(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)
Stay updated, free articles. Join our Telegram channelFull access? Get Clinical TreeGet Clinical Tree app for offline access |