Nonfamilial bilateral axillary nevus comedonicus in a 24-year-old lady – a case report

Authors

  • J. Chowdhury
  • A.K. Roy
  • S. Das
  • S. Hansda

Keywords:

Nevus comedonicus, axillary, bilateral

Abstract

Nevus comedonicus is a rare hamartoma of the pilosebaceous unit. Bilateral involvement is relatively uncommon and is usually associated with other non-cutaneous anomalies. We report a case of non-familial nevus comedonicus affecting both axillae and ears only in a 24-year-old lady without any other anomalies. 

References

Kofmann S, Ein Fall Von, Seltener. Localization and verbretung of comedones. Arch Dermatol Syphilis. 1895;32:177-8.

Bhagwat PV, Tophakhane RS, Rathod RM et al. Nevus comedonicus along Blaschko's lines. Indian J Dermatol Venereol Leprol. 2009;75:330.

Pavithra S, Pai H, Mallya H, Pai GS. Nevus comedonicus syndrome. Indian J Dermatol. 2011;56:771-2.

Ghorpade A, Ramanan C. Penile nevus comedonicus. Indian J Dermatol Venereol Leprol. 1991;57:237-9.

Molho-Pessach V, Schaffer JV. Blaschko lines and other patterns of cutaneous mosaicism. Clin Dermatol. 2011;29:205-25.

Köse O, Calikan E, Kurumlu Z. Three different epidermal naevi with no organ involvement: Sebaceous naevus, naevus comedonicus and Becker's naevus. Acta Derm Venereol. 2008;88:67-9.

Larralde M1, Abad ME, Muñoz AS, Luna P. Childhood flexural comedones: a new entity. Arch Dermatol. 2007;143:909-11.

Kuruvila M, Kumaresan M. Extensive nevus comedonicus. Indian J Dermatol. 2007;52:210-2.

Mahajan RS, Shah MM, Ninama KR, Bilimoria FE. Extensive nevus comedonicus. Indian Dermatol Online J. 2014;5:520-1.

Yadav P, Mendiratta V, Rana S, Chander R. Nevus comedonicus syndrome. Indian J Dermatol. 2015;60:421.

Downloads

Published

2016-11-18

How to Cite

1.
Chowdhury J, Roy A, Das S, Hansda S. Nonfamilial bilateral axillary nevus comedonicus in a 24-year-old lady – a case report. J Pak Assoc Dermatol [Internet]. 2016Nov.18 [cited 2024Apr.19];26(1):66-8. Available from: http://jpad.com.pk/index.php/jpad/article/view/77

Issue

Section

Case Reports