A progressive sclerotic depigmenting congenital melanocytic nevus in a Chinese patient^☆

Dear Editor,

Congenital Melanocytic Nevi (CMN) present in approximately 1%-2% of newborns.¹ They are usually brown to black, hairy lesions with a consistency similar to that of the surrounding normal skin. CMN is classified according to the diame-ter of the lesion: <1.5 cm is classified as Small Congenital Melanocytic Nevi (SCMN), 1.5-20 cm as Medium Congeni-tal Melanocytic Nevi (MCMN), 20-40 cm as Large Congenital Melanocytic Nevi (LCMN), and >40 cm as Giant Congenital Melanocytic Nevi (GCMN).

Spontaneous regression of medium-to-large congenital melanocytic nevi is rare, but regression presenting as depig-mentation with sclerosis, alopecia, or pruritus is exceedingly so.

Herein, we present a 15-month-old Chinese child with progressive regression of pigmentation and hardness of a hairless pruritic medium-sized CMN. This male infant rep-resents the first reported case in China of progressive sclerosing hypopigmented Congenital Melanocytic Nevus (CMN). The lesion has been present on his occipital scalp since birth. At 1-month of age, the lesion presented as a hard, slightly raised, black plaque measuring 10 × 8 cm, with a hypopigmented area in the upper left quadrant (Fig. 1A).

Fig. 1
(A) Lesion at 1-month of age: A 10 × 8 cm, hard, slightly raised black plaque with a hypopigmented area in the upper left quadrant. (B) Lesion at 15-months of age: A 14 × 11 cm, hardened, hairless surface with irregular dark-brown pigmentation and a bordered area of mild erythema.

As he grew older, the lesion exhibited progressive changes: hypopigmentation, sclerosis, hair loss, and pruri-tus. By 15-months, it had expanded to 14 × 11 cm, featuring a hardened, hairless surface with irregular dark-brown pigmentation and a bordered area of mild erythema. The periphery was accompanied by small-sized, scattered lesions and areas of hypopigmentation (Fig. 1B).

Histopathology demonstrated nests of melanocytes in the dermoepidermal junction and superficial dermis with markedly reduced skin appendages (Fig. 2A); the reticular dermis exhibited abundant collagen bundles and fibroblasts surrounding the nevus cell nests (Fig. 2B).

Fig. 2
(A) Nevus cell nests in the superficial dermis (Hematoxylin & eosin, ×100). (B) Collagen bundles and fibroblasts surrounding nevus cell nests (Hematoxylin & eosin, ×400).

Immunohistochemistry (Fig. 3A-D) confirmed nevus cell positivity for S100, Melan-A, and HMB45, negativity for p53, and a Ki-67 proliferation index <10%. Both biopsied lymph nodes showed reactive hyperplasia.

Fig. 3
Immunohistochemical staining (A) S100 Staining, ×200. (B) Melan-A Staining, ×200. (C) HMB45 Staining, ×200. (D) Ki-67 Staining, ×200.

PubMed was searched, and 13 cases of spontaneous regression of CMN with sclerosis. This cohort comprised eight females and five males. The onset age ranged from birth to three years, and the depigmentation process lasted less than eight years. The lesions were most commonly present on the trunk (10/13), then were found on the scalp (2/13), feet, and ankles (1/13). All the lesions were >1.5 cm in diameter. Sclerosis and pigmentation regres-sion occurred in all 13 cases. Hair loss (9/13), pruritus (6/13), and ulcer (4/13) were also observed. The mech-anism for these has been proposed as an autoimmune reaction. The autoimmune response targeting melanocytes may be responsible for the regression of pigmentation. Meanwhile, this autoimmune response would produce large amounts of inflammatory factors that induce collagen prolif-eration, resulting in sclerosis.² There was induration in a few cases,³,⁴ but no nodular lesions. Usually, induration denotes local hardening, whereas sclerosis means diffuse hardening. Localized induration on a CMN raises the possibility of malig-nant transformation, in contrast to the diffuse hardening of sclerotic CMNs, which is considered benign.⁴,⁵ In our case, we performed immunohistochemistry staining and observed a low proliferation index with Ki-67. In addition, none of the CMNs described so far have progressed to melanoma; the longest recorded follow-up is 17-years.⁵

In conclusion, we reported the first case of progressive sclerotic hypopigmented CMN in a Chinese patient. Contin-uous monitoring is required for this rare disease, but there is no need for excessive panic and extensive excision due to the low possibility of malignant transformation.

• ☆
  Study conducted at the Department of Dermatology, Union Hos-pital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
• Financial support
  This work was supported by Science and Technology Program of XPCC (2024ZD042, 2023ZD023).

Research data availability

All data supporting the findings are included within the arti-cle.

References

• ¹ Castilla EE, da Graca Dutra M, Orioli-Parreiras IM. Epidemiology of congenital pigmented naevi: II. risk factors. Br J Dermatol. 1981;104:421-7.
• ² Martin JM, Jorda E, Calduch L, Alonso V, Revert A. Pro-gressive depigmentation of a palmar congenital melanocytic nevus without an associated halo phenomenon. Dermatology. 2006;212:198-9.
• ³ Pattee SF, Hansen RC, Bangert JL, Joganic EF. Giant congeni-tal nevus with progressive sclerodermoid reaction in a newborn. Pediatr Dermatol. 2001;18:320-4.
• ⁴ Patsatsi A, Kokolios M, Pikou O, Lambropoulos V, Efstratiou I, Sotiriadis D. Sclerotic regressing large congenital nevus. Pediatr Dermatol. 2016;33:e366-7.
• ⁵ Ruiz-Maldonado R, Orozco-Covarrubias L, Ridaura-Sanz C, DurAn-McKinster C, Del Mar Sáez De Ocariz Gutiérrez M, Tamayo-Sánchez L. Desmoplastic hairless hypopigmented naevus: a variant of giant congenital melanocytic naevus. Br J Dermatol. 2003;148:1253-7.

Edited by

• Editor
  Sílvio Alencar Marques.

Publication Dates

• Publication in this collection
  03 Aug 2026
• Date of issue
  2026

History

• Received
  03 Oct 2025
• Accepted
  28 Nov 2025
• Published
  28 Apr 2026