"Hyperpigmentation" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Excessive pigmentation of the skin, usually as a result of increased epidermal or dermal melanin pigmentation, hypermelanosis. Hyperpigmentation can be localized or generalized. The condition may arise from exposure to light, chemicals or other substances, or from a primary metabolic imbalance.
Descriptor ID |
D017495
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MeSH Number(s) |
C17.800.621.430
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Hyperpigmentation".
Below are MeSH descriptors whose meaning is more specific than "Hyperpigmentation".
This graph shows the total number of publications written about "Hyperpigmentation" by people in this website by year, and whether "Hyperpigmentation" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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2002 | 0 | 1 | 1 |
2003 | 0 | 1 | 1 |
2005 | 1 | 0 | 1 |
2011 | 1 | 1 | 2 |
2013 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hyperpigmentation" by people in Profiles.
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Mashayekhi A, Kaliki S, Walker B, Park C, Sinha N, Kremer FZ, Shields CL, Shields JA. Metastasis from uveal melanoma associated with congenital ocular melanocytosis: a matched study. Ophthalmology. 2013 Jul; 120(7):1465-8.
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Saedi N, Chan HH, Dover JS. Treating lentigines in Asian patients with the Q-switched Alexandrite laser. J Drugs Dermatol. 2011 Dec; 10(12 Suppl):s14-5.
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Truong SV, Chen JK, Reinstadler A, Saedi N. Nephrogenic systemic fibrosis: a case report and review of the literature. J Drugs Dermatol. 2011 Jun; 10(6):622-4.
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Ang GC, Lee JB. Linear atrophoderma of Moulin: is it a single disease? J Am Acad Dermatol. 2005 May; 52(5):923-4; author reply 924-5.
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Jabbour SA. Cutaneous manifestations of endocrine disorders: a guide for dermatologists. Am J Clin Dermatol. 2003; 4(5):315-31.
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Sprecher E, Itin P, Whittock NV, McGrath JA, Meyer R, DiGiovanna JJ, Bale SJ, Uitto J, Richard G. Refined mapping of Naegeli-Franceschetti- Jadassohn syndrome to a 6 cM interval on chromosome 17q11.2-q21 and investigation of candidate genes. J Invest Dermatol. 2002 Sep; 119(3):692-8.