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Vol. 116. Issue 3.
Pages T307-T309 (March 2025)
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Vol. 116. Issue 3.
Pages T307-T309 (March 2025)
Practical Dermoscopy
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Exophytic Tumor on the Foot Dorsal Region
Tumor exofítico en la región dorsal del pie
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871
I.R. Camardella
Corresponding author
ileanacamardella@gmail.com

Corresponding author.
, M.V. Marin, S. Rodriguez Saa
Hospital El Carmen, Godoy Cruz, Mendoza, Argentina
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Actas Dermosifiliogr. 2025;116:307-910.1016/j.ad.2024.03.038
I.R. Camardella, M.V. Marin, S. Rodriguez Saa
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Case report

A 48-year-old woman with type 2 diabetes mellitus presented with a >2-year history asymptomatic tumor on the dorsolateral region of her right foot. Physical examination revealed a 1.5cm in diameter exophytic, pedunculated, skin-colored lesion with erythematous areas and verrucous zones (Fig. 1).

Figure 1.

Two-year history exophytic, erythematous tumor lesion with verrucous zones and some hemorrhagic crusts, located on the dorsolateral region of the foot.

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Polarized light dermoscopy revealed reddish areas resembling a vascular bed, branched vessels with rounded ends, yellowish structureless areas, and intertwined white areas encircling the vessels (Fig. 2).

Figure 2.

Polarized light dermoscopic images of the lower region of the lesion. Red vascular bed-like areas (white circle), branched vessels with rounded ends (black circles), yellowish structureless areas (blue circle), and intertwined white areas surrounding the vessels (black arrow) are observed.

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What is your diagnosis?

Diagnosis

Dermoscopic diagnosis suggested eccrine poroma, and histological analysis confirmed this suspicion. The histology showed an epidermis with focal hyperkeratosis and anastomosing cords of cuboidal cells with hyperchromatic, basaloid-appearing nuclei connected by intercellular bridges. These cords were located in the lower third of the epidermis toward the dermis (Fig. 3).

Figure 3.

Epidermis with focal hyperkeratosis. Anastomosing cords spreading toward the dermis are visible. H&E stain, ×10.

(0.2MB).
Commentary

Eccrine poroma is a rare benign adnexal tumor. It typically presents in older adults without gender preference. Clinically, it appears as a solitary papule, plaque, tumor, or nodule with a smooth, scaly, or verrucous surface. Ulcerations and erosions can occur secondary to friction. Although most lesions are pink, they may also appear reddish, blue, or even black when pigmented.1 They are usually located in acral regions, particularly on palms and soles, due to the high density of eccrine glands, though they can also occur in other areas.2

Dermoscopy is a valuable diagnostic tool. The hallmark findings suggestive of eccrine poroma include branched vessels with rounded ends—formerly called “chalice-shaped” or “cherry blossom” vessels—and intertwined white areas surrounding the vessels. Yellowish structureless areas and reddish vascular bed-like areas are also characteristic,3,4 all of which were present in our patient.

Less common dermoscopic findings include irregular linear vessels, glomerular vessels, bright white areas, atypical reticulation, hemorrhagic crusts, brown structureless areas, keratin, white circles, and regression structures.3,4

In a multicenter study by Marchetti et al.,4 4 dermoscopic patterns were identified: Pattern #1: Most common on hands and feet, showing reddish vascular bed-like areas, branched vessels with rounded ends, and yellowish structureless areas. This pattern was observed in our patient. Pattern #2: Found on the trunk and extremities, with polymorphic vessels, intertwined white areas around vessels, and branched vessels with rounded ends. Pattern #3: Characterized by small lesions anywhere on the body, often without vessels, clinically mimicking basal cell carcinoma. Pattern #4: Found anywhere on the body, featuring large lesions, sometimes pigmented, with blood spots, keratin, and atypical forked vessels.

Eccrine poroma is considered a great mimic, and its primary clinical differential diagnoses include amelanotic melanoma, squamous cell carcinoma, and basal cell carcinoma. Other differentials include pyogenic granuloma, hemangioma, seborrheic keratosis, wart, and melanocytic nevus.1

Treatment of choice is surgical excision. Complete removal is necessary, as a small percentage of lesions may progress to porocarcinom.5

Funding

None declared.

References
[1]
E. Kyrmanidou, C. Fotiadou, C. Kemanetzi, M.G. Trakatelli, A. Trigoni, A. Patsatsi, et al.
Eccrine poroma: pathogenesis, new diagnostic tools and association with porocarcinoma—a review.
Diagnostics (Basel), 13 (2023), pp. 2689
[2]
M.A.C. Alfredo, M.R.R. Lai, L.D.B. Miot, G.R. Haddad, A.L. Garcia, H.A. Miot.
Pigmented eccrine poroma in an atypical location.
An Bras Dermatol, 97 (2022), pp. 624-627
[3]
M. Chessa, A. Patrizi, C. Beraldi, P. Fanti, A. Brissani, S. Vaccari.
Dermoscopic-histopathological correlation of eccrine poroma: an observational study.
Dermatol Pract Concept, 9 (2019), pp. 283-291
[4]
M.A. Marchetti, M.L. Marino, P. Virmani, S.W. Dusza, A.A. Marghoob, G. Nazzaro, et al.
Dermatoscopic features and patterns of poromas: a multicentre observational case–control study conducted by the International Dermatoscopy Society.
J Eur Acad Dermatol Venereol, 32 (2018), pp. 1263-1271
[5]
A.M. Mohamed, B.J. Mohamed, K. Rania, G. Montassar.
Eccrine poroma localized in the second toe.
Radiol Case Rep, 17 (2022), pp. 4108-4110
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