it can be fatal, many survivors of lower exposure show apart from many debilitating effects show reddish coloration.

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Tuesday, November 30

Kinds of skin discoloration

Pictures of skin discoloration

Patchy irregular skin discoloration can be caused by various reasons.

The skin discoloration pictures and their brief description gives us a clear idea about the conditions and the ways to tackle them.
Changes in melanin pigmentation, diet, pregnancy, inflammation, growth of foreign organisms, diseases, hypercarotenemia, hypervascularization, cyanosis, mineral overload, medicines and jaundice can cause these various hues of discoloration.

Skin discoloration can be different and versicolor like white, brown, dark, red, pink, black, blue, orangish, yellowish, bronze and slate colors.

Skin discoloration and hyperpigmentation in Addison disease

Addison's disease, which is a disorder of adrenal gland insufficiency, increased tanning can be noted.
The manifestation of Addison disease in the skin primarily by hyperpigmentation.

Sunburn

Sunburn is a burn to skin tissue due to over exposure to sun light. There is malady and pain with hot, red or reddish skin and associated fatigue and mild dizziness.

Tanning

Tanning is a process by which skin color is darkened due to exposure to ultraviolet rays.
Moderate exposure to sun light has benefits like enhancing the vitamin D production by the dermis.

Freckles

Freckles are often visible in people with fair complexion and are concentrated clusters of melanin deposits.
Freckles contrast from moles and lentigines in that there is no increase in the number of melanin producing cells.

Lentigo

Lentigo (plural lentigines) is a benign hyperplasia (proliferation of cells) of melanocytes.
Regardless of sun exposure lentigo is stable in color and differ from moles in its linear spread, whereas moles are multi-layer nests of melanocytes.

Acanthosis nigricans

Acanthosis nigricans is brown to black, velvety, poorly defined skin discoloration.
Acanthosis nigricans dark brown coloration is usually found in the body folds like groins, armpits, neck folds etc.

Scleroderma diabeticorum

Scleroderma diabeticorum is a rare disorder affecting people with type 2 diabetes.
Scleroderma diabeticorum causes thickening of epidermis on the upper back and the back of the neck with excess black or dark brown melanin deposits.

Albinism

(achromia) is a hypopigmentary disorder which is congenital.
Albinism results from defect in production of melanin pigment due to dysfunction of melanocytes (melanin producing cells) in the skin, hair and eyes.

Leucism

Leucism, white skin coloration, is a result of defects in neural crest pigment cell differentiation.
Unlike albinism wherein the melanocytes are very much present but they fail to produce melanin pigment only, here the discoloration is caused due to defect in the embryonic development and there is partial or complete absence of pigment cells.

Vitiligo

In , a chronic disorder, loss of pigment (depigmentation) occurs in patches leading aesthetic disfigurement of the affected individual.
These depigmentation patches occur usually on the extremities and around body orifices like umbilicus, mouth, genitalia, nostrils and eyes.

Tinea versicolor

is caused by yeasts (fungi) Malassezia globosa and .
The first signs of tinea versicolor infection are small spots of pale discoloration, usually lighter than the surrounding area, developing on the oily areas of the body, such as back, upper arms and shoulder giving rise to itching.
Nevus depigmentosus are harmless non-progressive hypopigmented stable localised patches.
Nevus depigmentosus patches result from localised abnormalities in the function of melanocytes which fail to produce pigments.

Mongolian spot

, also known as "Mongolian blue spot," is a benign, flat, congenital birthmark with wavy borders and irregular shape.
The blue discoloration is caused by melanocytes, melanin containing cells, that are deep under the skin.


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Monday, November 29

Black, dark discoloration of skin - Brown spots and patches

Black, dark brown skin discoloration spots and patches

Dark brown discoloration of skin and patches is due to hyperpigmentation.

Brown discoloration of skin and formation of pigmented patches in most of the cases is caused by excessive production of the melanin pigment.

Sun damage, diseases, inflammation, hormonal imbalances, injuries etc. can cause excess pigmentation leading to skin discoloration and the incidence of dark brown skin patches. People with dark skin tones as with Mediterranean, African or Asian origins are more prone for excess pigmentation.

Sun exposure

Sun exposure, which has ultraviolet A and ultraviolet B radiation, brings about color changes in two different ways. Initially the Ultraviolet A (UVA) radiation which is usually in the range of 320 to 400 nm., by oxidative stress, causes the release of melanin from the melanocytes and causes its oxidation by combining with oxygen leading to rapid darkening discoloration patches of melanin.

Secondly, melanogenesis, which is skin reaction to photo-damage from UV radiation (CPD-DNA damage or direct DNA damage), increases the production of melanin pigment. The tanning or darkening by melanogenesis is a delayed reaction and the brown patches become visible only about three days after exposure. Sunscreens, umbrellas and hats can go a long way in protection from sun damage.

Freckles, age or liver patches and lentigines

Freckles (aka ephelis) are brown discoloration often visible in people with fair complexion and are concentrated clusters of melanin deposits.
Though many people have freckles, their origin is genetic in nature and freckles are triggered by exposure to sun.

Freckles contrast from moles and lentigines in that there is no increase in the number of melanin producing cells. Lentigo (plural lentigines) is a benign hyperplasia (proliferation of cells) of melanocytes. Regardless of sun exposure lentigo is stable in color and differ from moles in its linear spread, whereas moles are multilayer nests of melanocytes.

Liver patches are associated with aging and are blemishes on the skin associated with exposure to UV radiation from the sun. These dark brown liver patches particularly form on the face, hands, neck, shoulders and head. Freckles, lentigines and liver patches are benign and harmless and if required can be treated with skin whitening treatments

Melasma - brown patches

Chloasma or melasma are dark hyperpigmentation patches particularly common in women. Melasma are irregular dark, brown patches of excess pigment found on the nose, upper cheek, lips and forehead causing cosmetic discoloration. Melasma is usually prevalent in pregnant women (mask of pregnancy), women using contraceptives or women under HRT (hormone replacement therapy) medications.

Melasma patches also prevalent in men and women of Jewish descent, Russian descent, German descent and Native American descent. Genetic predisposition, thyroid diseases and female hormones (estrogen and progesterone) are the determining factors of developing melasma.

Melanocytic nevus (mole) skin discoloration

Melanocytic nevus is a common dark brown growth of the epidermis which are known as birth mark. Melanocytic nevus may form subdermal under the skin or form a pigmented growth on the dermis. Melanocytic nevi present at the time of birth or around the time of birth are called congenital nevi.

Melanocytic nevi may also appear in the childhood or later stages of life and their discoloration may range fromlight to very dark brown. Though in most of the cases Melanocytic nevi are harmless, any mole which changes color, shape, size or hurts may have to be investigated as some can turn into melanoma (a type of skin cancer).

Addison's disease

Addison's disease, a chronic adrenal insufficiency disease, is a rare endocrine disorder wherein adrenal glands malfunction or show functional insufficiency. Apart from the symptoms like weight loss, weakness, nausea, fever, diarrhea, muscle pains and headache, the Addison's disease affected person suffers from dark brown skin discoloration patches. It can give rise to brown freckles on the face, neck and shoulders and also dark brown skin discoloration patches on the knees, elbows, toes, knuckles and forehead.

Alkaptonuria

Alkaptonuria or dark urine disease is a rare inherited disorder leading to degradation of tyrosine and production and accumulation of homogentisic acid. Alkaptonuria causes damage to cartilage and heart valves and precipitates formation of kidney stones. Alkaptonuria disorder leads to dark brown patches of skin in sun exposed areas and around sweat glands.

Acanthosis nigricans is brown to dark, velvety, poorly defined skin discoloration. Acanthosis nigricans dark brown skin discoloration patches usually found in the body folds like groins, armpits, neck folds etc. Acanthosis nigricans, typically occurs in persons below 40 years and it is associated with obesity, hormonal anamallies and insulin resistance. Control of blood sugar and obesity improves the symptoms.

Scleroderma diabeticorum and dark brown patches

Scleroderma diabeticorum is a rare disorder affecting people with type 2 diabetes. Scleroderma diabeticorum causes thickening of epidermis on the upper back and the back of the neck with excess of dark brown patches melanin deposits. Scleroderma diabeticorum can be treated by bringing blood sugar under control and using moisturizers for softening the epidermis.

Dark, brown skin discoloration between thighs and in armpits

In some persons, especially in obese persons, the skin between the thighs and also in the armpits gets dark brown discoloration patches due excess melanocyte deposit as a result of excessive sweating and dead cells build-up leading to dermatitis and related fungal infections. Use of antifungal preparations followed by exfoliation and dermabrasion, if necessary, can remove the excess skin pigmentation and the dark brown patches to a great extent.


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White discoloration on skin - Pale skin discoloration

White skin discoloration
White or pale discoloration on skin occurs due to hypopigmentation (diminished pigmentation). The epidermis layer of skin has melanin pigment which gives different hues ranging right from white to dark black.
The amount of melanin to be produced by the skin and the color of a person are decided by the genetic factors.

There are also conditions wherein white hypopigmentation occurs due to some other factors like lack of vitamins, congenital conditions, autoimmune diseases, injuries, infections etc.

White discoloration on skin due to albinism

Albinism (achromia) is a hypopigmentary disorder which is congenital. Albinism results from defect in production of melanin pigment due to dysfunction of melanocytes (melanin producing cells) in the skin, hair and eyes. Albinism can be complete or partial leading to degrees of absence of melanin pigment in the hair, epidermis and eyes.

Two main clinical phenotype categories of albinism are ocular albinism and oculocutaneous albinism which are further categorized into subtypes based on specific genetic mutations. This genetic white color occurs due to mutations to the tyrosinase gene and several different types of mutations can occur. Certain mutations can lead to completely inactive tyrosine enzyme production resulting in total albinism.

In some mutations tyrosine enzyme may have reduced activity (leaky mutations) and partial albinism may result. Mutations to P protein gene and human gene coding for TRP-1 also produce varying degrees of albinism.

Leucism

This type of white discoloration on the skin is a result of defects in neural crest pigment cell differentiation. Unlike albinism wherein the melanocytes are very much present but they fail to produce melanin pigment only, here the discoloration is caused due to defect in the embryonic development. There is partial or complete absence of pigment cells.

In partial absence of skin pigment cells 'piebald' effect is seen with varying degree of pigment absence leading to spotted pigmentation. Another difference between albinism and leucism is that albinos lack skin pigment in both iris and the retinal pigmented epithelium (RPE) leading to red color of the internal blood vessels showing up as red eyes.

However the formation of iris and the retinal pigmented epithelium is by the outpouching of the neural tube during development and is not affected by the neural crest aberration. Hence the eye color is not affected and has normal pigmentation in leucism.

White discoloration on skin due to vitiligo

In this chronic disorder loss of pigment (depigmentation) occurs in patches leading aesthetic disfigurement of the affected individual. Though the very exact cause of this white hypopigmentation - hypomelanosis is not known, most of the researchers agree that autoimmunity, neural, oxidative stress, genetic or viral causes precipitate the death and destruction of melanocytes.

These depigmentation patches affecting the normal human skin color, occur usually on the extremities and around body orifices like umbilicus, mouth, genitalia, nostrils and eyes.There are different types of vitiligo and now various treatments are available for eradication or camouflage of the white patches.

Leprosy and white discoloration on skin

Leprosy or Hansen's disease (HD), which is now on the verge of eradication from the world population, is a chronic disease caused by the bacteria Mycobacterium leprae and Mycobacterium lepromatosis. Dermal lesions are the initial external signs, characterized by one or more hypopigmented macules or patches.

These white patches are anaesthetic in nature where sensations are lost. This is due to damage caused by human immune cells on the peripheral nerves. Leprosy can be cured completely and if detected early damages to nerves, dermis, eyes and limbs can be prevented.

White discoloration on skin due to tinea versicolor

Tinea versicolor is caused by yeasts (fungi) Malassezia globosa and Malassezia furfur. Tinea versicolor, though a common microbe living on the skin, sometimes over grows in some people and the exact reason is not clear. However, tinea versicolor is found to affect people with oily epidermis and in tropical and humid climates.

The first signs of tinea versicolor infection are small hypopigmented spots, usually lighter than the surrounding area, developing on the oily areas of the body, such as back, upper arms and shoulder giving rise to itching. The white coloration caused by tinea versicolor can be effectively treated and cured with anti-fungal lotions.

Idiopathic guttate hypomelanosis

Idiopathic guttate hypomelanosis is a non-infectious common benign acquired disorder of the skin affecting women more frequently than men. Idiopathic guttate hypomelanosis white discoloration appears to affect the exposed areas of the body, more particularly forearms and legs, in late twenties.

Idiopathic guttate hypomelanosis appears as small drops-like spots of white discoloration, the exact cause of which is not clear. However, as they appear on the exposed parts of the body, exposure to sun may have some role on the melanocytes making them effete.

Nevus depigmentosus

Nevus depigmentosus are harmless non-progressive hypopigmented stable localized skin patches. Nevus depigmentosus patches result from localized abnormalities in the function of melanocytes which fail to produce pigments. Most of the nevus depigmentosus patches are usually present right from birth.

Pityriasis alba

Pityriasis alba is a common and highly prevalent facial condition occurring in children. Pityriasis alba appears as dry, fine-scaled, white patches especially on the face. Pityriasis alba is a non-contagious condition and resolves by itself after sometime. Use of moisturizers improves the scaly condition especially in winter.

Avitaminosis and white skin discoloration

The chronic lack of certain vitamins, especially vitamins of the B complex group in the diet can cause hypopigmentation.
This white skin hypopigmentation can be corrected by improving the quality of diet and taking vitamin supplements.
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