ANSWER:BECKER NEVUS
An acquired, sharply demarcated, brownish patch with geographical borders and overhanging hypertrichosis is characteristic of a Becker nevus. This disorder is named after Samuel William Becker, who in 1949 reported 2 cases of a hyperpigmented and hypertrichotic lesion with unilateral distribution.1
PREVALENCE AND ETIOLOGY
A Becker nevus occurs in about 0.5% of adolescent boys and young men.2 The male to female ratio is approximately 5:1.2 The exact pathogenesis is not known; however, a target tissue increase in androgen receptors or sensitivity to androgens may be responsible.3
HISTOPATHOLOGY
Histopathological features include regular elongation of rete ridges, hyperpigmentation of the basal layer, acanthosis, and hyperkeratosis.2 Although the lesion is called a nevus, nevus cells are absent in the dermis. Thus, malignant transformation is not a concern.
CLINICAL MANIFESTATIONS
A Becker nevus typically begins in the second decade of life as a circumscribed brownish macule or patch that gradually enlarges in an irregular fashion, similar to a geographical configuration. Hypertrichosis usually develops a few years after the pigmentation. The hairs generally appear in the region of the pigmentation but are not necessarily confined to that area; they become coarser and darker with time. The lesion is typically asymptomatic and unilateral, with a predilection for the shoulder and upper chest.2
Although Becker nevus is usually an acquired disorder, congenital and familial cases have been described. Occasionally, it may be associated with ipsilateral breast hypoplasia, smooth muscle hamartoma, lipoatrophy, and musculoskeletal anomalies (including ipsilateral aplasia of pectoralis major, ipsilateral limb shortening, scoliosis, hemivertebrae, and spina bifida occulta).4 The term "Becker nevus syndrome" has been used to describe the association of a Becker nevus with noncutaneous anomalies.
DIFFERENTIAL DIAGNOSIS
The Table lists the differential diagnosis of Becker nevus. Of the conditions included, congenital melanocytic nevus, café au lait patch, and Albright syndrome are present at birth or appear shortly thereafter. Nevus spilus generally develops within the first year of life.
TREATMENT
Except for cosmesis, no treatment is necessary. The hyperpigmentation can be treated with Q-switched lasers. The hypertrichosis can be treated with depilation.
| Table — Differential diagnosis of Becker nevus | |
| Condition | Characteristics |
| Becker nevus | Acquired, sharply demarcated, brownish patch with geographical borders and overhanging hypertrichosis |
| Congenital melanocytic nevus | Dark-colored, elevated lesion with regular border |
| Café au lait patch | Hyperpigmented, sharply demarcated patch that is present at birth; usually tan to light brown in light-skinned persons and dark brown in dark-skinned persons |
| Albright syndrome | Triad of polyostotic fibrous dysplasia, hyperfunctioning endocrine system (notably precocious puberty and hyperthyroidism), and a hyperpigmented lesion on the same side as the bony lesion; the skin lesion is present at birth and has a serrated border |
| Nevus spilus | Circumscribed pigmentation that is stippled with dark-brown punctuate macules or papules; most lesions develop within the first year of life |
