1009 Users are discussing this topic

PatientPlus articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use, so you may find the language more technical than the condition leaflets.

Lentigines (plural of lentigo) are flat brown lesions which do not darken following sun exposure (thus differentiating them from ephelides, or true freckles).

One study of Caucasian women found that lentigines were signs of photo-damage whereas there was a genetic component in true freckles.[2] They may be any size from 5-20 mm and may be irregular in shape. They occur over the shoulders in young people, especially those who have had a lot of sun exposure and in the elderly on the sun-exposed sites such as the dorsum of the hands and forearms, the face and the neck.


The histopathology may include hyperplasia of the epidermis and pigmentation of the basal layer. A number of different types are found:

  • Lentigo simplex - the most common type, mainly seen in children and not associated with sun exposure. The spots are 5-15 mm in diameter.
  • Solar lentigo - related to sun exposure. Seen on skin normally exposed to sunlight (eg, face, hands), they are benign lesions, <5 mm in diameter but may merge to form larger spots. Former peak age of 30-50 is becoming younger with increasing sun exposure. The colour may vary from yellow-brown to black.
  • Ink spot lentigo - this lesion, so called because it resembles a spot of ink, is a benign lesion limited to sun-exposed areas. They are usually solitary lesions and may be mistaken for melanomas.
  • PUVA lentigo - these brown macules can appear six months or more after the start of psoralen combined with ultraviolet A (PUVA) treatment for psoriasis in areas exposed to treatment. The macules are usually 3-8 mm in diameter and persist for 3-6 months after treatment has finished. There is also a larger stellate form (which can be up to 3 cm in diameter) which may persist for two years or more.
  • Radiation lentigo - this appears after a single large exposure to radiation (of Chernobyl proportions rather than post-radiotherapy). There may be other histological signs of radiation damage, such as epidermal atrophy and subcutaneous fibrosis. The malignant potential for such lesions is not known.
  • Sunbed lentigo - lentigines can appear rapidly after intense exposure, or they may appear after long-term use. They are 2-5 mm in diameter and are most common on the anterior aspects of the arms and legs.
  • Labial and oral melanotic macules - labial macules usually appear as single lesions on the vermillion of the lower lip. Oral lesions occur on the gingival and buccal mucosa, palate and tongue.
  • Genital lentigo - in men, this can present as a tan to dark-brown macule anywhere on the glans, shaft or corona. They can achieve a size of 15 mm. In women, lentigines can occur anywhere on the genital mucosa and are usually between 5-15 mm in size.
  • Lentigines profusa - in this condition, there are widespread lentigines over the arms, legs and genitalia. There are no trigger factors or associated abnormalities (thus differentiating them from a number of lentigo-associated syndromes - see below). The lesions can be 5 mm-2 cm in diameter. The appearance is of dark brown or black freckles but with a more generalised distribution.
  • Agminated lentiginosis - in this condition, which can be associated with a number of childhood diseases, lentigines appear in a sharply demarcated distribution which often follows the outline of dermatomes. They are tan or dark brown in colour and may be present at birth or develop in early childhood.

A number of lentigo-associated conditions can occur:

  • LEOPARD - lentigines, electrocardiographic conduction defects, ocular hypertelorism, pulmonary stenosis, abnormal genitalia, restriction of growth, deafness.
  • Peutz-Jeghers syndrome - gastrointestinal polyps and pigmented macules.
  • Laugier-Hunziker syndrome - a variable number of pigmented macules appearing commonly around the oral mucosa or lower lip and in other areas.
  • Myxoma syndromes - a group of disorders including:
    • LAMB - lentigines, atrial myxomas, mucocutaneous myxomas and blue naevi.
    • NAME - naevi, atrial myxoma, myxoid neurofibroma and ephelides.
    • Carney's syndrome - cardiac, cutaneous and mammary myxomatous masses; lentigines; blue naevi; endocrine disorders; testicular tumours.

NEW - log your activity

  • Notes
    Add notes to any clinical page and create a reflective diary
  • Track
    Automatically track and log every page you have viewed
  • Print
    Print and export a summary to use in your appraisal
Click to find out more »
  • Actinic keratosis.
  • Ephelides (freckles) - become darker after sun exposure.
  • Seborrhoeic wart.
  • Xeroderma pigmentosum.
  • Melanoma of the skin.
  • Lentigo maligna - seen mainly on the sun-exposed areas of the face and neck in the elderly; it is slow-growing and sometimes grows to a size of several centimetres. Their size and site differentiates them from lentigines. Lentigo maligna is a pre-cancerous condition. Conversion to a lentigo maligna melanoma can take from a few months to up to 15 years. Transformation to malignancy is lower than in other forms of melanoma, occurring in approximately 5% of patients. However, the risk is higher in larger lesions with a risk of 50% in lesions larger than 4 cm. Identifying lesions that require referral is not easy but worrying signs include changes in size or colour, itching, burning, bleeding, or pain.[4] The ABCDE rule of melanoma may be helpful:
    • Asymmetry.
    • Border irregularity.
    • Colour variegation.
    • Diameter greater than 6 mm (the end of a pencil head), although melanoma can occur in lesions less than 6 mm.
    • Enlargement.

See separate Malignant Melanoma of Skin article.

  • Biopsy and histology may be used to differentiate the various types of lentigines.
  • A dermatoscope is occasionally used in the diagnosis of solar lentigo.
  • The diagnosis of lentigo maligna has been improved by the use of reflectance confocal microscopy (a non-invasive imaging technique that enables in vivo visualisation of the epidermis down to the papillary dermis) and immunohistochemical stains.
  • Unsightly lesions of the face can be lightly frozen, which often improves the cosmetic result.
  • Tretinoin is occasionally employed to lighten lesions (unlicensed use).[6] 
  • Cryotherapy can be used for isolated lentigines. One study found it was more effective than 40% trichloracetic acid for the treatment of solar lentigines although the difference was not significant.
  • Lasers are useful for a variety of lentigines. Aggressive therapy for using quality-switched lasers is effective in the treatment of solar lentigines but carries the risk of post-inflammatory hyperpigmentation (PIH). For darker skin types, less intensive irradiation reduces this risk, with no reduction in efficacy.[7] 
  • Intense pulsed light (IPL) is another option.
  • For doubt over diagnosis and for diagnostic biopsy.
  • When treatment is required but cannot be provided within primary care - eg, treatment with local chemical peel or lasers (Q-switched Nd:YAG or ruby) are effective when available.[8][9] 

Lentigines tend to worsen over time but do not become malignant.

  • New lesions can be prevented to some extent by sun avoidance. Clothing is more effective than sunscreens.
  • Avoiding the excessive use of sunbeds helps to prevent tanning-bed lentigines.
  • Avoidance of a large single dose of ionising radiation helps to prevent radiation lentigines.

Further reading & references

  1. Lentigo; DermNet NZ
  2. Ezzedine K, Mauger E, Latreille J, et al; Freckles and solar lentigines have different risk factors in Caucasian women. J Eur Acad Dermatol Venereol. 2012 Aug 28. doi: 10.1111/j.1468-3083.2012.04685.x.
  3. Barkal C et al; Clinical Atlas of Skin Tumors, 2014.
  4. Lentigo maligna and lentigo maligna melanoma; DermNet NZ
  5. Kasprzak JM, Xu YG; Diagnosis and management of lentigo maligna: a review. Drugs Context. 2015 May 29;4:212281. doi: 10.7573/dic.212281. eCollection 2015.
  6. Kircik LH; Safety and efficacy evaluation of tretinoin cream 0.02% for the reduction of photodamage: a pilot study. J Drugs Dermatol. 2012 Jan;11(1):83-90.
  7. Negishi K, Akita H, Tanaka S, et al; Comparative study of treatment efficacy and the incidence of post-inflammatory hyperpigmentation with different degrees of irradiation using two different quality-switched lasers for removing solar lentigines on Asian skin. J Eur Acad Dermatol Venereol. 2011 Dec 20. doi: 10.1111/j.1468-3083.2011.04385.x.
  8. Madan V, August PJ; Lentigo Maligna-Outcomes of Treatment with Q-Switched Nd:YAG and Alexandrite Lasers. Dermatol Surg. 2009 Mar 20.
  9. Rendon MI, Berson DS, Cohen JL, et al; Evidence and considerations in the application of chemical peels in skin disorders and aesthetic resurfacing. J Clin Aesthet Dermatol. 2010 Jul;3(7):32-43.

Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. EMIS has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.

Original Author:
Dr Laurence Knott
Current Version:
Peer Reviewer:
Dr Helen Huins
Document ID:
4055 (v23)
Last Checked:
Next Review:

Did you find this health information useful?

Yes No

Thank you for your feedback!

Subcribe to the Patient newsletter for healthcare and news updates.

We would love to hear your feedback!

Patient Access app - find out more Patient facebook page - Like our page