Tattoo
Reactions
Author: Terrence Keaney, MD, FAAD; Chief Editor:
Dirk M Elston, MD Fuente: Medscape
Nota: sin traducción al español para respetar el artículo original
Overview
A tattoo is the deposition of exogenous pigment into the skin or the
accidental entry of pigmented material. Accidental tattooing may occur after
abrasion injuries introducing asphalt, graphite, or carbon into the injured
skin. Rare iatrogenic tattoos have developed after the use of ferrous
subsulfate solution (Monsel solution) for coagulation purposes. While traumatic
tattoos are not rare, decorative tattoos are more common.
Decorative tattooing has been practiced for thousands of years for
artistic and cosmetic purposes. Tattoos are executed by professional tattoo
artists using an electric needle to introduce particles of pigment into the
dermis. The amateur tattoo artist may use any pointed object to place particles
of ink. Tattooing remains a common custom in various countries and cultures. It
gained popularity in many western countries throughout the 1990s. In the past,
decorative tattoos were primarily seen in men, especially in groups such as
sailors and members of the armed forces; however, they are increasingly
observed in young professionals of both sexes. The components of many tattoo
pigments have been identified, although new formulations continue to be
formulated (see Tattoo Pigments).
Complications resulting from decorative tattoos are rare, but the
incidence is increasing.[1, 2] The introduction of foreign substances into the skin can result in a
range of adverse effects, including a toxic or immunologic reaction to the
tattoo pigments, transmission of infectious disease, and the localization of
skin disease within the tattoo. The immunologic reaction to tattoos can vary
from an acute inflammatory reaction to allergic hypersensitivity. The
histopathologic pattern can be granulomatous, lichenoid, or pseudolymphomatous.
See the image below.
Transmission of Infection
Although significant infection secondary to tattoos is currently
unusual, infection may be introduced into the skin during the breach of the
epidermal barrier. Pyogenic infection resulting in erysipelas and gangrene were
a problem in the past, but localized skin infection secondary to gram-positive
bacteria is seldom observed today. Transmission of tuberculosis, syphilis,
leprosy, hepatitis, and HIV has also been recorded. By using a previously used
and infected tattoo needle, inoculation and person-to-person transmission of
viruses, including vaccinia and human papilloma virus, have been reported.[3, 4]
Certain types of tattoo inks and potential contamination of tattoo inks
can cause reactions that range from relatively mild to very severe,
particularly in individuals with preexisting comorbidities (cardiovascular
disease, diabetes, immune compromise). On August 7, 2014, the US Food and Drug
Administration issued a consumer warning about the potential health hazards associated
with tattoos following reports of infections from a line of home tattoo kits.
Testing revealed bacterial contamination in unopened tattoo ink bottles.[5]
See the image below.
Types of Reactions
Acute inflammatory reactions
Acute inflammatory reactions are associated with physical tissue injury
and the injection of pigment dyes or metals into the skin. This reaction
usually recedes without consequence within 2-3 weeks and is an expected adverse
effect of the tattooing process.
Eczematous hypersensitivity
reactions
Once acute inflammatory changes have resolved, the most frequent
reaction observed with tattoos is an allergic sensitivity to one of its
pigments. Individuals may manifest sensitivity to a particular pigment in
several ways. Histopathologic evaluation of involved skin may reveal a
spongiotic, granulomatous, or lichenoid type of tattoo reaction.
Commonly, hypersensitivity reactions to a tattoo pigment result in a
contact dermatitis or photoallergic dermatitis. These conditions may manifest
clinically as localized eczematous eruptions or, rarely, as an exfoliative
dermatitis. Histopathologic findings include acanthosis, spongiosis, and a
lymphocytic perivascular infiltrate.
See the image below.
Organic vegetable dyes are used more often than red pigments containing
mercury and have been associated with eczematous reactions and negative patch
test results. Because organic dyes are insoluble, little penetration into the
epidermis occurs; therefore, a negative patch test result occurs. Allergic
reactions may occur when organic dyes are injected into the dermis during tattoo
placement. One report describes allergic contact
dermatitis from a temporary henna tattoo.[6]
See the image below.
Photo-aggravated reactions
Photo-aggravated reactions are most commonly caused by yellow (cadmium
sulfide) tattoo pigment. Edema and erythema may develop upon exposure to
sunlight. Although the mechanism is not clear, cadmium sulfide is the
light-sensitive material used in photoelectric cells; therefore, the reaction
is believed to be phototoxic. Red tattoos have been associated with photo-aggravated
tattoo reactions less frequently than yellow tattoos, and most likely, these
reactions are related to the trace amounts of cadmium added to brighten the red
pigment.
In contrast to hypersensitivity reactions to red tattoos, reactions to
pigments used to create green, blue, and black tattoos are much less common.
Chromium in green tattoo pigment is associated with localized eczematous
reactions at the site of the pigment, eczema of the hands, and generalized
eczematous reactions. Patients may be sensitized primarily by exposure to
cement. Patch testing to 0.5% potassium dichromate is often positive.
Previously quiescent green-colored tattoos may become inflamed during patch
testing in potassium dichromate–sensitive individuals.[7]
Blue tattoos that contain cobalt have been linked to localized
hypersensitivity reactions and (rarely) spontaneous development of uveitis.
Allergic reactions to black tattoo pigment are very rare, with fewer
than 5 cases reported. Presumably, these patients were sensitive to carbon.[8, 9, 10]
Granulomatous reactions may take 2 forms. Foreign body reaction to
pigment can produce numerous pigment-filled giant cells. This reaction may be
viewed as the counterpart to an irritant contact
dermatitis. An immunologic granulomatous reaction is characterized
by aggregates of epithelioid cells, a ring of lymphocytes, and a few giant
cells. An immunologic granulomatous reaction may be indistinguishable from
tattoo involvement seen as a Köbner response in sarcoidosis;
therefore, further investigation, such as a complete review of systems and
possibly chest radiography, may be warranted to exclude systemic disease.
Most commonly, mercury (red pigment) is associated with a granulomatous
tattoo reaction; however, several reactions involving chromium (green pigment)
and cobalt (blue pigment) have also been reported.[13] In contrast to an eczematous hypersensitivity tattoo reaction in which
patch test results may be positive, granulomatous tattoo reactions are most
likely associated with negative patch test results.
Manganese reportedly causes a granulomatous reaction in purple tattoos,
but sufficient evidence is not available to establish manganese as the
definitive etiologic agent.[14, 15] One patient was documented with a granuloma occurring in the violet
areas of a tattoo shown to contain aluminum particles.[16] Intradermal provocation testing to aluminum was positive in this
patient.
Granulomatous reactions have been reported in permanent eyeliner tattoos
in several patients. Treatment is difficult because of the proximity to the lid
margin.[17]
Lichenoid hypersensitivity tattoo reactions are less common than
eczematous reactions. Evidence exists that the lichenoid reaction is an
expression of delayed hypersensitivity to a lymphocytic T-cell infiltrate,
which may simulate the graft-versus-host response. Mercury (red pigment) is
responsible for most lichenoid tattoo reactions. Clinically, warty papules or
plaques typical of hyperkeratotic lichen planus are usually confined to the red
portion of the tattoo, although a generalized lichen planus reaction developed
in one patient with a history of a lichenoid tattoo reaction.[21] This patient had occupational exposure to mercury.
Histopathologically, the pattern of inflammation is consistent with that
of lichen planus, including a bandlike infiltrate at the dermoepidermal
junction, liquefaction degeneration, hyaline bodies, and sawtooth rete ridges.
Similar to granulomatous tattoo reactions, lichenoid reactions are associated
with negative patch test results.
Delayed hypersensitivity to tattoo pigment may result in a
pseudolymphomatous reaction. Lymphadenosis benigna cutis (pseudolymphoma) can
develop after a variety of foreign substance exposures including insect bites,
acupuncture, antigen injections, earrings, and tattoos.[26] Tattoo-induced pseudolymphoma occurs primarily within red portions of
the tattoo. This reaction is rarely induced by green or blue tattoos.
Clinically, most reactions are characterized by flesh-to-plum or
plum-red indurated nodules and plaques similar to cutaneous B-cell lymphoma. Be
alert to this type of reaction to tattoo pigment to prevent an erroneous
diagnosis of lymphoma. Pseudolymphoma may be distinguished from cutaneous
lymphoma at histologic examination. Important features of a pseudolymphoma
include germinal centers, a mixed cell infiltrate, prominent vasculature, and
predominant involvement of the upper dermis compared with the lower dermis.
Immunohistochemical studies may provide additional information that helps
distinguish pseudolymphoma from malignant B-cell proliferation in the skin.
Monotypic light-chain expression highly suggests malignant lymphoma, while the
lymphocytes in pseudolymphoma primarily are polyclonal.
Localization of Disease in
Tattoos
Several cutaneous disorders show a predilection for tattooed skin. The
eruption may represent the initial manifestation of the disease or the
accentuation of an existing disorder in the area of the tattoo. Lichen planus,
psoriasis,
sarcoidosis,
and lupus erythematosus have been associated with localization to the site of a
tattoo.[27] No color predilection is demonstrated in this localization response.
Whether disease localized to the tattoo represents the Köebner phenomenon or
results from a locus minoris resistentiae that predisposes the area to disease
is unclear.
Several patients with malignant
melanoma occurring in a tattoo have been reported.[28] Most of these documented cases include melanomas found in tattoo sites
used for marking an irradiation field. The combination of India ink and
irradiation may be responsible for carcinogenesis. The association may be coincidental
in the patients without predisposing injury.
Keratoacanthoma, a keratinizing squamous cell neoplasm of
unknown origin characterized by rapid growth, have been observed with various
types of skin injury. Although rare, eruptive keratoacanthoma have been
reported in both red and multicolored tattoos.[29, 30]
Tattoo removal may be required when complications develop. If an
allergic reaction is noted, some cases resolve with topical or intralesional
steroids, but permanent removal may be necessary.
Most often, tattoo removal is sought for cosmetic reasons. Decorative
tattoo removal can be accomplished by a variety of methods. Treatment
modalities used in the past included cryosurgery, dermabrasion, carbon dioxide
lasers, and cold steel surgical excision. These destructive methods replaced
the tattoo with a permanent scar. In 1964, Goldman et al were the first to
describe the removal of tattoos with the Q-switched ruby laser.[31] These experiments were successful; however, the technique did not gain
popularity until the 1990s. Laser tattoo removal often requires multiple
treatments, and complete resolution of color may not be achieved in all cases.
Laser tattoo removal targets tattoo pigment-containing structures in the
skin using the theory of selective photothermolysis. To achieve selective
photothermolysis, sufficient energy to damage the target needs to be delivered
with a pulse duration that is less than the thermal relaxation time of the
target, which is itself defined by the size and shape of the target. The
smaller the target, the shorter the thermal relaxation time and therefore the
shorter the laser pulse duration required. The thermal relaxation time of
tattoo pigment particles is less than 10 nanoseconds, suggesting that energy
delivery in the picosecond range (1 trillionth of a second, 10-12 seconds)
should be effective.
Historically, the Q-switched lasers (nanosecond duration, 10-9 seconds)
ruby (694 nm), Q-switched Nd:YAG (1064 nm), Q-switched alexandrite (755 nm),
Q-switched frequency-doubled Nd:YAG (532 nm), and the pigmented lesion pulsed
dye (510 nm) lasers have been used to remove various tattoo pigments.
Recently developed picosecond laser systems generate significant
photomechanical effects, which leads to a more effective mechanical breakup of
the ink or pigment particles. Using picosecond pulses allows lower treatment
fluences to be used, while keeping the peak tensile stress induced
substantially higher than that typically produced with Q-switched lasers.
Selection of the appropriate wavelength is determined by the colors of
tattoo pigment to be targeted. Based on “complementary matching” of tattoo
pigment, green tattoo pigment is most effectively removed by 694-nm or 755-nm
wavelengths and red tattoo pigment is best removed with 532-nm wavelength. Blue
and black pigments are removed with any wavelength. More difficult to remove
are yellow and orange pigments, but these are often treated with 532-nm
wavelength.
Before laser treatment, tattoo pigment is localized within perivascular
fibroblasts, mast cells, and macrophages. After treatment with a Q-switched or
picosecond laser, rapid thermal expansion fragments the pigment-containing
cells causing the pigment to become extracellular.
The release of ink particles into the extracellular space allows for
lymphatic drainage and rephagocytosis of smaller residual ink particles. To a
lesser extent, elimination of pigment by formation of scale-crust may be
involved.
Complications following laser treatment of tattoos have been well
documented. Laser treatment infrequently may cause a localized tattoo reaction
to become generalized.[32, 33, 34] Pigment released into the extracellular space after laser treatment may
be viewed as foreign by the immune system, causing a hypersensitivity response.[35]
Laser-induced photochemical changes can occur in tattoo inks resulting
in irreversible immediate darkening of the tattoo. Pigments, including red,
brown, and white, used for cosmetic tattoos are at highest risk for this type
of reaction. The darkening reaction may be masked by an immediate whitening
action after laser treatment. The immediate whitening of the tattoo is likely
caused by the formation of gas bubbles that intensely scatter light. A small test
area is advised because this transient whitening reaction may obscure the
darkening reaction.[36] Most cosmetic tattoos contain iron (or titanium) oxide inks that, on
laser irradiation, are reduced from ferric oxide to the ferrous oxide form; the
latter being black and insoluble. Although this reaction pattern can usually be
improved with continued laser treatments or vaporization with a carbon dioxide
laser, the darkened color may be permanent.
Tattoo Pigments
The composition of tattoo pigment colors is as follows:
- Black - Carbon (India ink), iron oxide, logwood
- Blue - Cobalt aluminate
- Brown - Ferric oxide
- Green - Chromic oxide, lead chromate, phthalocyanine dyes
- Purple - Manganese, aluminum
- Red - Mercuric sulfide (cinnabar), sienna (ferric hydrate),
sandalwood, brazilwood, organic pigments (aromatic azo compounds)
- White - Titanium oxide, zinc oxide
- Yellow - Cadmium sulfide
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