Day: April 24, 2024

Neurofibromatosis Type 1 (NF1) (von Recklinghausen disease) This is a complex multi-system disorder, caused by loss of protein Neurofibromin needed in many cells– An autosomal dominant condition which is caused by a mutation/deletion of NF-1 gene on Chromosome 17 Skin features:>5 Café au lait marks >1.5cm diameter (uniformly pigmented brown macules)– Due to a collection of pigment producing melanocytes in the epidermis of the skin– Freckles found in the axilla and groin region– Peripheral neurofibromas Other Organs:– Spine –> Scoliosis– Eye –> Lisch nodules (dome shaped gelatinous masses on iris surface)– Endocrine –> Pheochromocytoma (adrenaline secreting tumour of the chromaffin

Urticaria + Angioedema This is a type 1 hypersensitivity reaction which gives a local release of histamine– This increases the permeability of small capillaries and venules resulting in fluid shift to the extracellular space and pruritus, causing swelling of tissues. Symptoms:– Urticaria –> Swelling of the superficial dermis– Presents as itchy red wheals which appear all over the body – Angioedema –> deeper swelling of the dermis– Presents as a swelling of tongue and lips Management:– Urticaria –> Antihistamines– Angioedema –> Corticosteroids   Hereditary angioedema This is an autosomal dominant condition which occurs due to a deficiency in C1-INH (Complement 1 inhibitor)–

Benign Lesions Seborrheic keratosis This is a benign squamous cell proliferation, common in elderly– Sudden onset of many lesions suggests GI carcinoma, known as the Leser-Trelat sign Appearance– Raised brown/black plaques on extremities/face– Coin like, “stuck on” appearance that can be very variable ManagementCompletely benign but can be removed if suspicion of cancer   Dermatofibroma This is an overgrowth of fibrous tissue in the dermis– Made up of fibroblasts, it is thought to be a reactive process or a neoplasm– It is completely benign and does not turn into cancer Appearance– Single dermal firm nodule found usually on the legs

Bacterial Infections Acne Vulgaris This is a condition where there is increased sebum production due to increased androgens– This causes excess keratin production which block follicles making comedones-Anaerobic bacteria Propionibacterium acnes colonise plugs giving inflammation Appearance– Red spots with pustules on face, cheeks, neck and upper trunk N.B. Can become disseminated around the body with fever, malaise.– This is known as acne fulminans and needs to be treated in hospital.   Management:– 1st line is single topical creams –> Benzoyl peroxide (antimicrobial action) or Vitamin A derivative–  If not successful –> try multiple topical agents together– If still uncontrolled –> oral antibiotics – tetracyclines (unless pregnant

Acne Rosacea        This is a chronic skin disease of unknown cause in adults which characteristically affects the nose, cheeks and forehead, most often between the ages of 30-60. – It is more common in white people with blue eyes, made worse by sunlight Appearance– Starts with flushing before giving persistent redness– Gives pustule formation and prominent blood vessels (telangiectasia)– Can lead to rhinophyma – bulbous nose due to chronic inflammation   Management– Reduce the factors which cause flushing such as sun exposure– Tetracycline antibiotics for 6-12 weeks –> doxycycline, minocycline– If resistant –> co-trimoxazole or metronidazole– If

Neurofibromatosis Type 1 (NF1) (von Recklinghausen disease) This is a complex multi-system disorder, caused by loss of protein Neurofibromin needed in many cells– An autosomal dominant condition which is caused by a mutation/deletion of NF-1 gene on Chromosome 17 Skin features:>5 Café au lait marks >1.5cm diameter (uniformly pigmented brown macules)– Due to a collection of pigment producing melanocytes in the epidermis of the skin– Freckles found in the axilla and groin region– Peripheral neurofibromas Other Organs:– Spine –> Scoliosis– Eye –> Lisch nodules (dome shaped gelatinous masses on iris surface)– Endocrine –> Pheochromocytoma (adrenaline secreting tumour of the chromaffin

These conditions are marked by an intrinsic problem with melanocytes, the pigment producing cells. Vitiligo This is an acquired autoimmune condition which leads to the destruction of melanocytes causing depigmentation of the skin (leukoderma).– In people with darker skin, it can be very apparent and psychologically scarring– It is more common in India and the onset is usually in youths before the age of 30. Associations:Type 1 diabetes, Addison’s disease, thyroid disease– Connective tissue disorders –> SLE, rheumatoid arthritis Appearance:Well-defined patches of depigmentation (on face, neck fingers and toes)– Koebner phenomenon occurs –> development of lesions on sites of injury–

Bullous pemphigoid This is an autoimmune skin condition causing blisters under the epidermis.– Due to a type II hypersensitivity reaction which gives destruction of hemi- desmosomes between basal cells and basal membrane.– IgG antibody is directed against BP180 and BP 230 of basement membrane – More common in elderly patients >70 years but there is no obvious cause  Appearance– Starts as a non-specific rash a month before the blisters– Then itchy blisters form around the skin folds.– Blisters are sup-epidermal and quite tense (do not rupture very easily) and heal without scarring – Blisters contains clear or cloudy yellowish fluid,

Eczema (Dermatitis) This is the general term which describes a condition which causes general inflammation of the skin.   Atopic Eczema (Atopic dermatitis) This is the most common type of eczema and most common inflammatory disease of early childhood– It affects about 20% of children under 5 and 2% of adults– It is an immunologically mediated inflammatory skin reaction, mediated by increased Th2 cells– This promotes pathogen specific IgE antibodies (type I hypersensitivity) increasing eosinophils and mast cells Cause: Underpinned by a genetic defect in skin barrier function– Associated with a loss of function variant of protein filaggrin.– This leads to

Bullous pemphigoid This is an autoimmune skin condition causing blisters under the epidermis.– Due to a type II hypersensitivity reaction which gives destruction of hemi- desmosomes between basal cells and basal membrane.– IgG antibody is directed against BP180 and BP 230 of basement membrane – More common in elderly patients >70 years but there is no obvious cause  Appearance– Starts as a non-specific rash a month before the blisters– Then itchy blisters form around the skin folds.– Blisters are sup-epidermal and quite tense (do not rupture very easily) and heal without scarring – Blisters contains clear or cloudy yellowish fluid,

Benign Lesions Seborrheic keratosis This is a benign squamous cell proliferation, common in elderly– Sudden onset of many lesions suggests GI carcinoma, known as the Leser-Trelat sign Appearance– Raised brown/black plaques on extremities/face– Coin like, “stuck on” appearance that can be very variable ManagementCompletely benign but can be removed if suspicion of cancer   Dermatofibroma This is an overgrowth of fibrous tissue in the dermis– Made up of fibroblasts, it is thought to be a reactive process or a neoplasm– It is completely benign and does not turn into cancer Appearance– Single dermal firm nodule found usually on the legs

Bacterial Infections Acne Vulgaris This is a condition where there is increased sebum production due to increased androgens– This causes excess keratin production which block follicles making comedones-Anaerobic bacteria Propionibacterium acnes colonise plugs giving inflammation Appearance– Red spots with pustules on face, cheeks, neck and upper trunk N.B. Can become disseminated around the body with fever, malaise.– This is known as acne fulminans and needs to be treated in hospital.   Management:– 1st line is single topical creams –> Benzoyl peroxide (antimicrobial action) or Vitamin A derivative–  If not successful –> try multiple topical agents together– If still uncontrolled –> oral antibiotics – tetracyclines (unless pregnant

Children often present with a variety of birthmarks – these can be asymptomatic or develop into diseases. They can be categorised by their colour.   Blue birthmarks   Mongolian Blue spots These are congenital marks, which occur mainly in Asian/African children– Colour occurs as dermal melanocytes become interrupted in their migration from neural crest to epidermis in utero. They are completely asymptomatic Appearance – Blue-grey macules, usually lumbosacral    Brown birthmarks   Congenital Melanocytic naevi These are congenital marks which occur due to congenital proliferation of melanocytes Appearance– Present as a brown plaque which can be hairy.– Size ranges Small/medium/ Large/

Urticaria + Angioedema This is a type 1 hypersensitivity reaction which gives a local release of histamine– This increases the permeability of small capillaries and venules resulting in fluid shift to the extracellular space and pruritus, causing swelling of tissues. Symptoms:– Urticaria –> Swelling of the superficial dermis– Presents as itchy red wheals which appear all over the body – Angioedema –> deeper swelling of the dermis– Presents as a swelling of tongue and lips Management:– Urticaria –> Antihistamines– Angioedema –> Corticosteroids   Hereditary angioedema This is an autosomal dominant condition which occurs due to a deficiency in C1-INH (Complement 1 inhibitor)–

There are many skin conditions which are associated with an underlying systemic pathology. Diabetic Skin Conditions   Diabetic dermopathy This is the presence of atrophic brown patches on shins, “shin spots”– It occurs due to changes in the microvasculature and leakage of blood into the skin – Occurs in about a third of diabetic patients   Necrobiosis Lipiodica These are yellow/brown waxy plaques that are slow growing and can ulcerate– They are also seen in rheumatoid arthritis– Lesions occur usually on the patient’s shins due to collagen degeneration– Appears as hardened, raised area of skin with yellowish tint Treatment– PUVA

Neurofibromatosis Type 1 (NF1) (von Recklinghausen disease) This is a complex multi-system disorder, caused by loss of protein Neurofibromin needed in many cells– An autosomal dominant condition which is caused by a mutation/deletion of NF-1 gene on Chromosome 17 Skin features:>5 Café au lait marks >1.5cm diameter (uniformly pigmented brown macules)– Due to a collection of pigment producing melanocytes in the epidermis of the skin– Freckles found in the axilla and groin region– Peripheral neurofibromas Other Organs:– Spine –> Scoliosis– Eye –> Lisch nodules (dome shaped gelatinous masses on iris surface)– Endocrine –> Pheochromocytoma (adrenaline secreting tumour of the chromaffin

These conditions are marked by an intrinsic problem with melanocytes, the pigment producing cells. Vitiligo This is an acquired autoimmune condition which leads to the destruction of melanocytes causing depigmentation of the skin (leukoderma).– In people with darker skin, it can be very apparent and psychologically scarring– It is more common in India and the onset is usually in youths before the age of 30. Associations:Type 1 diabetes, Addison’s disease, thyroid disease– Connective tissue disorders –> SLE, rheumatoid arthritis Appearance:Well-defined patches of depigmentation (on face, neck fingers and toes)– Koebner phenomenon occurs –> development of lesions on sites of injury–

Benign Lesions Seborrheic keratosis This is a benign squamous cell proliferation, common in elderly– Sudden onset of many lesions suggests GI carcinoma, known as the Leser-Trelat sign Appearance– Raised brown/black plaques on extremities/face– Coin like, “stuck on” appearance that can be very variable ManagementCompletely benign but can be removed if suspicion of cancer   Dermatofibroma This is an overgrowth of fibrous tissue in the dermis– Made up of fibroblasts, it is thought to be a reactive process or a neoplasm– It is completely benign and does not turn into cancer Appearance– Single dermal firm nodule found usually on the legs

Burns injury In a burn, there is local response with progressive tissue loss and release of inflammatory cytokines– Loss of capillary membrane integrity leads to fluid leading into interstitial space, leading to hypovolaemic shock– There is increased risk of bacterial infections (S. Aureus), acute peptic stress ulcers and lung injury   Before treating the burn, it is essential to measure the extent and depth of the burnExtent – Measured by Wallace’s Rule of Nines, divided body into 11 sections each measuring 9% surface area– Used to generate burn measurement quantified by the total body surface area (TBSA)   Depth – This is measured by the depth

Bullous pemphigoid This is an autoimmune skin condition causing blisters under the epidermis.– Due to a type II hypersensitivity reaction which gives destruction of hemi- desmosomes between basal cells and basal membrane.– IgG antibody is directed against BP180 and BP 230 of basement membrane – More common in elderly patients >70 years but there is no obvious cause  Appearance– Starts as a non-specific rash a month before the blisters– Then itchy blisters form around the skin folds.– Blisters are sup-epidermal and quite tense (do not rupture very easily) and heal without scarring – Blisters contains clear or cloudy yellowish fluid,

Bacterial Infections Acne Vulgaris This is a condition where there is increased sebum production due to increased androgens– This causes excess keratin production which block follicles making comedones-Anaerobic bacteria Propionibacterium acnes colonise plugs giving inflammation Appearance– Red spots with pustules on face, cheeks, neck and upper trunk N.B. Can become disseminated around the body with fever, malaise.– This is known as acne fulminans and needs to be treated in hospital.   Management:– 1st line is single topical creams –> Benzoyl peroxide (antimicrobial action) or Vitamin A derivative–  If not successful –> try multiple topical agents together– If still uncontrolled –> oral antibiotics – tetracyclines (unless pregnant

Acne Rosacea        This is a chronic skin disease of unknown cause in adults which characteristically affects the nose, cheeks and forehead, most often between the ages of 30-60. – It is more common in white people with blue eyes, made worse by sunlight Appearance– Starts with flushing before giving persistent redness– Gives pustule formation and prominent blood vessels (telangiectasia)– Can lead to rhinophyma – bulbous nose due to chronic inflammation   Management– Reduce the factors which cause flushing such as sun exposure– Tetracycline antibiotics for 6-12 weeks –> doxycycline, minocycline– If resistant –> co-trimoxazole or metronidazole– If

Eczema (Dermatitis) This is the general term which describes a condition which causes general inflammation of the skin.   Atopic Eczema (Atopic dermatitis) This is the most common type of eczema and most common inflammatory disease of early childhood– It affects about 20% of children under 5 and 2% of adults– It is an immunologically mediated inflammatory skin reaction, mediated by increased Th2 cells– This promotes pathogen specific IgE antibodies (type I hypersensitivity) increasing eosinophils and mast cells Cause: Underpinned by a genetic defect in skin barrier function– Associated with a loss of function variant of protein filaggrin.– This leads to

The skin functions as a barrier – made of the dermis and epidermis: The epidermis can be split into 4 main layers:1. Stratum corneum – composed of dead keratinocytes2. Stratum granulosum – has granules in keratinocytes3. Stratum spinosum – this layer is characterized by desmosomes between keratinocytes4. Stratum basalis – regenerative stem cell layer   When taking an assessment of the skin, the history is very important. i) Nature of the problem ii) Duration of the problem iii) Treatments so far iv) Allergies or Sensitivities:– Including atopy (eczema, asthma, allergy)   v) Sun exposure:– Skin response to sun– Can be