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خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
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Key histopathologic findings in selected hyperpigmentation disorders

Key histopathologic findings in selected hyperpigmentation disorders
Selected disorders Key histopathologic findings
Acanthosis nigricans
  • Hyperkeratosis and papillomatosis of the epidermis
  • Basal layer hyperpigmentation
  • Minimal acanthosis (misnomer)
Actinic lichen planus
  • Variable with typical findings of lichen planus including hyperkeratosis without parakeratosis, hypergranulosis, irregular acanthosis with "saw-toothed" rete ridges, liquefaction degeneration of the basal layer, and band-like lymphocytic infiltrate at the dermal-epidermal junction
Addison's disease[1]
  • Increased basal layer melanin, sometimes melanin incontinence
Becker's melanosis[2]
  • Variable papillomatosis, acanthosis, and hyperkeratosis
  • Regular elongation of the rete ridges with or without pilosebaceous unit hyperplasia
  • May have increased hair follicles or smooth muscle
Café-au-lait macules[1]
  • Increased melanin in the basal layer
  • Normal number of hyperactive melanocytes
Dermal melanocytosis[1]
  • Spindle-shaped dendritic melanocytes in the deep dermis with abundant fine granules of melanin
Diabetes mellitus - diabetic dermopathy[1]
  • Dermal hemosiderin, increased papillary dermal blood vessels, sparse perivascular lymphocytes
Diabetes mellitus - necrobiosis lipoidica
  • Diffuse palisaded and interstitial granulomatous dermatitis with tiers of granulomatous inflammation (includes multinucleated histiocytes) aligned parallel to the surface
Dowling-Degos
  • Delicate, elongated, hyperpigmented rete ridges
  • Sometimes resembles a reticulated seborrheic keratosis
Drug-induced hyperpigmentation[1]
  • Variable depending on drug or chemical:
    • Minocycline: brown dermal pigment that is positive with iron and melanin stains
    • Gold: chrysiasis pigment appears as black particles
    • Bleomycin: basal layer with increased melanin
    • Clofazimine: brown lipofuscin that stains with PAS
    • Amiodarone: brown pigment that stains with PAS
Ephelides[1]
  • Increased melanin in basal layer
  • Normal or decreased number of hyperactive melanocytes
Erythema dyschromicum perstans[1]
  • Liquefaction degeneration of the basal layer
  • Melanin incontinence
  • Interface changes with perivascular or interface lymphocytes
Erythromelanosis follicularis faciei et colli[3]
  • Hyperkeratosis
  • Dilatation of superficial dermal blood vessels
  • Follicular plugging
  • Variable melanin in basal layer
Exogenous ochronosis[1]
  • Yellow-brown "banana-shaped" deposits on homogenized collagen bundles
  • Small yellow-brown granules in endothelial cells and sweat glands
Hemochromatosis[1]
  • Increased melanin in the basal layer
  • Hemosiderin deposits scattered in the dermis, usually around blood vessels and sweat glands, best seen with Perl's stain
Lentigines[1]
  • Hyperpigmented, often elongated rete ridges, usually with increased melanocytes
Lichen planus pigmentosus
  • Similar to erythema dyschromicum perstans with marked pigment incontinence and epidermal atrophy
Melasma[4]
  • Increased melanin deposition in all layers of the epidermis
  • Solar elastosis
  • More abundant mast cells
Nevus of Ota, Nevus of Ito, Hori's nevi[1]
  • Normal epidermis
  • Spindle-shaped dendritic melanocytes in the dermis with abundant fine granules of melanin
Nevus spilus
  • Lentiginous melanocytic hyperplasia
  • Papular foci represent junctional, compound, blue, Spitz, and/or atypical nevi
Periorbital hyperpigmentation[5,6]
  • Dermal melanocytosis and melanin in upper dermal macrophages (melanophages)
Post-chikungunya pigmentation[7,8]
  • Intact basal layer with diffuse hypermelanosis of the entire epidermis
Postinflammatory hyperpigmentation
  • Increased or normal amount of melanin at basal layer, with or without melanin incontinence based on etiology
Primary cutaneous amyloidosis[1]
  • Macular amyloidosis with subtle amyloid globules in the papillary dermis in areas of melanin incontinence
  • Lichen amyloidosis with small deposits of amyloid in the dermal papillae
Riehl's melanosis[1]
  • Lymphocytic perivascular or interface dermatitis with melanin incontinence
Smoker's melanosis
  • Mucosal surface with basal layer melanosis, with or without melanin incontinence
Terra firma-forme dermatosis[9]
  • Prominent lamellar hyperkeratosis with focal areas having compact orthokeratosis in whorls
PAS: periodic acid-Schiff.
References:
  1. Rapini RP. Practical Dermatopathology, 2nd ed, Saunders, Philadelphia 2012.
  2. Cohen PR. Becker's nevus. Am Fam Physician 1988; 37:221.
  3. Kim MG, Hong SJ, Son SJ, et al. Quantitative histopathologic findings of erythromelanosis follicularis faciei et colli. J Cutan Pathol 2001; 28:160.
  4. Kang WH, Yoon KH, Lee ES, et al. Melasma: histopathological characteristics in 56 Korean patients. Br J Dermatol 2002; 146:228.
  5. Malakar S, Lahiri K, Banerjee U, et al. Periorbital melanosis is an extension of pigmentary demarcation line-F on face. Indian J Dermatol Venereol Leprol 2007; 73:323.
  6. Watanabe S, Nakai K, Ohnishi T. Condition known as "dark rings under the eyes" in the Japanese population is a kind of dermal melanocytosis which can be successfully treated by Q-switched ruby laser. Dermatol Surg 2006; 32:785.
  7. Khanna N, Rasool S. Facial melanoses: Indian perspective. Indian J Dermatol Venereol Leprol 2011; 77:552.
  8. Inamadar AC, Palit A, Sampagavi VV, et al. Cutaneous manifestations of chikungunya fever: observations made during a recent outbreak in south India. Int J Dermatol 2008; 47:154.
  9. Browning J, Rosen T. Terra firma-forme dermatosis revisited. Dermatol Online J 2005; 11:15.
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