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There is no cure for EDP. While multiple various topical and systemic therapies have been tried, none have been consistently successful. In children, spontaneous resolution of EDP over the course of months to years is possible; however, this outcome is less likely if EDP presents in adulthood.
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EDP initially presents as grey or blue-brown circumferential or irregularly shaped macules or patches that appear. While the lesions of EDP are generally non-elevated, they may initially have a slight raised red margin as they first begin to appear. These lesions usually arise in a symmetric
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distribution and involve the trunk, but also commonly spread to the face and extremities. EDP does not usually have symptoms beside the macules and patches of discolored skin; however, some itching in these areas may occur.
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Because EDP is an uncommon disease of the skin, it is important to consider other skin diseases that may resemble erythema dyschromicum perstans, such as infectious diseases (i.e.
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with peak age of onset being young adults, but it may also be seen in children or adults of any age. EDP is characterized by
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macules that are ash-grey in color and may vary in size and shape. While agents such as certain medications,
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have been implicated in the occurrence of this disease, the cause of this skin disease remains unknown.
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121:), reaction to drugs, post inflammatory hyperpigmentation, or
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James, William D.; Berger, Timothy G.; et al. (2006).
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Presentation of the condition in a 20 year old female.
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709:Inherited patterned lentiginosis in black persons
918:Eczematid-like purpura of Doucas and Kapetanakis
570:Yemenite deaf-blind hypopigmentation syndrome
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638:Reticular pigmented anomaly of the flexures
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914:Doucas and Kapetanakis pigmented purpura
643:Naegeli–Franceschetti–Jadassohn syndrome
653:X-linked reticulate pigmentary disorder
633:Reticulate acropigmentation of Kitamura
628:Pigmentatio reticularis faciei et colli
155:
1025:Dyschromatosis universalis hereditaria
830:Familial progressive hyperpigmentation
1020:Dyschromatosis symmetrica hereditaria
855:Transient neonatal pustular melanosis
7:
845:Photoleukomelanodermatitis of Kobori
623:Dermatopathia pigmentosa reticularis
850:Postinflammatory hyperpigmentation
770:Poikiloderma vasculare atrophicans
25:
555:Postinflammatory hypopigmentation
499:Progressive macular hypomelanosis
489:Idiopathic guttate hypomelanosis
973:Titanium metallic discoloration
729:Partial unilateral lentiginosis
746:Erythema dyschromicum perstans
72:Erythema dyschromicum perstans
33:Erythema dyschromicum perstans
1:
935:Hemosiderin hyperpigmentation
894:Pigmented purpuric dermatosis
840:Periorbital hyperpigmentation
336:Vogt–Koyanagi–Harada syndrome
802:Shiitake mushroom dermatitis
144:List of cutaneous conditions
889:Iron metallic discoloration
565:Vagabond's leukomelanoderma
1112:
835:Pallister–Killian syndrome
484:Albinism–deafness syndrome
751:Lichen planus pigmentosus
699:Centrofacial lentiginosis
456:Griscelli syndrome type 3
451:Griscelli syndrome type 2
431:Hermansky–Pudlak syndrome
123:lichen planus pigmentosus
54:
45:
704:Generalized lentiginosis
436:Chédiak–Higashi syndrome
765:Poikiloderma of Civatte
401:Oculocutaneous albinism
909:Gougerot–Blum syndrome
792:Incontinentia pigmenti
648:Dyskeratosis congenita
575:Wende–Bauckus syndrome
494:Phylloid hypomelanosis
265:Pigmentation disorders
331:Alezzandrini syndrome
310:Quadrichrome vitiligo
167:. Saunders Elsevier.
92:radiographic contrast
80:dermatosis cinecienta
18:Dermatosis cinecienta
928:Angioma serpiginosum
820:Acanthosis nigricans
359:Waardenburg syndrome
1096:Lichenoid eruptions
658:Galli–Galli disease
550:Nevus depigmentosus
904:Majocchi's disease
797:Scratch dermatitis
724:Mucosal lentigines
524:Vasospastic macule
441:Griscelli syndrome
208:External resources
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963:Arsenic poisoning
899:Schamberg disease
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756:Café au lait spot
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446:Elejalde syndrome
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174:978-0-7216-2921-6
98:, infection with
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27:Medical condition
16:(Redirected from
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714:Ink spot lentigo
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884:Hemochromatosis
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776:Riehl melanosis
734:PUVA lentigines
719:Lentigo maligna
689:Lentigo simplex
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663:Revesz syndrome
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560:Pityriasis alba
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529:Woronoff's ring
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968:Lead poisoning
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474:Cross syndrome
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186:External links
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88:hyperpigmented
84:skin condition
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517:hypomelanosis
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761:Poikiloderma
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685:Lentiginosis
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989:Carotenosis
616:Reticulated
347:development
293:melanocytes
65:Dermatology
38:Other names
1041:Skin color
1012:Dyschromia
958:Chrysiasis
694:Liver spot
513:Leukoderma
421:Melanosome
354:Piebaldism
345:Melanocyte
269:Dyschromia
150:References
96:pesticides
813:ungrouped
603:Melanosis
543:Ungrouped
411:in humans
384:amelanism
324:Syndromic
217:eMedicine
100:parasites
61:Specialty
1090:Category
1034:See also
870:pigments
672:Diffuse/
608:Melanism
424:transfer
393:Albinism
377:Loss of
302:Vitiligo
133:See also
1068:removal
1056:Sunless
1051:Tanning
953:Argyria
825:Freckle
741:Melasma
681:Lentigo
598:Melanin
379:melanin
290:Loss of
282:leucism
115:leprosy
1063:Tattoo
946:metals
811:Other/
785:Linear
589:Hyper-
171:
102:, and
78:, and
982:Other
944:Other
868:Other
467:Other
277:Hypo-
119:pinta
877:Iron
169:ISBN
515:w/o
117:or
104:HIV
41:EDP
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257:e
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200:D
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Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.
