International Journal of Trichology

CASE REPORT
Year
: 2018  |  Volume : 10  |  Issue : 1  |  Page : 24--25

Whorled scarring alopecia – The only adult marker of incontinentia pigmenti


Urvi Popli, Paul Devakar Yesudian 
 Departments of Dermatology, Wrexham Maelor Hospital, Wrexham, Wales, UK

Correspondence Address:
Dr. Urvi Popli
Department of Dermatology, Wrexham Maelor Hospital, Wrexham LL13 7TD
UK

Abstract

Incontinentia pigmenti (IP) is a rare X-linked dominant disease that affects the ectodermal tissues. It is associated with a whorled pattern of scarring alopecia, which is possibly underreported. This scarring alopecia could be used as a marker to identify adult women affected with IP as older patients may have minimal cutaneous manifestations. We report an unusual case of an 8-year-old girl who had recurrent inflammatory stage IP and later developed whorled scarring alopecia in the vertex of the scalp.



How to cite this article:
Popli U, Yesudian PD. Whorled scarring alopecia – The only adult marker of incontinentia pigmenti.Int J Trichol 2018;10:24-25


How to cite this URL:
Popli U, Yesudian PD. Whorled scarring alopecia – The only adult marker of incontinentia pigmenti. Int J Trichol [serial online] 2018 [cited 2022 Sep 29 ];10:24-25
Available from: https://www.ijtrichology.com/text.asp?2018/10/1/24/223389


Full Text

 Introduction



Incontinentia pigmenti (IP) is a rare genodermatosis that is lethal in males. It is a multisystem disorder, which affects ectodermal structures including cutaneous, ocular, dental, cerebral, and skeletal manifestations. A comprehensive review of 600 published clinical reports classified the skin findings in IP into four different stages.[1] An initial inflammatory or vesiculobullous eruption is followed by a verrucous phase, leading onto a hyperpigmented and finally an atrophic stage. Hair and scalp involvement, particularly whorled alopecia, was uncommon in a series of 40 patients with only 11 (28%) manifesting evidence of alopecia in the vertex.[2]

 Case Report



An 8-year-old female child was clinically diagnosed with IP at birth. Genetic testing revealed the mutation of IKBKG gene (inhibitor of nuclear factor kappa-B kinase subunit gamma), confirming the diagnosis. Her clinical course was of interest as she experienced reactivation of her IP rash in a blaschkoid pattern on the trunk every time she developed a viral infection from 11 months of age.[3] The flares eventually subsided, with no exacerbations after the age of 2. Over the past 2 years, her mother noted an area of alopecia near the vertex of the scalp. She was unsure of the duration of the hair loss but felt that it has become increasingly noticeable. On examination, she had subtle areas of whorled pigmentation in a blaschkoid distribution on the lower trunk and groin. A linear to whorled area of scarring alopecia was evident near the vertex of the scalp [Figure 1] and [Figure 2]. Hair texture and structure was normal under the dermatoscope. The nail, teeth, and rest of the skin showed no abnormality. Neurological and ophthalmological assessments revealed no systemic features of IP.{Figure 1}{Figure 2}

 Discussion



A review of all manifestations of IP identified whorled alopecia as a recognized feature of the condition,[1] but diffuse alopecia was aborted. In a case series by Hadj-Rabia et al., alopecia was identified in 11 (28%) of the 40 patients occurring at the site of previous blistering and generally unnoticed. Abnormal hair tended to be lusterless, wiry, and coarse, mainly in the vertex. Woolly hair has also been reported, but the hair shaft was normal on microscopic examination. Thin or sparse hair early in childhood did not seem to correlate with the quality or quantity of hair in later life.

In 1990, Happle argued that the linear and patchy alopecia seen in the patients with IP can be a manifestation of functional X chromosome mosaicism. They appeared to correspond to Blaschko's lines. Functional X chromosome mosaicism was recognized as a genetic mechanism underlying cutaneous anomalies seen in a number of X-linked diseases such as IP. It has been hypothesized that the segmental and streaked manifestations of IP may be consequential to tissue mosaicism from random X inactivation, with the normal X chromosome active in uninvolved skin and the IP X chromosome active in involved skin.[4] A similar pathogenesis could also explain the whorled pattern of alopecia in our patient.

This phenomenon may be underreported and dermatologist should specifically seek this sign as it could be hidden under the scalp hair. The scarring alopecia tends to be permanent and can be a useful marker to ascertain affected adult women who may no longer have cutaneous manifestations. In our patient, with the gradual resolution of cutaneous features and in the absence of systemic findings, scarring alopecia may be the only indication of IP as an adult.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

References

1Carney RG. Incontinentia pigmenti. A world statistical analysis. Arch Dermatol 1976;112:535-42.
2Hadj-Rabia S, Froidevaux D, Bodak N, Hamel-Teillac D, Smahi A, Touil Y, et al. Clinical study of 40 cases of incontinentia pigmenti. Arch Dermatol 2003;139:1163-70.
3Salako K, Yesudian PD. Recurrence of inflammatory stage incontinentia pigmenti: An example of cytokine-mediated apoptosis in a genodermatosis. Br J Dermatol 2011;165(S1):121.
4Happle R. Lyonization and the lines of Blaschko. Hum Genet 1985;70:200-6.