Hyperpigmented Lesions




(1)
Hôpital Universitaire de Strasbourg, Strasbourg, France

 




Abstract

Lesions which are darker than normal skin can be brown, black, or sometimes blue-gray.


Lesions which are darker than normal skin can be brown, black, or sometimes blue-gray.

The distribution and arrangement of lesions are important semiological elements to be specified, as well as the circumscribed or diffuse nature of the pigmentary disorder. A mucous involvement must also be investigated. Certain topographies are noteworthy.

Circumscribed disorders correspond to macules or pigmented patches that are clearly individualized, whereas diffuse lesions are poorly defined and generally widespread. Pigmentary disorders are often diffuse; they usually first appear and predominate in sun-exposed areas. When a pigmentary disorder is diffuse, it can sometimes be difficult to determine whether the pathological component is the one which is too pigmented or, on the contrary, the one which is lighter. History taking, comparison to naturally less pigmented skin (e.g., inner arms), and comparison to other members of the family can thus be decisive.

Sometimes hyper- and hypopigmented lesions may ­coexist in what is known as dyschromatosis.

The color of the lesions gives an indication of the type of pigmentary disorder:



  • Brown or brown black for epidermal and dermo-­epidermal hypermelaninosis.


  • Blue or blue-gray, sometimes with a metallic sheen, for dermal melanoses (also known as ceruleoderma) and certain exogenous and endogenous deposits of non-melanin pigments (also known as dyschromia).

In general, the cutaneo-conjunctival yellow coloration of icterus (jaundices), the orange-yellow color which spares the conjunctivae in carotenemias, as well as the ochre, light brown, or reddish brown coloration due to hemosiderin deposits, readily suggests the diagnosis.

The distribution, arrangement, and topography of the lesions provide an important help to diagnosis (Tables 17.1 and 17.2).


Table 17.1
Diagnostic approach to a brown hyperpigmentation (melanoderma) according to the arrangement, distribution and the circumscribed or diffuse nature of a lesion (non-exhaustive list)

















































































Special arrangement

Absence of any notable arrangement

Blaschkolinear hyperpigmentations

Circumscribed hyperpigmentation, well-defined

Incontinentia pigmenti

Tumors, hyperplasias, and pigmented hamartomas

McCune-Albright syndrome

Urticaria pigmentosa (mastocytosis)

Linear and whirled nevoid hypermelanosis

Interface dermatitides, often pigmented at advanced stage

Early stage of a verrucous epidermal nevus

Fixed drug eruption

Linear atrophoderma of Moulin

Lichen (planus)

Focal dermal hypoplasia

Ashy dermatosis (of Ramirez)

Partington X-linked cutaneous amyloidosis (in girls)

Others: lupus erythematosus, dermatomyositis, etc.

Segmental neurofibromatosis

Macular amyloidosis

Pigmented sequelae of inflammatory blaschkolinear dermatoses (fixed drug eruption, lichen, psoriasis, etc.)

Acanthosis nigricans

Chimerism

Notalgia paresthetica and frictional pigmentation and other physical causes: radiodermatitis, erythema ab igne (hot water bottle rash), etc.

Other linear pigmentations

Phototoxic reactions: phytophotodermatitis, Berloque dermatitis, Riehl’s melanosis, poikiloderma of Civatte, perioral dermatitis

Pigmentary demarcation lines

Idiopathic eruptive pigmentation

Pigmentary sequelae of exogenous dermatoses,e.g., phytophotodermatitis

Pigmented variants of certain dermatoses: morphea (atrophoderma of Pasini and Pierini), granuloma annulare, etc.

Pigmented sequelae of linear endogenous dermatoses: lymphangitis, superficial venous thrombosis, zoster, etc.

Pigmented form of mycosis fungoides

Reticulate hyperpigmentation

Pigmented form of common infections: erythrasma, pityriasis versicolor, tinea nigra, etc.

Zinsser-Cole-Engman syndrome

Dermal melanocytosis

Naegeli-Franceschetti-Jadassohn syndrome

Tattoo

Dyschromatoses (universalis hereditaria, acropigmentation of Dohi)

Postinflammatory pigmentation

Dermatopathia pigmentosa reticularis

Diffuse hyperpigmentation, poorly defined, photo-exposed, or generalized

Dowling-Degos disease

Hypermelaninosis

Reticulate acropigmentation of Kitamura

Metabolic and overload

Confluent and reticulated papillomatosis of Gougerot and Carteaud

Hemochromatosis (hemosiderosis and hypermelaninosis)

Partington-type X-linked cutaneous amyloidosis (in boys)

Only gold members can continue reading. Log In or Register to continue

Stay updated, free articles. Join our Telegram channel

Oct 6, 2016 | Posted by in Dermatology | Comments Off on Hyperpigmented Lesions

Full access? Get Clinical Tree

Get Clinical Tree app for offline access