- Nevus anemicus
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Nevus Anemicus Classification and external resources Nevus anemicus is a congenital disorder characterized by macules of varying size and shape that are paler than the surrounding skin and cannot be made red by trauma, cold, or heat.[1][2] The paler area is due to the blood vessels within the area which are more sensitive to the body’s normal vasoconstricting chemicals.[3]
Contents
Symptoms
This benign patch appears on the skin at birth or in early childhood. In most people these are under 10cm in size. If there is doubt about the diagnosis, rubbing the area causes the skin around the lesion to become red while the lesion itself does not change in color.[4] Often the patches are difficult to see against the background color of the patient’s skin, but if sunburn develops, then the white area stands out prominently.[5] The involved area is lighter than the normal skin, not because of a loss of pigment occurs, but because blood vessels are constricted, producing a perment blanching of the area. This blanching is a functional rather than a structual abnormality, presumed to be caused by local increased sensitivity to catecholamines.[6] Although the cutaneous vasculature appears normal histologically, the blood vessels within the nevus do not respond to injection of vasodilators. It has been postulated that the persistent pallor may represent a sustained localized adrenergic vasoconstriction.[7] Results of a skin biopsy would be interpreted as normal and only physiological testing can reveal the nevus in contrast to normal skin. Stroking the patch elicits no red flare. Only the normal skin would react with a characteristic erythematous response. Examination under a Wood lamp can also reveal the nevus anemicus patch will not emphasize as a patch of vitiligo would.[8]
Treatment
Since the histopathology of nevus anemicus is normal, nevus anemicus is a pharmacologic nevus and not an anatomic one.[9][10] and in most people a nevus anemicus is on a covered area and so light in appearance that no treatment is needed.[11]
See also
References
- ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. Page 582. ISBN 0-7216-2921-0.
- ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
- ^ "Dermatologic Disease Database". http://www.aocd.org/skin/dermatologic_diseases/nevus_anemicus.html. Retrieved 25 October 2011.
- ^ "Dermatologic Disease Database". http://www.aocd.org/skin/dermatologic_diseases/nevus_anemicus.html. Retrieved 25 October 2011.
- ^ "Global Skin Atlas". http://www.globalskinatlas.com/imagedetail.cfm?TopLevelid=682&ImageID=1775&did=182. Retrieved 25 October 2011.
- ^ McMillan , Julia A; DeAngelis, Catherine D.; Feigin, Ralph D.; Warshaw, Joseph B. (2006). Oski's Pediatrics, Principles & Practice. (4th ed.). Page 458. ISBN-13: 978-0781716185 0.
- ^ Nelson Textbook of Pediatrics 19th. (10th ed.). W.B. Saunders Company. Page 640. ISBN:1437707556.
- ^ Barber Kirk (2010). Consultant For Pediatricians '. Page 9:233, 237.
- ^ Mountcastle EA, Diestelmeier MR, Lupton GP. Nevus anemicus. J Am Acad Dermatol 1986;14:628-32..
- ^ Requena L, Sangueza OP. Cutaneous vascular anomalies. Part 1. Hamartomas, malformations and dilation of preexisting vessels. J Am Acad Dermatol 1997;37:523-49,quiz 549-52.
- ^ "Dermatologic Disease Database". http://www.aocd.org/skin/dermatologic_diseases/nevus_anemicus.html. Retrieved 25 October 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
hypomelanosisVasospastic macule · Woronoff's ring · Nevus anemicusUngroupedungrouped: 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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