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SYMPOSIUM DERMATOPATHOLOGY
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Year : 2013  |  Volume : 79  |  Issue : 3  |  Page : 367-375

Clinicopathological correlation of acquired hyperpigmentary disorders

Anisha B Patel1, Raj Kubba2, Asha Kubba2,  
1 Department of Dermatology, Oregon Health Sciences University, Portland, Oregon, USA
2 Delhi Dermatology Group, Delhi Dermpath Laboratory, New Delhi, India

Correspondence Address:
Asha Kubba
10, Aradhana Enclave, R.K. Puram, Sector 13, New Delhi - 110 066
India

Abstract

Acquired pigmentary disorders are group of heterogenous entities that share single, most significant, clinical feature, that is, dyspigmentation. Asians and Indians, in particular, are mostly affected. Although the classic morphologies and common treatment options of these conditions have been reviewed in the global dermatology literature, the value of histpathological evaluation has not been thoroughly explored. The importance of accurate diagnosis is emphasized here as the underlying diseases have varying etiologies that need to be addressed in order to effectively treat the dyspigmentation. In this review, we describe and discuss the utility of histology in the diagnostic work of hyperpigmentary disorders, and how, in many cases, it can lead to targeted and more effective therapy. We focus on the most common acquired pigmentary disorders seen in Indian patients as well as a few uncommon diseases with distinctive histological traits. Facial melanoses, including mimickers of melasma, are thoroughly explored. These diseases include lichen planus pigmentosus, discoid lupus erythematosus, drug-induced melanoses, hyperpigmentation due to exogenous substances, acanthosis nigricans, and macular amyloidosis.



How to cite this article:
Patel AB, Kubba R, Kubba A. Clinicopathological correlation of acquired hyperpigmentary disorders.Indian J Dermatol Venereol Leprol 2013;79:367-375


How to cite this URL:
Patel AB, Kubba R, Kubba A. Clinicopathological correlation of acquired hyperpigmentary disorders. Indian J Dermatol Venereol Leprol [serial online] 2013 [cited 2020 Oct 25 ];79:367-375
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Full Text

 Introduction



Acquired pigmentary disorders are found all over the world, but can be particularly distressing in patients with skin of color. Classic morphologies of these conditions have been reviewed in the global dermatology literature with an emphasis on treating these difficult diseases. [1] The importance of accurate diagnosis is emphasized here as the underlying diseases have varying etiologies that need to be addressed in order to effectively treat the dyspigmentation. In this review, we describe and discuss the utility of histology in the diagnostic work of hyperpigmentary disorders and how, in many cases, it can lead to targeted and more effective therapy. We focus on the most common acquired hyperpigmentary disorders seen in Indian patients as well as a few uncommon diseases with distinctive histological traits.

 Facial Melanoses



This group of diseases has been the focus of many review and management-focused articles, both in Indian dermatology literature and abroad. Pigmentary alterations of the face can be extremely distressing to the patient, making their effective management a priority for both the patient and the physician.

 Melasma



Melasma (chloasma) is the most common clinical diagnosis made among the facial melanoses. It occurs mostly in women, and is clinically characterized by patterned, symmetric, brown to grayish-brown, hyperpigmented patches of the face in malar and centro-facial areas [1] [Figure 1]a. However, in India, in one reported series, one out of every five patients was male. [2]{Figure 1}

Hyperpigmentation is largely epidermal, causing accentuation of the lesions under Wood's lamp. Melasma may, in some cases, present with significant dermal pigmentation, and this is clinically suggested by grayish hue and the lack of accentuation under Wood's light examination. The clinical and histopathological correlation of increased dermal melanin and negative Wood's lamp examination is controversial, Sanchez et al. [3] showing the correlation and Grimes [4] denying it.

The diagnosis of melasma is usually made on the basis of clinical features alone. However, this approach is unsatisfactory as there are many pigmentary disorders that, clinically, mimick melasma and the distinction between them invariably requires astute histopathological evaluation and subsequent clinical correlation. The histopathological features of melasma per se are subtle and only when control skin biopsies are available for comparison, they are truly appreciated [3],[4] [Figure 1]b and c. Increased epidermal melanin is the key feature and this requires Masson Fontana stain. This increase is seen mainly in the basal/suprabasal cells as pigmentary caps [3],[4] but in a Korean study increased melanization was noted in all layers of the epidermis [5] Dermal melanin is observed in some cases (dermal melasma) mainly in macrophages (also called melanophages) but also as free melanin deposits around superficial and deep vascular plexuses. [3] Increased melanocytic activity has been documented in melasma using Mel-5 immuno-staining. [4],[5] It reportedly varies from actual increase in the number of melanocytes [5] to merely enlargement of melanocytes with increased staining and prominent dendrites indicative of increased melanogenesis. [4]

Melasma pathology also includes additional dermal changes, namely solar elastosis and telengiectasia. These changes are best appreciated when uninvolved skin is available for comparison. Solar elastosis is evaluated with Verhoeff-van Gieson stain (VVG) and it has been observed in melasma as clumps of thick and fragmented elastic fibers in the papillary dermis. Sarkar et al. [2] in their series, reported solar elastosis in 85% of 20 biopsies from melasma patients. The histopathological evaluation of melasma should be done to exclude melasma mimickers. The best practice is to compare the pigmentary alteration of lesional skin with patient's normal skin as control.

 Lichen Planus Pigmentosus



Lichen planus pigmentosus (LPP) is a macular variant of lichen planus reported mostly from the Indian subcontinent and the Middle-East. [6],[7] It is characterized by focal or coalescing gray-blue patches or subtle plaques arising on the exposed areas, [Figure 2]a especially the neck and the adjacent torso. [1],[6] It is typically bilaterally symmetrical. [7] Rarely, LPP can mimick melasma. Photosensitivity is reported by some patients. The hyperpigmentation is mainly dermal, resulting in lesions that do not accentuate under Wood's lamp. Ashy dermatosis/erythema dyschromicum perstans bears similar morphology and is pathologically indistinguishable except it has predilection for non-sun exposed areas and has been reported mostly from South America. [8] LPP inversus is yet another similar entity in which intertriginous areas are predominantly involved. [9]{Figure 2}

LPP being a subset of lichen planus may, on occasion, exhibit typical lichenoid pathology if palpable lesions are present and are sampled. In most instances, however, that is not the case. Histopathological evaluation of a macular lesion shows a relatively flat epidermis with loss of rete pattern, focal basal cell vacuolization with occasional necrotic keratinocyte and Civatte body, dermal melanophages, and a sparse lymphohistiocytic inflammation [Figure 2]b. Foci of squamatized epidermis are sometimes encountered and indicate preceding vacuolar damage of the basal layer in a relatively aged lesion.

In a study, [7] in which 65 skin biopsies of LPP were examined, basal cell vacuolization was documented in 78.5%, dermal melanophages in 63%, and perivascular infiltrate in 81.5% of the cases. In the same study, band-like lichenoid infiltrate was observed in only 18.5% of the cases. The histopathology of LPP is, in general, subtle with sparse inflammation, requiring thorough evaluation of the biopsy. Therefore, diagnosis of LPP is based on clinicopathological correlation.

 Discoid Lupus Erythematosus



Discoid lupus erythematosus (DLE) may present as hyperpigmented plaques on the face and neck in a focal distribution without attendant erythema, induration, adherent scaling or scarring. This presentation of DLE is rarely reported in the literature. [10],[11] In a clinical study of LE from India, pigmented macular form was recorded in 25% of 65 cases. [10] We illustrate this entity with a case of a 31-year-old female who over a 3-year period progressively developed hyperpigmented plaques on the forehead, temples, cheeks, ears, and eyelids associated with photosensitivity [Figure 3]a. She was unsuccessfully treated for melasma. The diagnostic clues were bilateral asymmetry and follicular plugs. Wood's lamp examination showed accentuation. Histopathology showed a relatively thin epidermis with focal basal cell vacuolization, necrotic keratinocytes, pigment incontinence along with superficial and deep perivascular and perifollicular infiltrate of lymphohistiocytes [Figure 3]b and c. Follicular ostia were dilated and plugged. The clinical diagnosis of LE was validated using direct immunofluorescence study which showed a granular band of IgM and C3 along the basement membrane zone.

Melanotic LE as a melasma mimicker is hitherto unreported. Melanotic LE as a subset of DLE is, in our opinion, more common than the paucity of published literature would suggest. Both hypopigmentation and hyperpigmentation are recognized sequelae of LE. A good history and evidence of scarring would readily identify this group. A true melanotic LE would be when the hyperpigmentation arises de novo without preceding clinical signs of inflammation. Melanotic LE is more likely to be confused with LPP. However, with histopathology and DIF, it is not difficult to distinguish between them.{Figure 3}

 Drug-Induced Melanosis



Pigmentation as a side effect of medications is well recognized. Clofazimine, minocycline, and antimalarial-induced hyperpigmentation show varying pathologies but all are time-sensitive to the onset of the medication.

Most notable is clofazimine-induced brown pigmentation that is accentuated in sun-exposed areas and at times may appear like melasma , [Figure 4]a but typically it is generalized and nails are commonly involved [Figure 4]b. Two types of pigments accumulate in the skin, namely, redox dye and lipofuscin-ceroid. Redox dye is deposited in the skin, fat, gut, and lymph nodes usually within weeks of starting therapy. Discoloration of urine and sweat may also occur. Lipofuscin-ceroid pigment appears later, typically after 6-12 months, and is reversible. [12]{Figure 4}

Histopathology of clofazimine-induced pigmentation is characterized by large collections of foamy macrophages in the dermis bearing brownish granular pigment [Figure 4]c. The two pigments are indistinguishable and do not stain with acid fast stain, melanin stain, or iron stain. Under ultraviolet light, the pigments appear golden brown. Redox dye is best visualized in frozen sections as red auto-fluorescent deposits and it appears as birefringent crystals by light microscopy. [13] Lipofuscin-ceroid is identified by Mallory's hemofuscin stain in paraffin-embedded sections. Epidermis shows loss of rete pattern.

Minocycline-induced pigmentation is seen as perivascular granular brown pigment that stains positive with Perl's and Masson Fontana. Antimalarial-induced yellow-brown pigment is distributed within histiocytes throughout the dermis. It is weakly positive with Perl's stain.

 Argyria



Argyria is an exotic cause of hyperpigmentation. It results from deposition of silver in the skin subsequent to prolonged ingestion of silver. [14],[15],[16] In India, the exposure is mainly through ingestion of silver-coated sweets (mithai with silver virq) and silver-coated cardamom, beetle nut, and fennel seeds (consumed as mouth freshners for years on end). Argyria produces distinctive gray-blue discoloration in a photo pattern. Similar discoloration can also be seen over ear cartilage, in the nails, mucous membranes, and sclera [1],[15] [Figure 5]a and b.{Figure 5}

Localized cutaneous argyria due to prolonged contact with silver salts or silver jewelry, or from penetration of acupuncture needles is also reported. Such lesions may mimick melanocytic lesions including melanoma. [17],[18] Argyria lesions do not accentuate on Wood's lamp examination.

Histopathology shows brown-black granules deposited in a band-like fashion along the basement membrane of the eccrine glands [Figure 5]c. Occasionally, similar granules may be seen in the papillary dermis corresponding to elastic fibers, and around pilosebaceous units. Additional sites to examine are blood vessel wall and arrector pili muscle. Granules are refractile under dark field microscopy. [15],[16] Argyria pathology is subtle and may present as an invisible dermatosis. There is no obvious evidence of pigmentary pathology such as interface damage or dermal melanophages. Silver being inert, inflammation is minimal or absent. Gold and mercury granules are also refractile. However, granules in chrysiasis are larger, irregular in shape, mostly intracellular within macrophages and endothelial cells, and show orange-red birefringence on fluorescent microscopy. Mercury granules are larger, irregular, and are found in upper dermis mostly within macrophages. Positive identification of silver in the tissue can only be done by atomic absorption spectrophotometry. [19],[20] In argyria, serum silver levels reportedly range from 4 to 40 g, whereas the total silver content in the body is 1 mg. [14] Diagnosis can be established by histopathology and positive history of silver intake.

 Ochronosis



Exogenous ochronosis is a blue-black dermal discoloration secondary to prolonged use of skin bleaching creams containing hydroquinone. Bleaching occurs at first, followed by hyperpigmentation with papules over the treated areas. Clinically, pigmentation occurs over bony prominences, forehead, temples, nose, lower jaws, and sides of neck. [21] Exact pathogenesis of exogenous ochronosis is not known. It is believed that hydroquinone inhibits homogentisate 1, 2-dioxygenase in skin with formation of the pigment. Endogenous ochronosis (alkaptonuria) is an autosomal recessive disorder caused by inherited deficiency of homogentisic acid oxidase resulting in progressive deposition of polymerized homogentisic acid in the connective tissues of the skin and internal organs.

Histopathology of an early lesion shows swollen and basophilic collagen fibers. Older lesions show characteristic yellow-brown ochronotic pigment (homogentisic acid) coating collagen fibers and appearing as banana-shaped bodies [Figure 6]. Pigment granules are often also present in epithelium and basement membrane of sweat glands. The pigment is auto-fluorescent and it does not stain with Masson Fontana or Perl's stain. Ochronotic fibers do not stain with elastic stain. [21] Yellow collagen fibers eventually become amorphous eosinophilic material resembling colloid milium. Melanophages may be observed in upper dermis. [21] Histopathological features are common to both endogenous and exogenous ochronosis. [22]{Figure 6}

 Acanthosis Nigricans



Acanthosis nigricans (AN) is characterized by hyperpigmented, velvety thickening of skin predominantly affecting nape of neck and intertriginous/flexural areas of the body. Acquired AN is associated with a variety of conditions especially insulin resistance, metabolic syndrome, and malignancies. Obesity associated with AN was reported in 70% of patients in an Indian study. [23] AN is also a feature of several genetic syndromes.

Clinically, AN lesions present as symmetrical velvety plaques with predilection for back of neck, axillae, and groins [Figure 7]a. Less common sites include face, back of hands, fingers, or rarely palms. Oral lesions may involve tongue and lip. [23],[24]{Figure 7}

Histopathological features are subtle. Hyperkeratosis covers a papillomatous epidermis with finger-like projections forming peaks and valleys. Acanthosis is subtle [Figure 7]b. Features seen less often are perivascular chronic inflammatory infiltrate in upper dermis and occasionally keratin cysts reminiscent of seborrhoeic keratosis. In a study of 30 patients of AN, dermal inflammation was seen in 60% and pseudocysts in 30% cases. [23] Clinically, hyperpigmentation does not reflect in the pathology which shows minimal increase in melanin. Pathology of AN is similar to epidermal naevi. The distinction is made on the basis of clinicopathological correlation.

 Poikiloderma of Civatte



Poikiloderma of Civatte is most commonly seen in middle-aged, postmenopausal Caucasian women, but has also been reported in individuals with skin of color. [1] Skin lesions typically involve sun-exposed parts of face, neck, and V of the chest. Clinically, it presents as reticulate spots of hyperpigmentation and atrophic hypopigmentation with telengiectasia [25] [Figure 8]a.{Figure 8}

Histology is characterized by telengiectasia, fibrosis, and melanophages in the papillary dermis with prominent solar elastosis [Figure 8]b. Mild epidermal atrophy may be present particularly in older lesion. Accumulated elastotic material can be better visualized with an Orcein stain. Occasional mild vacuolar change is associated with melanin incontinence. [26] Poikiloderma associated with connective tissue disease shows interface dermatitis. Poikiloderma atrophicans vasculare displays band-like inflammation.

 Riehl's Melanosis (Pigmented Contact Dermatitis)



Riehl's melanosis is thought to be a pigmented contact dermatitis to allergens present in cosmetics, fragrances, and kumkum. [27],[28] It presents as patches of diffuse gray-brown pigmentation on forehead, scalp, face, and neck [Figure 9]a. Erythema, scaling, or pruritus is occasionally present. Henna application has been implicated in some patients. [1]{Figure 9}

Contrary to its name, histopathology, of pigmented contact dermatitis is not spongiotic but an, interface dermatitis with basal cell vacuolization [29] [Figure 9]b and c. Superficial perivascular lymphocytic infiltrate and melanophages are present in the dermis. Interface dermatitis overlaps with lupus erythematosus (LE) and LPP. [1],[30] LE typically shows deep perivascular and perifollicular inflammation, and lupus band on direct immunofluorescence study. LPP, on the other hand, is difficult to distinguish from Riehl's melanosis. The diagnosis is based on clinical correlation. Spongiosis and lymphocytic exocytosis are diagnostic features of contact dermatitis.

 Hori's Nevus (Acquired Bilateral Nevus of Ota Like Macules)



Hori's nevus was first described in 1984 in Japanese women. [31] Unlike Nevus of Ota, it is an acquired condition that occurs late in life. It is an example of circumscribed melanocytosis, similar to nevus of Ota/Ito and Mongolian spot. It typically presents with large pigmented macule(s) on the face. Ocular and mucosal membranes are not involved. Clinical features most commonly are bilateral, on the malar cheeks, forehead, temples, and eyelids, as blue-brown or slate gray patches. Facial macules are similar to melasma and Riehl's melanosis [Figure 10]a. Pigmentation is not photosensitive. Skin lesions do not accentuate on Wood's lamp examination as pigmentation is largely dermal. [31] Clinical similarity between melasma and Acquired bilateral nevus of Ota like macules (ABNOM) was further investigated for possibility of shared pathogenesis between the two entities. [32]{Figure 10}

Histopathology is subtle on scanning power. A close scrutiny will show melanophages in the mid- and upper dermis [Figure 10]b. Dermal melanocytes are hard to see as they are scattered diffusely in upper and mid-dermis, as single cells in between dermal collagen fibers. Elongated melanocytes may appear pigmented. The subtle pathology can be highlighted with Masson Fontana stain that highlights melanin pigment. [33] S-100 stain identifies the dermal melanocyte [Figure 10]c. Melasma and Riehl's melanosis do not show melanocytic pathology.

 Macular amyloidosis



Macular amyloidosis is an example of cutaneous variant of amyloidoses, which is common in Middle-East and India. Women are affected more often than men. Macular dark brown, symmetrical pigmentation occurs on central, upper back, chest, extremities, and face. Characteristic lesions consist of rippled or reticulated pigmentation which is typically pruritic [Figure 11]a. It is not photosensitive and Wood's lamp examination does not accentuate the dermal pigmentation.{Figure 11}

Histology shows small, sometimes subtle, globular deposits of eosinophilic amyloid and melanophages, confined within a few distended dermal papillae. Additional features include sparse vacuolar damage and apoptotic keratinocytes. [34] Amyloid is highlighted by Congo red and crystal violet stains [Figure 11]b and c. Amyloid deposits are focal and may be small enough to escape detection in the biopsy.

 Fixed Drug Eruption



Fixed drug eruption (FDE) is clinically distinctive. It presents as recurrent plaque(s) at fixed locations, commonly lips, genitalia, and acral areas subsequent to each exposure to the offending drug. Fixed drug eruption (FDE) plaques are erythema multiforme (EM)-like, even targetoid, usually non-itchy and resolve spontaneously with postinflammatory hyperpigmentation (PIH). Less commonly, FDE may present as pigmented macules. Many drugs are implicated in FDE, some notable being barbiturates, ibuprofen, and sulfonamides.

Histologically, vacuolar type of interface pathology observed is associated with necrotic keratinocytes and lymphocytic infiltrate that obscures the dermo epidermal junction (DEJ). Pigment incontinence is a prominent feature. Subepidermal vesiculation may be seen. Upper dermal inflammation consists of lymphohistiocytes, neutrophils, and eosinophils. Dermal melanophages may be the only tell-tale sign of a resolved lesion of FDE. [35]

 Confluent Reticulate Papillomatosis of Gougerot-Carteaud



Confluent reticulate papillomatosis (CRP) is an uncommon pigmentary disorder characterized by asymptomatic, persistent, coalescing brown papules, and small plaques forming a characteristic reticulate pattern. It has predilection for upper chest, upper back, shoulders, and neck, and is bilaterally symmetrical [36] [Figure 12]a.{Figure 12}

Histopathology shows a low papillomatous lesion covered by basket weave keratin. Epidermis is acanthotic at the base of the valleys between the papillomatous areas. Mild basal hyperpigmentation may be apparent in some cases [Figure 12]b. The pathology of CRP overlaps with mild forms of AN.

 Becker's Nevus



Becker's nevus (melanosis) is an acquired melanosis that presents in late childhood or early adolescence. A hyperpigmented patch gradually evolves into a plaque and usually displays variable degree of hypertrichosis. It typically arises in the vicinity of the large joints especially shoulders, elbows, and hips. Rarely, multiple sites may be affected. [37] Once fully evolved, Becker's nevus persists unchanged through life.

Histopathologically, Becker's nevus shows both epidermal and dermal abnormalities. The epidermal changes include acanthosis, mild papillomatosis, and variable basal hyperpigmentation. The rate ridges in Becker's nevus are flat in contradistinction to epidermal nevus. Dermal changes include increased number of hair follicles and sebaceous glands. Hypertrophy of arrector pilorum muscle along with bundles of smooth muscle fibers independent of adnexa are the distinctive pathological features. Dermal melanophages are also noted. [37]

 Ephelides (Freckles)



Ephelides are small pigmented macules that occur on the face and less commonly on other sun-exposed areas of light complexioned individuals. They are increasingly being observed in Indians with skin type IV and V. Ephelides are irregular, discrete, small macules, about 1-2 mm in size, typically distributed over the nose and malar areas. The pigmentation varies corresponding to seasons and level of sun exposure. [38]

Histological features show hypermelanization of basal epidermis with otherwise normal epidermal architecture. There is no increase in the number of melanocytes. Electron microscopy studies have shown increased melanin production by the affected melanocytes in contrast to normal skin. [39]

Psoralens and ultraviolet-A light (PUVA) therapy [40] is known to stimulate melanogenesis and causes ephelide-like pigmentation in some individuals which histologically is indistinguishable from classic ephelides. Cafι-au-lait spots also share the same pathological features.

 Conclusion



Disorders of hyperpigmentation discussed above focus on the acquired diseases and cover the most common diagnoses and demonstrate the utility of histopathology as the clinical presentations overlap significantly. Facial melanoses are group of heterogenous disorders, mistaken clinically as melasma The benefit from histopathological evaluation, is not only to confirm but exclude related disorders because management of these differs significantly. Discoid lupus erythematosus requires systemic therapy, as does LPP and AN. Some conditions are extremely resistant to treatment such as exogenous ochronosis and argyria, but cessation of the causative factors can halt progression of the disease. Targeted diagnosis and therapy can prevent progression of disease and years of failed treatments in patients. More importantly, it can reveal potentially disfiguring skin diseases such as DLE or highlights metabolic disease such as in AN.

This review, of most common acquired disorders, highlights the value of histopathology in evaluating hyperpigmentary disorders that afflicts so many of Indians seeking medical assistance. The key histopathological features are highlighted with emphasis on differential diagnosis that come into consideration. In conclusion, a specific diagnosis of hyperpigmentary disorder is possible based on histopathological findings and its interpretation in the context of clinical presentation.

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