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Linear morphea scleroderma

Morphea Genetic and Rare Diseases Information Center

Linear scleroderma Genetic and Rare Diseases Information

  1. A third subtype of morphea scleroderma, linear morphea, typically presents in children. It frequently appears as a linear patch of thickened, discolored skin on the arms or legs, but patches may also appear on an individual's forehead
  2. When involving the scalp and face, linear morphea has been referred to as morphea en coup d'sabre (linear scleroderma can produce a scarred appearance on the face and scalp similar to what might result from the strike of a sword). Linear morphea is the most common subtype of morphea in children
  3. Linear scleroderma is more common in children 10 and younger. These tight, thick bands can appear on the extremities, the back and front of the trunk, the buttocks or the face. They often appear as a single band in one body area and can be seen mixed with patches of morphea. Linear scleroderma can affect the bones and the muscles
  4. The cause of morphea is unknown. It may be caused by an unusual reaction of your immune system. In people at increased risk of morphea, it could be triggered by injury to the affected area, medications, chemical toxins, an infection or radiation therapy. The condition isn't contagious
  5. For severe or widespread morphea, your doctor may prescribe an immunosuppressive medication, such as oral methotrexate (Trexall), corticosteroid pills or both. Or your doctor may suggest hydroxychloroquine (Plaquenil) or mycophenolate mofetil. Each of these drugs has potential side effects

Linear Scleroderma - Dr

  1. Results: Linear morphea was the most common morphea subtype (50.1%, 291/581) in the cohort. Deep involvement was more common in linear (64.3%, 187/291) than other morphea subtypes. Linear morphea participants with deep involvement were more likely to have a limitation in range of motion (28.6%, 55/192) than those without (11.1%, 11/99, P <.001)
  2. Linear Scleroderma Linear scleroderma is a type of localized scleroderma that is most commonly diagnosed in children. Instead of patches of thickened skin commonly seen in the morphea -type of localized scleroderma, patients with the linear type have thick streaks of skin usually affecting the limbs and torso
  3. Linear scleroderma is a progressive loss of subcutaneous fat with pigment changes in the skin. It is a type of localized scleroderma in which the area of skin affected appears in a band. It typically first appears in young children on one side of the body. It can affect the trunk, arms, legs, face or neck, or multiple parts of the body
  4. Linear atrophoderma of Moulin is a rare subtype of atrophic and pigmented linear morphoea. Craniofacial linear morphoea was previously sub-classified as: En coup de sabre (linear atrophic band +/- sclerosis, classically on the forehead or scalp
  5. Morphea is a specific type of scleroderma that presents with dermal thickening and fibrotic plaques in the absence of internal organ involvement. 1 The lesions evolve through different phases, beginning with an inflammatory phase, which consists of erythematous, fibrotic plaques. Soon after, the center becomes white, while the edges remain red and active. 2 As the active phase subsides and the.
  6. Morphoea en coup de sabre is a variant of linear morphoea (a localised form of scleroderma) restricted to the frontoparietal region (forehead). The name 'en coup de sabre' (the blow of a sword) derives from the characteristic scar that indents the skin of the scalp and the underlying bone

Unlike systemic scleroderma or scleroderma, which affects an individual's internal organs, localized form of scleroderma/morphea does not cause any problem to internal organs. Instead, localized form of scleroderma affects the skin of a person only, while in some cases, it involves the underlying tissue and muscles of affected skin. The four types are: A) morphea B) generalized morphea C) linear scleroderma and D) en coup de sabre. A) Morphea - This is the most common type of localized scleroderma. It presents as one or a few (3-4) patches of skin thickening with different degrees of pigment changes. Some areas are dar Morphea is a localized form of scleroderma and affects primarily just the skin. Lesions are usually limited and most commonly just one lesion is found. However morphea can occur in a generalized form as well as guttate, nodular, subcutaneous and linear forms. Morphea is relatively uncommon and women are affected about three times as often as men

Frontal linear scleroderma (also known as en coup de sabre or morphea en coup de sabre) is a type of linear scleroderma characterized by a linear band of atrophy and a furrow in the skin that occurs in the frontal or frontoparietal scalp Linear scleroderma, also known as scleroderma en coup de saber, is a very focal form of scleroderma classically characterized by a linear band of atrophy involving the frontal or frontoparietal scalp and subjacent thinned calvaria associated with ipsilateral focal brain abnormalities.. In the brain beneath the skin lesion, focal atrophy and blurring of the gray-white matter interface can be. Linear morphea is the most common type of morphea found in school-aged children. The lesions may extend to the tissue under their skin, even to their muscles and bones, leading to deformities These include morphea and linear. Morphea. In localized morphea scleroderma, patches of hard, tight skin form on the body. These patches may enlarge or spread over time, but also may spontaneously disappear. Linear. This is a little more serious, and involves lines of hard, tight skin that form along the body

Linear Scleroderma - an overview ScienceDirect Topic

Scleroderma is a rare connective tissue disorder categorized into systemic sclerosis and localized scleroderma, also called morphea. Linear scleroderma of the scalp, also called en coup de sabre, is infrequently associated with neurologic symptoms. We describe a case of linear scleroderma en coup de Linear scleroderma manifests as a linear induration involving the dermis and subcutaneous tissue (possibly down to the fascia), muscles, tendons, and bones. Generalized morphea is characterized by four or more plaques larger than 3 cm, which tend to become confluent and affect two or more anatomic sites Linear scleroderma and morphea can coexist in the same patient. Other fibrosing conditions mentioned in this article include retroperitoneal fibrosis, mediastinal fibrosis, and Dupuytren contracture. The causes of localized fibrosing disorders are unknown. Genetic, infectious, and autoimmune mechanisms have been proposed

Morphea Scleroderma: What Is It, Causes, Treatment, and

Linear scleroderma is a focal atrophy of the skin, muscle and fat of the forehead and scalp heralded by the en coup de sabre (Strike of the Sabre) - a vertical, linear indentation of the forehead. Linear scleroderma also falls under the same umbrella diagnosis of morphea Localized scleroderma or morphea may be subdivided into 5 main types: bullous morphea, plaque morphea, generalized morphea, deep morphea, and linear scleroderma.2 Unlike most forms of localized scleroderma, which lack extracutaneous manifestations, a subset of linear scleroderma referred to as en coup de sabre has been associated with several.

Morphea Information for Patients RD

We describe the case of a 4-year-old girl with multiple morphea showing remarkable unilateral systematized distribution and whose linear lesions in the limbs appeared to follow Blaschko's lines. We suggest that linear scleroderma of the limbs, as well as frontoparietal scleroderma, may occur along the lines of Blaschko Morphea en coup de sabre is a form of linear scleroderma that primarily affects the head and neck and is named from its linear shape and characteristic lesions that resemble the wound from a saber. It is an inflammatory disease that results in excessive collagen deposition, sclerosis of involved skin and tissues, and progressive atrophy of involved areas

In linear morphea, skin irritation appears in a linear, rather than an oval shape. Damage can penetrate to the tissues below the skin, including muscle and bone. Pansclerotic morphea , the rarest and most severe form, usually affect children and involves the entire body, also penetrating through the skin into the bone Morphea may present at any age. In children, the linear subtype predominates while in adults' plaque and generalized subtypes are most common. Morphea occurs more frequently in women, especially in adults where female predominance is marked (5:1). Morphea is not the same as scleroderma (systemic sclerosis), and it does not become scleroderma

Morphea is a form of localized scleroderma that exists on a distinct part of the skin. The condition exists on the trunk and sometimes on the extremities and face. There are four different types of morphea, generalized morphea, pansclerotic morphea, linear morphea, and morphea of children Linear morphea on lower leg and foot. Linear scleroderma: Often beginning in childhood or the teenage years, this type causes a line of thickening skin, usually on an arm or leg. The hardening can extend beyond the skin, going deep into to the muscle and sometimes the bone Regardless of the type, morphea generally fades out in 3-5 years. However, people are often left with darkened skin patches and, in rare cases, muscle weakness. Morphea usually appears in people between the ages of 20 and 40. 2) Linear Scleroderma. Linear scleroderma describes a single line or band of thickened or abnormally colored skin Linear morphea en coup de sabre (ECDS) is a form of localized scleroderma that predominantly affects the pediatric population, with a median age of 10 years at presentation. The existence of neurologic findings in association with ECDS has been well described in the literature. Here we describe 4 patients with ECDS who presented with headaches, which were typical migraines in 3 of the patients

Treatment of Recalcitrant Generalized Morphea WithAtlas of Ophthalmology: Orbital haemangioma by Professor

Types of Scleroderma Johns Hopkins Medicin

Localized scleroderma, or morphea, is a rare condition that can present in different morphologies, including plaque, generalized, bullous, linear and deep.1 It is a discrete entity to systemic scleroderma in that it almost exclusively involves the skin and subcutaneous tissues, with cases of muscle and bone involve Localized scleroderma, often termed morphea in the dermatology literature, refers to a number of autoimmune conditions characterized by skin thickening and increased collagen deposition.It is the most common form of scleroderma, occurs generally in young adults, and has a predominance in the female sex. In morphea, the lesions are usually limited to the skin and subcutaneous fatty tissue. Morphea or localized scleroderma is a rare disorder with characteristic clinical features. The treatment of this disease involves the use of long term immunomodulators. Learn more about the clinical features, pathophysiology, laboratory diagnosis, treatment, and the prognosis. Learn more about it in our topic Scleroderma 1. Localised scleroderma/Morphea. Only affects the skin. Systemic sclerosis. Affects the organs in the body, including the skin. There are four types: Subtypes of systemic sclerosis. Limited cutaneous. 'Cutaneous' means skin and in limited cutaneous systemic sclerosis, the affected skin is limited to the hands, face, feet and.

Linear morphea of the forehead or en coup de sabre (ECDS) is an unusual variant of morphea. Morphea has an estimated annual population incidence of 2.7 per 100,000, although this incidence has been increasing slightly since the 1960s. Morphea is divided into subgroups that are based on clinical appearance and distribution Scleroderma is a condition that causes areas of the skin to become harder than usual. Hence the name scleroderma, which means hard skin. There are two kinds of scleroderma. Localised scleroderma (also known as morphoea or morphea) only affects the skin. In some cases it can spread to the tissues underneath the skin, such as muscles and bones Morphea is defined as a localized form of scleroderma which may include muscles as well. It does not occur commonly. It is a rare condition that leads to redness or purplish patches on your skin. It causes discoloration of skin to difficulty with the function of joints and muscles and other connective tissues

Morphea - Symptoms and causes - Mayo Clini

  1. ates in pediatric patients, followed by the plaque (25%) and generalized (5%) subtypes. Mechanism of the condition The most important thing to know about the mechanism of this disease is that overproduction of collagen by fibroblasts in affected tissues is common to all forms of morphea
  2. Morphea is a cutaneous fibrosing connective tissue disorder that represents a localized form of scleroderma (or systemic sclerosis). Morphea is distinguished from systemic sclerosis by the absence of sclerodactyly, Raynaud phenomenon, and nail fold capillary changes. The pathogenesis of morphea is not fully understood, but autoimmune.
  3. Linear morphea (linear scleroderma) is a form of localized scleroderma characterized by sclerotic lesions distributed in a linear, band-like pattern. A band-like linear induration, often with hypo or hyperpigmented areas, linear morphea most commonly seen on the leg but also arm and forehead (en coup de sabre) is characteristic
  4. Localized scleroderma can be divided into 3 main subtypes: morphea, linear scleroderma, and generalized morphea. Plaque morphea usually has a good prognosis and often does not require treatment
  5. Morphea or localized scleroderma is an idiopathic disorder characterized by local inflammation followed by fibrotic changes in the skin and subcutaneous tissues. Joint involvement has traditionally been thought to be related to the extent of skin disease, manifesting as arthralgia, impaired joint mobility, or joint contracture [ 1 , 2 ]
  6. Linear morphea (sometimes called linear scleroderma): Most common subtype in children However, clinicians have also used other descriptions for specific manifestations of morphea. Other forms of morphea you might hear mentioned are generalized morphea, bullous morphea, guttate morphea, pansclerotic morphea, deep morphea, and mixed morphea
  7. The two types of localized scleroderma are morphea and linear scleroderma. Scleroderma In recent decades, autologous fat tissue grafting has been successfully used to regenerate atrophic or fibrotic skin for a large number of clinical conditions such as radio dermatitis, burning scars, linear scleroderma , and different types of morphea [8]

Morphea - Diagnosis and treatment - Mayo Clini

Linear morphea is most common in children and affects the limbs, face, and/or scalp, typically as a single lesion ( Fig. 3-2 ). In children, linear morphea of the limbs can cause focal growth arrest and limb length discrepancies due to disruption of the growth plate. Joint contractures are a particular concern when the lesion crosses a joint Depending on the shape and area of skin affected, localized scleroderma can be divided into two groups: morphea and linear scleroderma. Symptoms of localized scleroderma . Morphea is characterized by thick, hard patches of skin that are white or yellow, and ringed with a purplish halo that may itch but is usually not painful

Linear morphea: Clinical characteristics, disease course

  1. En coup de sabre: This is a deep-seated form of linear scleroderma affecting the scalp and temple like from a sabre (sword). The hair is lost permanently and the underlying skull bone may shrink. Generalized morphea: This is a very rare form of morphea with widespread skin thickening over the body
  2. This primarily involves the deep dermis, subcutaneous tissue, fascia, or superficial muscle. The lesions are more diffuse than in linear scleroderma and do not demonstrate a linear pattern. Subtypes include subcutaneous morphea, morphea profunda, disabling pansclerotic morphea of childhood, and eosinophilic fasciitis
  3. Go to Tammy: Mother of Son with Linear and Morphea Scleroderma. SCLERO.ORG is the world's leading nonprofit for trustworthy research, support, education and awareness for scleroderma and related illnesses. We are a 501 (c) (3) U.S.-based public charitable foundation, established in 2002. Meet Our Team

Morphea is localized scleroderma confined to the skin. It most commonly affects the trunk but also occurs on the face and extremities. The four clinical variants include plaque-type morphea, generalized morphea, linear morphea (en coupe de sabre), and pansclerotic morphea of children (morphea profunda) which case it is called morphea or linear scleroderma. Medications used to treat scleroderma include peni-cillamine and other immunosuppressive agents, col-chicine, and glucocorticoids. Table 1 illustrates the scleroderma subtypes. Dietary Factors Pathological changes in the gastrointes-tinal tract in patients with scleroderma can resul

Under the term localized scleroderma a spectrum of conditions is classified, ranging from localized plaques of morphea of cosmetic importance only, to deep lesions of linear scleroderma and eosinophilic fasciitis, which can result in considerable morbidity. The etiology is unknown; environmental, infectious, and autoimmune causes have been. Morphea, also known as localized scleroderma, is an idiopathic, inflammatory disorder that causes sclerotic changes in the skin. Morphea is distinct from systemic sclerosis (scleroderma), an autoimmune connective tissue disorder characterized by acral or diffuse cutaneous sclerosis and frequent systemic manifestations

*Viewer Discretion Advised- Some medical images may not be suitable for all audiences.Discussion of the different subtypes of localized scleroderma (morphea).. Localized scleroderma, or morphea, is a chronic disease that causes a thickening and induration of the skin. For plaque type morphea, the treatments include super-potent corticosteroids and calcipotriol. For the more generalized forms, as well as the linear forms, UVA is currently the best therapeutic modality Morphea is the most common form of scleroderma in children. It presents in irregular patches on the skin, that initially appear small and pink and will eventually harden, leading to a diagnosis of scleroderma. The outlook is excellent for children with morphea, because these patches will eventually soften and fade, leaving no serious, long-term.

Linear Scleroderma - Scleroderma New

Linear Scleroderma: As suggested by its name, linear scleroderma is characterized by a single line or band of thickened, unusually coloured skin. Typically, the line runs down an arm or leg, but in some people it runs down the forehead. Some people have both morphea and linear scleroderma linear scleroderma localized scleroderma in a bandlike lesion with discoloration of the skin and atrophy of skin, subcutaneous tissue, muscle, and bone. See also coup de sabre. Called also linear morphea Linear scleroderma en coup de sabre is a rare subset of localized scleroderma, a distinct and separate disease entity from systemic scleroderma (1). Localized scleroderma is also referred to as Morphea, and is differentiated from systemic sclerosis by the absence of sclerodactyly, Raynaud's phenomenon, capillaroscopi Localized scleroderma is a milder type. Localized scleroderma rarely spreads and rarely affects your internal organs. Localized scleroderma is either morphea or linear in type. If you have morphea scleroderma, you may have waxy patches of skin that vary in size and shape. Linear scleroderma begins as a streak or line of hardened, waxy skin Morphea en coup de sabre is a type of linear scleroderma that has a tendency to leave disfiguring atrophic scars. A variety of treatments have been used for linear morphea, with varying degrees of success. Treatments consist of those intended to inhibit the progression and inflammatory phase of the disease and those to treat the residual atroph

Linear Scleroderma Children's Hospital of Philadelphi

  1. Linear morphea Also known as linear scleroderma, this is the most common variant of morphea or localized scleroderma in childhood comprising up to 65% of cases of juvenile morphea. It appears usually as a single unilateral indurated lesion with a linear distribution
  2. Scleroderma (from the Greek scleros, to harden) is a term that describes the presence of thickened, hardened skin.It may affect only limited areas of the skin (morphea), most or all of the skin (scleroderma), or also involve internal organs (systemic sclerosis)
  3. Generalized morphea involves more than four patches on several areas of the body. Linear morphea involves linear lesions on the skin surface and also deeper beneath the skin. Pansclerotic morphea affects deeper skin tissue and muscles, joints or bones. This type of morphea may also restrict movement because it affects the joints

Linear scleroderma is the most common subtype of localized scleroderma (LoS) in children. It can be associated with extracutaneous manifestations and long-term sequelae. Thus, appropriate diagnosis and management are key to improve the prognosis. linear scleroderma , morphea , Parry-Romberg syndrome , progressive hemifacial atroph The reason that localized scleroderma (other than linear) was not included in the orange card definition was 2‐fold. First, it was anticipated that nonspecialists would find difficulty in diagnosing variants of localized scleroderma/morphea other than linear, which is generally easier to diagnose than other forms of localized scleroderma Topical calcipotriene for morphea/linear scleroderma. Localized scleroderma is characterized by circumscribed fibrotic plaques. 1 If overlying joints, localized scleroderma can also lead to contractures and limb shortening. Localized scleroderma is treated most commonly with potent topical corticosteroids that may sometimes cause improvement.

Morphoea DermNet N

Linear morphea (LM) is a rare localized variant of scleroderma, and the term en coup de sabre (ECDS) refers to atrophic linear depression of the frontal or frontoparietal forehead extending to the scalp. The underlying etiology of LM is still poorly understood, although some have suggested that morphea represents a mosaic form of systemic. Linear morphea: Trunk/limb variant: Linear indurations: Dermis and subcutaneous tissue (may involve muscle and bone) Trunk/limb (linear scleroderma) Head variant (en coup de sabre) Linear indurations: Dermis of the frontoparietal area (may involve muscle, bone, and central nervous system) Face and scalp: Parry-Romberg syndrom plaque-morphea; linear scleroderma en coup de sabre central nervous system nflammation; Linear scleroderma en coup de sabre (LSCS) and plaque-morphea are both variants of localised scleroderma. 1 LSCS presents as band-like sclerotic skin lesions, usually involving a single unilateral change in the frontoparietal area of the head. This is characterised by atrophy and a furrow of the. In linear morphea erythematous or violaceous patches or plaques are seen with central sclerosis and active red border distributed in linear configuration which over time become sclerotic, white or hypopigmented. We report a series of cases encompassing all the three clinical variants of linear morphea

A Case of Minocycline-induced Linear Morphea Reactivation

Morphea, also known as localized scleroderma, is a rare disease seen in both adults and children. Most pediatric patients have the linear subtype, which can extend deeply into the subcutaneous tissue, muscle, and bone. Linear morphea on the head and neck, called en coup de sabre (ECDS), and Parry-Romberg syndrome (PRS), also called progressive. Morphea, also called localized scleroderma, is a sclerosing skin disorder that resembles scleroderma (systemic sclerosis) in terms of cutaneous histopathological features, but differs demographically and clinically. Hallmark clinical and serological features of scleroderma (sclerodactyly, Raynaud's phenomenon, internal organ involvement, and. Maybe: While it is not given in high doses as in chemotherapy, methotrexate can be used to treat coup en sabre, a linear form of scleroderma which resembles a cut of the sword. It may work in some cases but risk versus benefit needs to be carefully analyzed

Linear morphea on lower leg and foot: Linear scleroderma: Often beginning in childhood or the teenage years, this type causes a line of thickening skin, usually on an arm or leg. The hardening can extend beyond the skin, going deep into to the muscle and sometimes the bone Scleroderma is a rare disease of the connective tissue. It can cause the tissue in skin, joints, and internal organs to thicken and stiffen. There are three major forms of the disease: Localized scleroderma (can be morphea or linea) — Usually affects only the skin in isolated parts of the body

Morphea is characterized by skin thickening with increased quantities of collagen in the indurative lesion. 2 This entity is subdivided into linear scleroderma, plaque morphea, deep morphea, bullous morphea, and generalized morphea. 3, 4, 5 Each one of these subtypes may affect the face with varying intensity. LoS is the most common subtype of. Morphea is a type of localised scleroderma, it affects the skin and sometimes underlying muscles and joints which can cause disability but it never affects i..

Morphoea en coup de sabre DermNet N

Linear scleroderma: lt;p|>||||| | |||Morphea|||| |Classification and external resources||||| 10|| 9|| DiseasesDB|| eM... World Heritage Encyclopedia, the aggregation. Linear morphea: This is the most common type of morphea seen in children. It causes long, linear-like plaque areas to appear across the body. These linear patches might travel in the same direction as the arms or legs SCLERODERMA LOCALIZED-. a term used to describe a variety of localized asymmetrical skin thickening that is similar to those of systemic scleroderma but without the disease features in the multiple internal organs and blood vessels. lesions may be characterized as patches or plaques morphea bands linear or nodules Scleroderma is a complex, multisystem disease that often progressively affects the skin, blood vessels, lungs, digestive tract, kidneys, heart, muscles and bones. Scleroderma is inflammatory and has an autoimmune component. It has been associated with exposure to a variety of chemical agents, but the exact cause is not yet known

Is Morphea The Same As Scleroderma? - ePainAssis

linear morphea - induration is linear, may involve dermis, subcutaneous tissue, muscle, and bone . linear morphea (linear scleroderma) primarily affects extremities ; contractures may occur when lesion crosses joint ; en coup de sabre - on face or scalp with appearance of stroke from a sword, usually on paramedian forehead. Together, we are more than scleroderma. Scleroderma (also known as systemic sclerosis) is a rare, autoimmune disease that can affect connective tissue throughout the whole body, both inside and out. 1,2 Everyone with scleroderma has a slightly different combination of symptoms, which is why there are many different experiences with scleroderma. 2 Scleroderma is a progressive disease that can produce complications ranging from mild to severe. Its two main forms are: Localized scleroderma, which affects a local area of the skin (and is most often treated by dermatologists) Systemic sclerosis, which can affect the skin, joints, blood vessels and internal organs En coup de sabre is a rare subtype of linear morphea that involves the frontoparietal scalp and forehead. 7,12,13 It manifests as a solitary, linear, fibrous plaque that involves the skin, underlying muscle, and bone. 7 Although most cases present with a single lesion, multiple lesions can occur. 8 The exact etiology of this disease remains to.

Localized scleroderma: clinical spectrum and therapeuticScleroderma Research Papers on the Six Different StrandsMorphoeaRare Skin Diseases: Orphan Market Opportunities 17 Orphan

Linear scleroderma tends to affect children and adolescents, while morphea is more common in adults. However, both can coexist in the same patient. First, areas of hard and dry skin develop in the hands, arms, face, or leg. Then, plaques (morphea) or wide strips (linear scleroderma) appear. Plaques are round or oval, often with a white. Morphea involves isolated patches of hardened skin and discriminates from systemic sclerosis by its supposed lack of internal organ involvement. Classification. The most widely used classification divides morphea into five general subtypes: plaque morphea, generalized morphea, linear scleroderma, bullous morphea, and deep morphea title = Pediatric morphea (localized scleroderma): Review of 136 patients, abstract = Background: Morphea is an autoimmune inflammatory sclerosing disorder that may cause permanent functional disability and disfigurement. Objectives: We sought to determine the clinical features of morphea in a large pediatric cohort Localized scleroderma [morphea] L94.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2021 edition of ICD-10-CM L94.0 became effective on October 1, 2020. This is the American ICD-10-CM version of L94.0 - other international versions of ICD-10 L94.0 may differ Localized scleroderma is different from systemic scleroderma, in that it only affects the skin, related tissues, and muscles below the tissues. It can go away on its own; however, serious and disabling cases can also occur. There are two subtypes of this form of scleroderma: morphea and linear Localized Scleroderma: A term used to describe a variety of localized asymmetrical SKIN thickening that is similar to those of SYSTEMIC SCLERODERMA but without the disease features in the multiple internal organs and BLOOD VESSELS. Lesions may be characterized as patches or plaques (morphea), bands (linear), or nodules