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This is a PatientPlus article. PatientPlus articles are written for doctors and so the language can be technical. However, some people find that they add depth to the articles found in the other sections of this website which are written for non-medical people.

Synonyms: Localised scleroderma, morphea

Morphoea is a rare, persistent condition where the patient has areas of thickened skin.

MORPHOEA -CLOSE UP (DIS73.jpg)

Adults or children may be affected.

Aetiology

In most cases the cause of morphoea is unknown. It can however sometimes occur with systemic sclerosis or follow:1

  • Tick bites - it has been associated with Lyme disease2 - see our dedicated record.
  • Measles and other viral infections
  • Localised injury
  • Pregnancy
  • Autoimmune diseases including lichen sclerosus and lichen planus
Presentation
  • Plaques:
    • This is the most common type of morphoea.
    • Plaques are thickened, usually oval patches of skin between 1- 20 cm (or greater) in diameter.
    • They start as a mauve colour, then change to ivory white in the middle with a lilac edge over several months. Long-standing plaques may be brown.
    • Their surface is hairless, smooth and shiny. They tend not to sweat. Several asymmetrical plaques may be present on both sides of the trunk and limbs.
    • Sometimes the surface is hyper-pigmented with very little to feel.
  • Superficial morphoea:
    • Middle-aged women usually present with symmetrical mauve-coloured patches in the skin folds.
    • They are particularly common in the groin, armpits and under the breasts.
  • Linear morphea:
    • This may present on the scalp/forehead and limbs. This is most often found on the limb of a child.
    • A long and narrow plaque may be associated with underlying contractures.
    • A deep form affecting the scalp is called 'En coup de sabre' - a sabre cut. The hair is lost permanently and the underlying skull bone may shrink.
  • Pansclerotic disabling morphoea:
    • This affects children and results in extensive hardening of skin and underlying muscle.
    • The growth of bones may be affected.
  • Generalised morphoea:
    • This a rare condition with widespread skin thickening over the trunk.
Investigations

Blood tests have little role in assessment of morphoea.

Although a presumptive diagnosis can frequently be made on clinical findings, a biopsy can be used to confirm the diagnosis and delineate the depth of involvement.3

  • For plaque-type and generalised morphoea, a deep punch biopsy (including subcutaneous fat) is usually sufficient.
  • For linear and deep morphoea, an incisional biopsy extending down to muscle is required.

Radiography may be helpful in cases of linear or deep morphoea where involvement of the underlying bone is suspected. It can also be used to monitor paediatric patients for potential growth defects.

Differential diagnosis
Management

All suspected cases should be referred for diagnosis.

Unfortunately there is no available, effective treatment for most cases of morphoea. Although several have shown benefit in research, few controlled trials have been performed.
Therapy aimed at reducing inflammatory activity in early disease is more successful than attempts to decrease sclerosis in well-established lesions.3 Treatment of active lesions with superpotent topical or intralesional corticosteroids may help reduce inflammation and prevent progression. Topical tacrolimus has also been successful with mild to moderate lesions.4

Therapy with topical calcipotriene may also be beneficial. Night occlusion e.g. with plastic wrap is used to increase penetration of the medication.
Patients with potentially disabling generalised, linear or deep morphoea typically require more aggressive therapy.5
Occasionally the following are found helpful:

Prognosis

Generally the lesions gradually improve over a period of years and may even resolve spontaneously.

  • Plaque-type morphoea is usually active for several years then slowly softens, leaving brown staining and sometimes depressed areas of skin.
  • Linear morphoea tends to be more progressive and lasts longer, but also eventually improves, although sometimes deposits of calcium arise within the lesions.
  • Limbs affected by severe morphoea may be stiff and weak if there is muscle wasting.


Document references
  1. DermNet NZ; Morphoea. December 2006.
  2. Prinz JC, Kutasi Z, Weisenseel P, et al; "Borrelia-associated early-onset morphea": A particular type of scleroderma in childhood and adolescence with high titer antinuclear antibodies? Results of a cohort analysis and presentation of three cases. J Am Acad Dermatol. 2008 Nov 18. [abstract]
  3. Bergstrom KD, Schaffer JV; Morphoea. eMedicine, August 2006.
  4. Stefanaki C, Stefanaki K, Kontochristopoulos G, et al; Topical tacrolimus 0.1% ointment in the treatment of localized scleroderma. An open label clinical and histological study. J Dermatol. 2008 Nov;35(11):712-8. [abstract]
  5. Dutz J; Treatment options for localized scleroderma. Skin Therapy Lett. 2000;5(2):3-5. [abstract]

Internet and further reading
  • Oh CK, Lee J, Jang BS, et al; Treatment of atrophies secondary to trilinear scleroderma en coup de sabre by autologous tissue cocktail injection. Dermatol Surg. 2003 Oct;29(10):1073-5. [abstract]
  • Scleroderma Society
  • No authors listed; How can treatment of systemic sclerosis be improved?. By setting up a national database of all cases and entering patients into trials. UK Scleroderma Study Group. BMJ. 1998 Aug 1;317(7154):294-5.
  • Badea I, Taylor M, Rosenberg A, et al; Pathogenesis and therapeutic approaches for improved topical treatment in localized scleroderma and systemic sclerosis. Rheumatology (Oxford). 2008 Nov 20. [abstract]
Acknowledgements EMIS is grateful to Dr Hayley Willacy for writing this article. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2009.
Document ID: 434
Document Version: 23
Document Reference: bgp25994
Last Updated: 22 Jan 2009
Planned Review: 22 Jan 2011

The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest. Find out more about updating.

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