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Scleroderma DermNet

The general term ' scleroderma ' is often used for both morphoea (localised scleroderma) and systemic sclerosis (systemic scleroderma). Distinguishing these two conditions is very important, as they vary greatly and require different treatment. Key features of systemic sclerosi Scleroedema (American spelling scleredema) is a type of cutaneous mucinosis of unknown cause. Scleroedema should not be confused with ' scleroderma ', in which the skin is fibrotic (morphoea and systemic sclerosis) It is also known as localised scleroderma. The term 'scleroderma' covers various types of morphoea and systemic sclerosis . Subtypes of morphoea vary according to the location of involved skin. Any subtype of morphoea can also result in deep or subdermal involvement of the underlying fat, fascia, muscle, or bone 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 Dermnet.com and the Dermnet Skin Disease Atlas are to be used only as a reference. Dermnet does not provide medical advice, diagnosis or treatment. Use of images for any purpose including but not limited to research, commercial, personal, or non-commercial use is prohibited without prior written consent

Systemic sclerosis DermNet N

  1. 102P Systemic sclerosis, commonly called scleroderma, CREST syndrome, Raynaud phenomenon. Watch later. Share. Copy link. Info. Shopping. Tap to unmute. If playback doesn't begin shortly, try.
  2. Summary: Scleromyxedema is a rare mucinous deposition disorder that shares clinical features with scleroderma but has important distinguishing features in clinical presentation and major organ complications that should be recognized. Patients typically respond well to therapy as highlighted in several larger series, but poor outcomes are reported in a few cases
  3. Dermnet is the largest independent photo dermatology source dedicated to online medical education though articles, photos and video. Dermnet provides information on a wide variety of skin conditions through innovative media
  4. Scleroderma is a long-lasting disease that affects your skin, connective tissue, and internal organs. It happens when your immune system causes your body to make too much of the protein collagen.

Scleroderma is an uncommon condition that results in hard, thickened areas of skin and sometimes problems with internal organs and blood vessels. Scleroderma is caused by the immune system attacking the connective tissue under the skin and around internal organs and blood vessels. This causes scarring and thickening of the tissue in these areas 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 Scleroderma (sklair-oh-DUR-muh) is a group of rare diseases that involve the hardening and tightening of the skin and connective tissues. Scleroderma affects women more often than men and most commonly occurs between the ages of 30 and 50. While there is no cure for scleroderma, a variety of treatments can ease symptoms and improve quality of life It is a form of localized scleroderma, which is an inflammatory condition that causes hard and thickened patches of skin on different areas of the body, with no involvement of internal organs. Morphea scleroderma is classified according to the shape and location of the patches, the amount of skin affected, and the depth of tissue involvement. The various classifications of morphea include circumscribed morphea, generalized morphea, and linear morphea

Limited scleroderma can cause tiny calcium deposits (calcinosis) to develop under your skin, mainly on your elbows, knees and fingers. You can see and feel these deposits, which sometimes are tender or become infected. Swallowing difficulties. Limited scleroderma commonly causes problems with the tube that connects the mouth and stomach (esophagus) Sclerosing or Morpheaform Basal Cell Carcinoma. Morpheaform BCC is an insidious tumor possessing innocuous surface characteristics that can mask its potential for deep, wide extension. The tumor is waxy, firm, flat-to-slightly raised, either pale white or yellowish, and resembles localized scleroderma, thus the designation morpheaform Systemic scleroderma, or systemic sclerosis, is an autoimmune rheumatic disease characterised by excessive production and accumulation of collagen, called fibrosis, in the skin and internal organs and by injuries to small arteries. There are two major subgroups of systemic sclerosis based on the extent of skin involvement: limited and diffuse. The limited form affects areas below, but not above, the elbows and knees with or without involvement of the face Scleroderma renal crisis is a rapidly progressive form of renal failure associated with hypertensive encephalopathy, severe headaches, seizures, retinopathy, microangiopathic haemolytic anaemia (MHA), and left ventricular failure. It is an uncommon (10% patients with diffuse SD) but serious complication of scleroderma, heralded by a ris This Guide for New and Future Patients™ is a companion document to the Scleroderma FAQ™, also available through the Scleroderma Education Project website: www.SclerodermaInfo.org.. Think of the main Scleroderma FAQ as the 50-page User Manual that came with your shiny new 65-inch ultra high definition TV. This Guide is the equivalent of the Getting Started Guide that also came with the TV

Atrophoderma of Pasini and Pierini (also known as Dyschromic and atrophic variation of scleroderma, Morphea plana atrophica, Sclérodermie atrophique d'emblée) is a disease characterized by large lesions with a sharp peripheral border dropping into a depression with no outpouching, which, on biopsy, elastin is normal, while collagen may be thickened Scleromyxedema is a rare, severe skin disorder. Signs and symptoms include abnormal accumulation of mucin in the skin ( mucinosis ), causing papular and sclerodermoid bumps; increased production of fibroblasts (connective tissue cells) in the absence of a thyroid disorder; and monoclonal gammopathy (abnormal proteins in the blood) Scleredema dermnet nz псориазис. dermnet nz nail psoriasis laser treatment for psoriasis in india; psoriasis and enemas psoriasis an vulva; scleromyxedema, scleredema, and eosinophilic fasciitis.dermatology services at Germain Dermatology include DermNet NZ. Venous eczema is a Necrolytic migratory erythema c. Psoriasis d Scleroderma is rare, and the signs and symptoms are similar to many other diseases. Doctors who most commonly diagnose scleroderma are dermatologists and rheumatologists. Dermatologists have expertise in diagnosing diseases that affect the skin, and rheumatologists specialize in diseases that affect the joints, muscles, and bones Sjukdom/tillstånd. Systemisk skleros är en ovanlig bindvävssjukdom som karaktäriseras av förändrat immunförsvar, försämrad blodcirkulation och ökad bindvävsproduktion i hud och inre organ, framför allt i mag-tarmkanal, lungor, hjärta och njurar. Sjukdomen kallades tidigare sklerodermi (skleros=förhårdning, derma=hud)

Scleroderma Temporal Arteritis: Dermnet.com and the Dermnet Skin Disease Atlas are to be used only as a reference. Dermnet does not provide medical advice, diagnosis or treatment. Use of images for any purpose including but not limited to research, commercial, personal, or non-commercial use is prohibited without prior written consent.. Systemic scleroderma is an autoimmune disorder that affects the skin and internal organs.It is characterized by the buildup of scar tissue (fibrosis) in the skin and other organs. The fibrosis is caused by the body's production of too much collagen, which normally strengthens and supports connective tissues Morphea is a skin condition that causes patches of reddish skin that thicken into firm, oval-shaped areas.It is a form of scleroderma.. Patches most often occur on the abdomen, stomach, and back, and sometimes on the face, arms and legs. Morphea is classified according to the localization of the lesions and the depth of tissue involvement into localized or circumscribed (limited to one or. Diagnosis. Because scleroderma can take so many forms and affect so many different areas of the body, it can be difficult to diagnose. After a thorough physical exam, your doctor may suggest blood tests to check for elevated levels of certain antibodies produced by the immune system Pseudoepitheliomatous hyperplasia (PEH) is a benign condition, characterized by hyperplasia of the epidermis and adnexal epithelium, closely simulating squamous cell carcinoma. PEH may be present in a number of conditions characterized by prolonged inflammation and/or chronic infection, as well as i

scleroderma). It tells you what it is, what causes it, what can be done about it, and where you can find out more about it. What is morphoea? Morphoea is a rare skin disorder where areas of skin become much thicker and firmer than normal. It is sometimes called 'localised scleroderma.' This ter Frontal linear scleroderma (en coup de sabre) Kenneth A Katz MD MSc Dermatology Online Journal 9(4): 10 From the Ronald O. Perelman Department of Dermatology, New York University Abstract. En coup de sabre is a type of linear scleroderma that presents on the frontal or frontoparietal scalp Scleroderma, often referred to as morphoea, is a term used to describe sclerosis of the skin, either localised or generalised, occurring in patients as the only or prominent feature. Scleroderma is best considered as a separate entity to systemic sclerosis, which unlike scleroderma results in Raynaud's phenomenon, sclerodactyly (spindled fingers), nailfold capillary changes and systemic.

Systemic sclerosis (scleroderma) is an autoimmune, collagen vascular disease of unknown aetiology that can be difficult to diagnose and treat. Skin manifestations include skin tightness and induration, often preceded by oedema. Skin induration initially affects the fingers and extends proximally - Scleroderma Image courtesy of www.dermnet.com. Used with permission. Swelling Around the Nail • Mucus cyst • Fibroma • Malignant melanoma. Masses • Pyogenic granuloma • Warts • Fibroma • Malignant melanoma. PreTest 1 • What disease would most likely produce these nails Sjögren's syndrome is a condition named after Henrik Sjögren, MD following the 1933 publication of his observations and characterization of the condition. It is the second most common autoimmune disorder, affecting 3 percent of the population 50 years or older.. In Sjögren's syndrome, the immune system mistakenly attacks the glands that produce fluids in the body

Scleroedema DermNet N

  1. Systemisk sklerose (sklerodermi) Systemisk sklerose er en bindevevssykdom som angriper mange organer og gir uttalt bindevevsdannelse, såkalt sklerose. Huden angripes nesten alltid. Prognosen avhenger av hvilken type systemisk sklerose det er. Systemisk sklerose kan gi mange ulike symptomer, blant annet hudforandring, svelgvansker, kortpustet.
  2. Erythema nodosum, a painful disorder of the subcutaneous fat, is the most common type of panniculitis. Generally, it is idiopathic, although the most common identifiable cause is streptococcal.
  3. Noninfectious penile lesions are classified by clinical presentation as papulosquamous (e.g., psoriasis), inflammatory (e.g., lichen sclerosus, lichen nitidus, lichen.
  4. Definition / general. Either localized (morphea) or systemic (involving skin of face, upper trunk, hands and arms, esophagus, heart and lungs) May have visceral disease without skin disease. May be associated with Raynaud phenomenon, Borrelia burgdorferi infection
  5. The three primary features of Aspirin Exacerbated Respiratory Disease (AERD) are asthma, chronic nasal polyps, and severe reactions to aspirin and other NSAIDs. A majority of patients also experience respiratory reactions to alcohol and an impaired sense of smell. It is estimated that 7 to 10% of adults with asthma have AERD. Among those with.
  6. Clinical signs reflect the sheer and close observatory quality of an astute physician. Many new dermatological signs both in clinical and diagnostic aspects of various dermatoses are being reported and no single book on dermatology literature gives a comprehensive list of these signs and postgraduate students in dermatology finds it difficult to have access to the description, as most of.

Morphoea DermNet N

  1. The Juvenile Scleroderma Network is an organization dedicated to provide emotional support and educational information to parents and their children living with juvenile scleroderma, to support pediatric research to identify the cause of and the cure for..
  2. DermNet NZ is an online resource about skin diseases developed by the New Zealand Dermatological Society Incorporated. DermNet NZ provides information about this condition. The National Organization for Rare Disorders (NORD) has a report for patients and families about this condition. NORD is a patient advocacy organization for individuals with.
  3. The word scleroderma means hard skin. There are two kinds of scleroderma: Localised scleroderma (also known as morphoea). This only affects the skin. It causes some areas of the skin to become harder than usual. This type of scleroderma is more common in children. See separate leaflet called Localised Scleroderma (Morphoea) for more details
  4. تليف. صورة مجهرية للقلب تظهر تليف (باللون الأصفر - على يسار الصورة) وترسب نشواني (باللون البني - على يمين الصورة). صبغة موفات. التليف هو عبارة عن تشكل زائد للنسيج الضام الليفي في نسيج أو عضو خلال.
  5. Thomas O. Willcox, Gregory J. Artz, in Neurology and Clinical Neuroscience, 2007 Tympanic Membrane. Pathology of the tympanic membrane includes perforations, atelectasis, and tympanosclerosis.Aside from its role in protecting the middle ear, the tympanic membrane is critical in receiving sound waves and efficiently transmitting them through the ossicular chain to the endolymph of the cochlea

Morphoea en coup de sabre DermNet N

Dermnet: Dermatology Pictures - Skin Disease Picture

The 1980 American College of Rheumatology Classification Criteria for Rheumatic Diseases is the most widely used system for systemic scleroderma. Because it was designed for research applications and not for clinical diagnosis, it has been criticized for its low sensitivity in identifying early disease and milder forms of systemic scleroderma such as CREST syndrome Kelsey CE, Torok KS. The Localized Scleroderma Cutaneous Assessment Tool: responsiveness to change in a pediatric clinical population. J Am Acad Dermatol 2013; 69:214. Teske NM, Jacobe HT. Using the Localized Scleroderma Cutaneous Assessment Tool (LoSCAT) to classify morphoea by severity and identify clinically significant change Localised scleroderma treatments. There are different types of localised scleroderma, mostly affecting the skin so many which involve creams for treatment as listed below.. Plaque morphoea. The most common form, plaque morphoea, does not always need treatment. This form often does not cause symptoms and often gradually improves or clears away after a number of years Raynaud's is a common condition thought to affect up to ten million people in the UK. Raynaud's symptoms are: A colour change in the extremities such as the hands or feet, often in response to cold conditions. Cold and numbness in the affected areas, such as the fingers and toes. Tingling or pain, especially as the circulation returns to the.

Morphea, also known as localized scleroderma, is a disorder characterized by excessive collagen deposition leading to thickening of the dermis, subcutaneous tissues, or both. Morphea is classified into circumscribed, generalized, linear, and pansclerotic subtypes according to the clinical presentation and depth of tissue involvement The sclera is the white part of the eye.When the sclera is swollen, red, tender, or painful (called inflammation), it is called scleritis.It is common for people with scleritis to have another disease, like rheumatoid arthritis or other autoimmune disease. This underlying disease causes many of the symptoms of scleritis Lichen sclerosus is a disorder that usually affects skin on the vulva (the area outside the vagina), anus or penis. It causes the skin to become discolored, thin, irritated and itchy. Blisters and sores may also form on the genitals. Rarely, these symptoms can appear on other parts of the body Poikiloderma vasculare atrophicans (PVA), is a cutaneous condition (skin disease) characterized by hypo- or hyperpigmentation (diminished or heightened skin pigmentation, respectively), telangiectasia and skin atrophy. Other names for the condition include prereticulotic poikiloderma and atrophic parapsoriasis. The condition was first described by pioneer American pediatrician Abraham Jacobi.

Lichen sclerosus is a relatively common chronic condition classically associated with the vulva.On the vulva is also known as chronic atrophic vulvitis.. On the glans penis it was referred to as balanitis xerotica obliterans, abbreviated BXO Lichen sclerosus (LS) is a chronic, inflammatory skin disease of unknown cause which can affect any body part of any person but has a strong preference for the genitals (penis, vulva) and is also known as balanitis xerotica obliterans (BXO) when it affects the penis.Lichen sclerosus is not contagious. There is a well-documented increase of skin cancer risk in LS, potentially improvable with. DermNet / CC BY-NC-ND Infant Symptoms . Many infants develop a type of seborrheic dermatitis called cradle cap, which causes redness and thick, scaly patches to form on the baby's scalp, ears, neck, or even in the diaper area. Like with adults, these patches are greasy and yellow to brown in color Pyoderma gangrenosum is a rare, inflammatory skin disease where painful pustules or nodules become ulcers that progressively grow. Pyoderma gangrenosum is not infectious. Treatments may include corticosteroids, ciclosporin, infliximab, or canakinumab.. The disease was identified in 1930. It affects approximately 1 person in 100,000 in the population

102P Systemic sclerosis, commonly called scleroderma

Raynaud's phenomenon is episodic vasospasm of the arteries or arterioles in the extremities (usually the digits) which leads to colour change including pallor, followed by cyanosis and/or rubor. Primary Raynaud's phenomenon (80-90% of cases) which occurs without an associated underlying condition. Secondary Raynaud's phenomenon (10-20% of. Morphea is a rare skin condition characterized by small red or purple patches that develop firm white or ivory centers. The affected skin becomes tight and less flexible. Morphea (mor-FEE-uh) is a rare condition that causes painless, discolored patches on your skin. Typically, the skin changes appear on the belly, chest or back INTRODUCTION. Lichen sclerosus (LS) is a benign, chronic, progressive dermatologic condition characterized by marked inflammation, epithelial thinning, and distinctive dermal changes accompanied by symptoms of pruritus and pain (picture 1A-C) [].The previous designation was lichen sclerosus et atrophicus; the et atrophicus was dropped because areas of thickening and hyperplasia often occur Morphea is a skin condition that involves a patch or patches of discolored or hardened skin on the face, neck, hands, torso, or feet

Scleromyxedema - PubMe

  1. Cheilitis, or lip inflammation, is a condition that manifests as red, dry, scaling, and itchy lips. Many different factors can cause cheilitis, such as an infection, chronic lip licking, or exposure to an allergen or irritant (including sun damage, lip cosmetics, oral hygiene products, fragrances, certain foods, as well as certain medications, such as accutane)
  2. Lichen sclerosus is a chronic inflammatory skin disorder that most commonly affects women before puberty or after menopause. Although rare, it can also be seen in men. When found in males, the disease is known as balanitis xerotica obliterans. Lichen sclerosus is characterized by skin changes of the external genitalia
  3. La morfea o esclerodermia localizada es un trastorno en el que los depósitos excesivos de colágeno conducen al engrosamiento de la dermis y a veces de los tejidos subcutáneos.. La grasa, fascias, músculos y huesos también pueden verse afectados, pero no los órganos internos como en la esclerosis sistémica. La morfea casi siempre evoluciona hacia la inactividad de forma natural
  4. 5 Skin Problems Associated With Scleroderma. DermNet NZ does not provide an online consultation service. If you have any concerns with your skin or its treatment, see a dermatologist for advice. Pustular skin conditions — codes and concepts open
  5. Toata luna iunie este luna constientizarii Sclerodermiei. Sclero = tare si derma = piele. Scleroza pielii este insa doar una din manifestarile acestei afectiuni. Complicatiile articulare, digestive,..

Dr. Mihai Lupu, Bukarest. 2 188 gillar · 65 pratar om detta. Sunt Mihai Lupu, medic dermatolog, pasionat de tot ce inseamna piele si bunastarea acesteia. Impreuna putem gasi cea mai buna solutie.. ea. To pre-qualify for this study you must: • Be over 18 years of age. • Have been diagnosed by a physician with Atopic Dermatitis (Eczema) at least one year ago. • Have tried topical treatments for Eczema that did not work for you or have used tablets or injectable drugs for Eczema Dermnet: Dermatology Pictures Skin Disease Pictures . Progresive systemic sclerosis . Von Madonnen, Rattenbissen und Tabaksbeuteln Die . CREST syndrome Pathology Student . Dr Amir s Blog: CREST Syndrome . Pin on Home Remedies . Sklerodaktylie und Raynaud Symptomatik bei CREST Syndrom

Systemic sclerosis | DermNet NZ

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Scleroderma: Definition, Types, Symptoms, Causes, and

Scleroderma - NH

Health Resources for Community Outreach. Find free resources and help spread the word about health conditions that affect the bones, joints, muscles, and skin. Find Resources for Community Outreach. Featured. Information on the Coronavirus (COVID-19) NIAMS Bone health information. NIAMS Coalition raises awareness about NIAMS research Are You Confident of the Diagnosis? Characteristic findings on physical examination Generalized myxedema is a manifestation of severe hypothyroidism developing over an extended period of time causing skin that appears waxy, doughy, swollen (although non-pitting) and dry. The initial symptoms include mental and physical sluggishness, constipation, loss of appetite, hoarseness in voice, leg.

Localised Scleroderma (Morphoea)

Sclerodactyly is a hardening of the skin of the hand that causes the fingers to curl inward and take on a claw-like shape. It is brought on by a condition called systemic scleroderma, or systemic. Postinflammatory hypopigmentation is a common cause of acquired hypopigmentary disorders. It can be a result of cutaneous inflammation, injury or dermatological treatment Bier spots were originally described in 1898 by Bier1 and are also called physiologic anemic macules, angiospastic macules and exaggerated physiologic speckled mottling of the skin.2 The condition is usually seen in people 20 to 40 years old and is more common in women than men.2 Clinically, the lesions appear as transient, small white macules with surrounding blanching erythema when the.

Scleroderma - Symptoms and causes - Mayo Clini

Porokeratosis is a rare skin disorder that is usually benign. Find out more about its six subtypes, who's at risk, how it's treated, and more Lichen simplex chronicus (see comment) Comment: Sections demonstrate hyperkeratosis, focal parakeratosis, a thickened granular layer and marked acanthosis. Characteristic vertically oriented, thickened collagen bundles are seen in the superficial dermis. The underlying dermis shows mild to moderate chronic inflammation Scleroderma, also known as systemic sclerosis, is an autoimmune connective tissue disorder characterised by multisystem fibrosis and soft tissue calcification. As such, it affects many separate organ systems, which are discussed separately: The remainder of this article is a general discussion of scleroderma Diagnosis. Treatment. Tophi are chunks of uric acid (monosodium urate) crystals that accumulate in and around joints and other parts of the body as the result of advanced gout. 1  A tophus around a joint can cause it to become swollen and misshapen and the skin that covers it to become stretched and taut, sometimes to the point of ulceration التهاب الجلد الدهني أو الأكزيما الدهنية أو النملة الدهنية ويعرف أيضًا بالتهاب الجلد المثي (بالإنجليزية: Seborrheic dermatitis أو seborrheic eczema أو seborrhea)‏ هو مرض مزمن، منتكس ويكون عادةً التهابًا جلديًا خفيفًا، ويسمى لدى الأطفال.

The term calcinosis cutis describes the deposition of insoluble calcium salts in the skin and subcutaneous tissue. There are five subtypes of calcinosis cutis: dystrophic, metastatic, idiopathic, iatrogenic, and calciphylaxis. The treatment of calcinosis cutis is often challenging and the subtype influences the approach to treatment Drugs.com provides accurate and independent information on more than 24,000 prescription drugs, over-the-counter medicines and natural products. This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. Data sources include IBM Watson Micromedex (updated 2 Aug 2021), Cerner Multum™ (updated 3 Aug 2021), ASHP (updated 30 July 2021.

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

Limited scleroderma - Symptoms and causes - Mayo Clini

Raynaud's - Getting Diagnosed. Raynaud's phenomenon is often diagnosed by a GP based upon your symptoms and your medical history. It is likely that they will also arrange some blood tests, so that any underlying health conditions can be ruled out Glossitis - Pictures, Symptoms, Treatment and Causes. Glossitis is a medical problem that consists of a smooth-looking, swollen tongue which also develops a color change.. The diagnosis of pernio can often be made on clinical grounds. Patients typically report the development of tender, pruritic, and/or painful digits following exposure to nonfreezing cold, damp conditions. The dorsal surfaces of the toes and fingers are the most common sites, but the ear, nose, thighs, or buttocks may also be affected

Sclerosing or Morpheaform Basal Cell Carcinoma - dermnet

Scleroderma Photo - Skin Disease PicturesMorphoea | DermNet NZExamining the Fingernails When Evaluating Presentinglook at my profile pic - Scleroderma - Inspire

Lichen planus (LP) is a pruritic, papular eruption characterised by its violaceous colour and polygonal shape, sometimes with a fine scale. It is most often found on the flexor surfaces of the upper extremities, genitalia and on the mucous membranes Histoplasmosis is an infection caused by a fungus called Histoplasma. The fungus lives in the environment, particularly in soil that contains large amounts of bird or bat droppings Melasma is a skin condition characterized by brown or blue-gray patches or freckle-like spots. It's often called the mask of pregnancy. Melasma happens because of overproduction of the cells that make the color of your skin Dermatomyositis is an idiopathic inflammatory myopathy with characteristic cutaneous findings that occur in children and adults (see the image below). This systemic disorder most frequently affects the skin and muscles but may also affect the joints; the esophagus; the lungs; and, less commonly, the heart. [ 1, 2] Dystrophic calcinosis may. Gangrene occurs when there is death and decay of body tissue. It is caused by a lack of blood supply and is most common in the lower limbs, but can occur in the upper limbs and intestine. Lack of blood supply is caused by three major mechanisms: infection, vascular or trauma Symptoms of pustular [PUHS-choo-lar] psoriasis include pustules (white, pus-filled, painful bumps) that may be surrounded by inflamed or reddened/discolored skin. The pus in pustules is caused by inflammation and is not contagious. Those with pustular psoriasis generally go in a cycle of the reddening/discoloring of the skin, followed by pustules and scaling