A chronic skin disease characterized by small follicular papules, disseminated reddish-brown scaly patches, and often, palmoplantar hyperkeratosis. The papules are about the size of a pin and topped by a horny plug.
A mild exanthematous inflammation of unknown etiology. It is characterized by the presence of salmon-colored maculopapular lesions. The most striking feature is the arrangement of the lesions such that the long axis is parallel to the lines of cleavage. The eruptions are usually generalized, affecting chiefly the trunk, and the course is often self-limiting.
A name originally applied to a group of skin diseases characterized by the formation of fine, branny scales, but now used only with a modifier. (Dorland, 27th ed)
Group of mostly hereditary disorders characterized by thickening of the palms and soles as a result of excessive keratin formation leading to hypertrophy of the stratum corneum (hyperkeratosis).
A malignant skin neoplasm that seldom metastasizes but has potentialities for local invasion and destruction. Clinically it is divided into types: nodular, cicatricial, morphaic, and erythematoid (pagetoid). They develop on hair-bearing skin, most commonly on sun-exposed areas. Approximately 85% are found on the head and neck area and the remaining 15% on the trunk and limbs. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1471)
A medical specialty concerned with the skin, its structure, functions, diseases, and treatment.
Studies in which the presence or absence of disease or other health-related variables are determined in each member of the study population or in a representative sample at one particular time. This contrasts with LONGITUDINAL STUDIES which are followed over a period of time.
Tumors or cancer of the SKIN.
The indelible marking of TISSUES, primarily SKIN, by pricking it with NEEDLES to imbed various COLORING AGENTS. Tattooing of the CORNEA is done to colorize LEUKOMA spots.
Abnormal responses to sunlight or artificial light due to extreme reactivity of light-absorbing molecules in tissues. It refers almost exclusively to skin photosensitivity, including sunburn, reactions due to repeated prolonged exposure in the absence of photosensitizing factors, and reactions requiring photosensitizing factors such as photosensitizing agents and certain diseases. With restricted reference to skin tissue, it does not include photosensitivity of the eye to light, as in photophobia or photosensitive epilepsy.
A syndrome characterized by headache, neck stiffness, low grade fever, and CSF lymphocytic pleocytosis in the absence of an acute bacterial pathogen. Viral meningitis is the most frequent cause although MYCOPLASMA INFECTIONS; RICKETTSIA INFECTIONS; diagnostic or therapeutic procedures; NEOPLASTIC PROCESSES; septic perimeningeal foci; and other conditions may result in this syndrome. (From Adams et al., Principles of Neurology, 6th ed, p745)

The relationship between pityriasis rubra pilaris and inflammatory arthritis: case report and response of the arthritis to anti-tumor necrosis factor immunotherapy. (1/12)

Pityriasis rubra pilaris (PRP) refers to a group of erythematous, scaling dermatologic conditions that have been associated with seronegative arthritis. We report a case of polyarthritis in a young man with PRP in which magnetic resonance imaging suggested an entheseal-based pathology for the joint disease. The arthritis, but not the skin condition, demonstrated dramatic response to anti-tumor necrosis factor immunotherapy.  (+info)

Pityriasis rubra pilaris. (2/12)

Pityriasis rubra pilaris is a chronic, papulosquamous dermatosis of unclear etiology. The case of a 61-year-old man with pityriasis rubra pilaris is presented. The clinical forms, histopathologic features, and treatment options of pityriasis rubra pilaris are reviewed.  (+info)

A review of pityriasis rubra pilaris and rheumatologic associations. (3/12)

Pityriasis rubra pilaris (PRP) is a rare group of hyperkeratotic, papulosquamous disease that can be acquired or inherited. There have been reported cases of rheumatologic associations, mainly arthritis and dermatomyositis. In this review article, we will explore the clinical presentation and classification, rheumatologic associations and treatment modalities of PRP. In addition, we will also report a case of PRP with seronegative arthritis.  (+info)

Pityriasis rubra pilaris, type 1. (4/12)

A 57-year-old woman presented with a history of dry skin with an associated sensation of burning and itching. It had been previously diagnosed as psoriasis. Clinical and histopathologic examination were consistent with pityriasis rubra pilaris, and treatment consisted of acitretin and narrow-band ultraviolet B phototherapy. Pityriasis rubra pilaris is a papulosquamous disorder of unknown etiology, which can be treated with retinoids, methotrexate, cyclosporine, and narrow-band phototherapy.  (+info)

Pityriasis rubra pilaris, type IV. (5/12)

A 4-year-old girl presented with a 3-year history of demarcated, salmon-pink, hyperkeratotic plaques, which were symmetrically distributed on the elbows, knees, ankles, and dorsal aspects of the hands and feet. A diffuse, orange-pink palmoplantar keratoderma was also evident. Clinical and histologic findings were consistent with a diagnosis of pityriasis rubra pilaris (PRP), type IV (circumscribed juvenile). Type IV PRP develops in prepubertal children, is typically localized to the distal aspects of the extremities, and has an unpredictable course. Although ultraviolet (UV) radiation can potentially exacerbate PRP, our patient has improved with broad-band UVB phototherapy.  (+info)

Adult onset pityriasis rubra pilaris. (6/12)

Pityriasis rubra pilaris (PRP) has always been an intriguing topic ever since its inception. It is a group of chronic disorders characterized by reddish orange plaques with pityriasiform scaling showing follicular keratoses, palmoplantar keratoderma, and sometimes, erythroderma. It occurs all over the world but with racial variations. Its incidence might vary and the age at onset, behavior, clinical appearance, and prognosis are considered to be very important for its classification. It may manifest either as Type I classical adult onset PRP, Type II atypical adult (onset) PRP, or Type VI PRP (HIV-associated PRP pityriasis rubra pilaris) in contrast to classical juvenile (Type III) and circumscribed juvenile (Type IV) encountered among children. Its diagnosis is largely clinical with microscopic pathology being a useful supplement, but it continues to be a therapeutic dilemma. We review the epidemiology of adult onset PRP here and take stock of the prevalent treatment options.  (+info)

Systemic sclerosis in a patient with pityriasis rubra pilaris. (7/12)

Pityriasis rubra pilaris (PRP) is a rare, chronic erythematous squamous disorder of unknown etiology. It has been found in association with several autoimmune diseases, including thyroiditis, myositis, myasthenia gravis and vitiligo. Herein we report a case of systemic sclerosis in a patient with classic adult pityriasis rubra pilaris. A 38 year old woman with classic adult type 1 pityriasis rubra pilaris (PRP) developed progressive skin thickening of the trunk, face, upper and lower extremities after 2 years of PRP treatment with topical emollients and steroids. Clinical examination and immunological findings were consistent with SSc. Co-existence of these two rare conditions is documented for the first time.  (+info)

Letter: Adenocarcinoma of the lung associated with pityriasis rubra pilaris. (8/12)

We describe a case of pityriasis rubra pilaris refractory to conventional treatment, found to be associated with an unrecognized primary adenocarcinoma of the lung. Complete resolution of the eruption followed surgical resection of the tumor.  (+info)

Pityriasis rubra pilaris (PRP) is a rare, chronic inflammatory skin disorder characterized by the development of reddish orange scaly patches and thickened plaques on the skin. It primarily affects the scalp, face, knees, elbows, and palms and soles. The condition can also cause reddening and thickening of the skin over the entire body in severe cases.

The key features of PRP include follicular papules (small bumps around hair follicles) that may be surrounded by a white collarette of scale, and areas of skin that are redder than normal (erythema). The condition can also cause nail changes, such as thickening and ridging.

PRP is thought to be caused by an abnormal immune response, although the exact cause is not known. It can affect people of all ages, but it is most commonly seen in children and adults between 40-60 years old. The condition typically progresses through several stages, with periods of worsening symptoms followed by periods of improvement or remission.

Treatment for PRP may include topical therapies, such as corticosteroids or retinoids, as well as systemic treatments, such as immunosuppressive drugs or biologics. The choice of treatment depends on the severity and extent of the condition, as well as other factors.

Pityriasis rosea is a common, self-limited skin condition characterized by the development of oval or round, scaly, pinkish, inflamed patches on the skin. The initial lesion, known as the "herald patch," often appears before other lesions and measures 2-10 cm in diameter. It usually starts as a single, solitary, scaly, raised patch on the trunk that precedes the generalized eruption by about 1-2 weeks. The rash typically spreads to involve the chest, abdomen, back, arms, and legs, sparing the face, palms, and soles.

The rash is often asymptomatic but can be pruritic (itchy) in some cases. It usually resolves within 6-12 weeks without any treatment, although topical treatments such as corticosteroids or antihistamines may be used to relieve itching. The exact cause of pityriasis rosea is not known, but it is thought to be caused by a viral infection. It is more common in young adults and is more prevalent in the spring and fall seasons.

Pityriasis is a general term used to describe a group of skin conditions characterized by scaling. It includes several specific types, the most common being Pityriasis rosea and Pityriasis simplex capillitii (also known as dandruff).

1. Pityriasis rosea: This is a temporary skin rash that often begins with a single, round, scaly patch on the chest, abdomen, or back. A few days to weeks later, more patches appear. These patches are oval and scaly, and they may be pink, red, or tan. The rash usually lasts about 6-8 weeks.

2. Pityriasis simplex capillitii: This is a very common condition characterized by flaking or scaling of the scalp, which is often referred to as dandruff.

The term "pityriasis" comes from the Greek word "pitýrios," which means "bran."

Keratoderma, palmoplantar is a medical term that refers to a group of skin conditions characterized by thickening and hardening (hyperkeratosis) of the skin on the palms of the hands and soles of the feet. This condition can affect people of all ages, but it's most commonly seen in children.

The thickening of the skin is caused by an overproduction of keratin, a protein that helps to form the tough, outer layer of the skin. In palmoplantar keratoderma, this excess keratin accumulates in the stratum corneum, the outermost layer of the epidermis, leading to the formation of rough, scaly, and thickened patches on the palms and soles.

There are several different types of palmoplantar keratoderma, each with its own specific symptoms and causes. Some forms of the condition are inherited and present at birth or develop in early childhood, while others may be acquired later in life as a result of an underlying medical condition, such as atopic dermatitis, lichen planus, or psoriasis.

Treatment for palmoplantar keratoderma typically involves the use of emollients and keratolytic agents to help soften and remove the thickened skin. In some cases, oral retinoids or other systemic medications may be necessary to manage more severe symptoms. It's important to consult with a healthcare provider for an accurate diagnosis and treatment plan.

Carcinoma, basal cell is a type of skin cancer that arises from the basal cells, which are located in the lower part of the epidermis (the outermost layer of the skin). It is also known as basal cell carcinoma (BCC) and is the most common form of skin cancer.

BCC typically appears as a small, shiny, pearly bump or nodule on the skin, often in sun-exposed areas such as the face, ears, neck, hands, and arms. It may also appear as a scar-like area that is white, yellow, or waxy. BCCs are usually slow growing and rarely spread (metastasize) to other parts of the body. However, they can be locally invasive and destroy surrounding tissue if left untreated.

The exact cause of BCC is not known, but it is thought to be related to a combination of genetic and environmental factors, including exposure to ultraviolet (UV) radiation from the sun or tanning beds. People with fair skin, light hair, and blue or green eyes are at increased risk of developing BCC.

Treatment for BCC typically involves surgical removal of the tumor, along with a margin of healthy tissue. Other treatment options may include radiation therapy, topical chemotherapy, or photodynamic therapy. Prevention measures include protecting your skin from UV radiation by wearing protective clothing, using sunscreen, and avoiding tanning beds.

Dermatology is a medical specialty that focuses on the diagnosis, treatment, and prevention of diseases and conditions related to the skin, hair, nails, and mucous membranes. A dermatologist is a medical doctor who has completed specialized training in this field. They are qualified to treat a wide range of skin conditions, including acne, eczema, psoriasis, skin cancer, and many others. Dermatologists may also perform cosmetic procedures to improve the appearance of the skin or to treat signs of aging.

A cross-sectional study is a type of observational research design that examines the relationship between variables at one point in time. It provides a snapshot or a "cross-section" of the population at a particular moment, allowing researchers to estimate the prevalence of a disease or condition and identify potential risk factors or associations.

In a cross-sectional study, data is collected from a sample of participants at a single time point, and the variables of interest are measured simultaneously. This design can be used to investigate the association between exposure and outcome, but it cannot establish causality because it does not follow changes over time.

Cross-sectional studies can be conducted using various data collection methods, such as surveys, interviews, or medical examinations. They are often used in epidemiology to estimate the prevalence of a disease or condition in a population and to identify potential risk factors that may contribute to its development. However, because cross-sectional studies only provide a snapshot of the population at one point in time, they cannot account for changes over time or determine whether exposure preceded the outcome.

Therefore, while cross-sectional studies can be useful for generating hypotheses and identifying potential associations between variables, further research using other study designs, such as cohort or case-control studies, is necessary to establish causality and confirm any findings.

Skin neoplasms refer to abnormal growths or tumors in the skin that can be benign (non-cancerous) or malignant (cancerous). They result from uncontrolled multiplication of skin cells, which can form various types of lesions. These growths may appear as lumps, bumps, sores, patches, or discolored areas on the skin.

Benign skin neoplasms include conditions such as moles, warts, and seborrheic keratoses, while malignant skin neoplasms are primarily classified into melanoma, squamous cell carcinoma, and basal cell carcinoma. These three types of cancerous skin growths are collectively known as non-melanoma skin cancers (NMSCs). Melanoma is the most aggressive and dangerous form of skin cancer, while NMSCs tend to be less invasive but more common.

It's essential to monitor any changes in existing skin lesions or the appearance of new growths and consult a healthcare professional for proper evaluation and treatment if needed.

Tattooing is defined medically as the process of inserting pigment into the skin's dermis layer to change its color. This procedure creates a permanent design or image. The equipment used for tattooing includes an electrically powered tattoo machine, needles, and ink. Tattooing can carry potential risks such as infection, allergic reactions, and scarring. It is essential to ensure that all tattooing procedures are performed under sterile conditions and by a licensed professional to minimize these risks.

Photosensitivity disorders refer to conditions that cause an abnormal reaction to sunlight or artificial light. This reaction can take the form of various skin changes, such as rashes, inflammation, or pigmentation, and in some cases, it can also lead to systemic symptoms like fatigue, fever, or joint pain.

The two main types of photosensitivity disorders are:

1. Phototoxic reactions: These occur when a substance (such as certain medications, chemicals, or plants) absorbs light energy and transfers it to skin cells, causing damage and inflammation. The reaction typically appears within 24 hours of exposure to the light source and can resemble a sunburn.

2. Photoallergic reactions: These occur when the immune system responds to the combination of light and a particular substance, leading to an allergic response. The reaction may not appear until several days after initial exposure and can cause redness, itching, and blistering.

It is important for individuals with photosensitivity disorders to avoid excessive sun exposure, wear protective clothing, and use broad-spectrum sunscreens with a high SPF rating to minimize the risk of phototoxic or photoallergic reactions.

Aseptic meningitis is a type of meningitis (inflammation of the membranes covering the brain and spinal cord) that is not caused by bacterial infection. Instead, it can be due to viral infections, fungal infections, or non-infectious causes such as certain medications, chemical irritants, or underlying medical conditions. In aseptic meningitis, the cerebrospinal fluid (CSF) analysis may show increased white blood cells, typically lymphocytes, but no bacterial growth on culture. Common viral causes include enteroviruses, herpes simplex virus, and varicella-zoster virus. Treatment depends on the underlying cause and may include supportive care, antiviral medications, or immunosuppressive therapy in some cases.

Pityriasis pilaris, a skin disease not described by dermatologists] (Pityriasis pilaris, maladie de la peau non décrite par les ... Griffith (June 1998). "Pityriasis rubra pilaris". In Champion R.H.; Burton J.L.; Burns D.A.; Breathnach S.M. (eds.). Textbook ... Pityriasis rubra pilaris refers to a group of chronic disorders characterized by reddish orange, scaling plaques and keratotic ... M. G. A. Devergie and the eponymous named Devergie's disease at Who Named It? "Pityriasis rubra pilaris". DermNZ (New Zealand ...
Treatment of pityriasis rubra pilaris with etanercept". Dermatol Ther. 24: 285-6. doi:10.1111/j.1529-8019.2011.01404.x. PMID ... In 1856 Devergie was the first to describe a chronic papulosquamous disorder known as pityriasis rubra pilaris, also referred ...
Pityriasis rubra pilaris List of cutaneous conditions Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). ...
"Pityriasis Rosea, Pityriasis Rubra Pilaris, and Other Papulosquamous and Hyperkeratotic Diseases". Andrews' Diseases of the ... Retinoids and immunosuppressive drugs can be used when it is caused by psoriasis or pityriasis rubra pilaris. A sedative ... pityriasis rubra pilaris or a drug reaction, such as the use of topical steroids. Primary erythroderma is less frequent and is ... The classification of exfoliative dermatitis into Wilson-Brocq (chronic relapsing), Hebra or pityriasis rubra (progressive), ...
... was a Benedictine nun who died after a three-year battle with the skin disease Pityriasis rubra pilaris. Prior to the 1960s, ... where she was diagnosed with Pityriasis Rubra Pilaris. At the time, there was neither a cure nor specific treatment. According ...
... among the first to use large doses of Vitamin A which he used in the treatment of Darier's disease and pityriasis rubra pilaris ...
In this congress, various dermatological diseases such as lichen, pityriasis rubra pilaris, pemphigus, trichophytosis, syphilis ...
... or pityriasis rubra pilaris, or, in some cases, hereditary.: 783 Onycholysis List of cutaneous conditions James, William; ...
... a skin disease marked by small and itchy rashes Pityriasis rubra pilaris, the Devergie's disease, lichen ruber acuminatus or ... Rubra, red in Latin, may refer to : Rubra, an Edenist serpent, a character of the Night's Dawn trilogy and also : Folliculitis ... a genodermatose Granulosis rubra nasi, a rare familial disease of children occurring on the nose, cheeks, and chin Lochia rubra ... United States Turritopsis rubra, a type of jellyfish Ulmus rubra, the slippery elm This disambiguation page lists articles ...
... a Streptococcus species resistant to antibiotics Pityriasis rubra pilaris, a rare skin disorder Platelet-rich plasma Prion ...
... disorders 696.2 Parapsoriasis 696.3 Pityriasis rosea 696.4 Pityriasis rubra pilaris 696.5 Other and unspecified pityriasis ...
Pituitary dwarfism 1 Pityriasis lichenoides chronica Pityriasis lichenoides et varioliformis acuta Pityriasis rubra pilaris ...
... pityriasis rosea MeSH C17.800.859.600.685 - pityriasis rubra pilaris MeSH C17.800.859.675 - psoriasis MeSH C17.800.859.675.175 ... pityriasis lichenoides MeSH C17.800.859.575.650.580 - lymphomatoid papulosis MeSH C17.800.859.600 - pityriasis MeSH C17.800. ... pityriasis lichenoides MeSH C17.800.859.475.650.580 - lymphomatoid papulosis MeSH C17.800.859.575 - parapsoriasis MeSH C17.800. ... 859.600.650 - pityriasis lichenoides MeSH C17.800.859.600.650.580 - lymphomatoid papulosis MeSH C17.800.859.600.675 - ...
It is seen in: Psoriasis Pityriasis rubra pilaris Lichen planus Flat warts Lichen nitidus Vitiligo Lichen sclerosus Elastosis ... pityriasis rubra pilaris, and keratosis follicularis (Darier disease).[citation needed] The Koebner phenomenon describes skin ...
... rubra pilaris, reddish-orange patches (Latin: rubra) on the skin Pityriasis versicolor, a skin eruption on the trunk ... pale patches on the face Pityriasis lichenoides chronica, caused by a hypersensitivity reaction to infectious agents Pityriasis ... historically called Pityriasis capitis Pityriasis amiantacea, condition of the scalp in which thick tenaciously adherent scale ... Pityriasis commonly refers to flaking (or scaling) of the skin. The word comes from the Greek πίτυρον "bran". Types include: ...
... pityriasis rosea Gibert) Pityriasis rubra pilaris (Devergie's disease, lichen ruber acuminatus, lichen ruber pilaris) Pure hair ... folliculitis rubra, keratosis pilaris rubra atrophicans faciei, lichen pilare, lichen pilaire ou xerodermie pilaire symmetrique ... Pityriasis lichenoides et varioliformis acuta (acute guttate parapsoriasis, acute parapsoriasis, acute pityriasis lichenoides, ... Pityriasis lichenoides chronica (chronic guttate parapsoriasis, chronic pityriasis lichenoides, dermatitis psoriasiformis ...
Bornean bristlehead, Pityriasis gymnocephala Order: Passeriformes Family: Malaconotidae Bushshrikes are similar in habits to ... Rallina rubra White-striped forest-rail, Rallina leucospila Forbes's rail, Rallina forbesi Mayr's rail, Rallina mayri Red- ... Turdus pilaris White-collared blackbird, Turdus albocinctus Chestnut thrush, Turdus rubrocanus Ring ouzel, Turdus torquatus ... Pityriasis gymnocephala), also variously known as the bristled shrike, bald-headed crow or the bald-headed wood-shrike, is the ...

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