Dermatology Flashcards
<p>Define basal cell carcinoma.</p>
<p>Basal cell carcinoma (BCC) of the skin is a common neoplasm, related to exposure to sunlight.</p>
<p>Explain the aetiology/risk factors of basal cell carcinoma.</p>
<p>Ultraviolet (UV) radiation<br></br>Sun exposure<br></br>X Ray exposure<br></br>Arsenic exposure<br></br>Xeroderma pigmentosum<br></br>Basal cell nevus syndrome (Gorlin-Goltz syndrome)<br></br>Transplant patients</p>
<p>Summarise the epidemiology of basal cell carcinoma.</p>
<p>BCC is the most common malignancy of the skin in fair-skinned adults in the US, Australia, and Europe and its incidence is increasing.</p>
<p>Recognise the presenting symptoms of basal cell carcinoma.</p>
<p>Papules with associated telangiectasias<br></br>Plaques, nodules, and tumours with rolled borders<br></br>Small crusts and non-healing wounds<br></br>Non-healing scabs<br></br>Pearly papules and/or plaques</p>
<p>Recognise the signs of basal cell carcinoma on physical examination.</p>
<p>Metastases associated with large or neglected BCC</p>
<p>Local destruction with advanced lesion</p>
<p>Identify appropriate investigations for basal cell carcinoma and interpret the results.</p>
<p>Biopsy for dermatohistopathology</p>
<p>Define candidiasis.</p>
<p>Oral candidiasis involves a local infection of oral tissues by yeasts of the genus Candida, mostly C albicans.</p>
<p>Explain the aetiology/risk factors of candidiasis.</p>
<p>Hyposalivation/xerostomia<br></br>Poor oral hygiene, especially among denture wearers<br></br>Malabsorption and malnutrition<br></br>Advanced malignancy<br></br>Cancer chemotherapy and radiotherapy<br></br>HIV infection<br></br>Endocrine disturbance (e.g., diabetes mellitus, hypoparathyroidism, pregnancy, hypoadrenalism)<br></br>Immunosuppressive agents (e.g., systemic corticosteroid therapy)<br></br>Current or recent past use of broad-spectrum or multiple narrow-spectrum antibiotics</p>
<p>Summarise the epidemiology of candidiasis.</p>
<p>It is the most common oral fungal infection and is commonly seen in infants and older adults, and also with states of local and systemic immunological suppression.</p>
<p>Recognise the presenting symptoms of candidiasis. Recognise the signs of candidiasis on physical examination.</p>
<p>Creamy white or yellowish plaques, fairly adherent to oral mucosa<br></br>Cracks, ulcers, or crusted fissures radiating from angles of the mouth (angular cheilitis).<br></br>Spotty red areas on the buccal mucosa<br></br>Lesions confined to the outline of a dental prosthesis</p>
<p>Identify appropriate investigations for candidiasis and interpret the results.</p>
<p>Superficial smear of lesion for microscopy</p>
<p>Define cellulitis.</p>
<p>Cellulitis is an acute spreading infection of the skin with visually indistinct borders that principally involves the dermis and subcutaneous tissue. It is characterised by erythema, oedema, warmth, and tenderness, and commonly occurs in an extremity.</p>
<p>Define erysipelas.</p>
<p>Erysipelas is a distinct form of superficial cellulitis with notable lymphatic involvement and is raised, sharply demarcating it from uninvolved skin.</p>
<p>Explain the aetiology/risk factors of cellulitis and erysipelas.</p>
<p>Prior episode of cellulitis<br></br>Ulcer/wound<br></br>Dermatosis<br></br>Tinea pedis interdigitalis<br></br>Lymphoedema<br></br>Venous insufficiency/chronic leg oedema</p>
<p>Summarise the epidemiology of cellulitis and erysipelas.</p>
<p>Cellulitis is a common condition; a general practice with approximately 2000 people will have about 30 consultations for 'cellulitis and abscess' each year.</p>
<p>Recognise the presenting symptoms of cellulitis and erysipelas. Recognise the signs of cellulitis and erysipelas on physical examination.</p>
<p>Skin discomfort<br></br>Macular erythema with indistinct borders on the skin<br></br>Disruption of cutaneous barrier<br></br>Raised erythema with clearly demarcated margins (erysipelas)</p>
<p>Identify appropriate investigations for cellulitis and erysipelas and interpret the results.</p>
<p>FBC<br></br>Purulent focus culture and molecular diagnostic procedures</p>
<p>Generate a management plan for cellulitis and erysipelas.</p>
<p><strong>1st line: </strong>Parenteral antibiotic with MRSA cover</p>
<p><u>Plus:</u><br></br>Antibiotic with Pseudomonas cover if immunocompromised</p>
<p>Identify the possible complications of cellulitis and erysipelas and its management.</p>
<p>Sepsis<br></br>Chronic oedema in affected extremity</p>
<p>Summarise the prognosis for patients with cellulitis and erysipelas.</p>
<p>The prognosis of cellulitis is excellent. Most episodes of cellulitis resolve with therapy, and major sequelae are absent. However, it is believed that an episode of cellulitis may leave residual damage to draining lymphatics and perhaps increase the likelihood of recurrence in the future.</p>
<p>Define eczema.</p>
<p>Eczema is an inflammatory skin condition characterised by dry, pruritic skin with a chronic relapsing course.</p>
<p>Explain the aetiology/risk factors of eczema.</p>
<p>Age <5<br></br>Asthma<br></br>Family history of eczema<br></br>Allergic rhinitis<br></br>Active and passive exposure to smoke</p>
<p>Summarise the epidemiology of eczema.</p>
<p>It can affect all age groups, but it is most commonly diagnosed before 5 years of age and affects 10% to 20% of children. Eczema usually presents in childhood, with 45% of patients diagnosed by 6 months of age, and 70% to 85% by 5 years of age.</p>
<p>Recognise the presenting symptoms of eczema. Recognise the signs of eczema on physical examination.</p>
<p>Pruritus<br></br>Xerosis (dry skin)<br></br>Erythema<br></br>Scaling<br></br>Vesicles<br></br>Papules<br></br>Keratosis pilaris<br></br>Excoriations<br></br>Lichenification<br></br>Hypopigmentation</p>
<p>Identify appropriate investigations for eczema and interpret the results.</p>
<p>No investigations are needed.</p>
<p>Define epidermoid and pilar cysts.</p>
<p>Epidermoid cysts, also called sebaceous, keratin, or epithelial cysts, are small, hard lumps that develop under the skin. These cysts are common. They grow slowly. They do not cause other symptoms and are nearly never cancerous. About 1% of these may progress to SCC or BCC.</p>
<p>Explain the aetiology/risk factors of epidermoid and pilar cysts.</p>
<p>HPV infection<br></br>Acne<br></br>Excessive exposure to the sun<br></br>Other skin conditions</p>
<p>Summarise the epidemiology of epidermoid and pilar cysts.</p>
<p>Epidermoid cysts are the most common cutaneous cysts and typically occur in the third and fourth decades of life.</p>
<p>Recognise the presenting symptoms of epidermoid and pilar cysts. Recognise the signs of epidermoid and pilar cysts on physical examination.</p>
<p>Epidermoid cysts are often found on the face, head, neck, back, or genitals. They can range in size from 1/4 inch to 2 inches across. They look like a small bump, are tan to yellow in color, and are filled with thick, smelly matter. They do not cause any pain and can usually be ignored.</p>
<p>Identify appropriate investigations for epidermoid and pilar cysts and interpret the results.</p>
<p>No investigations are necessary. They can be diagnosed by examination only. Sometimes an ultrasound may be used.</p>
<p>Define erythema multiforme.</p>
<p>Erythema multiforme (EM) is typically an acute, self-limiting but often relapsing, mucocutaneous inflammatory condition. It is a hypersensitivity reaction associated with certain infections, vaccinations, and, less commonly, medications.</p>
<p>Explain the aetiology/risk factors of erythema multiforme.</p>
<p>Prior occurrence<br></br>Herpes simplex virus (HSV) infection<br></br>Mycoplasma pneumonia</p>
<p>Summarise the epidemiology of erythema multiforme.</p>
<p>The incidence of EM is not known, although it is considered to be relatively common. Peak incidence occurs in the second and third decades, and it rarely occurs in patients under 3 or over 50 years of age.</p>
<p>Recognise the presenting symptoms of erythema multiforme. Recognise the signs of erythema multiforme on physical examination.</p>
<p>Target lesions of the extremities<br></br>Recurrent disease<br></br>Mucosal erosions<br></br>Rapid onset of lesions<br></br>Self-limiting course<br></br>Clustered vesicles on an erythematous base<br></br>Rhonchi, rales, and/or wheezes</p>
<p>Identify appropriate investigations for erythema multiforme and interpret the results.</p>
<p>FBC<br></br>Serum electrolytes<br></br>Herpes simplex virus (HSV) serology<br></br>Rapid PCR<br></br>Cold-haemagglutination serology<br></br>M pneumoniae titres<br></br>CXR</p>
<p>Define erythema nodosum.</p>
<p>Erythema nodosum (EN) is a common cutaneous hypersensitivity reaction consisting of erythematous, tender nodules most commonly located over the shins, but also reported over the thighs, upper extremities, calves, buttocks, and face.</p>