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Acne vulgaris

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Hamid Qazi, MD, BSc [2] Jesus Rosario Hernandez, M.D. [3] Tayyaba Ali, M.D.[4]

Synonyms and keywords: Common acne

Overview

Main article: Acne Vulgaris

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2]Tayyaba Ali, M.D.[3]

Overview

Acne Vulgaris is a skin disease caused by changes in the pilosebaceous units (skin structures comprising a hair follicle and its related sebaceous gland). Severe acne is inflammatory, but acne can also manifest in noninflammatory forms.[1] Acne lesions are defined as pimples, spots, or zits. Acne diminishes with age, by early twenties acne disappears. There is no set age for acne to disappear, some individuals have acne decades later, into their thirties and forties and even beyond.[2] The term acne comes from a Greek word άκμή (acme in the sense of a skin eruption) in the writings of Aëtius Amidenus. The vernacular term bacne or backne is often used to show acne found specifically on one’s back.[3]

Classification

There are multiple grading scales for rating the severity of acne vulgaris. [4] Three techniques include the Leeds acne grading technique, which counts and categorizes lesions into inflammatory and non-inflammatory (ranges from 0 to 10.0), Cook’s acne grading scale, which uses photographs to rate severity from 0 to 8 (0 being the least severe and 8 being the most severe), and the Pillsbury scale, which classifies the severity of the acne from 1 (least severe) to 4 (most severe). [5]

Epidemiology and Demographics

In the United States, acne affects 17 million people. It is most common during adolescence, affecting more than 85% of teenagers, and frequently continues into adulthood. [6]

Risk Factors

Acne is the most common skin disease that occurs in all races and ages, including teenagers and young adults. About 80 percent of all people between the ages of 11 and 30 have acne outbreaks in life. Some people in their forties and fifties still suffer from acne.[7]

References

  1. http://www.emedicine.com/DERM/topic2.htm
  2. Anderson, Laurence. 2006. Looking Good, the Australian guide to skin care, cosmetic medicine, and cosmetic surgery. AMPCo. Sydney. ISBN 0 85557 044 X.
  3. Cure forAcne
  4. Leeds, Cook’s and Pillsbury scales obtained from here
  5. “zit – docdud”.
  6. James WD (2005). “Clinical practice. Acne”. N Engl J Med. 352 (14): 1463–72. PMID 15814882.
  7. “Acne – Aesthetipedia”.

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Historical Perspective

Main article: Acne Vulgaris

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2] Tayyaba Ali, M.D.[3]

Overview

Historical Perspective

The historical backdrop of skin acne compasses back to the beginning of written history. In Ancient Egypt, it is recorded that few pharaohs were skin inflammation victims. From Ancient Greece comes the English word ‘acne’ (signifying ‘point’ or ‘pinnacle’). Skin inflammation medicines are likewise of the significant relic: :

  • Ancient Rome: Taking a hot bath, and frequently sulfurous, mineral water was one of only a handful few accessible skin acne medicines. Probably the soonest text to specify skin issues is De Medicina by the Roman author Celsus.
  • The 1800s: Nineteenth-century dermatologists used sulfur in the treatment of acne. It was believed to dry the skin.
  • The 1920s: Benzoyl Peroxide is used.
  • The 1930s: Laxatives were used as a cure for ‘chastity pimples’. Radiation also was used.
  • The 1950s: At the point when anti-toxins opened up, it was found that they effectively affected acne. They were taken orally, regardless. A significant part of the advantage was not from eliminating microscopic organisms but from the mitigating effects of antibiotic medication and its family drugs. Effective antimicrobial opened up later.
  • 1970s: Tretinoin (original Trade Name Retin A) was found effective for acne.[1] This preceded the development of oral isotretinoin (sold as Accutane and Roaccutane) in 1980.[2]
  • The 1980s: Accutane is introduced in America.
  • The 1990s: Laser treatment introduced.
  • The 2000s: Blue/red light therapy.

References

  1. “Tretinoin (retinoic acid) in acne”. The Medical letter on drugs and therapeutics. 15 (1): 3. 1973. PMID 4265099.
  2. Jones H, Blanc D, Cunliffe WJ (1980). “13-cis retinoic acid and acne”. Lancet. 2 (8203): 1048–9. PMID 6107678.

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Classification

Main article: Acne Vulgaris

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2] Tayyaba Ali, M.D.[3]

Overview

There are multiple grading scales for rating the severity of acne vulgaris.[1] Three techniques include the Leeds acne grading technique, which counts and categorizes lesions into inflammatory and non-inflammatory (ranges from 0 to 10.0), Cook’s acne grading scale, which uses photographs to rate severity from 0 to 8 (0 being the mildest or least severe and 8 being the most severe), and the Pillsbury scale, which classifies the severity of the acne from 1 (least severe) to 4 (most severe).[2]

References

  1. Leeds, Cook’s and Pillsbury scales obtained from here
  2. “zit – docdud”.

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Pathophysiology

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

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Pathophysiology

Inside the pore are sebaceous glands which produce sticky sebum. When the outer layers of skin shed (as it does continuously), the dead skin cells left behind may become ‘glued’ together by the sticky sebum. This causes a blockage in the pore, especially when the skin becomes thicker at puberty.[1] The sebaceous glands produce more sebum which builds up behind the blockage, and this sebum harbors various bacteria including the species Propionibacterium acnes. Since the body’s natural defense against bacteria is primarily phagocytes (white blood cells), these rush to the site behind the blockage (where the bacteria are). This is what gives some pimples the ‘whiteheads’ (unless the phagocytes are deeper in the skin, which means you can’t see the ‘white’ caused by them). The white blood cells then destroy (by phagocytosis) the bacteria to prevent infection. The pain one may feel when a pimple is present is caused by the widening of skin around the white blood cells.

Video

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References

  1. Anderson, Laurence. 2006. Looking Good, the Australian guide to skin care, cosmetic medicine and cosmetic surgery. AMPCo. Sydney. ISBN 0 85557 044 X.

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Causes

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]; Associate Editor(s)-in-Chief: Ogheneochuko Ajari, MB.BS, MS [3] Tayyaba Ali, M.D.[4]

Causes

Common Causes

Acne develops because of occlusion of follicles. The earliest change in acne development is hyperkeratinization and formation of a plug of keratin and sebum (a micro-comedo). Sebaceous glands enlarge, and sebum production increases with increased androgen (DHEA-S) production at the adrenarche. The micro-comedo may enlarge to form an open comedo (blackhead) or closed comedo (whitehead). Increased sebum production provides an environment for the overgrowth of Propionibacterium acnes. Bacterial overgrowth of Propionibacterium acnes can cause inflammation, leading to inflammatory lesions (papules, pustules, or nodules) in the dermis around the micro-comedo or comedo, which may cause scarring or hyperpigmentation.[1]

There are many misconceptions and myths about acne.

Primary Causes

Exactly why some people get acne and some do not is not fully known. It is known to be partly hereditary. Several factors are known to be linked to acne:

  • Family/Genetic history: The tendency to develop acne runs in families. For example, school-age boys with acne have other members of their family with acne. I associate a family history of acne with an earlier acne occurrence and increased acne lesions. [2]
  • Hormonal activity, such as menstrual cycles and puberty: During puberty, increased male sex hormones called androgens, cause the glands to get larger and make more sebum. [3]
  • Stress: The increased output of hormones from the adrenal (stress) glands.
  • Hyperactive sebaceous glands, secondary to the three hormone sources above.
  • Accumulation of dead skin cells.
  • Bacteria in the pores, to which the body becomes ‘allergic.’: Propionibacterium acnes (P. acnes) is the anaerobic bacterium that causes acne. In-vitro resistance of P. acnes to commonly used antibiotics has been increasing. [4]
  • Skin irritation or scratching of any sort will activate inflammation.
  • Use of anabolic steroids.
  • Any medication containing halogens (iodides, chlorides, bromides), lithium, barbiturates, or androgens.
  • Exposure to high levels of chlorine compounds, particularly chlorinated dioxins, can cause severe, long-lasting acne, known as Chloracne.
  • Exposure to certain drugs and chemical compounds, including narcotics (opiates and opioids), especially when taken intravenously

Several hormones have been linked to acne: the androgens testosterone, dihydrotestosterone (DHT) and dehydroepiandrosterone sulfate (DHEAS), 17-hydroxyprogesterone, and insulin-like growth factor 1 (IGF-I). Besides, acne-prone skin is insulin resistant.

In later years, the development of acne vulgaris is uncommon, although this is the age group for Rosacea, which may have similar appearances. True acne vulgaris in adults may be a feature of an underlying condition such as pregnancy and disorders such as polycystic ovary syndrome or the rare Cushing’s syndrome. Menopause-associated acne occurs as the production of the natural anti-acne ovarian hormone estradiol fails at menopause. The lack of estradiol also causes thinning hair, hot flashes, thin skin, wrinkles, vaginal dryness, predisposes to osteopenia and osteoporosis, and triggering acne (known as acne climacteric in this situation).

Diet

Milk

A recent study, based on a survey of 47,335 women, did find a positive epidemiological association between acne and consumption of partially skimmed milk, instant breakfast drink, sherbet, cottage cheese and cream cheese.[5] The researchers hypothesize that the association may be caused by hormones (such as several sex hormones and bovine IGF-I) present in cow milk. Though there is evidence of an association between milk and acne, the exact cause is unclear. Most dermatologists are awaiting confirmatory research linking diet and acne but some support the idea that acne sufferers should experiment with their diets, and refrain from consuming such fare if they find such food affects the severity of their acne.[6]

Seafood

Seafood often contains relatively high levels of iodine. Iodine is known to make existing acne worse but there is probably not enough to cause an acne outbreak.[7] Still, people who are prone to acne may want to avoid excessive consumption of foods high in iodine.

High Carbohydrates/High GI

It has also been suggested that there is a link between a diet high in refined sugars and other processed foods and acne. The theory is that rapidly digested carbohydrate food such as white bread and refined sugars produces an overload in metabolic glucose that is rapidly converted into the types of fat that can build up in sebaceous glands. According to this hypothesis, the startling absence of acne in non-westernized societies could be explained by the low glycemic index of these cultures’ diets. Others have cited possible genetic reasons for there being no acne in these populations, but similar populations shifting to these diets do develop acne. Note also that the populations studied consumed no milk or other dairy products.[8] Further research is necessary to establish whether a reduced consumption of high-glycemic foods (such as soft drinks, sweets, white bread) can significantly alleviate acne, though consumption of high-glycemic foods should in any case be kept to a minimum, for general health reasons.[9] Avoidance of ‘junk food’ with its high fat and sugar content is also recommended.[10] On the other hand there is no evidence that fat alone makes skin oilier or acne worse.

The University of Pennsylvania and the US Naval Academy conducted experiments that fed subjects chocolate or a bar with similar amounts of macronutrients (fat, sugar etc.) and found that consumption of chocolate, frequent or not, had no effect on the developing of acne. [11]

A 2005 systematic review found “surprisingly little evidence exists for the efficacy or lack of efficacy of dietary factors, face-washing and sunlight exposure in the management of acne.”[12] A study in November 2006 in Australia gave a 50% reduction in 12 weeks in mild-moderate facial acne by introducing its subjects to a high protein, low GI diet. [13]

The American Medical Association says chocolate does not contribute to acne. [14]

A recent study[15] shows that a diet high enough in sugars triggers the liver to convert these sugars into lipid; as a side-effect this stops production of sex hormone binding globulin– a chemical which reduces the level of testosterone in the blood. Since high testosterone levels generally trigger acne, the researchers believe that this can be a cause.

Vitamins A and E

Studies have shown that newly diagnosed acne patients tend to have lower levels of vitamin A circulating in their bloodstream than those that are acne free.[16] In addition people with severe acne also tend to have lower blood levels of vitamin E.[17]

Hygiene

Acne is not caused by dirt. This misconception probably comes from the fact that blackheads look like dirt stuck in the openings of pores. The black color is simply not dirt but compact keratin. In fact, the blockages of keratin that cause acne occur deep within the narrow follicle channel, where it is impossible to wash them away. These plugs are formed by the failure of the cells lining the duct to separate and flow to the surface in the sebum created there by the body.

Sex

Common myths state that masturbation causes acne and, conversely, that celibacy or sexual intercourse can cure it. Acne has not been linked to any type of sexual activity.

Causes by Organ System

Cardiovascular No underlying causes
Chemical / poisoning Dioxins, Industrial exposure to halogenated hydrocarbons
Dermatologic Chloracne, Skin irritation or scratching
Drug Side Effect 17-hydroxyprogesterone, antiepileptics, bromides, Cidofovir, Dactinomycin, dehydroepiandrosterone sulfate (DHEAS), Desogestrel and Ethinyl Estradiol, dihydrotestosterone (DHT), Eflornithine, Estradiol valerate and estradiol valerate/dienogest, Ethynodiol diacetate and ethinyl estradiol, Fluoxymesterone, gefitinib, Goserelin, iodides, isoniazid, Ivacaftor, leflunomide, lithium, low Vitamin A levels, low Vitamin E levels, methyltestosterone, nabumetone, Nafarelin, Oxandrolone, oxcarbazepine, phenytoin, pramipexole, prednisolone, steroids, testosterone, Chlorides

Cosmetic agents

Ear Nose Throat No underlying causes
Endocrine Congenital adrenal hyperplasia, Cushing’s syndrome, increased androgen production, insulin-like growth factor 1 (IGF-I), polycystic ovary syndrome, Dioxins
Environmental Increased stress levels
Gastroenterologic No underlying causes
Genetic Genetic, congenital adrenal hyperplasia
Hematologic No underlying causes
Iatrogenic No underlying causes
Infectious Disease Propionibacterium acnes infection, Staphylococcus epidermidis
Musculoskeletal / Ortho No underlying causes
Neurologic Dioxins
Nutritional / Metabolic

A diet high in glycemic index foods and dairy products, consumption of cottage cheese and cream cheese, consumption of partially skimmed milk, low Vitamin A levels, low Vitamin E levels

Obstetric/Gynecologic Menstrual cycles, oral contraceptives, pregnancy, Dioxins
Oncologic Dioxins
Opthalmologic No underlying causes
Overdose / Toxicity No underlying causes
Psychiatric No underlying causes
Pulmonary No underlying causes
Renal / Electrolyte No underlying causes
Rheum / Immune / Allergy Dioxins
Sexual Puberty, Dioxins
Trauma No underlying causes
Urologic No underlying causes
Dental Dioxins
Miscellaneous No underlying causes

Causes in Alphabetical Order

References

  1. Simpson, Nicholas B.; Cunliffe, William J. (2004). “Disorders of the sebaceous glands”. In Burns, Tony; Breathnach, Stephen; Cox, Neil; Griffiths, Christopher. Rook’s textbook of dermatology (7th ed. ed.). Malden, Mass.: Blackwell Science. pp. pp. 43.1-75. ISBN 0-632-06429-3.
  2. F. Ballangera, P. Baudrya, J.M. N’Guyenb, A. Khammaria, B. Dréno Heredity: A Prognostic Factor for Acne 5/2/2005
  3. US Dept Health and Human Services January 2005
  4. National Guideline Clearinghouse 11/12/2007
  5. Adebamowo CA, Spiegelman D, Danby FW, Frazier AL, Willett WC, Holmes MD (2005). “High school dietary dairy intake and teenage acne”. J Am Acad Dermatol. 52 (2): 207–14. PMID 15692464.
  6. Fries JH (1978). “Chocolate: a review of published reports of allergic and other deleterious effects, real or presumed”. Ann Allergy. 41 (4): 195–207. PMID 152075.
  7. Danby FW (2007). “Acne and iodine: Reply”. J Am Acad Dermatol. 56 (1): 164–5. PMID 17190637.
  8. Loren Cordain, et al. “Acne Vulgaris – A Disease of Western Civilization” Arch Dermatol. 2002;138:1584-1590. Observation
  9. Smith R, Mann N, Makelainen H, Braue A, Varigos G (2004). “The effect of short-term altered macronutrient status on acne vulgaris and biochemical markers of insulin sensitivity”. Asia Pac J Clin Nutr. 13 (Suppl): S67. PMID 15294556.
  10. Anderson, Laurence. 2006. Looking Good, the Australian guide to skin care, cosmetic medicine and cosmetic surgery. AMPCo. Sydney. ISBN 0-85557-044-X.
  11. “Sweet news about chocolate”. usaweekend.com. 1998-06-05. Retrieved 2007-05-27.
  12. Magin P, Pond D, Smith W, Watson A (2005). “A systematic review of the evidence for ‘myths and misconceptions’ in acne management: diet, face-washing and sunlight”. Fam Pract. 22 (1): 62–70. PMID 15644386.
  13. RMIT acne study
  14. JAMA Patient Page – Acne
  15. [1]
  16. Naweko San-Joyz (April 11, 2007). “How Does Vitamin A Prevent Acne Outbreaks?”. American Chronical. Retrieved 2007-09-17.
  17. El-Akawi Z, Abdel-Latif N, Abdul-Razzak K (2006). “Does the plasma level of vitamins A and E affect acne condition?”. Clin. Exp. Dermatol. 31 (3): 430–4. doi:10.1111/j.1365-2230.2006.02106.x. PMID 16681594.

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Differentiating Acne Vulgaris from other Diseases

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: João André Alves Silva, M.D. [2]

Overview

Acne vulgaris must be differentiated from other diseases that cause scaly red skin, comedones, papules, nodules, and possibly scarring, including chickenpox, herpes zoster, erythema multiforme, among others.

Differentiating Acne Vulgaris from other Diseases

Different rash-like conditions can be confused with acne and are thus included in its differential diagnosis. The various conditions that should be differentiated from acne include:[1][2][3][4][5][6][7]

Disease Features
Impetigo 
  • It commonly presents with pimple-like lesions surrounded by erythematous skin. Lesions are pustules, filled with pus, which then break down over 4-6 days and form a thick crust. It’s often associated with insect bites, cuts, and other forms of trauma to the skin.
Insect bites
  • The insect injects formic acid, which can cause an immediate skin reaction often resulting in a rash and swelling in the injured area, often with formation of vesicles.
Kawasaki disease
Measles
Monkeypox
  • The presentation is similar to smallpox, although it is often a milder form, with fever, headache, myalgia, back pain, swollen lymph nodes, a general feeling of discomfort, and exhaustion. Within 1 to 3 days (sometimes longer) after the appearance of fever, the patient develops a papular rash, often first on the face. The lesions usually develop through several stages before crusting and falling off.
Rubella
Atypical measles
Coxsackievirus
  • The most commonly caused disease is the Coxsackie A disease, presenting as hand, foot and mouth disease. It may be asymptomatic or cause mild symptoms, or it may produce fever and painful blisters in the mouth (herpangina), on the palms and fingers of the hand, or on the soles of the feet. There can also be blisters in the throat or above the tonsils. Adults can also be affected. The rash, which can appear several days after high temperature and painful sore throat, can be itchy and painful, especially on the hands/fingers and bottom of feet.
Acne
Syphilis It commonly presents with gneralized systemic symptoms such as malaise, fatigue, headache and fever. Skin eruptions may be subtle and asymptomatic It is classically described as:
Molluscum contagiosum
  • The lesions are commonly flesh-colored, dome-shaped, and pearly in appearance. They are often 1-5 millimeters in diameter, with a dimpled center. Generally not painful, but they may itch or become irritated. Picking or scratching the lesions may lead to further infection or scarring. In about 10% of the cases, eczema develops around the lesions. They may occasionally be complicated by secondary bacterial infections.
Mononucleosis
Toxic erythema
  • It is a common rash in infants, with clustered and vesicular appearance.
Rat-bite fever
  • It commonly presents with fever, chills, open sore at the site of the bite and rash, which may show red or purple plaques.
Parvovirus B19
  • The rash of fifth disease is typically described as “slapped cheeks,” with erythema across the cheeks and sparing the nasolabial folds, forehead, and mouth.
Cytomegalovirus
Scarlet fever
Rocky Mountain spotted fever
Stevens-Johnson syndrome
  • The symptoms may include fever, sore throat and fatigue. Commonly presents ulcers and other lesions in the mucous membranes, almost always in the mouth and lips but also in the genital and anal regions. Those in the mouth are usually extremely painful and reduce the patient’s ability to eat or drink. Conjunctivitis of the eyes occurs in about 30% of children. A rash of round lesions about an inch across, may arise on the face, trunk, arms and legs, and soles of the feet, but usually not on the scalp.
Varicella-zoster virus
  • It commonly starts as a painful rash on one side of the face or body. The rash forms blisters that typically scab over in 7-10 days and clears up within 2-4 weeks.
Chickenpox
  • It commonly starts with conjunctival and catarrhal symptoms and then characteristic spots appearing in two or three waves, mainly on the body and head, rather than the hands, becoming itchy raw pox (small open sores which heal mostly without scarring). Touching the fluid from a chickenpox blister can also spread the disease.
Meningococcemia
Rickettsial pox
Meningitis

References

  1. Hartman-Adams H, Banvard C, Juckett G (2014). “Impetigo: diagnosis and treatment”. Am Fam Physician. 90 (4): 229–35. PMID 25250996.
  2. Mehta N, Chen KK, Kroumpouzos G (2016). “Skin disease in pregnancy: The approach of the obstetric medicine physician”. Clin Dermatol. 34 (3): 320–6. doi:10.1016/j.clindermatol.2016.02.003. PMID 27265069.
  3. Moore, Zack S; Seward, Jane F; Lane, J Michael (2006). “Smallpox”. The Lancet. 367 (9508): 425–435. doi:10.1016/S0140-6736(06)68143-9. ISSN 0140-6736.
  4. Ibrahim F, Khan T, Pujalte GG (2015). “Bacterial Skin Infections”. Prim Care. 42 (4): 485–99. doi:10.1016/j.pop.2015.08.001. PMID 26612370.
  5. Ramoni S, Boneschi V, Cusini M (2016). “Syphilis as “the great imitator”: a case of impetiginoid syphiloderm”. Int J Dermatol. 55 (3): e162–3. doi:10.1111/ijd.13072. PMID 26566601.
  6. Kimura U, Yokoyama K, Hiruma M, Kano R, Takamori K, Suga Y (2015). “Tinea faciei caused by Trichophyton mentagrophytes (molecular type Arthroderma benhamiae ) mimics impetigo : a case report and literature review of cases in Japan”. Med Mycol J. 56 (1): E1–5. doi:10.3314/mmj.56.E1. PMID 25855021.
  7. CEDEF (2012). “[Item 87–Mucocutaneous bacterial infections]”. Ann Dermatol Venereol. 139 (11 Suppl): A32–9. doi:10.1016/j.annder.2012.01.002. PMID 23176858.

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Epidemiology and Demographics

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

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Overview

In the United States, acne affects 17 million people. It is most common during adolescence, affecting more than 85% of teenagers, and frequently continues into adulthood. [1]

References

  1. James WD (2005). “Clinical practice. Acne”. N Engl J Med. 352 (14): 1463–72. PMID 15814882.

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Risk Factors

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

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Overview

Acne is the most common skin disease. People of all races and ages get acne. But it is most common in teenagers and young adults. An estimated 80 percent of all people between the ages of 11 and 30 have acne outbreaks at some point. Some people in their forties and fifties still get acne.

References

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Natural History, Complications and Prognosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

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Complications

Acne Scars

See Acne scarring.

Severe acne often leaves small scars where the skin gets a “volcanic” shape. Acne scars are difficult and expensive to treat, and it is unusual for the scars to be successfully removed completely.

Physical acne scars are often referred to as “Icepick” scars. This is because the scars tend to cause an indentation in the skin’s surface. There are a range of treatments available.

Although quite rare, the medical condition Atrophia Maculosa Varioliformis Cutis results in “acne like” depressed scars on the face.

Ice pick scars – Deep pits, that are the most common and a classic sign of acne scarring.
Box car scars – Angular scars that usually occur on the temple and cheeks, and can be either superficial or deep, these are similar to chickenpox scars.
Rolling scars – Scars that give the skin a wave-like appearance.
Hypertrophic scars – Thickened, or keloid scars. [1]

Pigmentation

Pigmented scars is a slightly misleading term, suggesting a change in the skin‘s pigmentation, and that they are true scars. Neither is true. Pigmented scars are usually the result of nodular or cystic acne (the painful ‘bumps’ lying under the skin). They often leave behind an inflamed red mark. Often, the pigmentation scars can be avoided simply by avoiding aggravation of the nodule or cyst. When sufferers try to ‘pop’ cysts or nodules, pigmentation scarring becomes significantly worse, and may even bruise the affected area. Pigmentation scars nearly always fade with time taking between 3 months to two years to do so, although rarely can persist.

On the other hand, some people, particularly people with naturally tanned skin do develop brown hyperpigmentation scars which is caused by a local increased production of the pigment melanin. These too typically fade over time.

Prognosis

Acne usually goes away after the teenage years, but it may last into middle age. The condition often responds well to treatment after 6 – 8 weeks, but it may flare up from time to time. Scarring may occur if severe acne is not treated. Some people, especially teenagers, can become very depressed if acne is not treated.

References

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Diagnosis

Diagnosis

History and Symptoms | Physical Examination | Laboratory Findings | Other Diagnostic Studies

Treatment

Treatment

Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies

Case Studies

Case Studies

Case #1

Related Chapters
External Links

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