Disseminated blue naevus and malignant blue naevus associated with excessive aromatase syndrome
被引:4
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作者:
Lobo, A. Z. C.
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Univ Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, BrazilUniv Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, Brazil
Lobo, A. Z. C.
[1
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Martin, R. M.
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Univ Sao Paulo, Sch Med, Mol Genet & Hormones Lab LIM 42, Endocrinol & Dev Unit, Sao Paulo, BrazilUniv Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, Brazil
Martin, R. M.
[3
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Belda, W., Jr.
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Univ Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, BrazilUniv Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, Brazil
Belda, W., Jr.
[1
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Michi, M. M.
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Univ Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, BrazilUniv Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, Brazil
Michi, M. M.
[1
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Arnone, M.
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Univ Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, BrazilUniv Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, Brazil
Arnone, M.
[1
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Festa-Neo, C.
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Univ Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, BrazilUniv Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, Brazil
Festa-Neo, C.
[1
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Sotto, M. N.
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Univ Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, BrazilUniv Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, Brazil
Sotto, M. N.
[1
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Vilela, M. A. C.
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Univ Sao Paulo, Sch Med, Hosp Clin, Dept Endocrinol, Sao Paulo, BrazilUniv Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, Brazil
Vilela, M. A. C.
[2
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Sanches, J. A., Jr.
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Univ Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, BrazilUniv Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, Brazil
Sanches, J. A., Jr.
[1
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机构:
[1] Univ Sao Paulo, Dept Dermatol, Hosp Clin, Sao Paulo, Brazil
[2] Univ Sao Paulo, Sch Med, Hosp Clin, Dept Endocrinol, Sao Paulo, Brazil
[3] Univ Sao Paulo, Sch Med, Mol Genet & Hormones Lab LIM 42, Endocrinol & Dev Unit, Sao Paulo, Brazil
We report a case of a 17-year-old boy who had a giant congenital blue naevus with multiple satellite pigmented lesions. Later the patient developed melanoma arising in the pre-existing lesion. He also had gynaecomastia and was diagnosed as having aromatase excess syndrome. To our knowledge, the association of these two rare conditions has not been previously reported. Further studies should be performed to investigate this unusual combination, which may have a genetic, endocrine or local cutaneous link leading to its occurrence.