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Anais Brasileiros de Dermatologia

Print version ISSN 0365-0596

An. Bras. Dermatol. vol.85 no.3 Rio de Janeiro June 2010

http://dx.doi.org/10.1590/S0365-05962010000300015 

CASE REPORT

 

Becker nevus syndrome*

 

 

Fabiane Eiras CosendeyI; Nayibe Solano MartinezII; Gabriela Alice BernhardIII; Maria Fernada Reis Gavazzoni DiasIV; David Rubem AzulayV

ICurrently participating in the postgraduate program at the Professor Rubem David Azulay Institute of Dermatology, Santa Casa de Misericórdia, Rio de Janeiro, Brazil, Medical Residency Program in Clinical Medicine, Military Police Central Hospital, Rio de Janeiro, Brazil
IICurrently participating in the postgraduate program at the Professor Rubem David Azulay Institute of Dermatology, Santa Casa de Misericórdia, Rio de Janeiro, Brazil
IIICurrently participating in the postgraduate program at the Professor Rubem David Azulay Institute of Dermatology, Santa Casa de Misericórdia, Rio de Janeiro, Brazil
IVProfessor of Dermatology, Professor Rubem David Azulay Institute of Dermatology, Santa Casa de Misericórdia, Rio de Janeiro, Brazil, Doctorate and Master's Degree from the Federal University of Rio de Janeiro, Rio de Janeiro, Brazil
VHead, Professor Rubem David Azulay Institute of Dermatology, Santa Casa de Misericórdia, Rio de Janeiro, Brazil, Head Professor, Pontifical University, Coordinator, Professor of Dermatology, Fundação Técnico-Educacional Souza Marques, Assistant Professor, Federal University of Rio de Janeiro, Brazil

Mailing Address

 

 


ABSTRACT

Becker nevus syndrome is a phenotype characterized by the fundamental presence of Becker's nevus with ipsilateral hypoplasia of the breast or other skin, skeletal and/or muscular disorders. This syndrome generally originates at birth, intensifies significantly in adolescence and is one of the syndromes that constitute epidermal nevus syndrome. To the best of our knowledge, this is the first case published in the Brazilian literature of Becker nevus syndrome associated with Becker's nevus, ipsilateral breast hypoplasia and scoliosis in a 14-year-old girl.

Keywords: hamartoma; hypertrichosis; nevus; scoliosis.


 

 

INTRODUCTION

Becker's nevus (BN) is a cutaneous hamartoma characterized by circumscribed hyperpigmentation with hypertrichosis, which was described for the first time by Becker in 1949.1,2

In the past, many authors have observed the association between BN and other disorders such as breast hypoplasia or scoliosis.1 However, it was only in 1995 that the term hairy epidermal nevus syndrome or Becker nevus syndrome was described for the first time by Happle as an association of BN with unilateral breast hypoplasia and muscle, skin and/or skeletal abnormalities. 1 This recently described entity forms part of the epidermal nevus syndrome.

 

CASE REPORT

A 14-year-old female patient from Realengo, Brazil reported a small, slightly brownish mark on her left breast that had been present since birth. She reported that in adolescence the lesion had spread onto her back and right leg with a concomitant increase in body hair in that region. She reported no hirsutism, irregular menstruation or any similar cases in the family. At dermatological examination, a hyperchromic macule with well-defined, irregular borders was found in the right scapular region, extending towards the shoulder and anterior chest region and a hyperchromic macule with hypertrichosis on her right ipsilateral leg (Figures 1 and 2A). Clinical examination showed hypogenesis of the right breast and scoliosis (Figure 2B). Gynecological examination was normal. Histopathology of the macule showed moderate acanthosis, hyperpigmentation of the basal layer with coarse granules of melanin, presence of melanophages in the papillary dermis and hyperplasia of the arrector pili muscle, compatible with Becker's nevus (Figure 3). The following laboratory tests were performed: full blood count, liver function tests, kidney function tests, 17 OH progesterone, LH, FSH, prolactin, free T4 and TSH, which were all normal. Imaging exams performed included radiography of the spinal column, which confirmed the presence of scoliosis, and breast ultrasonography, which revealed thickened fibroglandular tissue in the left breast and hypotrophy of the right breast.

 


 

 

DISCUSSION

Becker's nevus is a hyperpigmented hamartoma with hypertrichosis and well-defined borders that may appear in any part of the body, but is more common on the trunk and upper limbs.1-3 Spontaneous regression of the lesion may occur. In 1984, Person and Longcope detected an increase in androgen receptor levels in Becker's nevus. Later studies confirmed this increase, leading to the hypothesis of hormonal hyperresponsiveness in this cutaneous hamartoma. There have been reports in the literature of some patients with acneiform lesions of Becker's nevus and the hypothesis is that this lesion may be mediated by androgens. As an androgen- dependent disorder, it is much more common in males (5:1) and in adolescence. 1,4

In the epidermis, histopathology shows acanthosis and hyperpigmentation of the basal layer and in the dermis there is hyperplasia of the arrector pili muscle with melanophages, as seen in this patient.1,2,4

Despite the hyperchromia, Becker's nevus does not belong to the group of melanocytic lesions. It is considered a particular form of epidermal nevi similar to verrucous epidermal nevus, sebaceous nevus of Jadassohn, nevus comedonicus, eccrine nevus, apocrine nevus and white sponge nevus, which are named in accordance with the preponderant structure (Table 1).1,5

 

 

Conceptually, epidermal nevi are considered to constitute a hamartomatous proliferation developed from the embryonic ectoderm and characterized by hyperplasia of the epidermal structures such as keratinocytes, apocrine and eccrine glands, hair follicles and sebaceous glands.5

In 1968, Solomon et al. described epidermal nevus syndrome, which consists of the association of epidermal nevi, which are generally more extensive, with various abnormalities of the skin, eyes, central nervous system and skeleton that originate in the ectoderm and that may, albeit rarely, be accompanied by abnormalities in the urogenital tract and cardiovascular system, which originate in the embryonic mesoderm.5-7

The cutaneous appearance of epidermal nevi depends partly on the predominant type of cell involved, on the patient's age, the area of the body affected and the degree of cell differentiation. Epidermal nevi follow the lines of Blaschko. The association of epidermal nevi with abnormalities of the central nervous system was described for the first time by Schimmelpenning and later by Feuerstein and Mims.3 The greater the number of extracutaneous lesions and the more disseminated the epidermal nevus, the greater the probability that the central nervous system will be involved and that there will be other systemic manifestations, which may be a reflex of the severity of the biological inheritance caused by mutation during development.5,6,8 There is systemic involvement in around 8% of patients with epidermal nevi. In addition to the epidermal nevus, other skin abnormalities may occur in epidermal nevus syndrome such as café-au-lait spots, speckled lentiginous nevus, multiple melanocytic nevi and vascular malformations (phakomatosis pigmentovascularis)5 The following entities described by Happle are part of an even larger concept of epidermal nevus syndrome: Proteus syndrome, sebaceous nevus syndrome, Becker nevus syndrome, phacomatosis pigmentokeratotica, CHILD syndrome and nevus comedonicus syndrome (Table 2).5,6,8

 

 

In 1995, Happle first described Becker nevus syndrome or hairy epidermal nevus syndrome. The presence of Becker's nevus is fundamental in characterizing the syndrome; however, its association with breast hypoplasia or other skin, muscle and/or skeletal disorders is also necessary (Table 3).1,2 In general, these disorders involve the same side of the body; however, they may be bilateral. Breast hypogenesis, scoliosis or any other findings alone are insufficient to establish diagnosis of the syndrome.1

 

 

Becker nevus syndrome is also an androgendependent disorder as is Becker's nevus and is therefore more commonly found in adolescence due to the increased hyperpigmentation of the nevus and the hair.1-5 The proportion of women sufferers is the same as that of men, although it is more easily diagnosed in women due to the more visible breast hypoplasia.1,2

Many of the findings associated with this syndrome are believed to be the result of the increase in the number of androgen receptors in certain areas. Androgen is one of the hormones responsible for hair growth, bone development and muscle mass. Person and Nirde et al. measured androgen receptors in a lesion of Becker's nevus and in the normal skin of a patient with Becker's nevus and found an increase in these receptors in the lesion. They proposed that Becker's nevus could be considered a component of the androgen receptor hypersensitivity syndrome spectrum.9 The pathogenesis of breast hypoplasia remains to be clarified; however, it is possible that it could be the same as that of Becker's nevus, although androgen receptor levels in the breast may counterbalance the effect of estrogen on the growth of the normal breast, resulting in hypoplasia. Spironolactone is an antiandrogen used to treat acne, hirsutism and androgenic alopecia. Its mechanism of action is still not fully understood; however, it is believed that it may result from negative feedback of androgen receptors and may therefore improve hypoplasia. In the present study, an increase in the breast with hypoplasia was found following use of spironolactone 50 mg/day.9 This finding corroborates the hypothesis of an increase in androgen receptors in Becker's nevus and in the hypoplastic breast. Nevertheless, this could not be evaluated in the patient in the present study because she preferred to undergo breast implant surgery.

In the majority of cases, the syndrome occurs sporadically and a family association has rarely been found. Heterozygotic individuals would be phenotypically normal and the allele responsible would then be transmitted through several generations. Genetic studies suggest that the nevus and its associated disorders would only originate when a somatic recombination occurred in the early stage of embryogenesis, resulting in a population of homozygotic cells. 1,6 However, the genetic basis of this syndrome has yet to be fully clarified. Becker nevus syndrome involves extremely subtle clinical findings and many cases may have remained undetected.

 

REFERENCES

1.  Happle R, Koopman RJJ. Becker nevus syndrome. Am J Med Genetics. 1997;68:357-61.         [ Links ]

2.  Alfaro A, Torrelo A, Hernández A, Zambrano A, Happle R. Síndrome del nevo de Becker. Actas Dermosifiliogr. 2007;98:624-6.         [ Links ]

3.  Ferreira MJ, Bajanca R, Fiadeiro T. Congenital melanosis and hypertrichosis in a bilateral distribution. Pediatri Dermatol. 1998;15:290-2.         [ Links ]

4.  Santos-Juanes J, Galache C, Curto JR, Carrasco MP, Ribas A, Sánchez del Río J. Acneiform lesions in Becker's nevus and breast hypoplasia. Int J Dermatol. 2002;41:699-700.         [ Links ]

5.  Thomas VD, Swanson NA, Lee KK. Benignan epithelial tumors, hamartomas and hyperplasias. In: Wolff K, Goldsmith LA, Katz SI, Gilchrest BA, Paller AS, Lefell D, editors. Fitzpatrick's Dermatology in General Medicine; 7th ed. New York: McGraw-Hill; 2008. p.1057-62.         [ Links ]

6.  Sugarman JL. Epidermal nevus syndromes. Semin Cutan Med Surg. 2007;26:221-30.         [ Links ]

7.  Noronha L, Neto JF, Nones RB, Taniguchi K. Nevo epidérmico: análise clínica e histológica de seis casos. An Bras Dermatol.1999;74:259-62.         [ Links ]

8.  Vidaurri-de la Cruz H, Tamayo-Sánchez L, Durán- McKinster C, de la Luz Orozco-Covarrubias M, Ruiz- Maldonado R. Epidermal nevus syndromes: Clinical findings in 35 patients. Pediatr Dermatol. 2004;21:432-9.         [ Links ]

9.  Hoon Jung J, Chan Kim Y, Joon Park H, Woo Cinn Y. Becker's nevus ipsilateral breast hypoplasia: improvement with Spironolactona. J Dermatol. 2003;30:154-156.         [ Links ]

 

 

Mailing Address:
Fabiane Eiras Cosendey
Rua Mariz e Barros,71 - Ap. 902 - Icaraí
24220 120 Niterói - RJ
Tel.: 21 2612 1620 7895 0462
E-mail: fabianecosendey@yahoo.com.br

Received on 07.05.2009.
Approved by the Advisory Board and accepted for publication on 27.11.2009.
Conflict of interest: None
Financial funding: None

 

 

* Study conducted at the Professor Rubem David Azulay Institute of Dermatology, Santa Casa de Misericórdia, Rio de Janeiro, Brazil.