|Year : 2019 | Volume
| Issue : 6 | Page : 247-250
Isolated patchy heterochromia of the scalp hair: A rare entity with literature review
Priyadarshini Sahu, Surabhi Dayal, Rupinder Kaur, Jayanti Singh
Department of Dermatology, Venereology and Leprology, Pt B D Sharma University of Health Science, Rohtak, Haryana, India
|Date of Web Publication||14-Jan-2020|
Dr. Surabhi Dayal
18, Vikas Nagar, Rohtak - 124 001, Haryana
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Scalp hair heterochromia involves the presence of two different colors of the scalp hair in the same individual. It may be of three types: patchy, diffuse, and segmental. Isolated patchy heterochromia of the scalp hair is a rare entity, and a very few cases have been described in the literature. Hereby, we report one such case of isolated patchy scalp hair heterochromia in a 2-year-old healthy male child with black hairs presenting with a bunch of blond hairs without any underlying abnormalities along with the literature review.
Keywords: Blond hairs, heterochromia, scalp
|How to cite this article:|
Sahu P, Dayal S, Kaur R, Singh J. Isolated patchy heterochromia of the scalp hair: A rare entity with literature review. Int J Trichol 2019;11:247-50
| Introduction|| |
Heterochromia of the scalp hair is a rare phenomenon characterized by the presence of two distinct colors of the scalp hair in the same person. Typically, colors such as brown, blond, red, and yellow hair presenting in the background of dark color hairs have been described in previous studies.,,,,,,,,,, Here, we present a pediatric patient with scalp hair heterochromia without any underlying abnormalities.
| Case Report|| |
A 2-year-old male child of Indian origin with black hairs presented with a bunch of blond hairs of the same length on the right and left parietal region of the scalp since birth [Figure 1]. The patch of blond hairs approximately measured about 6 cm × 8 cm. The patient was in a good health with normal developmental milestones. Family and past history was also unremarkable. There was no history of exposure to any other chemicals, trauma, or inflammatory disease of the scalp.
|Figure 1: Tuft of blond hairs on the right and left parietal region with black hairs on the rest of the scalp in a 2.year.old male child|
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General physical examination revealed normal physical development. On cutaneous examination, the patient had tuft of blond hair on the bilateral parietal region of the scalp following Blaschko's lines with normal color of the underlying skin. As the underlying skin of blond hairs was normal, the diagnosis of melanocytic nevi, halo nevus, and vitiligo was excluded. The hair of the eyelashes and eyebrows were of black color. Nails, teeth, and oral mucosa were normal. No ophthalmologic, audiologic, or neurological abnormalities were found. Routine blood investigations were normal. On light microscopy, the lighter hair appears to be slightly thinner than the darker hair and the pigmentation was homogenous along the entire hair shaft [Figure 2]. As the pigmentation was homogenous throughout the hair shaft, the diagnosis of segmental heterochromia was excluded. Based on these findings, diagnosis of patchy heterochromia of the scalp hair was made.
|Figure 2: Under light microscopy, (a) showing blond hair and (b) showing black hair; blond hair is thinner than black hair and pigmentation is uniform in black hair as compared to blond hair (×10 magnification)|
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| Discussion|| |
Follicular melanogenesis of hairs is tightly coupled with hair growth cycle, i.e., melanocytic proliferation (during early anagen), maturation (mid-to-late anagen), and melanocytic death via apoptosis (during early catagen). The process of melanogenesis is controlled by complex genetic mechanisms. Melanin pathway divides into two pathways after the formation of dopaquinone from tyrosine. Dopaquinone converts to 5,6-dihydroxyindole and 5,6-dihydroxyindole-2-carboxylic acid oligomers to form eumelanin. Another pathway leads to the formation of benzothiazinyl alanine which forms pheomelanin and trichochromes. Tyrosinase activity determines the color of individual hair. The skin phototype does not determine the hair color as can be seen by the co-expression of eumelanic hair color in the Fitzpatrick skin type 1 and 2. Melanosome structure correlates with the type of melanin produced. Black hair follicle melanocytes have the largest number of eumelanosomes (melanosomes containing eumelanin) and red hair follicle melanocytes contain pheomelanosomes. Whereas, melanosomes in blond hair are weakly melanized. The author also speculates that hair follicles individually may have remarkable autonomy in terms of their pigment type, which may be the cause of variable polymorphisms in hair pigmentation.
There are various etiologies of scalp hair heterochromia, which includes genetic basis, metabolic defects, nutritional defects, or drugs [Table 1]. The distribution of heterochromic hair can be symmetric or asymmetric. When the heterochromic hair is symmetric such as difference in scalp and body hairs, it is considered as physiologic. On the contrary, asymmetric distribution indicates an underlying pigmentary disorder.,
There are three different clinical types of asymmetrical scalp hair heterochromia: patchy, segmental, and diffuse type. Patchy heterochromia of hairs which is not associated with any detectable skin pigmentary mosaicism, not characterized by poliosis and not resulting from the presence of an underlying melanocytic nevus, is known as isolated patchy heterochromia (IPH).
Patchy and diffuse heterochromia are assumed to have genetic basis, whereas segmental heterochromia, which is characterized by alternating dark and light segments on each hair, is mostly associated with iron-deficiency anemia. The review of literature of all the cases of patchy heterochromia of the scalp hair is given in [Table 2].,,,,,,,,,, In all these cases, the heterochromic hairs follow the Lines of Blaschko More Details. Our patient is a case of IPH along the lines of Blaschko, which might be secondary somatic mosaicism of one or more genes involved in pigmentation and skin pigmentation (hypo- or hyperpigmentation) due to the fact that such cutaneous mosaicism may not be present at birth but may develop later in life.
There are only a few case reports of scalp hair heterochromia in the literature and none of them are from India. To the best of the authors' knowledge, ours might be the first case report of IPH of the scalp hair from India. This might be due to the fact that this condition is asymptomatic and may be underdiagnosed so far. However, such IPH may be associated with other abnormalities of skin pigmentation. Further, genetic analysis of such pigmentary mosaicism is difficult as there is involvement of heterogeneous genes. Thus, dermatologist fraternity must be always aware of such possible pigmentary changes and keep these patients on regular follow-up.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient's parents have given their consent for the patient's images and other clinical information to be reported in the journal. The patient's parents understand that the patient's name and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2]
[Table 1], [Table 2]