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Classification of juvenile localized scleroderma

Classification of juvenile localized scleroderma
Main group Subtype Description
(1) Circumscribed morphea (a) Superficial Oval or round circumscribed areas of induration limited to epidermis and dermis, often with altered pigmentation and violaceous, erythematous halo (lilac ring). They can be single or multiple.
(b) Deep Oval or round circumscribed deep induration of the skin involving subcutaneous tissue extending to fascia and may involve underlying muscle. The lesions can be single or multiple. Sometimes the primary site of involvement is in the subcutaneous tissue without involvement of the skin.
(2) Linear scleroderma (a) Trunk/limbs Linear induration involving dermis, subcutaneous tissue and, sometimes, muscle and underlying bone and affecting the limbs and the trunk.
(b) Head En coup de sabre (ECDS). Linear induration that affects the face and the scalp and sometimes involves muscle and underlying bone.
Parry Romberg or progressive hemifacial atrophy loss of tissue on one side of the face that may involve dermis, subcutaneous tissue, muscle, and bone. The skin is mobile.
(3) Generalized morphea   Induration of the skin starting as individual plaques (four or more and larger than 3 cm) that become confluent and involve at least two out of seven anatomic sites (head-neck, right upper extremity, left upper extremity, right lower extremity, left lower extremity, anterior trunk, posterior trunk).
(4) Panclerotic morphea   Circumferential involvement of limb(s) affecting the skin, subcutaneous tissue, muscle, and bone. The lesion may also involve other areas of the body without internal organs involvement.
(5) Mixed morphea   Combination of two or more of the previous subtypes. The order of the concomitant subtypes, specified in brackets, will follow their predominant representation in the individual patient (ie, mixed morphea [linear-circumscribed]).
Associated conditions: lichen sclerosus et atrophicus (LSA) and atrophoderma of Pasini and Pierini (APP) can be associated with the previous subtypes but are not included in the above classification. Source: Consensus conference, Padua, Italy, 2004.
Reproduced with permission from: Laxer RM, Zulian F. Localized scleroderma. Curr Opin Rheumatol 2006; 18:606. Copyright © 2006 Lippincott Williams & Wilkins.
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