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Tumoral Calcinosis: An Uncommon Cause for a Mass in a Reconstructed Breast.
Koh, Eugene; Dean, Nicola R; Watson, David I; Carter, Christopher D.
Afiliação
  • Koh E; Department of Plastic and Reconstructive Surgery, Flinders Medical Centre, Bedford Park, South Australia, Australia; Department of Surgery, Department of Anatomical Pathology, SA Pathology, and Department of Pathology, Flinders University, Bedford Park, South Australia, Australia.
  • Dean NR; Department of Plastic and Reconstructive Surgery, Flinders Medical Centre, Bedford Park, South Australia, Australia; Department of Surgery, Department of Anatomical Pathology, SA Pathology, and Department of Pathology, Flinders University, Bedford Park, South Australia, Australia.
  • Watson DI; Department of Plastic and Reconstructive Surgery, Flinders Medical Centre, Bedford Park, South Australia, Australia; Department of Surgery, Department of Anatomical Pathology, SA Pathology, and Department of Pathology, Flinders University, Bedford Park, South Australia, Australia.
  • Carter CD; Department of Plastic and Reconstructive Surgery, Flinders Medical Centre, Bedford Park, South Australia, Australia; Department of Surgery, Department of Anatomical Pathology, SA Pathology, and Department of Pathology, Flinders University, Bedford Park, South Australia, Australia.
Plast Reconstr Surg Glob Open ; 4(5): e700, 2016 May.
Article em En | MEDLINE | ID: mdl-27579225
ABSTRACT
Tumoral calcinosis is a rare clinical and histopathological syndrome whose exact etiology is unknown. We present a case of a 57-year-old woman who presents with a painful lump in her right chest after bilateral breast reconstructions for bilateral asynchronous breast cancers. It is important to be aware of all possible differential diagnoses in a patient presenting with a chest mass after mastectomy and reconstruction for breast cancer as not all lesions of this type represent recurrent cancer.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article