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Post-inflammatory Hyperpigmentation of Skin

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Appearance

Hyperpigmentation occurs as brown macules or patches often with a poorly defined border, irregular in outline and usually with little surface change.1 The basic mechanism in response to various triggers (see Causes, below) is melanosis of the epidermal or dermal layer of the skin. Arachidonic acid in the epidermal layer is oxidised to leukotrienes, prostaglandins and other products that stimulates melanocytes to increase the production of melanin. In dermal melanosis, inflammation disrupts the basal layer, causing melanin to be released and trapped in the macrophages of the papillary dermis, a process with the delightful name of pigmentary incontinence.2

Pigmentary changes are much more common in darker skinned individuals of Asian or African origin and pigmentation follows many common inflammatory diseases such as eczema, psoriasis or acne. Where erythema is seen in white individuals, pigmentation occurs in dark skinned individuals.

Diagnosis

Pigmentation due to increased melanin is a dirty brown colour, as opposed to that due to haemosiderin pigmentation following purpura which is more a rusty brown colour.3 Hyperpigmentation on the face may be due to pregnancy or taking the contraceptive pill (melasma/chloasma).4

Other conditions which may enter into the differential diagnosis include:2

Causes
  • Inflammatory skin conditions Any inflammatory skin condition involving the dermo-epidermal junction can cause hyperpigmentation e.g. eczema, psoriasis, lichen planus, acne, systemic lupus erythematosus, chronic dermatitis and cutaneous T-cell lymphoma.
  • Trauma
  • Allergic reactions
  • Photoxocicity
  • Iatrogenic Hyperpigmentation can be a complication of treatment with a fully ablative laser device in dark skinned patients. (This risk can be reduced by the use of fractional CO2 laser).5
  • Drugs Chlorpromazine, chloroquine and arsenic are all common culprits. Other drugs which occasionally cause hyperpigmentation include tetracycline, bleomycin, doxorubicin, 5-fluorouracil, busulfan, antimalarial drugs and hormones (e.g. oestrogen).
  • Exposure to ultraviolet light
  • Exposure to chemicals such as silver, gold and arsenic
  • Idiopathic Occasionally no cause can be identified.
Investigations2
  • Wood's light may help to differentiate dermal from epidermal hyperpigmentation which may help to elucidate the cause.
  • Biopsy may be required, especially if there is no identifiable preceding inflammation to account for the pigmentation.
Primary Care Management
  • The condition may resolve in time without additional treatment.
  • Avoidance of sun exposure may prevent further hyperpigmentation occurring on the face. Daily use of a high factor sunscreen may be helpful.
  • The underlying cause should be treated if possible.
  • If treatment is required, skin lightening creams may help. Hydroquinone 2% is usually prescribed first line but may not be very effective.2
  • A retinoid such as tretinoin may be helpful, particularly in sun-damaged skin.6
  • A topical steroid may help if there is an underlying inflammatory process but caution should be used in applying steroid creams to the face due to skin thinning. Recently a triple therapy has been tried using a combination of steroid, retinoid and 4% hydroquinone.7
  • Other treatments being developed which have shown some depigmenting activity include a combination of retinaldehyde (a retinoic acid precursor) and glycolic acid8 and the peroxidase inhibitor methimazole, which inhibits the production of melanin.9
Prognosis

Patients should be warned that the pigmentation may be slow to resolve, even with treatment. Epidermal pigmentation may persist for 6-12 months. Dermal pigmentation may persist for years.

When to Refer

If the diagnosis is in doubt or the patient requests specialist advice, referral should be considered.


Document references
  1. Hyperpigmentation; acnesource.com 2005
  2. Schwartz R, Kihiczak N; Postinflammatory Hyperpigmentation eMedicine.com 2008.
  3. Haemosiderin; LaTrobe University Department of Podiatry - Vascular Assessment2001; Picture of haemosiderin deposits
  4. Chloasma; DermaNet NZ 2006; Pictures of chloasma
  5. Tan KL, Kurniawati C, Gold MH; Low risk of postinflammatory hyperpigmentation in skin types 4 and 5 after treatment with fractional CO2 laser device. J Drugs Dermatol. 2008 Aug;7(8):774-7. [abstract]
  6. Kang S, Bergfeld W, Gottlieb AB, et al; Long-term efficacy and safety of tretinoin emollient cream 0.05% in the treatment of photodamaged facial skin: a two-year, randomized, placebo-controlled trial. Am J Clin Dermatol. 2005;6(4):245-53. [abstract]
  7. Taylor SC, Burgess CM, Callender VD, et al; Postinflammatory hyperpigmentation: evolving combination treatment strategies. Cutis. 2006 Aug;78(2 Suppl):6-19. [abstract]
  8. Katsambas AD; RALGA (Diacneal), a retinaldehyde and glycolic acid association and postinflammatory hyperpigmentation in acne--a review. Dermatology. 2005;210 Suppl 1:39-45. [abstract]
  9. Kasraee B, Handjani F, Parhizgar A, et al; Topical methimazole as a new treatment for postinflammatory hyperpigmentation: report of the first case. Dermatology. 2005;211(4):360-2. [abstract]

Internet and further reading
  • Stulberg DL, Clark N, Tovey D; Common hyperpigmentation disorders in adults: Part I. Diagnostic approach, cafe au lait macules, diffuse hyperpigmentation, sun exposure, and phototoxic reactions. Am Fam Physician. 2003 Nov 15;68(10):1955-60. [abstract]
  • Stulberg DL, Clark N, Tovey D; Common hyperpigmentation disorders in adults: Part II. Melanoma, seborrheic keratoses, acanthosis nigricans, melasma, diabetic dermopathy, tinea versicolor, and postinflammatory hyperpigmentation. Am Fam Physician. 2003 Nov 15;68(10):1963-8. [abstract]
Acknowledgements EMIS is grateful to Dr Laurence Knott for writing this article. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2009.
Document ID: 4051
Document Version: 21
Document Reference: bgp25983
Last Updated: 12 May 2009
Planned Review: 11 May 2012

The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest. Find out more about updating.

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