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Congenital melanocytic nevus in Child
See also in: External and Internal Eye,Anogenital,Hair and Scalp
Other Resources UpToDate PubMed

Congenital melanocytic nevus in Child

See also in: External and Internal Eye,Anogenital,Hair and Scalp
Contributors: Youssef M. Salem, Lorena A. Mija, Sarah Hocker DO, Belinda Tan MD, PhD, William M. Lin MD, Susan Burgin MD
Other Resources UpToDate PubMed

Synopsis

Congenital melanocytic nevus (CMN) is a benign nevus present at birth or within the first few weeks of life. CMNs are often flat and tan in color, initially resembling an irregular café au lait macule. They may change in color, become papillated, or display hair growth during the first few years of life and can vary tremendously in size. CMNs have a slight female predominance (3:2) and are more common among Blacks and individuals of Japanese descent compared with Whites and individuals of Hispanic descent.

One of the principal categorizations of CMNs is by size based on the projected maximal diameter of the CMN in adulthood. Different size cutoffs have been used with a recent proposed categorization including the categories of small (< 1.5 cm), medium (M1: 1.5-10 cm, M2: > 10-20 cm), large (L1: > 20-30 cm, L2: > 30-40 cm), and giant (G1: > 40-60 cm, G2: > 60 cm). It is estimated that small CMNs occur in 1 in 100 newborns, that medium CMNs occur in 1 in 1000 newborns, and that large CMNs occur in 1 in 20 000 newborns. Giant CMNs can occur in very rare cases, estimated to occur in 1 in 500 000 newborns. Most CMNs are < 3-4 cm, with larger lesions being less common.

Most small or medium CMNs present with a smooth, well-defined ovoid shape and a uniform brownish color. Large CMNs may display irregular borders and variation in texture or pigmentation including black, gray, and blue, and dermal or subcutaneous. Hypertrichosis or pigmented hair growth occurs in approximately 75% of CMNs. CMNs with diffuse terminal hair growth are referred to as giant hairy nevi.

CMNs are mostly on the trunk or extremities and less commonly on the head and neck. Approximately 3% of patients have multiple CMNs. CMNs may also arise in the nail matrix. In these cases, they may present with features also displayed by subungual melanoma.

CMNs have been associated with many benign lesions, the most common of which include café au lait macules and mucosal nevi.

CMNs have also been reported to have an increased risk for transformation to melanoma. The risk of melanoma is believed to correlate with CMN size. The incident rate of melanoma arising in small or medium CMNs is reported to be less than 1%. In one meta-analysis, melanoma was estimated to develop in approximately 2% of large CMNs (> 20 cm). Melanomas were diagnosed at a mean age of 12 years (range: birth to 58 years old), with 82% cutaneous and 13% visceral. Most cutaneous melanomas were located on the trunk (68%), and most of the melanoma-associated CMNs exceeded 40 cm in diameter (74%), with 94% of patients also having satellite nevi.

Large CMNs overlying limbs can be associated with atrophy of the subcutaneous tissue. Large CMNs over the head or axial skeleton should alert the physician to assess for neurocutaneous involvement (developmental delays, seizures, hydrocephalus, intracranial hypertension). Larger CMNs may also present with pruritus and erosions or ulceration.

Neurocutaneous melanosis is when a CMN is associated with neuromelanosis, a congenital error in ectodermal morphogenesis resulting in melanocytic proliferation within the leptomeninges and brain parenchyma. This most commonly occurs in larger CMNs. While not all patients are symptomatic, there can be diverse neurologic findings that typically present by age 2.

CMN may also be associated with other syndromes such as Carney (pigmented skin lesions and atrial myxomas), LAMB (lentigines, atrial myxoma, mucocutaneous myxoma, blue nevi), NAME (nevi, atrial myxoma, myxoid neurofibromata, ephelides), neurocutaneous melanosis, premature aging syndrome, occult spinal dysraphism, and possibly neurofibromatosis type 1 and other malformation syndromes.

Related topic: Giant Congenital Nevus

Codes

ICD10CM:
D22.9 – Melanocytic nevi, unspecified

SNOMEDCT:
398696001 – Congenital melanocytic nevus

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Diagnostic Pearls

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Differential Diagnosis & Pitfalls

  • Lentigo simplex
  • Café au lait spot
  • Plexiform neurofibroma
  • Congenital dermal melanocytosis
  • Becker nevus
  • Blue nevus
  • Nevus sebaceus
  • Postinflammatory hyperpigmentation
  • Pigmented epidermal nevus
  • Acquired melanocytic nevus
  • Congenital Blue nevus
  • Congenital dermal melanocytosis
  • Cutis verticis gyrata
  • Melanoma, including Subungual melanoma

Best Tests

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Management Pearls

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Therapy

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References

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Last Reviewed:03/21/2023
Last Updated:03/22/2023
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Congenital melanocytic nevus in Child
See also in: External and Internal Eye,Anogenital,Hair and Scalp
A medical illustration showing key findings of Congenital melanocytic nevus : Present at birth
Clinical image of Congenital melanocytic nevus - imageId=2314374. Click to open in gallery.  caption: 'A large variegated, reddish, and brown plaque on the leg.'
A large variegated, reddish, and brown plaque on the leg.
Copyright © 2024 VisualDx®. All rights reserved.