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Dermoscopy in eczema: A magnified approach to diagnosis and management
*Corresponding author: Yasmeen Jabeen Bhat, Department of Dermatology, Venereology and Leprosy, Government Medical College, Srinagar, Jammu and Kashmir, India. yasmeenasif76@gmail.com
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Received: ,
Accepted: ,
How to cite this article: Bhat YJ, Qayoom M. Dermoscopy in eczema: A magnified approach to diagnosis and management. Indian J Skin Allergy. doi: 10.25259/IJSA_14_2025
Abstract
Eczema is a prevalent inflammatory skin condition characterized by barrier dysfunction, immune dysregulation, and environmental triggers. The disease manifests in acute, subacute, and chronic stages, presenting diagnostic challenges due to clinical overlap with other dermatoses. Dermoscopy, a noninvasive imaging tool traditionally used for pigmented lesions, has emerged as a valuable adjunct in diagnosing and monitoring eczema. This review explores the evolving role of dermoscopy in identifying disease-specific patterns across different stages of eczema, distinguishing it from mimickers, and assessing treatment response. Characteristic dermoscopic features, such as vascular patterns, pigmentary changes, and scaling variations, correlate with histopathological findings, improving diagnostic precision. Furthermore, dermoscopy aids in detecting eczema complications, including secondary infections and chronic skin changes. While it enhances diagnostic accuracy and disease monitoring, limitations include overlapping features with other inflammatory disorders and the need for clinical expertise. Future research and standardized dermoscopic criteria may further refine its application in eczema management, optimizing patient outcomes through early detection and tailored therapeutic interventions.
Keywords
Acute
Subacute
Chronic
Dermoscopy
Eczema
INTRODUCTION
Eczema is a common inflammatory skin disease that affects individuals across all age groups. Eczema, derived from the Greek words ek (out) and zema (boil), literally means “to boil out.”[1] Characterized by a relapsing course with exacerbations of erythema, scaling, pruritus, and vesiculation, eczema presents significant diagnostic and therapeutic challenges.
Eczema arises from a combination of epidermal barrier dysfunction, immune dysregulation, and environmental triggers. Disruption of the stratum corneum, due to intrinsic defects or external insults, leads to increased trans epidermal water loss and heightened permeability to irritants and allergens. This initiates an immune response, predominantly involving T cells, cytokines such as interleukin (IL)-1, IL-6, and tumor necrosis factor-alpha, and local inflammation. Chronicity results from repeated cycles of inflammation, pruritus, and scratching, further impairing barrier integrity and promoting secondary infections.
Eczema is classified into acute, subacute, and chronic stages, reflecting its evolving clinical presentation and histopathological features over time.[2] Acute phase manifests as intense itching, redness, swelling, and papulovesicular lesions. The subacute stage is marked by persistent swelling and scaling, while the chronic stage is characterized by dry, fissured, thickened, and lichenified skin.
Eczema is typically diagnosed through a thorough clinical examination. Patch testing may prove valuable in suspected cases of contact eczema affecting the face, hands, or feet, or when the dermatitis is atypical or asymmetrical. Biopsy is rarely necessary.
Effective management involves not only symptom control but also accurate diagnosis, disease monitoring, and timely identification of complications. In this regard, dermoscopy – a non-invasive technique traditionally used in dermatology for the evaluation of pigmented skin lesions, particularly melanomas – has been increasingly integrated into clinical practice for managing eczema.
Dermoscopy involves the use of a handheld device equipped with a light source and magnification lens to examine skin lesions. It provides an in-depth view of epidermal and superficial dermal features, which are not visible to the naked eye.[3,4] In recent years, this technique has been applied to a variety of dermatological conditions, extending its utility beyond the diagnosis of melanoma and non-melanoma skin cancers to include inflammatory skin disorders like eczema.[5,6]
DERMOSCOPY IN DIAGNOSIS OF ECZEMA
The diagnosis of eczema is primarily clinical, based on characteristic lesions, patient history, and environmental or genetic triggers. In eczema, dermoscopic findings depend on the stage of the disease (acute, subacute, or chronic). Some of the key dermoscopic and histopathological features identified in eczema are given in Table 1 and their co-relation is depicted in Table 2.
Dermoscopy | Histopathology | |
---|---|---|
Acute | • Irregular pigment • Linear and patchy arrangement of vessels • Pink-red background • White and yellow-orange clods (yellow clod sign) • Excoriation marks with adherent fibers (adherent fabric fiber sign) • Vascular changes with irregular dots |
• Marked spongiosis with intraepidermal vesicle formation • Mild acanthosis and hyperkeratosis • Focal parakeratosis • Exocytosis of lymphocytes • Prominent papillary dermal edema • Superficial perivascular lymphocytic infiltrate with eosinophils and histiocytes • Dilated, non-torous blood vessels • No fibrosis |
Subacute | • White scales or peripherally attached scales • Irregular pigment network • Brown–white background • Black/brown/gray dots • Vascular changes with irregular dots |
• Moderate spongiosis with fewer vesicles • Moderate acanthosis and hyperkeratosis • More prominent parakeratosis • Exocytosis of lymphocytes and occasional eosinophils • Moderate papillary dermal edema • More prominent lymphohistiocytic perivascular infiltrate • Dilated, non-tortuous blood vessels • Mild fibrosis |
Chronic | • Brown–white background • Irregular pigment network • Black/brown/gray blotches • White dots, clods, blotches |
• Minimal spongiosis • Marked acanthosis with irregular epidermal hyperplasia • Diffuse parakeratosis • Exocytosis of lymphocytes with occasional plasma cells • Minimal papillary dermal edema • Dense lymphocytic infiltrate with plasma cells and fibrosis • Subepidermal fibrinoid degeneration • Neovascularization may be present • Marked dermal collagen deposition |
Dermoscopic features | Histopathological features |
---|---|
Hypopigmented zones | Spongiosis |
Scales | Focal parakeratosis |
Brown dots | Epidermal melanin deposition and melanin incontinence |
Erythema, crown of branched vessels with central hypopigmentation, dotted vessels | Dilatation of dermal blood vessels |
Yellow–orange clods | Plasma exudate, neutrophilic debris |
Brown rim around clods | Hemosiderin deposition, RBC extravasation, and plasma globules |
Excoriation marks | Epidermal erosions and neutrophilic debris |
RBC: Red blood cell
The clinical presentation of eczema can overlap with other inflammatory skin conditions, such as psoriasis, or tinea corporis.[7,8] This overlap can make diagnosis challenging, especially in complex or atypical cases. Dermoscopy helps in overcoming these diagnostic challenges by providing a more detailed view of the skin’s surface features, thus increasing diagnostic precision.[6,9]
A summary of dermoscopic and histopathological features of eczema, as reported in previous studies, is presented in Table 3. Certain forms of eczematous dermatitis can present with distinct and unique features.
Authors and year | Study design | Sample | Key findings | Histopathology | Link |
---|---|---|---|---|---|
Nair et al. (2021)[10] |
Prospective observational study | 60 (Eczema in 35) | Eczema: Dull/light red or violaceous background; dotted vessels; patchy vascular pattern; yellow/white/mixed scales, yellow clod sign in nummular eczema | Not done | PMID: 34759408 |
Adabala et al. (2022)[8] | Cross-sectional study | 60 (Eczema in 14) | Diffuse scaling, white and yellow scales, and dotted vessels with a patchy distribution of vessels | Compact hyperkeratosis, intact granular layer, spongiosis with acanthosis, and irregular psoriasiform hyperplasia | PMID: 35198472 |
Chauhan et al. (2023)[7] | cross-sectional, comparative study | 81 (Eczema in 50) | Yellowish scales, with focal or absent vessels, brown/orange-brown dots and/or globules, yellow/yellow-orange crusts over a yellow/yellow-brown background | Not done | PMID: 37151275 |
Bhatt et al. (2023)[12] |
Cross-sectional Study | 252 | Atopic dermatitis: Hypopigmented zones, brown dots, crown of branched vessels with central hypopigmentation, dotted vessels. Yellow-orange clods, brown rim around clods Nummular dermatitis: Yellow-orange clods, crusting and red dots, scales Seborrheic dermatitis: hypopigmented zones, disturbed pigment network, diffuse pink background, yellow scales, grouped linear vessels |
Atopic dermatitis: Spongiosis with intercellular edema in the stratum spinosum, areas of pigment clumps in stratum corneum, hemosiderin, dilatation of dermal vessels, RBCs extravasation, hemosiderin and plasma globules, denuded epidermis Nummular dermatitis: Plasma globules, plasma, neutrophilic debris, and parakeratosis Seborrheic dermatitis: Spongiosis, psoriasiform hyperplasia of the epidermis, dilatation of capillaries with inflammatory infiltrate, exudate with plasma, dilated capillaries |
PMID: 38371584 |
Pakornphadungsit et al. (2023)[15] | Cross-sectional study | 102 (Eczema in 43) |
Dull red background, dotted vessel, patchy vessel distribution, whitish scales, patchy scale distribution |
Not done | PMID: 36718215 |
RBC: Red blood cell
Stasis dermatitis - globular or glomerular vessels are commonly observed due to elevated hydrostatic pressure.[9] Pityriasis alba is characterized by diffuse, dull white, structureless areas with blurred margins. Less frequently observed features include incomplete perieccrine brown pigmentation, brown dots, and white scales, which may appear patchy or confined to skin furrows. In addition, incomplete perifollicular brown pigmentation may be present in some cases.[11-13]
Nummular eczema typically reveals yellow serocrusts with characteristic yellow scales known as the “yellow clod sign.” [10] Seborrheic dermatitis - common dermoscopic findings include focal dull white structureless areas, patchy white scales, and patchy yellow scales or crusts. Less frequently observed features include patchy brown scales or crusts, protruding follicular plugs, and vascular patterns such as dotted or linear clustered vessels.[11]
Hand eczema and palmar psoriasis have significant overlapping clinical features. Both conditions commonly exhibit dotted vessels, though palmar psoriasis shows a higher prevalence of regularly distributed vessels, whereas hand eczema tends to have patchy vessel distribution. Scaling patterns also differ, white scales predominate in palmar psoriasis, while hand eczema often presents with both white and yellow scales or predominantly yellow scales. Background erythema in psoriasis is typically light red, whereas eczema shows a yellowish-dull red background. Additional findings in hand eczema include brownish-orange dots and yellow-orange clods.[8,9] [Figure 5]

- Dermoscopy of acute eczema: (a) Acute eczema with erythematous plaque with oozing and crusting with surrounding excoriation marks (b) Dermoscopy showing yellow scales and crusts (Yellow Clod Sign) – (red star), dotted vessels, both distributed in patches (blue arrow), pinkish-yellow background.

- Yellowish crusts (red star), pinkish yellow background, adherent fabric fiber sign (blue arrow) on dermoscopy of acute eczema.

- Dermoscopy of subacute eczema: (a) Subacute eczema with erythematous, mildly scaly plaques with excoriations (b) Dermoscopy showing red dots in a patchy and irregular distribution (star), white scales (arrow), yellow serocrusts, excoriations.

- Dermoscopy of chronic eczema: (a) Chronic eczema with lichenified, thickened, and hyperpigmented skin with scaling and excoriations due to repeated scratching or rubbing (b) Dermoscopy showing white and yellow scales (red star), greyish-white background and an irregular pigment network (blue arrow).

- Dermoscopy of palmoplantar eczema: (a) Palmoplantar eczema with erythema, scaling, hyperkeratosis, fissuring, and vesicles (b) Dermoscopy showing yellowish white scales (blue arrow) in a diffuse distribution with yellowish homogenous areas (star) on a pinkish white background. Faint yellow globules (green arrow) can be appreciated (Yellow clod sign).
Asteatotic eczema is frequently identified by the presence of white scales that have a double-free edge, creating a “rail-like” appearance.[9]
Follicular eczema - Multiple, round, whitish areas with blurry margins surrounding a normal hair follicle with perifollicular scales (author’s own observation) in comparison to perifollicular scales and dotted vessels in follicular psoriasis [Figure 6].

- Dermoscopy of follicular eczema: (a) Follicular eczema with multiple pruritic, skin-colored to erythematous perifollicular papules seen over the extensor surfaces (b) Dermoscopy showing multiple, round, whitish areas with blurry margins surrounding a normal hair follicle with perifollicular scales (arrow)
Pigmented contact dermatitis - reticular or patchy pseudo-network with varying shades of brown, gray, and violaceous pigmentation. The background may show gray-brown dots and globules, corresponding to pigment incontinence. Ill-defined patchy pigmentation is common, often with scaling and focal erythema. Fine dotted or linear vessels may be present, but vascular structures are generally sparse [Figure 7].

- Dermoscopy of pigmented contact dermatitis: (a) Pigmented contact dermatitis with ill-defined, patchy, brown to slate-gray hyperpigmented macules over face and neck, with minimal to no erythema or scaling. (b) Dermoscopy showing brownish background with accentuated pseudo-network and brownish dots and globules (red circle) and erythematous areas (red arrow)
Erythroderma - the dermoscopic features of underlying skin disorders are often preserved, particularly in cases secondary to psoriasis (especially pustular psoriasis), pityriasis rubra pilaris (PRP), eczema, scabies, and dermatophytosis.[14] Eczema in erythroderma is commonly characterized by dotted or pinpoint vessels in a patchy distribution, along with profuse white-yellow serocrusts (yellow clods) and scaling. These findings correlate with underlying spongiosis, which can be confirmed histopathologically.[14-16]
Table 4 mentions the differential diagnosis alongwith dermoscopic clues to differentiate from eczema.[6, 9, 16-22]
Category | Condition | Key features | Dermoscopic clues |
---|---|---|---|
Infections | Tinea corporis/cruris | Annular scaly plaques with central clearing; pruritic; KOH+hyphae | Peripheral white scaling; broken hairs, moth-eaten scales, broken hairs, peripheral dotted vessels, follicular micropustules[6,9,16,17] |
Scabies | Burrows, nocturnal itch; webspace/genital predilection | Delta-wing jet sign; tiny gray dots (mites)[18] | |
Autoimmune | Psoriasis | Well-demarcated plaques, silvery scale; auspitz sign; nail pitting | Uniform white scales, diffuse and regular dotted vessels, red globules[6,9,16] |
Lupus erythematosus (DLE) | Discoid plaques, follicular plugging; scarring | Follicular plugs (“strawberry pattern”), White scales, telangiectasia, white structureless areas, perifollicular scaling[6] | |
Lichen planus | Violaceous, flat-topped polygonal papules or plaques, intense pruritus, wickham striae | Wickham striae (white network-like pattern), peripheral dotted/linear vessels[6,9] | |
Malignancies | Paget’s disease | Unilateral nipple/perianal erythema; eczematous but refractory | Milky-red areas; serpentine/atypical vessels, pinkish-orange background, yellow/white scales, dotted vessels, blood spots, brown peppering, chrysalis-like structure[19] |
Mycosis fungoides (early) | Poikilodermatous patches; chronic, resistant to steroids | Orange-yellow patches; patchy whitish scales, short linear (“chicken-wire”) vessels, spermatozoa like vessels[20] | |
Genodermatoses | Hailey–Hailey disease | Erosions in intertriginous areas; family history | White clouds separated by pink furrows, “crumbled fabric pattern”[21] |
Drug reactions | Drug-induced eczema | Temporal link to medication; symmetric maculopapular rash | Morbilliform pattern; focal petechiae[22] |
Other | Lichen simplex chronicus | Localized lichenified plaque; psychogenic itch | Erythema and perifollicular scaling associated with hair shaft breakage, “broom fibers”[6] |
Pityriasis rosea | Herald patch; “christmas tree” pattern; self-limiting | Central white scaling; peripheral collarette[6,9,16] |
KOH: Potassium hydroxide, DLE: Discoid lupus erythematosus
DERMOSCOPY IN MONITORING DISEASE ACTIVITY AND TREATMENT RESPONSE
Eczema is a dynamic disease that exhibits fluctuating activity over time. Treatment strategies for eczema generally aim to control acute flares, reduce inflammation, and maintain long-term skin health. Monitoring disease activity is crucial for adjusting treatment protocols and ensuring optimal patient outcomes. Traditional methods of monitoring disease activity, including Eczema Area and Severity Index, Severity Scoring of Atopic Dermatitis, Patient-Oriented Eczema Measure, etc., are largely subjective, relying on clinical evaluation, patient-reported symptoms, and overall appearance.[16] Dermoscopy offers an objective, reproducible means to monitor disease progression and assess the response to therapy.[23]
Evaluation of inflammatory activity: Dermoscopy provides a detailed view of the extent of vascular changes and scale in eczema lesions, both of which correlate with the degree of inflammation. Increased vascularity and scaling may indicate an active flare, while a reduction in these features can suggest a positive response to treatment.[23]
Accuracy in patch testing: Dermoscopy can improve accuracy in the differential diagnosis between weak allergic and irritant patch test reactions.[24]
Early detection of disease resolution: As the lesions improve, dermoscopy can reveal a gradual reduction in erythema, exudation, and scaling. The disappearance of dilated blood vessels, scaling, and exudation is a positive indicator that the disease is resolving.
Assessing the efficacy of topical and systemic therapies: Dermoscopy can be used to evaluate the effectiveness of various therapies, such as topical corticosteroids, calcineurin inhibitors, and newer biologic agents. Changes in vascularity, scaling, and crusting may guide decisions regarding dose adjustments or the introduction of alternative treatments.[23]
Chronic eczema management: Chronic eczema patients often experience long-term skin changes, such as lichenification, thickening, and pigmentation alterations. Dermoscopy can help track these changes, providing a clearer picture of how the skin is adapting to chronic inflammation and whether further interventions are needed to prevent disease progression or complications.
DERMOSCOPY IN COMPLICATIONS OF ECZEMA
Eczema patients are at an increased risk of developing secondary complications. One of the most common complications of eczema is bacterial superinfection, particularly with Staphylococcus aureus. Dermoscopic features suggestive of bacterial involvement include the presence of pustules, crusting, and abscess formation. Pustules may appear as small, well-defined, white or yellowish globules, often surrounded by erythema and honey-colored crusts, which is a hallmark sign of a bacterial infection.[18] Besides, these patients are also prone to develop viral infections such as herpes simplex virus (HSV) or molluscum contagiosum, which can be identified on dermoscopy by the presence of vesicles, erosions, or hemorrhagic crusts. The characteristic dermoscopic appearance of HSV lesions – such as grouped vesicles and a “dappled” pattern of inflammation – can help distinguish viral infections from other eczema-related changes.[25]
LIMITATIONS OF DERMOSCOPY IN ECZEMA
Despite its advantages, dermoscopy does have limitations in the management of eczema. Some of these include:
Interpretation challenges: While dermoscopy can aid in diagnosing and monitoring eczema, the interpretation of findings may vary between clinicians. Expertise and training are required to correctly identify key features and avoid misdiagnosis.[26]
Overlapping features: Many inflammatory skin conditions share similar dermoscopic features with eczema. This overlap can complicate the diagnostic process, particularly when lesions are atypical.
Inability to replace histopathology: Dermoscopy is an adjunct tool, not a replacement for histopathology. In cases of atypical eczema or when the diagnosis is uncertain, biopsy and histopathological examination remain the gold standard for definitive diagnosis.
CONCLUSION
Dermoscopy has emerged as a valuable, non-invasive tool in the diagnosis and management of eczema, offering enhanced visualization of vascular, pigmentary, and structural changes that are not appreciable to the naked eye. Its utility extends beyond diagnosis to monitoring disease activity, assessing treatment response, and identifying complications such as secondary infections. By providing objective and reproducible findings, dermoscopy complements clinical evaluation, reducing diagnostic ambiguity and facilitating individualized treatment strategies. However, its interpretation requires expertise, and it remains an adjunct to traditional diagnostic methods rather than a replacement for histopathology. Future research and standardization of dermoscopic criteria may further refine its role in eczema management, improving patient outcomes through early detection and precise therapeutic interventions.
Ethical approval:
Institutional Review Board approval is not required.
Declaration of patient consent:
The authors certify that they have obtained all appropriate patient consent.
Conflicts of interest:
There are no conflicts of interest.
Use of artificial intelligence (AI)-assisted technology for manuscript preparation:
The authors confirm that there was no use of artificial intelligence (AI)-assisted technology for assisting in the writing or editing of the manuscript and no images were manipulated using AI.
Financial support and sponsorship: Nil.
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