- Nevus depigmentosus
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Nevus depigmentosus Classification and external resources Nevus depigmentosus or nevus achromicus[1] is a depigmentation problem in skin which can be easily differentiated from vitiligo. Although age factor has not much involvement in the nevus depigmentosus but in about 19% of the cases these are noted at birth. Their size may however grow in proportion to growth of the body. The distribution is also fairly stable and are nonprogressive hypopigmented patches.[2] The exact cause of nevus depigmentosus is still not clearly understood. A sporadic defect in the embryonic development has been suggested to be a causative factor.[3] It has been described[by whom?] as "localised albinism", though this is incorrect. Those with nevus depigmentosus may be prone to sunburn due to the lack of pigment, and the patient should use good sun protection.[4] Sunscreen should be applied to all exposed skin, since reduced tanning of normal skin will decrease the contrast with hypopigmented skin.[5] Most patients with nevus depigmentosus do not peruse treatment for their lesion.[6] There is no way to repigment the skin.[6] If, however, the lesion is of cosmetic concern, camouflage makeup is effective.[6] If the lesion is small one could also consider excision.[6]
Contents
Causes
These white spots result from abnormalities in the function of melanocytes which produce little pigment thereby resulting in characteristic white spots in skin.[2]
Symptoms
These are localized white spots on skin which may affect any area of the body, but these white spots are quite stable lesions.[2] In the majority of patients, the lesions are not completely achromic, but are hypopigmented and resemble splashed paint.[7] The individual lesions are permanent and there are no effective therapies for re-pigmenting this nevus.[7] If there is hair in an affected area, it is usually colourless or white.
Treatment
Different therapeutic modalities have been attempted to repigment the lesions of nevus depigmentosus such as PUVA, excimer laser, and different grafting techniques. PUVA therapy has not been shown to be beneficial.[8] Successful repigmentation was reported in a single case with 14 sessions of excimer laser treatment.[9] Though the repigmentation of nevus depigmentosus is possible by grafting techniques, the results are inconsistent and recurrence is possible. In consideration of the experience of other authors and us, the quality and retention of pigment are unpredictable. These factors need to be considered while consulting and offering any treatment to the patient of nevus depigmentosus.[10]
See also
- Nevus
- Vitiligo
- Alphos
- Albinism
- Leucism
- Melanism
- Pityriasis alba
- Quadrichrome vitiligo
- Selective ultraviolet phototherapy
- List of cutaneous conditions
References
- ^ PMID: 9922008
- ^ a b c Lee, H S; Chun, Y S & Hann, S K (January 1999). "Nevus depigmentosus: clinical features and histopathologic characteristics in 67 patients". J Am Acad Dermatol 40 (1): 21–26. doi:10.1016/S0190-9622(99)70524-4. PMID 9922008.
- ^ Disorders of hypopigmentation in children. U.S. National Library of Medicine. PMID 1870914.
- ^ J. Kwiatkowski, David. Tuberous Sclerosis Complex: Genes, Clinical Features and Therapeutics. p. 286. ISBN 978-3527322015.
- ^ J. Kwiatkowski, David. Tuberous Sclerosis Complex: Genes, Clinical Features and Therapeutics. p. 286. ISBN 978-3527322015.
- ^ a b c d J. Nordlund, James. The pigmentary system: physiology and pathphysiology. p. 651. ISBN 978-0195098617.
- ^ a b Clinical Pediatric Dermatology. p. 92. ISBN 9788131214893.
- ^ Berg M, Tarnowski W. Nevus pigmentosus. Arch Dermatol 1974;109:920.
- ^ Kim DY, Lee KY, Park YK. Use of the 308-nm excimer laser for nevus depigmentosus: A promising treatment for either nevus depigmentosus or vitiligo. J Dermatol 2007;34:217-8.
- ^ "Journal of Cutaneous and Aesthetic Surgery". Medknow Publications. 2008. http://www.jcasonline.com/article.asp?issn=0974-2077;year=2011;volume=4;issue=1;spage=29;epage=32;aulast=Mulekar#ref8. Retrieved 23 June 2011.
Pigmentation disorders/Dyschromia (L80–L81, 709.0) Hypo-/
leucismLoss of melanocytesvitiligo: Quadrichrome vitiligo · Vitiligo ponctué · syndromic (Alezzandrini syndrome · Vogt–Koyanagi–Harada syndrome)
melanocyte development: Piebaldism · Waardenburg syndrome · Tietz syndromeLoss of melanin/
amelanismalbinism: Oculocutaneous albinism · Ocular albinism
melanosome transfer: Hermansky–Pudlak syndrome · Chédiak–Higashi syndrome · Griscelli syndrome (Elejalde syndrome · Griscelli syndrome type 2 · Griscelli syndrome type 3)
other: Cross syndrome · ABCD syndrome · Albinism–deafness syndrome · Idiopathic guttate hypomelanosis · Phylloid hypomelanosis · Progressive macular hypomelanosisLeukoderma w/o
hypomelanosisUngroupedungrouped: Nevus depigmentosus · Postinflammatory hypopigmentation · Pityriasis alba · Vagabond's leukomelanoderma · Yemenite deaf-blind hypopigmentation syndrome · Wende–Bauckus syndromeHyper- ReticulatedDermatopathia pigmentosa reticularis · Pigmentatio reticularis faciei et colli · Reticulate acropigmentation of Kitamura · Reticular pigmented anomaly of the flexures · Naegeli–Franceschetti–Jadassohn syndrome · Dyskeratosis congenita · X-linked reticulate pigmentary disorder · Galli–Galli disease · Revesz syndromeDiffuse/
circumscribedLentigo/Lentiginosis: Lentigo simplex · Liver spot · Centrofacial lentiginosis · Generalized lentiginosis · Inherited patterned lentiginosis in black persons · Ink spot lentigo · Lentigo maligna · Mucosal lentigines · Partial unilateral lentiginosis · PUVA lentigines
Melasma · Erythema dyschromicum perstans · Lichen planus pigmentosus · Café au lait spot · Poikiloderma (Poikiloderma of Civatte · Poikiloderma vasculare atrophicans) · Riehl melanosisLinearOther/ungroupedAcanthosis nigricans (Acral acanthotic anomaly) · Freckle · Familial progressive hyperpigmentation · Pallister–Killian syndrome · Periorbital hyperpigmentation · Photoleukomelanodermatitis of Kobori · Postinflammatory hyperpigmentation · Transient neonatal pustular melanosisOther
pigmentsiron: Hemochromatosis · Iron metallic discoloration · Pigmented purpuric dermatosis (Schamberg disease, Majocchi's disease, Gougerot–Blum syndrome, Doucas and Kapetanakis pigmented purpura/Eczematid-like purpura of Doucas and Kapetanakis, Lichen aureus, Angioma serpiginosum) · Hemosiderin hyperpigmentationother metals: Argyria · Chrysiasis · Arsenic poisoning · Lead poisoning · Titanium metallic discolorationDyschromatoses Dyschromatosis symmetrica hereditaria · Dyschromatosis universalis hereditariaCategories:- Disturbances of human pigmentation
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