Dermatology: Practical and Conceptual


224 Observation  |  Dermatol Pract Concept 2018;8(3):14

DERMATOLOGY PRACTICAL & CONCEPTUAL
www.derm101.com

Asymptomatic heterogeneously black-pigmented 
plaque in a 58-year-old man: an unusual 
presentation of a melanoma mimicker

Daniela Majerson1, Paula Majluf1, Álvaro Abarzúa-Araya1 , Sergio González-Bombadiére1

1 Dermatology Department, Pontificia Universidad Católica de Chile, Santiago, Chile

Key words: melanoma, dermatofibroma, basal cell carcinoma, seborrheic keratosis, dermoscopy,

Citation: Majerson-Grinberg D, Majluf P, Abarzúa-Araya A, González-Bombadière. Asymptomatic heterogeneously black-pigmented 
plaque in a 58-year-old man: an unusual presentation of a melanoma mimicker. Dermatol Pract Concept. 2018;8(3):224-226. DOI: https://
doi.org/10.5826/dpc.0803a14

Received: November 2, 2017; Accepted: December 3, 2017; Published: July 31, 2018

Copyright: ©2018 Majerson-Grinberg et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are 
credited.

Funding: None.

Competing interests: The authors have no conflicts of interest to disclose.

All authors have contributed significantly to this publication.

Corresponding author: Daniela Majerson, MD, Dermatology Department, Pontificia Universidad Católica de Chile, Vicuña 
Mackenna 4686, Macul. Centro Médico San Joaquin UC, Santiago, Chile. Email: djamerson@gmail.com.

Case Presentation

A 58-year-old man with a history of nodular basal cell car-

cinoma presented with an asymptomatic black-pigmented 

lesion on his left shoulder, without variation in size over 

time, which had been present for years. Physical examination 

revealed an irregular black-bluish-pigmented plaque with a 

maximum diameter of 8 mm. The dimple sign was negative 

(Figure 1). Dermoscopy showed a pseudo-pigmentary net-

work and comedo-like openings at its center, asymmetrical 

peripheral streak-like structures, areas of brown-bluish 

pigmentation, fingerprint-like structures, and eccentric milia-

like cysts (Figure 2). The lesion was excised and histological 

examination was performed (Figure 3).

Diagnosis

Pigmented dermatofibroma

Figure  1. Physical examination revealed an irregular black-bluish-

pigmented plaque with a maximum diameter of 8 mm. [Copyright: 

©2018 Majerson-Grinberg et al.]



Observation  |  Dermatol Pract Concept 2018;8(3):14 225

nonmelanocytic lesions, the black color may correspond to 

hemosiderin deposits inside the skin (as in the case presented), 

or be derived from the oxidized plug of keratin masses (as 

in the pseudocysts in the seborrheic keratosis [SK]), or result 

from artificial tattoos. Other melanoma mimickers with blue 

pigmentation are vascular lesions, Kaposi sarcoma, basal cell 

carcinomas (BCC), and radiation tattoos [5]. Most of the der-

matoscopic criteria for MM were described in its superficial 

spreading variety. However, pigmented nodular melanoma 

could be recognized by the presence of a combination of blue 

and black color within the lesion (the “blue-black rule”). 

The presence of this feature plus one or more of the standard 

melanoma criteria reach a sensitivity of 84.6% [6].

Pigmented BCC may dermatoscopically simulate mela-

noma: when melanin from the tumor nest, as well as in 

stroma, is increased, the nests coalesce, forming an unstruc-

tured pigmented area. Other elements like ulceration, arboriz-

ing vessels, or maple-leaf-like or spoke-wheel areas can help 

identify it [7].

Clonal SK are characterized by milia cysts and sharply 

demarcated borders, but they often show areas of bluish 

pigmentation composed of multiple, variously sized, and 

irregularly distributed blue-gray ovoid roundish structures, 

which resemble the asymmetrical- globular pattern observed 

melanoma or the ovoid nests commonly described in BBC [8].

On the other hand, Ferrari et al described a group of 

atypical “non-DF like” patterns, including a melanoma-like 

subtype. One of the lesions showing this pattern was, as in 

this case, characterized by the presence of irregular streak-

like structures [1,9] and this group was histopathologically 

related with HDF [1]. The most frequent dermatoscopic 

Microscopic Findings

Histopathologically, the biopsy showed hyperorthokeratosis 

with acanthosis and hyperpigmentation of basal keratino-

cytes; small buds of basaloid cells and sebaceous glands were 

also visible. The dermis showed a fibrohistiocytic prolifera-

tion, with fibrous stroma, denser at the periphery, some blood 

vessels, and hemosiderophages consistent with hemosiderotic 

dermatofibroma with epidermal folliculosebaceous induction.

Discussion

Dermatofibroma (DF) is a common benign dermal lesion 

composed of fibroblasts, collagen, macrophages, and capil-

laries that presents with a wide clinicopathological variety. 

It appears as a firm papule, plaque, or nodule, with a vari-

able degree of pigmentation, more commonly on the lower 

extremities of young adults [1,2].

There are more than 40 histological variants. The pig-

mented or hemosiderotic type (HDF) represents 2% and was 

first described in 1938 as a differential diagnosis of melanoma 

(MM) [2]. It is composed of small vessels, extravasated eryth-

rocytes, and intra- and extracellular hemosiderotic deposits. 

Clinically it presents as a firm, hard, smooth-surface papule 

or nodule with reddish to bluish coloration, more frequently 

in middle-aged women, and its recurrence is about 19%. 

However, because of its rarity, it is not often suspected as a 

melanoma mimicker [2,3].

Dermoscopy improves the diagnostic accuracy in the 

clinical evaluation of pigmented skin disorders that mimic 

melanoma. Melanoma simulators comprise a heterogeneous 

group of melanocytic and nonmelanocytic lesions: Black 

or blue color does not always indicate melanoma [4]. In 

Figure 2. Dermatoscopy showed a pseudo-pigmentary network and 

comedo-like openings at its center, asymmetrical peripheral streak-

like structures, areas of brown-bluish pigmentation, fingerprint-like 

structures, eccentric milia-like cysts, and a peripheral milky red area. 

[Copyright: ©2018 Majerson-Grinberg et al.]

Figure 3. Hematoxylin and eosin (H&E) staining ×100. Hemosid-

erotic dermatofibroma with epidermal folliculosebaceous induction. 

Note the hyperpigmentation of basal keratinocytes, small buds of 

basaloid cells, and sebaceous glands. The dermis showed a fibrohis-

tiocytic proliferation, with fibrous stroma, denser at the periphery, 

some blood vessels, and hemosiderophages. [Copyright: ©2018 Ma-

jerson-Grinberg et al.]



226 Observation  |  Dermatol Pract Concept 2018;8(3):14

ickers. However, histopathological examination remains 

mandatory to reach an accurate diagnosis.

References

 1. Ferrari A, Argenziano G, Buccini P, et al. Typical and atypical der-

moscopic presentations of dermatofibroma. J Eur Acad Dermatol 

Venereol. 2013;27(11):1375-1380. doi: 10.1111/jdv.12019.

 2. Zaballos P, Llambrich A, Ara M, Olazarán Z, Malvehy J, Puig S. 

Dermoscopic findings of haemosiderotic and aneurysmal derma-

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250. doi: 10.1111/j.1365-2133.2005.06844.x.

 3. Scalvenzi M, Balato A, De Natale F, Francia MG, Mignogna C, 

De Rosa G. Hemosiderotic dermatofibroma: report of one case. 

Dermatology. 2007;214(1):82-84. doi: 10.1159/000096918.

 4. Kaminska-Winciorek G, Wydmanski J. Benign simulators of 

melanoma on dermoscopy – black colour does not always indicate 

melanoma. J Pre Clin Res. 2013;7(1):6-12.

 5. Scope A, Benvenuto-Andrade C, Agero AL, Marghoob AA. Non-

melanocytic lesions defying the two-step dermoscopy algorithm. 

Dermatol Surg. 2006;32(11):1398-1406.

 6. Argenziano G, Longo C, Cameron A, et al. Blue-black rule: a sim-

ple dermoscopic clue to recognize pigmented nodular melanoma. 

Br J Dermatol. 2011;165(6):1251-1255. doi: 10.1111/j.1365-

2133.2011.10621.x.

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081X(02)00229-8.

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ziano G. Unusual dermoscopic patterns of seborrheic keratosis. 

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tional dermoscopic presentation of haemosiderotic dermatofibro-

ma. Br J Dermatol. 2007;156(1):199-200. doi: 10.1111/j.1365-

2133.2006.07611.x.

10. Arpaia N, Cassano N, Vena GA. Dermoscopic patterns of der-

matofibroma. Dermatol Surg. 2005;31(10):1336-1339. doi: 

10.1097/00042728-200510000-00015.

features described of HDF are a homogeneous central bluish 

or reddish area, with white structures inside, and a delicate 

pigment network at the periphery with variable vascular 

structures [2]. Thus, melanoma cannot be ruled out, consider-

ing the multicomponent dermatoscopic pattern of this entity.

Various DF dermoscopic structures appear to corre-

late with evolutive stages histopathologically. In our case, 

the basal keratinocytes accumulating melanin pigment in 

response to the inflammatory process would correspond 

dermatoscopically to a pseudo-pigmentary network and 

irregular streak-like structures [1,10] as brown-bluish pig-

mentation that represents the blood phagocytosed by the 

tumor cells. We also propose that fingerprint-like structures 

are correlated with elongation of the rete ridges, as small buds 

of basaloid cells and sebaceous glands would reflect comedo-

like openings and eccentric milia-like cysts. Milky red areas 

would correspond to blood vessels in the peripheral stroma 

of the tissue.

Dermatoscopic features of our case were highly indicative 

for melanoma and shared some features with clonal SK, such 

as milia-like cysts and areas of brown-bluish pigmentation, 

and clinically, it can be confused with a superficial pigmented 

BCC.

Conclusions

The present case of pigmented dermatofibroma is the first 

reported, to our knowledge, to exhibit simultaneously a 

milia-like cyst and streak-like and fingerprint-like structures.

In conclusion, we report an HDF with different der-

moscopic features from previously reported observations, 

highlighting the importance of understanding that this rare 

subtype of DF presents polymorphic features at dermoscopy, 

so it should be included in the spectrum of melanoma mim-