This document discusses the dermo-epidermal junction (DEJ) and dermis. It describes the four layers of the basement membrane zone (BMZ) of the DEJ - the basal keratinocyte layer containing hemidesmosomes, the lamina lucida, lamina densa containing type IV collagen and laminins, and the lamina fibroreticularis containing anchoring fibrils made of type VII collagen. It also discusses the cells and extracellular matrix components of the dermis, including collagen, elastic fibers, proteoglycans, fibroblasts, macrophages, dendrocytes and mast cells. Disorders of the DEJ like epidermolysis bullosa are also mentioned.
This document discusses three genera of fungi (Trichophyton, Microsporum, Epidermophyton) that can cause infections of the skin, hair, and nails. It then describes different clinical presentations of tinea capitis (scalp ringworm), including nonscarring alopecia and scaling, as well as a boggy scalp swelling called kerion. Examples are given of tinea pedis (athlete's foot), along with general measures for treatment such as keeping the infected area dry and avoiding synthetic clothes. Specimen collection involves examining hair shafts for spores in tinea capitis or skin scrapings to view fungal hyphae.
Actinic keratoses: Erythematous scaly lesions on sun-damaged skin & considered precancerous lesions that have the potential to progress into invasive SCC.
Bowens disease: SCC in situ It has the potential to progress to invasive SCC.
Leukoplakia: Leukoplakia refers to a white patch or plaque on the oral mucosa that cannot be wiped off and cannot be characterized clinically or pathologically as any other disease.
Hereditary disorder of keratinization characterized by expanding atrophic anular patch(es) surrounded by prominent keratotic ridge called the cornoid lamella
Skin warts are benign tumours caused by infection of keratinocytes with HPV, visible as welldefined hyperkeratotic protrusions. We will explore the detailed types, presentation, and treatment modalities of most common warts.
Dyschromatosis and Reticulate pigmentary disorderssanjay singh
油
This document summarizes several rare pigmentary disorders including reticulate pigmentary disorders, dyschromatosis, and related conditions. Key points include:
- Reticulate pigmentary disorders involve freckle-like macules joined at margins in a net-like pattern, while dyschromatosis involves interspersed hyperpigmented and hypopigmented macules.
- Several conditions are classified including acral, flexural, generalized types like reticulate acropigmentation of Kitamura and dyschromatosis symmetrica hereditaria.
- Genetic mutations in genes like ADAM10, DSRAD, KRT5 are associated with these conditions. Histopathology often
This document provides a classification and overview of the differential diagnosis of papular lesions that can occur on the face. It categorizes potential causes into infections, inflammatory disorders, tumors, and others. Key points include descriptions of common infections like molluscum contagiosum and lupus vulgaris. Inflammatory conditions discussed are acne, rosacea, perioral dermatitis, and sarcoidosis. Benign and malignant tumors of the skin and adnexal structures are also reviewed. Differential diagnoses and treatment approaches are mentioned for many of the conditions.
Lichen planus is a chronic inflammatory skin disease that affects the skin, mucous membranes, and nails. It is characterized by flat-topped, violaceous papules and plaques that are extremely pruritic. Histologically, there is vacuolar degeneration of basal keratinocytes, band-like infiltrate obscuring the dermoepidermal junction, and degenerative keratinocytes known as colloid bodies in the lower epidermis. It has a worldwide distribution and can affect people of any age, race, or sex. While the exact cause is unknown, it is considered to have an autoimmune pathogenesis. Treatment involves topical corticosteroids as first line, with systemic cortic
This document discusses various types of cutaneous mucinoses, which are skin conditions characterized by abnormal deposition of mucin in the skin. It describes primary mucinoses such as lichen myxoedematosus and reticular erythematous mucinosis, as well as secondary causes. Key features, histopathology, complications, diagnostic evaluation and treatment approaches are provided for selected mucinoses like scleromyxoedema and scleredema.
Seborrheic dermatitis (SD) is a common chronic skin condition characterized by redness and scaling in areas with many sebaceous glands like the face, scalp, and skin folds. It causes mild flaking of the scalp known as dandruff. Lesions can be itchy or painful and look deep red or purple with pimple-like bumps or blisters. Treatment involves topical anti-fungal creams, steroid creams, or oral anti-fungal medication for deep infections.
Cutaneous tuberculosis can present in several forms based on the route of infection and immune status of the host. Lupus vulgaris is the most common form in adults, presenting as slowly expanding reddish plaques on the head and neck. Scrofuloderma results from contiguous spread from underlying bone or lymph node infection, causing ulcerating nodules. Tuberculosis verrucosa cutis, or warty tuberculosis, occurs through inoculation and presents as painless verrucous plaques. Diagnosis involves biopsy showing granulomatous inflammation with caseation necrosis and occasionally visualizing acid-fast bacilli. Treatment involves anti-tubercular therapy targeting Mycobacterium tuberculosis.
This document discusses disorders of pigmentation. It begins by explaining that skin color is determined primarily by melanin, which is produced by melanocytes and transferred to keratinocytes. It then covers an overview of pigmentation disorders and their social implications. The rest of the document delves into specific hyperpigmentation and hypopigmentation disorders, providing details on classification, causes, characteristics, and examples of each type.
Viral skin diseases are common and include infections caused by herpes simplex virus, varicella zoster virus, and human papillomavirus. Herpes simplex virus causes lesions such as cold sores, genital herpes, and eczema herpeticum. Varicella zoster virus causes chickenpox and shingles. Human papillomavirus causes warts, including common warts, flat warts, plantar warts, and genital warts. These viral infections are generally self-limiting but can be treated with antivirals to reduce symptoms and duration of infection.
Actinic lichen planus is a variant of lichen planus characterized by annular erythematous brownish plaques located predominantly on exposed areas of skin like the face. Histological examination shows features of interface dermatitis like mild vacuolar degeneration of the basal layer, perivascular lymphocytic infiltration in the mid-dermis, and significant pigmentary incontinence. The key diagnostic feature is annular lichenoid plaques confined to sun-exposed skin.
This document summarizes several bullous diseases:
1. It describes the locations and characteristics of vesicles and bullae. Vesicles can form within or under the epidermis or between the dermis and epidermis.
2. It then focuses on three main immunobullous diseases - pemphigus, pemphigoid, and linear IgA bullous disease. Pemphigus is caused by antibodies against desmoglein proteins and features flaccid blisters. Pemphigoid features tense blisters caused by antibodies against basement membrane proteins. Linear IgA bullous disease clinically resembles pemphigoid.
3. Dermatitis herpetiformis is described
Superficial fungal infections of the skin are common. The document discusses the classification, presentation, and management of several common fungal infections including tinea infections, pityriasis versicolor, candidiasis, and chronic paronychia. For tinea capitis, oral griseofulvin or other systemic antifungals for 6-8 weeks are recommended. Topical antifungals are used for localized fungal infections while systemic antifungals like itraconazole or fluconazole are used for more extensive or resistant cases.
This document provides an overview of erythroderma, also known as generalized exfoliative dermatitis. It defines erythroderma as an inflammatory dermatosis involving 90% or more of the skin surface. The clinical presentation includes patchy erythema becoming universal over 24-48 hours accompanied by malaise, shivering and pyrexia, followed by scaling after 2-6 days. Erythroderma can be caused by conditions like eczema, psoriasis, malignancy, and drug reactions. Complications can include edema, lymphadenopathy, cardiac failure, metabolic disturbance, hypothermia, and cutaneous or respiratory infection. Management involves close inpatient monitoring and initially topical st
1. Cutaneous photosensitivity reactions require absorption of light energy by molecules, leading to damage and clinical disease.
2. Common photosensitivity disorders include polymorphic light eruption (PLE), chronic actinic dermatitis (CAD), and solar urticaria.
3. Clinical features, histopathology, and phototesting help differentiate types of photosensitivity dermatoses.
This document describes a biopsy of an 80-year-old female with a clinical diagnosis of bullous pemphigoid. Microscopic examination showed a subepidermal bulla filled with plasma, neutrophils, and eosinophils. The dermis beneath showed a dense perivascular infiltrate of lymphocytes, eosinophils, and plasma cells. These features are consistent with bullous pemphigoid. Bullous pemphigoid is an autoimmune blistering disease that typically affects the elderly and presents as large, tense bullae on the trunk and extremities. Histologically, it shows a subepidermal blister often containing eosinophils and a superficial perivascular mixed inflammatory infiltrate
Pemphigus is a group of chronic autoimmune bullous diseases characterized by the presence of autoantibodies against desmosomal proteins. The main types are pemphigus vulgaris, pemphigus foliaceus, and pemphigus erythematosus. Pemphigus vulgaris presents with flaccid blisters and erosions especially in the oral cavity and skin folds. Pemphigus foliaceus presents with fragile superficial blisters that leave moist erosions and crusts mainly on the face and scalp. Diagnosis involves clinical features and detection of autoantibodies through laboratory tests. Nikolsky's sign, elicited by applying pressure to separate
Lichen planus is a chronic inflammatory skin condition that causes itchy, purple-colored papules and plaques. It is thought to be an autoimmune reaction targeting skin cells. The lesions typically appear on the wrists, legs, and oral mucosa. On microscopy, distinctive saw-tooth shaped keratinocytes (Civatte bodies) and band-like inflammatory infiltrate are seen. Treatment involves topical corticosteroids and immunomodulators. While usually self-limiting, lichen planus can lead to scarring and has a small risk of malignant transformation, especially in oral lesions.
This document provides information on pemphigus, an autoimmune blistering disease of the skin and mucous membranes. It discusses the various subtypes of pemphigus, including pemphigus vulgaris, pemphigus foliaceus, pemphigus vegetans, paraneoplastic pemphigus, and drug-induced pemphigus. It covers the clinical presentation, pathogenesis, histopathology, diagnosis and management of pemphigus. Key points include that pemphigus vulgaris presents with oral blisters/erosions in 50-70% of patients, while pemphigus foliaceus presents with superficial blisters that rupture and form scaly crust
This document discusses cutaneous porphyrias, which are metabolic disorders caused by defects in the heme biosynthesis pathway. There are several types of cutaneous porphyrias that can be classified as either acute or cutaneous/chronic. The document focuses on Porphyria Cutanea Tarda (PCT), Erythropoietic Protoporphyria (EPP), Congenital Erythropoietic Porphyria (CEP), Hepatoerythropoietic Porphyria (HEP), and Variegate Porphyria (VP). It describes the genetic causes, clinical features, diagnostic approaches, histopathological findings, and treatment options for these specific cut
Lichen planus (LP) is an inflammatory autoimmune disorder affecting the skin, hair, nails, and mucous membranes. It is characterized by small, polygonal, flat-topped papules that are purple, shiny, and have fine white lines. LP has no clear cause but may be triggered by viral infections, autoimmune disorders, medications, or dental materials. Histology shows basal cell damage and a band-like lympho-histiocytic infiltrate. Treatment includes topical corticosteroids and antihistamines or systemic corticosteroids, dapsone, or retinoids depending on severity.
This document discusses various types of cutaneous mucinoses, which are skin conditions characterized by abnormal deposition of mucin in the skin. It describes primary mucinoses such as lichen myxoedematosus and reticular erythematous mucinosis, as well as secondary causes. Key features, histopathology, complications, diagnostic evaluation and treatment approaches are provided for selected mucinoses like scleromyxoedema and scleredema.
Seborrheic dermatitis (SD) is a common chronic skin condition characterized by redness and scaling in areas with many sebaceous glands like the face, scalp, and skin folds. It causes mild flaking of the scalp known as dandruff. Lesions can be itchy or painful and look deep red or purple with pimple-like bumps or blisters. Treatment involves topical anti-fungal creams, steroid creams, or oral anti-fungal medication for deep infections.
Cutaneous tuberculosis can present in several forms based on the route of infection and immune status of the host. Lupus vulgaris is the most common form in adults, presenting as slowly expanding reddish plaques on the head and neck. Scrofuloderma results from contiguous spread from underlying bone or lymph node infection, causing ulcerating nodules. Tuberculosis verrucosa cutis, or warty tuberculosis, occurs through inoculation and presents as painless verrucous plaques. Diagnosis involves biopsy showing granulomatous inflammation with caseation necrosis and occasionally visualizing acid-fast bacilli. Treatment involves anti-tubercular therapy targeting Mycobacterium tuberculosis.
This document discusses disorders of pigmentation. It begins by explaining that skin color is determined primarily by melanin, which is produced by melanocytes and transferred to keratinocytes. It then covers an overview of pigmentation disorders and their social implications. The rest of the document delves into specific hyperpigmentation and hypopigmentation disorders, providing details on classification, causes, characteristics, and examples of each type.
Viral skin diseases are common and include infections caused by herpes simplex virus, varicella zoster virus, and human papillomavirus. Herpes simplex virus causes lesions such as cold sores, genital herpes, and eczema herpeticum. Varicella zoster virus causes chickenpox and shingles. Human papillomavirus causes warts, including common warts, flat warts, plantar warts, and genital warts. These viral infections are generally self-limiting but can be treated with antivirals to reduce symptoms and duration of infection.
Actinic lichen planus is a variant of lichen planus characterized by annular erythematous brownish plaques located predominantly on exposed areas of skin like the face. Histological examination shows features of interface dermatitis like mild vacuolar degeneration of the basal layer, perivascular lymphocytic infiltration in the mid-dermis, and significant pigmentary incontinence. The key diagnostic feature is annular lichenoid plaques confined to sun-exposed skin.
This document summarizes several bullous diseases:
1. It describes the locations and characteristics of vesicles and bullae. Vesicles can form within or under the epidermis or between the dermis and epidermis.
2. It then focuses on three main immunobullous diseases - pemphigus, pemphigoid, and linear IgA bullous disease. Pemphigus is caused by antibodies against desmoglein proteins and features flaccid blisters. Pemphigoid features tense blisters caused by antibodies against basement membrane proteins. Linear IgA bullous disease clinically resembles pemphigoid.
3. Dermatitis herpetiformis is described
Superficial fungal infections of the skin are common. The document discusses the classification, presentation, and management of several common fungal infections including tinea infections, pityriasis versicolor, candidiasis, and chronic paronychia. For tinea capitis, oral griseofulvin or other systemic antifungals for 6-8 weeks are recommended. Topical antifungals are used for localized fungal infections while systemic antifungals like itraconazole or fluconazole are used for more extensive or resistant cases.
This document provides an overview of erythroderma, also known as generalized exfoliative dermatitis. It defines erythroderma as an inflammatory dermatosis involving 90% or more of the skin surface. The clinical presentation includes patchy erythema becoming universal over 24-48 hours accompanied by malaise, shivering and pyrexia, followed by scaling after 2-6 days. Erythroderma can be caused by conditions like eczema, psoriasis, malignancy, and drug reactions. Complications can include edema, lymphadenopathy, cardiac failure, metabolic disturbance, hypothermia, and cutaneous or respiratory infection. Management involves close inpatient monitoring and initially topical st
1. Cutaneous photosensitivity reactions require absorption of light energy by molecules, leading to damage and clinical disease.
2. Common photosensitivity disorders include polymorphic light eruption (PLE), chronic actinic dermatitis (CAD), and solar urticaria.
3. Clinical features, histopathology, and phototesting help differentiate types of photosensitivity dermatoses.
This document describes a biopsy of an 80-year-old female with a clinical diagnosis of bullous pemphigoid. Microscopic examination showed a subepidermal bulla filled with plasma, neutrophils, and eosinophils. The dermis beneath showed a dense perivascular infiltrate of lymphocytes, eosinophils, and plasma cells. These features are consistent with bullous pemphigoid. Bullous pemphigoid is an autoimmune blistering disease that typically affects the elderly and presents as large, tense bullae on the trunk and extremities. Histologically, it shows a subepidermal blister often containing eosinophils and a superficial perivascular mixed inflammatory infiltrate
Pemphigus is a group of chronic autoimmune bullous diseases characterized by the presence of autoantibodies against desmosomal proteins. The main types are pemphigus vulgaris, pemphigus foliaceus, and pemphigus erythematosus. Pemphigus vulgaris presents with flaccid blisters and erosions especially in the oral cavity and skin folds. Pemphigus foliaceus presents with fragile superficial blisters that leave moist erosions and crusts mainly on the face and scalp. Diagnosis involves clinical features and detection of autoantibodies through laboratory tests. Nikolsky's sign, elicited by applying pressure to separate
Lichen planus is a chronic inflammatory skin condition that causes itchy, purple-colored papules and plaques. It is thought to be an autoimmune reaction targeting skin cells. The lesions typically appear on the wrists, legs, and oral mucosa. On microscopy, distinctive saw-tooth shaped keratinocytes (Civatte bodies) and band-like inflammatory infiltrate are seen. Treatment involves topical corticosteroids and immunomodulators. While usually self-limiting, lichen planus can lead to scarring and has a small risk of malignant transformation, especially in oral lesions.
This document provides information on pemphigus, an autoimmune blistering disease of the skin and mucous membranes. It discusses the various subtypes of pemphigus, including pemphigus vulgaris, pemphigus foliaceus, pemphigus vegetans, paraneoplastic pemphigus, and drug-induced pemphigus. It covers the clinical presentation, pathogenesis, histopathology, diagnosis and management of pemphigus. Key points include that pemphigus vulgaris presents with oral blisters/erosions in 50-70% of patients, while pemphigus foliaceus presents with superficial blisters that rupture and form scaly crust
This document discusses cutaneous porphyrias, which are metabolic disorders caused by defects in the heme biosynthesis pathway. There are several types of cutaneous porphyrias that can be classified as either acute or cutaneous/chronic. The document focuses on Porphyria Cutanea Tarda (PCT), Erythropoietic Protoporphyria (EPP), Congenital Erythropoietic Porphyria (CEP), Hepatoerythropoietic Porphyria (HEP), and Variegate Porphyria (VP). It describes the genetic causes, clinical features, diagnostic approaches, histopathological findings, and treatment options for these specific cut
Lichen planus (LP) is an inflammatory autoimmune disorder affecting the skin, hair, nails, and mucous membranes. It is characterized by small, polygonal, flat-topped papules that are purple, shiny, and have fine white lines. LP has no clear cause but may be triggered by viral infections, autoimmune disorders, medications, or dental materials. Histology shows basal cell damage and a band-like lympho-histiocytic infiltrate. Treatment includes topical corticosteroids and antihistamines or systemic corticosteroids, dapsone, or retinoids depending on severity.
Oral lichen planus is a chronic inflammatory disease that affects the oral mucosa. It is characterized by white striations (Wickham's striae) and varies in appearance from reticular to erythematous or ulcerative lesions. The cause is unknown but involves a cell-mediated immune response. Treatment focuses on reducing symptoms and includes topical corticosteroids, immunosuppressants, or retinoids. Malignant transformation may rarely occur so follow-up is important.
The document describes various normal anatomical structures and abnormalities that can present on the tongue, including different types of papillae, taste buds, and developmental variations. It then discusses many potential clinical findings involving the tongue related to deficiencies, infections, tumors, and other oral diseases. Specific conditions covered in detail include hairy tongue, leukoplakia, geographic tongue, candidiasis, macroglossia, ulcers, deviations and ties. Multiple images are also provided to illustrate key pathologies.
This document discusses several benign disorders of the oral cavity. It begins by defining common oral lesions including ulcers, erosions, abscesses, cysts, and more. It then categorizes benign oral disorders into congenital lesions, inflammatory/traumatic conditions, autoimmune diseases, precancerous lesions, and benign tumors. Specific conditions are discussed in detail such as torus, lingual thyroid, fibroma, aphthous ulcers, lichen planus, leukoplakia, hemangioma, and ranula. Treatment options are provided for each condition. The document serves as a comprehensive overview of benign oral pathology.
THE TONGUE IN HEALTH AND SICKNESS.pptxAisha lamido
油
The document provides an overview of the tongue's anatomy, functions, and clinical significance. It discusses the appearance of a healthy tongue and various abnormalities that may indicate underlying oral or systemic diseases. Color changes, surface features, moisture, size, ulcers, tumors, movement abnormalities, and developmental anomalies are described. The role of family physicians in examining the tongue and recognizing abnormalities that may assist in diagnosis is emphasized. The tongue is a useful clinical indicator and abnormalities can present diagnostic challenges requiring thorough history and examination.
This document discusses several connective tissue diseases:
- Lupus erythematosus can present as cutaneous, subacute, or chronic forms and is characterized by a butterfly rash. Systemic lupus erythematosus can involve multiple organ systems.
- Scleroderma involves skin thickening and fibrosis. It can be limited or diffuse and also cause lung, heart, gastrointestinal and renal involvement.
- Dermatomyositis is characterized by a violaceous rash over the knuckles, elbows and back along with progressive symmetric muscle weakness.
The tongue is made up of papillae and muscles that contain different types of taste buds. Appearances such as color, size, ulcers, and tremors can provide clues to underlying diseases or deficiencies. Common tongue conditions include hairy tongue, leukoplakia, candidiasis, fissures, and geographic tongue. Diseases like anemia, scurvy, cancer, and infections can cause changes to the tongue's color, surface, movements, and size. A thorough exam of the tongue is important for diagnosis.
This document discusses connective tissue diseases, specifically lupus erythematosus and scleroderma. It describes the different types of lupus, including discoid lupus erythematosus and systemic lupus erythematosus, and their characteristic manifestations, histology, and treatment. It also discusses scleroderma, differentiating between morphoea, systemic sclerosis, and chemically induced scleroderma. Systemic sclerosis is described in more detail, outlining its cutaneous features, systemic involvement affecting organs like the lungs and kidneys, and current limited treatment options.
Morphea and allied Sclerosing Inflammatory Dermatoses-1.pptxkainatusman3
油
This document discusses morphea and allied sclerosing inflammatory dermatoses. It defines morphea as characterized by varying degrees of sclerosis, fibrosis, and skin atrophy. It can affect the skin, subcutaneous tissue, and sometimes deeper tissues. Morphea is classified into limited and generalized types based on extent of skin involvement. Limited types include plaque, guttate, keloidal/nodular, and deep morphea variants. Generalized types are disseminated plaque and pansclerotic morphea. Linear morphea variants like en coup de sabre and linear atrophoderma of Moulin can also occur. Investigations and first, second, and third line treatment options are
1. Lupus erythematosus is an autoimmune disease where the immune system attacks healthy tissue. It is characterized by a red rash and can cause skin, joint, kidney, and other organ involvement.
2. The document discusses the classification, epidemiology, pathogenesis, clinical features, investigations, management, and prognosis of both cutaneous and systemic lupus erythematosus.
3. Treatment involves general measures, local and systemic medications like antimalarials, corticosteroids, and immunosuppressants to control disease activity and damage. Monitoring is important to assess disease status and damage over time.
Diseases of the throat by Dr. Kavitha Ashok Kumar MSU MalaysiaKavitha Ashokb
油
This document discusses diseases of the throat, including lesions of the oral cavity and pharynx. It describes various white and red lesions that can occur in the oral cavity, such as oral submucous fibrosis and candidiasis. It also discusses conditions like chronic tonsillitis, adenoid hypertrophy, and tonsillectomy. Chronic tonsillitis is characterized by recurrent sore throat, fever and neck swelling. Adenoid hypertrophy can cause nasal obstruction and mouth breathing. Tonsillectomy may be indicated for chronic tonsillitis, respiratory obstruction or peritonsillar abscess.
This document provides an overview of lichen planus, specifically oral lichen planus (OLP). It discusses the history, epidemiology, definition, etiology, predisposing factors, clinical features, clinical variants (reticular, erosive, atrophic, plaque-like, papular, bullous), and histopathology of OLP. OLP is a chronic immunological mucocutaneous disorder that commonly presents as white striations or plaques on the oral mucosa. It is believed to be mediated by T-cells that trigger apoptosis of epithelial cells, though the exact cause is still unknown.
A 22-year-old college student presents with symptoms including a malar rash, photosensitivity, arthritis, fatigue, and hair loss. Laboratory tests show a positive ANA, positive anti-Smith antibody, and low white blood cell and platelet counts. This constellation of clinical features and laboratory results makes systemic lupus erythematosus the most likely diagnosis for the patient.
The document discusses various oral pigmentations that can occur both exogenously and endogenously. Exogenous pigmentations include those caused by heavy metal poisoning from substances like lead, mercury, silver and bismuth. Endogenous pigmentations include conditions like smoker's melanosis caused by tobacco use, as well as pigmentations associated with medical disorders and neoplasms involving melanin deposition or hematological changes. A thorough history, examination and appropriate diagnostic tests are needed to identify the cause of oral pigmentation in each case.
This document provides an overview of genetic epidermolysis bullosa (EB), a group of inherited skin fragility disorders characterized by blistering of the skin from mild mechanical trauma. It defines the major types of EB - simplex, junctional, and dystrophic - based on the level in the skin where blistering occurs. For each type, it describes clinical features, molecular pathology, specific subtypes, management considerations, and prognosis. The document emphasizes EB is a genetically determined condition caused by mutations impacting proteins important for skin integrity.
Unit 1 Computer Hardware for Educational Computing.pptxRomaSmart1
油
Computers have revolutionized various sectors, including education, by enhancing learning experiences and making information more accessible. This presentation, "Computer Hardware for Educational Computing," introduces the fundamental aspects of computers, including their definition, characteristics, classification, and significance in the educational domain. Understanding these concepts helps educators and students leverage technology for more effective learning.
How to Configure Flexible Working Schedule in Odoo 18 EmployeeCeline George
油
In this slide, well discuss on how to configure flexible working schedule in Odoo 18 Employee module. In Odoo 18, the Employee module offers powerful tools to configure and manage flexible working schedules tailored to your organization's needs.
How to create security group category in Odoo 17Celine George
油
This slide will represent the creation of security group category in odoo 17. Security groups are essential for managing user access and permissions across different modules. Creating a security group category helps to organize related user groups and streamline permission settings within a specific module or functionality.
Managing expiration dates of products in odooCeline George
油
Odoo allows users to set expiration dates at both the product and batch levels, providing flexibility and accuracy. By using Odoo's expiration date management, companies can minimize waste, optimize stock rotation, and maintain high standards of product quality. The system allows users to set expiration dates at both the product and batch levels, providing flexibility and accuracy.
10. Lichen Planus Verrucosus
K/a Hypertrophic LP
Extremely pruritic
Hyperkeratotic plaques
on the shin and ankles
Can transform into
metastatic squamous cell
carcinoma (esp. distal
extremeties)
11. Atrophic Lichen Planus
Lower limbs
Violaceous papules and plaques with depressed
and atropic center
Usually occurs after resolution of typical LP &
Accentuate by potent topical steroids
13. Annular LP
Glans & trunk
Typical violaceous papules, in a
ring like fashion
Central clearing leaving behind
active raised border
Variant : AALP ( Annular Atrophic
LP)
Small violaceous papules
Slowly grow peripherally
Center:atrophic and hyperpigmented
Peripherally raised
Trunk, limbs
14. Linear LP
Spontaneous
Linear along
Lines of
Blaschko
children > adults
Rarely, occur at
the site of healed
herpes zoster scar
15. Bullous LP
Blisters within the papules
Liquefactive degeneration
of the basal layer of
epidermis, l/t sub
epidermal blisters, MAX
JOSEPH SPACES
Extremities, shin (97%) >
upper limbs > thigh
Chronic course
Family history present
17. LP Pemphigoides
Blisters on LP lesions + non
affected skin
Distal limbs
Histology
Direct Immunofluorescence
Deposition of IgG & C3 at BMZ
19. Actinic LP
Summer months
Sun exposed areas, forehead
and face, dorsal surface of
hands and neck
Blue, brownish plaque,
annular hypopigmented
border with central atrophy
Young adults & children
NO PRURITIS
NO KOEBNERIZATION
20. LP Pigmentosus
Slate grey to brownish-
black macules
sun exposed areas &
flexural folds
Types
Diffuse (most common)
Blotchy
Reticular
Perifollicular
21. Lichen Planopilaris
a/k/a Follicular LP
Chronic lymphocytic inflammation around the upper
portion of hair follicle
Irregular patchy loss of hair, with loss of follicular
ostia.
Multifocal, patchy > diffuse
Perifollicular erythema and scaling + on periphery of
the lesion
Disease activity, periphery>center of the alopecia patch
Pruritis with dysesthesia
Site frontocentral scalp & crown
24. Erosive LP
Mucosal surface
Oral cavity or genitalia
Erosions on the surface of papular lesions
Aggressive form of LP
Eruptive LP
A/k/a acute or exanthematous LP
Disseminated form
Trunk, dorsum of feet & wrist
Self-limiting
Heal in 3-9months with hyperpigmentation.
25. Nail LP
10%
Finger nails>toe nails
Adults ( 50-60 years )
In pediatric age , nail LP>skin LP
Chronic course
3 presentations
Typical Nail LP
Twenty Nail Dystrophy (trachyonychia)
Idiopathic Atrophy of Nails
26. TYPICAL NAIL LP
diffuse nail ridging
splitting
dorsal pterygium
TWENTY NAIL DYSTROPHY
Excessive longitudnal ridging l/t nail roughness
Beningn condition
No nail scarring
One to several nails affected
IDIOPATHIC ATROPHY OF THE NAIL
acute & rapid, painless, destruction of the nail
OTHERS
Yellow nail syndrome like changes
Nail bed erosions
Pigmentary changes : longitudnal melanonychia,
longitudnal erythronychia
28. TYPICAL NAIL LP
diffuse nail ridging
splitting
dorsal pterygium
TWENTY NAIL DYSTROPHY
Excessive longitudnal ridging l/t nail roughness
Beningn condition
No nail scarring
One to several nails affected
IDIOPATHIC ATROPHY OF THE NAIL
acute & rapid, painless, destruction of the nail
OTHERS
Yellow nail syndrome like changes
Nail bed erosions
Pigmentary changes : longitudnal melanonychia,
longitudnal erythronychia
30. TYPICAL NAIL LP
diffuse nail ridging
splitting
dorsal pterygium
TWENTY NAIL DYSTROPHY
Excessive longitudnal ridging l/t nail roughness
Beningn condition
No nail scarring
One to several nails affected
IDIOPATHIC ATROPHY OF THE NAIL
acute & rapid, painless, destruction of the nail
OTHERS
Yellow nail syndrome like changes
Nail bed erosions
Pigmentary changes : longitudnal melanonychia,
longitudnal erythronychia
32. Palmoplantar LP
Rare
Highly pruritic,
erythematous, scaly
plaque with/out
plamoplantar
keratoderma
Internal plantar arch
& hands (NO
FINGERTIPS)
Young adults (20-40
years age)
33. Oral LP
In 70-77% of cutaneous disease
25% present with oral LP
Middle age (40-70 years), women
6 types (ANDREASEN CLASSIFICATION)
RETICULAR
PLAQUE-LIKE
PAPULAR
EROSIVE
ATROPHIC
BULLOUS
Lateral margins of tongue, gingiva, lips and hard palate
Chronic course
STRESS, SPICY & ACIDIC FOOD- flare up
Association with HCV infection
Risk of malignant transformation in 0.4-1.5%
34. RETICULAR LP
Most common
Asymptomatic
Irregular patchy, plaque with white
streaks in a lacy pattern
posterior buccal mucosa
Bilateral
EROSIVE ORAL LP
Large, erythematous, well defines
erosions on buccal mucosa
with/out pseudomembrane
Buccal mucosa, Dorsum & lateral
borders of tongue, gingiva
ATROPHIC LP
Gingiva
Irritaion following eating & brushing
36. Genital LP
25% cases with skin LP
Males
Shaft of penis, glans penis, prepuce, scrotum
ANNNULAR LP (most common presentation)
37. Female
Vulval and vaginal
Vulval : on introitus, white lacy, reticular borders extending into vagina
Dyspareunia
a/w pruritis and pain
Loss of normal architecture and scarring on healing
VVG (VULVO-VAGINAL-GINGIVAL) SYNDROME
Erosive lesions
a/w HLA-DQB1*0201 allele
38. Esophageal LP
Rare
Middle age, women, with oral LP
c/o dysphagia, odynophagia, or both
Endoscopy
Strictures & malignant transformation to
Squamous cell carcinoma common
40. Treatment
FIRST LINE
Topical corticosteroids
First generation antihistaminics (hydroxyzine /
chloprpheniramine)
Intra-lesional steroids (hypertrophic , nail &
erosive LP)
Immunomodulator (tacrolimus, pacrolimus)
Topical minoxidil (LPP)
41. SECOND LINE
Systemic corticosteroids (oral or IM)
Oral prednisolone : 0.5-1mg/kg/day for 4-6 weeks
Oral mini pulse with betamethsone
IM inj. Of Triamcinolone :40-80mg, every 6-8
weeks
Phototherapy
NB-UVB
PUVA
Extracorporeal photopheresis, in recalcitrant & severe
erosive LP
43. MUCOSAL LP
First line : Topical steroids
Intralesional steroids used in localised ulcerative LP
Local phototherapy : NB-UVB and PUVA
excimer 308 nm laser with ECP in recalcitrant oral LP
Second line :
Systemic corticosteroids , short term
Hydroxycholoroquine