Volume 31, Issue 2 pp. 228-231

A case of focal dermal hypoplasia (Goltz) syndrome with exophytic granulation tissue treated by curettage and photodynamic therapy

R. Mallipeddi

R. Mallipeddi

Dermatological Surgery and Laser Unit, St John's Institute of Dermatology, St Thomas' Hospital, London, UK; and Department of Dermatology, Brighton General Hospital, Brighton, UK

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S. I. Chaudhry

S. I. Chaudhry

Dermatological Surgery and Laser Unit, St John's Institute of Dermatology, St Thomas' Hospital, London, UK; and Department of Dermatology, Brighton General Hospital, Brighton, UK

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C. R. Darley

C. R. Darley

Dermatological Surgery and Laser Unit, St John's Institute of Dermatology, St Thomas' Hospital, London, UK; and Department of Dermatology, Brighton General Hospital, Brighton, UK

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H. A. Kurwa

H. A. Kurwa

Dermatological Surgery and Laser Unit, St John's Institute of Dermatology, St Thomas' Hospital, London, UK; and Department of Dermatology, Brighton General Hospital, Brighton, UK

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First published: 08 February 2006
Citations: 18
Dr Raj Mallipeddi, Dermatological Surgery and Laser Unit, St John's Institute of Dermatology, St Thomas' Hospital, London, SE1 7EH, UK.
E-mail: [email protected]

Conflict of interest: none declared.

Summary

Focal dermal hypoplasia (Goltz) syndrome is a rare genetic disorder characterized by cutaneous, ectodermal and mesodermal defects. We present a case in which painful, exophytic granulation tissue has been the main symptom over the past 15 years. After unsatisfactory results with a number of treatment modalities including topical steroids, silver-nitrate applications, cryotherapy, curettage, excision and pulsed-dye laser, we achieved significant benefit with curettage in combination with photodynamic therapy. Although impaired wound healing has been described in focal dermal hypoplasia, this is, to our knowledge, the first time that pyogenic granuloma-like lesions have been reported.

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