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Giant morphea-form basal cell carcinoma of the umbilicus: Successful debulking with vismodegib.
Orduz Robledo, Mariana; Lebas, Eve; Reginster, Marie-Annick; Baghaie, Mahmoud; Groves, Sabine; Nikkels, Arjen F.
Afiliación
  • Orduz Robledo M; Department of Dermatology, Liège University Hospital (CHU), Liège, Belgium.
  • Lebas E; Department of Dermatology, Liège University Hospital (CHU), Liège, Belgium.
  • Reginster MA; Department of Dermatopathology, Liège University Hospital (CHU), Liège, Belgium.
  • Baghaie M; Department of Radiodiagnostics, Liège University Hospital (CHU), Liège, Belgium.
  • Groves S; Private Practitioner, Liège University Hospital (CHU), Liège, Belgium.
  • Nikkels AF; Department of Dermatology, Liège University Hospital (CHU), Liège, Belgium.
Rare Tumors ; 10: 2036361318772938, 2018.
Article en En | MEDLINE | ID: mdl-29760872
Basal cell carcinoma of the umbilicus is very rare. The nodular subtype is the main representative. Giant basal cell carcinomas represent around 1% of all basal cell carcinomas. The hedgehog pathway inhibitor vismodegib is indicated for advanced basal cell carcinoma and CD56-negative immunostaining seems indicative for successful treatment. A 54-year-old man presented a 10 cm × 14 cm large and 4.5 cm deep morphea-form basal cell carcinoma with faint immunohistochemical CD56 expression arising from the umbilicus. A sequential treatment was initiated with debulking using vismodegib 150 mg per day for 4 months, followed by reconstructive surgery. To the best of our knowledge, this is the first report of a giant basal cell carcinoma of the morphea-form type of the umbilicus. The sequential treatment plan reduces the duration of vismodegib inherent adverse effects and significantly reduces the tumor mass prior to surgery. Besides increasing adherence to vismodegib treatment, this approach facilitates the surgical technique and improves cosmetic outcome.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Rare Tumors Año: 2018 Tipo del documento: Article País de afiliación: Bélgica

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Rare Tumors Año: 2018 Tipo del documento: Article País de afiliación: Bélgica