|Year : 2015 | Volume
| Issue : 3 | Page : 131-132
A rare presentation and histopathologic findings of woolly hair nevus
Laura Miguel Gomez1, Lorea Bagazgotia1, Luis Requena2
1 Department of Dermatology, Ramon y Cajal Hospital, Madrid, , Europe, Spain
2 Department of Pathology, Fundación Jimenez Diaz Hospital, Madrid, , Europe, Spain
|Date of Web Publication||19-Oct-2015|
Laura Miguel Gomez
Department of Dermatology, Ramon y Cajal Hospital, Madrid, Spain. Carretera de Colmenar Viejo km 9,1, 28034 Madrid
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Woolly hair nevus is a rare disease whose diagnosis is challenging. We present a case of this condition presenting in a 27-year-old healthy male. We describe a histology pattern consisting in the presence of several terminal hair follicles ending in the same dilated follicular infundibulum, a perifollicular lymphocytic infiltrate and an excessive amount of normal apocrine glands in deep reticular dermis, some findings non-previously reported. Clinicopathological correlation is very important for making a correct diagnosis.
Keywords: Hair disorders, histopathologic pattern, woolly hair nevus
|How to cite this article:|
Gomez LM, Bagazgotia L, Requena L. A rare presentation and histopathologic findings of woolly hair nevus. Int J Trichol 2015;7:131-2
| Introduction|| |
Woolly hair nevus (WHN) is characterized by an area with fine, curly and often hypopigmented hair, on a circumscribed area of the scalp. Hutchinson et al. classified three variants of woolly hair: Hereditary woolly hair (autosomal dominant), familial woolly hair (autosomal recessive) and a WHN. Woolly hair syndrome (WHS) affects to the whole scalp and it may be associated with other cutaneous anomalies and extracutaneous anomalies, such as Noonan syndrome or carvajal disease.,, In contrast to the WHS, WHN is not a hereditary condition. Recently, it has been found in two cases of WHN, somatic HRAS c. 34G > A, p.G12S mutation in affected in hair. Interestingly, this mutation has also been observed in epidermal nevus. Also, a HRAS c. 37G > C, p. Gly13Arg mutation has been described in nevus of Jadassohn and Schimmelpenning syndrome.
| Case Report|| |
We report the case of a 27-year-old healthy male who presented with an area of curlier and thinner hair than the rest of his scalp localized on the right parietal area. He referred that just at that location, his hair had been different since childhood, curlier than the rest. Physical examination revealed a plaque with shorter and curlier hair on an area of 10 cm in diameter on the right parietal area of the scalp. A decreased density of hair was observed. The skin on the patch was apparently healthy. There were not exclamation mark hairs or miniaturization of hair follicles. A hair pull test was negative [Figure 1]. A skin biopsy showed a mild perifollicular lymphocytic infiltrate, telangiectatic capillaries in the superficial dermis and several terminal hair follicles emerged in the same dilated follicular infundibulum. Interestingly, an excessive amount of normal apocrine glands were found in the deep reticular dermis. Counting of hair follicles was normal [Figure 2]a,[Figure 2]b,[Figure 2]c. Based on clinical appearance and histopathologic studies, a diagnosis of WHN was established.
|Figure 1: (a) A plaque with shorter and curlier hair on an area of 10 cm in diameter on the right parietal area of scalp. Skin on the patch was apparently healthy. (b) An area of curlier hair than the rest of his scalp localized on the right parietal area since childhood|
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|Figure 2: (a) Several involved terminal hair follicles ending in the same infundibulum, a perifollicular lymphocytic infiltrate and an excessive amount of normal apocrine glands (H and E, ×4). (b) Several involved sterminal hair follicles ending in the same infundibulum and a perifollicular lymphocytic infiltrate (H and E, ×20). (c) An excessive amount of normal apocrine glands (H and E, ×20)|
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| Discussion|| |
WHN usually appears during the 1st years of life and it remains stable throughout adulthood. It may be associated with pigmented or epidermal nevus, usually on the neck, arm or even coexisting with WHN. Histopathologic findings of WHN are scarcely described in the literature, probably because most cases are diagnosed clinically. A wavy appearance of hair follicles with perifollicular infiltration of inflammatory cells has been described, but normal hairs and cutaneous appendages may also be observed. In our case, we found a different histopathological pattern, with several involved terminal hair follicles ending in the same infundibulum, a perifollicular lymphocytic infiltrate and an excessive amount of normal apocrine glands, findings similar to those of nevus of Jadassohn. It may be possible that WHN is the clinical manifestation of a wide range of different histopathologic hamartomatous lesions involving the hair follicles, some of them clearly evident, with thinner and curved hair follicles and accompanying epidermal nevus in the overlying epidermis, and subtle histopathologic changes in other cases, as in our case.
| Conclusion|| |
We described a case of WHN showing some nonpreviously reported histopathologic findings. These findings described indicate that clinicopathologic correlation is necessary to establish a diagnosis of WHN with confidence.
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Conflicts of interest
There are no conflicts of interest.
| References|| |
CG, Hernandez R EG, Galilea ON. Woolly hair nevus in a toddler. Int J Trichology 2014;6:187-8.
Hutchinson PE, Cairns RJ, Wells RS. Woolly hair. Clinical and general aspects. Trans St Johns Hosp Dermatol Soc 1974;60:160-77.
Legler A, Thomas T, Zlotoff B. Woolly hair nevus with an ipsilateral associated epidermal nevus and additional findings of a white sponge nevus. Pediatr Dermatol 2010;27:100-1.
Oliveira JR, Mazocco VM, Arruda L. Woolly hair nevus syndrome. An Bras Dermatol 2004;79:103-6.
Thomas J, Sindhu BR, Dinesh DK, Parimalam K. Type A woolly hair nevus. Indian J Paediatr Dermatol 2014;15:27-9.
Murao K, Miyajima O, Kubo Y. Woolly hair nevus associated with digital abnormalities and auditory disturbance. Int J Dermatol 2014;53:e164-6.
Levinsohn JL, Teng J, Craiglow BG, Loring EC, Burrow TA, Mane SS, et al.
Somatic HRAS p.G12S mutation causes woolly hair and epidermal nevi. J Invest Dermatol 2014;134:1149-52.
Groesser L, Herschberger E, Ruetten A, Ruivenkamp C, Lopriore E, Zutt M, et al.
Postzygotic HRAS and KRAS mutations cause nevus sebaceous and Schimmelpenning syndrome. Nat Genet 2012;44:783-7.
Hong H, Lee WS. Woolly hair nevus involving entire occipital and temporal scalp. Ann Dermatol 2013;25:396-7.
Venugopal V, Karthikeyan S, Gnanaraj P, Narasimhan M. Woolly hair nevus: A rare entity. Int J Trichology 2012;4:42-3.
[Figure 1], [Figure 2]