Indian Journal of Dermatology
  Publication of IADVL, WB
  Official organ of AADV
Indexed with Science Citation Index (E) , Web of Science and PubMed
Users online: 1178  
Home About  Editorial Board  Current Issue Archives Online Early Coming Soon Guidelines Subscriptions  e-Alerts    Login  
    Small font sizeDefault font sizeIncrease font size Print this page Email this page

Table of Contents 
Year : 2013  |  Volume : 58  |  Issue : 2  |  Page : 161
Congenital melanocytic nevus admixed with speckled lentiginous nevus

Department of Dermatology, School of Medicine, Chungnam National University, Daejeon, Korea

Date of Web Publication5-Mar-2013

Correspondence Address:
Myung Im
Department of Dermatology, School of Medicine, Chungnam National University, Daejeon
Login to access the Email id

Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0019-5154.108091

Rights and Permissions

How to cite this article:
Jeong NJ, Park SB, Lee Y, Seo YJ, Lee JH, Im M. Congenital melanocytic nevus admixed with speckled lentiginous nevus. Indian J Dermatol 2013;58:161

How to cite this URL:
Jeong NJ, Park SB, Lee Y, Seo YJ, Lee JH, Im M. Congenital melanocytic nevus admixed with speckled lentiginous nevus. Indian J Dermatol [serial online] 2013 [cited 2023 Oct 1];58:161. Available from:


Speckled lentiginous nevus (SLN) clinically presents as a circumscribed patch of hyperpigmentation that has features consistent with lentigines or café-au-lait macules, including scattered, more darkly-pigmented macular, and papular elements.[1] In some cases, dark spots from lentigines to compound or intradermal nevi may occur, and various types of nevi (blue nevi, Spitz nevi) may be present in the same lesion.[2] However, only a few cases of the presence of an SLN and concurrent congenital melanocytic nevus (CMN) since birth have been reported.[3],[4]

A 28-year-old male presented with a large pigmented lesion on his back, present since birth. This congenital lesion consisted of a 7 × 8 cm black hairy plaque on a large light brown patch with numerous scattered darker brown macules [Figure 1]. Its increase in size was solely in proportion to the patient's growth. The patient had no other skin abnormality, underlying disease, or family history. A biopsy was obtained from the black plaque on his back.

Histopathological examination of the specimen showed basal hyperpigmentation with a lentiginous pattern and nevus cells penetrating the dermis around hair follicles. There was no cytological or architectural atypia within the lesion [Figure 2]a and b.
Figure 1: A tannish-brown hyper pigmentation with superimposed dark macules, and black hairly plaques ranging up to 7 × 8 cm on the zback

Click here to view
Figure 2: Basal hyperpigmentation with rete ridge elongation and nevus cell within the reticular dermis ((a) H and E, ×100, (b) H and E, ×200)

Click here to view

A CMN usually has a somewhat speckled component because of an uneven melanocytic distribution. In such cases, the speckled component is frequently seen only at the peripheral portion of the nevus.[2],[3] Therefore, the speckled component of the CMN can be distinguished from an SLN clinically. The speckled component in our patient did not exhibit a peripheral distribution, and there was a classic CMN admixed with a speckled component at the centre of the lesion. A lentiginous pattern of rete ridges in CMN is uncommon. Therefore, CMN seems to have simultaneously occurred above the base of the SLN rather than the SLN spreading from the CMN. Moreover, the SLN and CMN had been present concurrently since birth. Therefore, we diagnosed CMN with concurrent SLN. A few cases of CMN hybrid with SLN have been reported previously. These reports emphasised that SLN that fall within the spectrum of CMN include the following observations. First, SLN present at birth or are noted soon thereafter. Second, the patterns of distribution reflect embryonic development. Third, SLN exhibit hamartomatous behaviour with various types of nevi (e.g. blue nevi, Spitz nevi, and junctional nevi) presenting within the same lesion over time.[2],[3],[4] We described a patient with a congenital pigmented lesion that had the clinical appearance of an SLN, and presented as a hybrid lesion with a CMN. The occurrence of CMN with SLN is rare. We believe that this case supports the hypothesis that SLN is a subtype of CMN.

   References Top

1.Wolff K, Goldsmith LA, Katz SI, Gilchrest BA, Paller AS, Leffell DJ. et al. Benign neopoasias and hyperplasias of melanocyte. In: Grichnik JM, Rhodes AR, Sober AJ, editors. Fitzpatrick's dermatology in general medicine. 7 th ed. New York, USA: McGraw-Hill; 2008. p. 1103-4.  Back to cited text no. 1
2.Elder DE, Elenitsas R, Johnson BL, Murphy GF, Xu X. Benign pigmented lesions and malignant melanoma. In: Elder DE, Elenitsas R, Murphy GF, Xu X. editors. Lever's histopathology of the skin. 10 th ed. Philadelphia, USA: Lippincott Williams and Wilkins; 2008. p. 709.  Back to cited text no. 2
3.Torrelo A, de Prada I, Zambrano A, Happle R. Extensive speckled lentiginous nevus associated with giant congenital melanocytic nevus: An unusual example of twin spotting? Eur J Dermatol 2003;13:534-6.  Back to cited text no. 3
4.Brufau C, Moran M, Armijo M. Nevus on nevus. Apropos of 7 case reports, 3 of them associated with other dysplasias, and 1 with an invasive malignant melanoma. Ann Dermatol Venereol 1986;113:409-18.  Back to cited text no. 4


  [Figure 1], [Figure 2]

This article has been cited by
1 Nevus Spilus (Speckled Lentiginous Nevus) in the Oral Cavity: Report of a Case and Review of the Literature
Karen G. Torres, Laura Carle, Michael Royer
The American Journal of Dermatopathology. 2017; 39(1): e8
[Pubmed] | [DOI]


Print this article  Email this article
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Article in PDF (842 KB)
    Citation Manager
    Access Statistics
    Reader Comments
    Email Alert *
    Add to My List *
* Registration required (free)  

    Article Figures

 Article Access Statistics
    PDF Downloaded44    
    Comments [Add]    
    Cited by others 1    

Recommend this journal