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{{Infobox disease | {{Infobox disease |
Name = Keloid Disorder | Name = Keloid |
Image = Verbrennungsnarbe keloid1.jpg | Image = Verbrennungsnarbe keloid1.jpg |
Caption = Keloid on the throat| Caption = Keloid on the throat|
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A '''keloid ''' ({{IPAc-en|ˈ|k|iː|l|ɔɪ|d}}; also '''keloidal scar''')<ref name="Bolognia">{{cite book |author=Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |pages=1499|isbn=1-4160-2999-0 |oclc= |doi= |accessdate=}}</ref>
'''Keloid ''' ({{IPAc-en|ˈ|k|iː|l|ɔɪ|d}}; is a very hard to treat fibro-proliferative disorder of cutaneous connective tissue secondary to dysregulation in various skin repair and healing processes. Keloid Disorder has a very diverse phenotype and presents itself for most part during childhood and teenage years.
is the formation that a type of ] which, depending on its maturity, is composed mainly of either type III (early) or type I (late) ]. It is a result of an overgrowth of granulation tissue (collagen type 3) at the site of a healed skin injury which is then slowly replaced by collagen type 1. Keloids are firm, rubbery lesions or shiny, fibrous ], and can vary from pink to flesh-coloured or red to dark brown in colour. A keloid scar is ] and not contagious, but sometimes accompanied by severe itchiness, pain,<ref>{{cite journal |author=Ogawa R |title=The most current algorithms for the treatment and prevention of hypertrophic scars and keloids |journal=Plast. Reconstr. Surg. |volume=125 |issue=2 |pages=557–68 |date=February 2010 |pmid=20124841 |doi=10.1097/PRS.0b013e3181c82dd5 |url=http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0032-1052&volume=125&issue=2&spage=557}}</ref> and changes in texture. In severe cases, it can affect movement of skin. Keloid scars are seen 15 times more frequently in highly-pigmented ethnic groups than in Caucasians.


Keloids should not be confused with ], which are raised scars that do not grow beyond the boundaries of the original wound.
Age of onset of Keloid Disorder is not well described in the literature and has not been subject of any prior research. Based on clinical observations, various authors have reported Keloid Disorder to be commonly seen between the ages of 10 and 30 with no indication of the age of onset of this disorder.

Keloid Disorder is one that has been neglected by the medical research community, as a result, our knowledge about this condition is very limited. Epidemiology of Keloid Disorder has never been studied. Although the disorder runs in families, its genetic basis has not been understood. In the same token, there has not been any advances in treatment of keloid in the past several decades.

Keloid Disorder results in excessive deposition of collagen (type 3) at the site of previous skin injury. Clinically Keloid lesions are firm, rubbery or shiny, fibrous ], and can vary from pink to flesh-coloured or red to dark brown in colour. Keloid Disorder is ] and not contagious, but sometimes accompanied by severe itchiness, pain,<ref>{{cite journal |author=Ogawa R |title=The most current algorithms for the treatment and prevention of hypertrophic scars and keloids |journal=Plast. Reconstr. Surg. |volume=125 |issue=2 |pages=557–68 |date=February 2010 |pmid=20124841 |doi=10.1097/PRS.0b013e3181c82dd5 |url=http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0032-1052&volume=125&issue=2&spage=557}}</ref> and changes in texture. In severe cases, it can affect movement of skin. Keloid scars are seen 15 times more frequently in highly-pigmented ethnic groups than in Caucasians.

Keloid Disorder should not be confused with ], which are raised scars that do not grow beyond the boundaries of the original wound. The term keloid scarring, although commonly used, it does not define this fascinating disorder.

This disorder can present itself as a single spot on the skin of the affected individual, or it can involve several areas of the skin. In some cases, presentation is limited to one or few small lesions of the skin; either round or linear; in other cases, keloid lesions can appear as large nodules, conglomerate of nodules, massive skin tumors, or appear as very large patches.

Most keloid lesions develop in an early age in genetically predisposed individuals subsequent to variety of injuries to the skin which span from acne, chicken pox, vaccination, surgical wound, burns, etc. Over time, the lesions grow in size and number and may cause a multitude of physical as well as psychological issues for the patients.

The diverse phenotype and multitude of factors that trigger keloid formation has led us to propose “Keloid Disorder” as the identifying name for this condition and the term “Keloid” to be reserved for referring to each individual skin lesion that patients have.
Although reported in individuals from almost all ethnic backgrounds, this disorder is more common among two distinct and genetically distant populations; Africans / African Americans and Asians. The only groups of individuals who may be spared from developing keloids are albinos, making the case for a relationship between melanin production and susceptibility to keloid formation at least among dark-skinned individuals.

Most patients, especially Africans and African Americans have a positive family history of keloid disorder. Development of keloids among twins also lends credibility to existence of a genetic susceptibility to develop keloids. Marneros et al. (5) reported four sets of identical twins with keloids; Ramakrishnan et al. (6) also described a pair of twins who developed keloids at the same time after vaccination. Case series have reported clinically severe forms of keloids in individuals with a positive family history and black African ethnic origin .

Although Keloid Disorder can occur at any age, it tends to develop more rapidly during and after puberty. Epidemiology and age of onset of Keloid Disorder has never been systematically studied. Indeed, Keloid Disorder is one of the most understudied disorders known to human. Our current understanding of the age of onset and age distribution of Keloid Disorder is solely based on observation or citations of very old literature, or studies that have had aims other than studying the true age of onset of Keloid Disorder. While studying genetics of Keloid Disorder, Clark et. al. studied 5 families with total of 35 affected individuals with various phenotypes and distribution of keloidal lesions. Age of onset of Keloid Disorder was obtained by taking history from the study subjects. The age reported for first keloid development varied from 5 to 52 years, although most subjects examined (50%) reported onset of their first keloid between 10 and 19 years. Similarly when individuals with multiple keloids were asked to recall onset age of each lesion, participants reported the largest number of keloids (46%) appearing between 10 and 19 years.

Knowing that keloid disorder has a very variable phenotype with a yet unknown genotype, and that it can occur in all races and among individuals of all ages, one can only assume that there may be some correlations between the age of onset of Keloid Disorder and variables such as race, heritage and country of origin, pattern of distribution of keloidal lesions on the skin as well as factors that trigger keloid formation.


==Signs and symptoms== ==Signs and symptoms==
In addition to formation of keloid lesions, most patients sufeer


Keloids expand in claw-like growths over normal skin.<ref>{{cite journal |doi=10.4103/0970-0358.19796 |author=Meenakshi J, Jayaraman V, Ramakrishnan KM, Babu M |title=Keloids and hypertrophic scars: a review |journal=Indian J Plast Surg |volume=38 |issue=2 |pages=175–9 |year=2005 |url=http://www.ijps.org/article.asp?issn=0970-0358;year=2005;volume=38;issue=2;spage=175;epage=179;aulast=Meenakshi}}</ref> They have the capability to hurt with a needle-like pain or to itch without warning, although the degree of sensation varies from person to person. Keloids expand in claw-like growths over normal skin.<ref>{{cite journal |doi=10.4103/0970-0358.19796 |author=Meenakshi J, Jayaraman V, Ramakrishnan KM, Babu M |title=Keloids and hypertrophic scars: a review |journal=Indian J Plast Surg |volume=38 |issue=2 |pages=175–9 |year=2005 |url=http://www.ijps.org/article.asp?issn=0970-0358;year=2005;volume=38;issue=2;spage=175;epage=179;aulast=Meenakshi}}</ref> They have the capability to hurt with a needle-like pain or to itch without warning, although the degree of sensation varies from person to person.


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Revision as of 03:15, 7 May 2014

Medical condition
Keloid
SpecialtyDermatology Edit this on Wikidata
Postoperative keloid

A keloid (/ˈkiːlɔɪd/; also keloidal scar) is the formation that a type of scar which, depending on its maturity, is composed mainly of either type III (early) or type I (late) collagen. It is a result of an overgrowth of granulation tissue (collagen type 3) at the site of a healed skin injury which is then slowly replaced by collagen type 1. Keloids are firm, rubbery lesions or shiny, fibrous nodules, and can vary from pink to flesh-coloured or red to dark brown in colour. A keloid scar is benign and not contagious, but sometimes accompanied by severe itchiness, pain, and changes in texture. In severe cases, it can affect movement of skin. Keloid scars are seen 15 times more frequently in highly-pigmented ethnic groups than in Caucasians.

Keloids should not be confused with hypertrophic scars, which are raised scars that do not grow beyond the boundaries of the original wound.

Signs and symptoms

Keloids expand in claw-like growths over normal skin. They have the capability to hurt with a needle-like pain or to itch without warning, although the degree of sensation varies from person to person.

If the keloid becomes infected, it may ulcerate. Removing the scar is one treatment option; however, it may result in more severe consequences: the probability that the resulting surgery scar will also become a keloid is high, usually greater than 50%. Laser treatment has also been used with varying degrees of success.

Gordon, with keloid from being whipped.

Keloids form within scar tissue. Collagen, used in wound repair, tends to overgrow in this area, sometimes producing a lump many times larger than that of the original scar. Although they usually occur at the site of an injury, keloids can also arise spontaneously. They can occur at the site of a piercing and even from something as simple as a pimple or scratch. They can occur as a result of severe acne or chickenpox scarring, infection at a wound site, repeated trauma to an area, excessive skin tension during wound closure or a foreign body in a wound. Keloids can sometimes be sensitive to chlorine. Keloid scars can grow, if they appear at a younger age, because the body is still growing.

Location

Keloids can develop in any place where an abrasion has occurred. They can be the result of pimples, insect bites, scratching, burns, or other skin trauma. Keloid scars can develop after surgery. They are more common in some sites such as the central chest, the back and shoulders and the ear lobes. They can also occur on body piercings. The most common spots are earlobes, arms, pelvic region, and over the collar bone.

Cause

Keloids usually result from piercings, implantations, etc. where metals with grades lower than surgical were used. There is also speculation that fibroblasts, MMP-2 (Matrix Metalloproteinase-2), and/or TIMP (Tissue Inhibitors of Metalloproteinases) could have some relation to the cause.

Pathology

Histologically, keloids are fibrotic tumors characterized by a collection of atypical fibroblasts with excessive deposition of extracellular matrix components, especially collagen, fibronectin, elastin, and proteoglycans. Generally, they contain relatively acellular centers and thick, abundant collagen bundles that form nodules in the deep dermal portion of the lesion. Keloids present a therapeutic challenge that must be addressed, as these lesions can cause significant pain, pruritus (itching), and physical disfigurement. They may not improve in appearance over time and can limit mobility if located over a joint.

Keloids affect both sexes equally, although the incidence in young female patients has been reported to be higher than in young males, probably reflecting the greater frequency of earlobe piercing among women. The frequency of occurrence is 15 times higher in highly pigmented people. African descendant people have increased risk of keloid occurrences.

Treatments

The best treatment is prevention in patients with a known predisposition. This includes preventing unnecessary trauma or surgery (including ear piercing, elective mole removal), whenever possible. Any skin problems in predisposed individuals (e.g., acne, infections) should be treated as early as possible to minimize areas of inflammation.

Should keloids occur, the most effective treatment is superficial radiotherapy (SRT), which can achieve cure rates of up to 90%.

Epidemiology

Persons of any age can develop a keloid. Children under 10 are less likely to develop keloids, even from ear piercing. Keloids may also develop from Pseudofolliculitis barbae; continued shaving when one has razor bumps will cause irritation to the bumps, infection, and over time keloids will form. Persons with razor bumps are advised to stop shaving in order for the skin to repair itself before undertaking any form of hair removal. The tendency to form keloids is speculated to be hereditary. Keloids can tend to appear to grow over time without even piercing the skin, almost acting out a slow tumorous growth; the reason for this is unknown. If a keloid grows too large, removal is the only solution, resulting in a scar or, in worst cases, amputation.

History

Keloids were described by Egyptian surgeons around 1700 BC. Baron Jean-Louis Alibert (1768–1837) identified the keloid as an entity in 1806. He called them cancroïde, later changing the name to chéloïde to avoid confusion with cancer. The word is derived from the Greek χηλή, chele, meaning "hoof", here in the sense of "crab pincers", and the suffix -oid, meaning "like". For many years, Alibert's clinic at Hôpital Saint-Louis was the world’s center for dermatology.

Gallery

Young male with bilateral keloid formation on the plantar surfaces of feet

References

  1. Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 1499. ISBN 1-4160-2999-0.{{cite book}}: CS1 maint: multiple names: authors list (link)
  2. Ogawa R (February 2010). "The most current algorithms for the treatment and prevention of hypertrophic scars and keloids". Plast. Reconstr. Surg. 125 (2): 557–68. doi:10.1097/PRS.0b013e3181c82dd5. PMID 20124841.
  3. Meenakshi J, Jayaraman V, Ramakrishnan KM, Babu M (2005). "Keloids and hypertrophic scars: a review". Indian J Plast Surg. 38 (2): 175–9. doi:10.4103/0970-0358.19796.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: unflagged free DOI (link)
  4. Kathleen Collins, "The Scourged Back," History of Photography 9 (January 1985):hy 43-45.
  5. Wound Healing, Keloids at eMedicine

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