全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Circumscribed Morphea and Breast Asymmetry in an Adolescent

DOI: 10.1155/2014/418257

Full-Text   Cite this paper   Add to My Lib

Abstract:

Morphea is a rare fibrosing disorder of the skin and underlying tissues. Circumscribed morphea presents with less than three discrete indurated plaques and breasts are commonly affected in women. We report the case of a 12-year-old female with a right infra-areolar, nontender, brownish patch and asymmetry of the right breast with 2 years of evolution. Skin biopsy showing thickening of the dermal collagen bundles confirmed the clinical diagnosis of morphea. After a 3-year follow-up period without progression of disease, reconstructive surgery is scheduled. Plaque morphea can involve all layers of the skin but associated breast deformity is rare. It can mimic benign and malignant breast disorders justifying the benefit for early tissue biopsy. Breast morphea generally has a good prognosis but hyperpigmentation and breast deformity in young girls have been rarely described. An early diagnosis can possibly lead to a therapeutic intervention with a different outcome, as it can be the source of severe psychological and social issues in a delicate period of development such as adolescence. 1. Introduction Morphea is a rare fibrosing disorder of the skin and underlying tissues, with equal prevalence both in adults and children, female predominance, and greater prevalence in caucasians. Circumscribed morphea presents with less than three discrete indurated plaques, predominantly on the trunk, and it can be superficial or deep [1–3]. Breasts are commonly affected in women, uniformly sparing the nipples [4]. 2. Case Presentation We report the case of a 12-year-old female patient who was referred to our outpatient clinic for evaluation of a patch in her right breast with 2 years of evolution. Pruritus and pain were denied. No musculoskeletal, respiratory, gastrointestinal, neurologic, and vascular symptoms were present. Her past medical history was irrelevant except for asthma and there was no family history of autoimmune diseases. At the physical exam, right breast asymmetry was noted, with an infra-areolar patch with 7 by 3?cm, with nontender, brownish, hyperpigmented, and hypopigmented areas (Figure 1). There were no other relevant cutaneous lesions. Figure 1: Right breast asymmetry, infra-areolar patch, with 7?cm, with nontender, brownish, hyperpigmented, and hypopigmented areas. A skin biopsy was performed, showing thickening of the collagen bundles in the dermis with a perivascular lymphohistiocytic infiltrate. No eccrine glands were present (Figure 2). These histologic findings confirmed the clinical diagnosis of morphea. Figure 2: Haematoxylin and

References

[1]  S. Christen-Zaech, M. D. Hakim, F. S. Afsar, and A. S. Paller, “Pediatric morphea (localized scleroderma): review of 136 patients,” Journal of the American Academy of Dermatology, vol. 59, no. 3, pp. 385–396, 2008.
[2]  J. J. Leitenberger, R. L. Cayce, R. W. Haley, B. Adams-Huet, P. R. Bergstresser, and H. T. Jacobe, “Distinct autoimmune syndromes in morphea: a review of 245 adult and pediatric cases,” Archives of Dermatology, vol. 145, no. 5, pp. 545–550, 2009.
[3]  A. V. Marzano, S. Menni, A. Parodi et al., “Localized scleroderma in adults and children. Clinical and laboratory investigations of 239 cases,” European Journal of Dermatology, vol. 13, no. 2, pp. 171–176, 2003.
[4]  N. Fett and V. P. Werth, “Update on morphea: part I. Epidemiology, clinical presentation, and pathogenesis,” Journal of the American Academy of Dermatology, vol. 64, no. 2, pp. 217–228, 2011.
[5]  C. J. Clark and D. Wechter, “Morphea of the breast—an uncommon cause of breast erythema,” The American Journal of Surgery, vol. 200, no. 1, pp. 173–176, 2010.
[6]  L. S. Peterson, A. M. Nelson, W. P. D. Su, T. Mason, W. M. O'Fallon, and S. E. Gabriel, “The epidemiology of morphea (localized scleroderma) in Olmsted County 1960–1993,” Journal of Rheumatology, vol. 24, no. 1, pp. 73–80, 1997.
[7]  K. J. Murray and R. M. Laxer, “Scleroderma in children and adolescents,” Rheumatic Disease Clinics of North America, vol. 28, no. 3, pp. 603–624, 2002.
[8]  D. A. Davis, P. R. Cohen, M. D. McNeese, and M. Duvic, “Localized scleroderma in breast cancer patients treated with supervoltage external beam radiation: radiation port scleroderma,” Journal of the American Academy of Dermatology, vol. 35, no. 6, pp. 923–927, 1996.
[9]  N. R. Bleasel, K. M. Stapleton, C. Commens, and V. A. Ahern, “Radiation-induced localized scleroderma in breast cancer patients,” Australasian Journal of Dermatology, vol. 40, no. 2, pp. 99–102, 1999.
[10]  J. Kushi and M. E. Csuka, “Generalized morphea after breast cancer radiation therapy,” Case Reports in Rheumatology, vol. 2011, Article ID 951948, 9 pages, 2011.
[11]  G. Shetty, F. Lewis, and S. Thrush, “Morphea of the breast: case reports and review of literature,” Breast Journal, vol. 13, no. 3, pp. 302–304, 2007.
[12]  T. Eidlitz-Markus, M. Mukamel, Y. Haimi-Cohen, J. Amir, and A. Zeharia, “Breast asymmetry during adolescence: physiologic and non-physiologic causes,” Israel Medical Association Journal, vol. 12, no. 4, pp. 203–206, 2010.
[13]  E. S. Treiber, N. S. Goldberg, and H. Levy, “Breast deformity produced by morphea in a young girl,” Cutis, vol. 54, no. 4, pp. 267–268, 1994.
[14]  S. A. Slavin and S. Gupta, “Reconstruction of scleroderma of the breast,” Plastic and Reconstructive Surgery, vol. 99, no. 6, pp. 1736–1741, 1997.
[15]  J. M. Weinberg, M. Russo, R. J. Hirsch, and P. C. Don, “Morphoea of the breast in a young girl,” Clinical and Experimental Dermatology, vol. 26, no. 6, pp. 497–498, 2001.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133