A two-year-old male patient, presented with a single LM on the left hallux that started at six months of age, with progressive growth. A light and dark brown band occupied 40% of the nail plate width, showing a triangular shape. Dermoscopy disclosed irregular lines regarding color, thickness and spacing, with blurred lateral edges. Intraoperative dermoscopy showed an irregular pattern. An excisional biopsy was performed, and histopathology was compatible with a junctional lentiginous ungual MN. The patient developed nail dystrophy after the biopsy and the melanonychia recurred two years later, with the presence of Hutchinson's sign in the hyponychium. Patient follow-up was chosen, with stability throughout the four-year follow-up (Fig. 1).

Figure 1.

(A), Clinical aspect of the LM, taking up 50% of the total thickness of the left hallux nail. (B), Dermoscopy at the first consultation. (C), Intraoperative dermoscopy, showing a pigmented lesion with an irregular pattern and eccentric blur. (D), Dermoscopy two years after the biopsy, Hutchinson's sign in the hyponychium.

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A 13-year-old female patient with a single LM present at birth and showing progressive growth. There was a light and dark brown band on the second left toe, measuring 3 mm, which occupied 20% of the nail width, with the presence of Hutchinson's sign in the proximal and lateral nail folds. Dermoscopy showed irregular lines in thickness and color, with loss of parallelism and blurred edges. A tangential biopsy was performed, which was compatible with a junctional MN. After the biopsy, the LM persisted on the lateral nail border without dystrophy and remained stable throughout five years of follow-up (Fig. 2).

Figure 2.

Clinical (A) and dermoscopic (B) aspect at the first consultation; (C–D) Clinical (C) and dermoscopic (D) aspect five years after the biopsy.

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A three-year-old female patient with LM on the fifth finger of the left hand for two years, with recurrence after a previous biopsy performed one year had shown a lesion compatible with a junctional MN on histopathology, and which had grown since then. A black to dark brown band occupied 50% of the nail width, with pseudo-Hutchinson's sign. Dermoscopy showed irregular lines regarding color and thickness, loss of parallelism, and blurred edges. A second evaluation of the histopathological examination did not detect any signs of malignancy. The LM remained stable throughout two years of follow-up (Fig. 3).

Figure 3.

(A), Clinical aspect. (B), Dermoscopy: irregular color and thickness, loss of parallelism and blurred edges.

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A nine-year-old female patient, presenting a LM for six years on the third left finger, with progressive growth. A light brown band was observed, which took up 40% of the nail plate (4 mm), with pseudo-Hutchinson's sign. Dermoscopy showed homogeneous lines, preserving parallelism. Follow-up was chosen, but there was a loss of follow-up, and the patient returned four years later, with a biopsy performed in another service compatible with acral lentiginous melanoma in situ. A second evaluation of the histopathology favored the hypothesis of lentiginous MN, but it was not possible to rule out melanoma in situ. The margins were widened by 5 mm, and the ungual complex was removed up to the periosteal level, with healing by second intention. She was maintained under strict clinical follow-up, with no signs of recurrence or metastasis during eight years of follow-up.(Fig. 4)

Figure 4.

(A-B), Clinical (A) and dermoscopic (B) aspect at the first consultation; (C), histopathology examination stained with H&E showing melanocyte proliferation in a continuous arrangement forming some nests at the dermoepidermal junction.

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In adults, clinical warning signs for subungual melanoma are considered to be the recent appearance of LM in a single nail, with heterogeneous coloration, history of changes in color, thickness or shape, width greater than 2/3 of the nail or greater than 3 mm, proximal width greater than the distal one (triangular shape), Hutchinson's sign, and associated nail dystrophy. Warning dermoscopic findings include heterogeneous brown to black color, irregular lines (regarding color, spacing, thickness, and loss of parallelism), blurring of edges, and micro-Hutchinson's sign.2,6

However, such findings are common in childhood LM, without translating into an increased risk of malignancy. The MN, a major cause of LM in children, often presents with rapid growth, wide bands, heterogeneous pigmentation, irregular lines, triangular shape, and Hutchinson's sign, as demonstrated in other studies.3,4,7–10 Its recurrence after excision is frequent, as in Cases 1 and 3. Subungual melanoma is extremely rare in children, with few reports in the literature, all in situ. Interestingly, Case 4, reported as subungual melanoma in situ, had less clinical and dermoscopic suspicion during the initial evaluation. The biopsy showed lentiginous melanocytic proliferation with rare nests, focal cytologic atypia, and preserved symmetry. Acral MN may present with cytoarchitectural atypia without indicating malignancy, while subungual melanoma may have few atypia in the initial phase, which makes the differential diagnosis between these two entities a difficult one. Considering the preservation of histological symmetry and the long period of 10 years of evolution with no evidence of progression to invasive melanoma, Case 4 is more likely to represent an MN than an in situ melanoma.

The cases described herein illustrate the challenge in managing children with LM. Although the appearance and behavior of the lesion can be challenging, simulating melanoma, some authors disagree with the systematic indication of biopsy.9 Management should be individualized, prioritizing clinical and dermoscopic follow-up, in addition to considering the family's level of anxiety. When, however, the biopsy is chosen, it is important that it is guided by intraoperative dermoscopy and performed tangentially when possible, minimizing the risk of nail distrophy. When facing an irregular pattern on intraoperative dermoscopy, however, excisional biopsy may be chosen, aiming at a lower risk of recurrence. Moreover, the analysis by a pathologist with expertise in melanocytic lesions is imperative.

None declared.

Isabela Boechat Morato: Design and planning of the study, data collection, drafting and editing of the manuscript, critical review of intellectual content, approval of the final version of the manuscript.

João Renato Vianna Gontijo: Drafting and editing of the manuscript and critical review of the relevant intellectual content, approval of the final version of the manuscript.

Glaysson Tassara Tavares: Drafting and editing of the manuscript and critical review of the relevant intellectual content, approval of the final version of the manuscript.

Flávia Vasques Bittencourt: Drafting and editing of the manuscript and critical review of the relevant intellectual content, approval of the final version of the manuscript.

None declared.