Home About us Editorial board Ahead of print Current issue Archives Instructions Submit article Search Subscribe Contacts Login
  • Users Online: 465
  • Home
  • Print this page
  • Email this page


 
 Table of Contents  
THE CLINICAL PICTURE
Year : 2022  |  Volume : 9  |  Issue : 2  |  Page : 141-142

Midline nevoid acanthosis nigricans


Department of Dermatology, Venereology, and Leprology, Government Medical College and Hospital, Nagpur, Maharashtra, India

Date of Submission23-Mar-2020
Date of Decision20-Jul-2020
Date of Acceptance14-Mar-2021
Date of Web Publication12-Aug-2022

Correspondence Address:
Dr. Vaishali H Wankhade
Associate Professor, Department of Dermatology, Venereology, and Leprology, Government Medical College and Hospital, Nagpur, Maharashtra
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/Pigmentinternational.Pigmentinternational_

Rights and Permissions

Keywords: Dermoscopy, nevoid, papillomatosis


How to cite this article:
Kowe PA, Agrawal SK, Wankhade VH. Midline nevoid acanthosis nigricans. Pigment Int 2022;9:141-2

How to cite this URL:
Kowe PA, Agrawal SK, Wankhade VH. Midline nevoid acanthosis nigricans. Pigment Int [serial online] 2022 [cited 2022 Sep 26];9:141-2. Available from: https://www.pigmentinternational.com/text.asp?2022/9/2/141/353668



A 16-year-old male presented with gradually progressive, asymptomatic, thick lesion over midline of abdomen and chest for 4 years. He was born to non-consanguineous parents with no other family members affected with similar disease. He was nonobese (body mass index: 18.2 kg/m2) and had no endocrinopathy. There was neither any history of drug intake prior to onset of lesion, nor significant weight loss. Examination revealed overlying well-demarcated, hyperpigmented velvety plaque with soft ridges in supra umbilical area extending linearly up to the chest [Figure 1]. Based on history and examination, we kept differential diagnosis of inflammatory linear verrucous epidermal nevus (ILVEN) and nevoid acanthosis nigricans (AN). Dermoscopy using 3Gen DermLite DL4 (CA, USA) 10× polarized mode, showed multiple linear crista cutis and sulcus cutis with hyperpigmented dots in the crista cutis [Figure 2]a. Histopathological examination revealed hyperkeratosis, irregular acanthosis, hyperpigmentation of basal layer, and papillomatosis with upward projection of dermal papillae. Dermis showed pigment incontinence and perivascular lymphocytic infiltrate [Figure 2]b. Based on history, clinical findings, dermoscopy, and skin biopsy we made the final diagnosis of nevoid variant of AN. Patient was counselled and advised tretinoin 0.05% cream at night and 12% urea containing moisturizers in daytime.
Figure 1 Hyperpigmented velvety plaque with soft ridging in supra umbilical area extending linearly up to the chest

Click here to view
Figure 2 (a) Dermoscopy showing multiple crista cutis (green arrow) and sulcus cutis (red arrow) with hyperpigmented dots in crista cutis (blue arrow) (polarized; original magnification: 10×). (b) H and E showing hyperkeratosis (red arrow), irregular acanthosis (green arrow), papillomatosis, increased basal layer pigmentation (blue arrow), and dermal melanophages (black arrow) (H and E, 10×)

Click here to view


Schwartz categorized AN into the eight variants: obesity associated, syndromic, benign, malignant, drug induced, acral, mixed, and unilateral.[1] Unilateral nevoid acanthosis nigricans (UNAN) is a term which denotes blaschkoid, linear, unilateral distribution of classic AN lesion. Inherited as irregularly autosomal dominant trait, it can present at birth, childhood, puberty, or in middle-aged adults. Sites of involvement reported previously are: scalp, face, back, chest, abdomen, periumbilical area, thigh, and flexures. There are very few reports of midline involvement which we observed in our case. The condition needs to be differentiated from verrucous epidermal nevus and ILVEN which resembles AN clinically. Dermoscopy plays an important bedside tool to differentiate and diagnose such similar looking entities. The closest dermoscopic differentials of AN include confluent and reticulated papillomatosis of Gougerot–Carteaud syndrome and idiopathic eruptive macular pigmentation.[2],[3] Further confirmation can be done by routine skin biopsy with hematoxylin and eosin staining. Various treatments that have been tried are keratolytics such as retinoid, ammonium lactate creams, calcipotriene, fish oil, cryotherapy, dermabrasion, excision, and long-pulse alexandrite lasers.[4] Recently Campos et al. treated a case of UNAN successfully with CO2 laser. Midline distribution of the lesion with characteristic linear pattern, absence of family history, and other systemic abnormalities prompted us to report this case.[5]

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Das A, Bhattacharya S, Kumar P et al. Unilateral nevoid acanthosis Nigricans: Uncommon variant of a common disease. Indian Dermatol Online J 2014;5(suppl 1):S40-3.  Back to cited text no. 1
    
2.
Errichetti E, Maione V, Stinco G. Dermatoscopy of confluent and reticulated papillomatosis (Gougerot‐Carteaud syndrome). J Dtsch Dermatol Ges 2017;15:836-8.  Back to cited text no. 2
    
3.
Vasani RJ. Idiopathic eruptive macular pigmentation-uncommon presentation of an uncommon condition. Indian J Dermatol 2018;63:409-11.  Back to cited text no. 3
[PUBMED]  [Full text]  
4.
Krishnaram AS. Unilateral nevoid acanthosis nigricans. Int J Dermatol 1991;30:452-3.  Back to cited text no. 4
    
5.
Campos MA, Varela P, Baptista A, Ferreira EO. Unilateral nevoid acanthosis nigricans treated with CO2 laser. BMJ Case Rep 2016;2016:bcr2016216073.  Back to cited text no. 5
    


    Figures

  [Figure 1], [Figure 2]



 

Top
 
 
  Search
 
Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
Access Statistics
Email Alert *
Add to My List *
* Registration required (free)

 
  In this article
References
Article Figures

 Article Access Statistics
    Viewed267    
    Printed10    
    Emailed0    
    PDF Downloaded31    
    Comments [Add]    

Recommend this journal


[TAG2]
[TAG3]
[TAG4]