Case report
Correction of facial linear scleroderma ‘coup de sabre’ with BoneSource®

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Summary

Linear scleroderma is a subtype of localised scleroderma. When linear scleroderma occurs on the anterior portion of the scalp and forehead, it may assume an ivory-like, depressed configuration similar to the stroke of a sabre and called ‘coup de sabre’. Atrophic changes affect subcutaneous tissue and skin, with later involvement of the muscles and osteocartilaginous framework. Various operative interventions, such as skin flap, fat graft, dermofat graft and bone graft could be used for correction of this deformity, but there is no definite satisfactory treatment modality. We report the case of a 19-year-old female with a band-like indurated skin lesion with depression in the frontoparietal region of the scalp. Through bicoronal incision and subperiosteal dissection the defect was fully exposed. The depressive lesion was slightly hyperaugmented using BoneSource® (calcium phosphate hydroxyapatite cement; Stryker Leibinger Corp., Kalamazoo, MI, USA), considering skin and soft tissue atrophy. Surgical outcome was excellent in cosmetic and functional aspects without any complication. The patient was followed for 36 months after the operation; the defect was satisfactorily corrected and no postoperative problems have been found.

Section snippets

Case report

A 19-year-old female presented with a 2 × 15 cm-sized depressive lesion on her right eyebrow and temporoparietal area which accompanied alopecia and pigmentation. This lesion first appeared around the age of 4 years, and there has been no family history or medical history. She has not had any treatment on this lesion before.

Evidence of systemic symptoms, such as subcutaneous nodule or Raynand's phenomonen, were not found. Preoperative laboratory tests, including complete blood cell count, blood

Discussion

Scleroderma is a chronic disease of unknown origin with characteristic sclerotic change, caused by excessive deposition of collagen fibres and matrix protein. Scleroderma can be divided into two types depending on the region involved: systemic type and localised type. Systemic type can be classified into diffuse and limited, and localised type can be further classified into morphea, generalised morphea, linear scleroderma and eosinophilic fasciitis.1

As systemic scleroderma induces sclerotic

References (8)

  • M.K. Connolly

    Scleroderma

    Dermatol Ther

    (2001)
  • M. Sengezer et al.

    Repair of ‘coup de sabre’, a linear form of scleroderma

    Ann Plast Surg

    (1996)
  • O. Ronald

    Frontal linear scleroderma (en coup de sabre)

    Dermatol Online J

    (2003)
  • S.W. Park et al.

    Survival of grafts in coup de sabre

    Dermatol Surg

    (2002)
There are more references available in the full text version of this article.

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