Benign/malignant dermatological lesions Flashcards
Solar keratosis
A: Pre-malignant abnormal skin proliferation due to prolonged UV exposure.
S: Usually multiple, flat or thickened scaly lesions, can be skin coloured or reddened. May be uncomfortable.
D: None-specific, biopsy if concern about progression to SCC
T: Cryotherapy, curettage, 5-fluorouracil or imiquimod
Keratocanthoma
A: Sun exposed areas commonly affected, can be triggered by a minor injury. Originates from hair follicle.
S: Dome-shaped, symmetrical lesion, often surrounded by inflamed skin and capped with keratin and debris
D: Difficult to discriminate from malignancy so biopsies are needed.
T: Includes cryotherapy, curettage and surgical excision.
Sebaceous cyst
A: Usually caused by blocked sebaceous glands or hair follicles
S: Usually asymptomatic lump, often on face, neck or trunk. The lump may become infected (red, hot and painful).
D: None, unless infection is suspected.
T: Surgical excision, can be removed with applications of heat pad.
Dermoid cyst
A: Benign tumours consisting of skin cells, hair follicles and sweat glands. They appear in early childhood due to a defect in skin tissue development.
S: Firm, dough-like lumps, usually 0.5-6cm and often occur on the face, neck or scalp.
D: US scan to plan surgery
T: Surgical removal
Lipoma
A: Benign tumours composed of fat cells, they may have a genetic element or arise from trauma.
S: Palpable soft, smooth lump beneath skin that is easily moved. Usually 2-10cm in size but can be bigger. Multiple tender lipomas are know as Dercum’s disease.
D: -
T: Usually none needed but can be removed surgically.
Basal cell carcinoma
A: Commonest skin malignancy, genetic susceptibility but it usually occurs with excessive sun exposure (more common in fair skinned individuals).
S: Slow growing, shiny, pearly nodule with ‘rolled edge’ and telangiectasia, commonly not the face. Very rarely metastasises.
D: Skin biopsy
T: Surgical excision, cryotherapy, radiotherapy and 5-fluorouracil. Excellent prognosis.
Squamous cell carcinoma
A: Second most common, originating in epidermis. Can be from excessive sun exposure, genetics, smoking, chronic ulceration (Marjolin’s ulcer), infections (HPV).
S: Usually appear on sun-exposed sites and are slow-growing tender, scaly or crusted lumps. May presents as ulcers that don’t heal.
D: Biopsy
T: Surgical excision and radiotherapy.
Good prognosis but 5% of tumours metastasise to local lymph nodes.
Bowen’s disease
A: SCC-in-situ, intradermal SCC. Can be from excessive sun exposure, genetics, smoking, chronic ulceration (Marjolin’s ulcer), infections (HPV).
S: Gradually enlarging, well demarcated erythematous plaque with an irregular border and surface crusting or scaling.
T: Cryotherapy, curettage, 5-fluorouracil, imiquimod cream or photodynamic therapy.
Reoccurrence is fairly common, a can progress to SCC.
Malignant melanoma
A: Malignant proliferation of melanocytes. Can be from sun damage, genetics, or from other moles. Highest mortality of skin cancers.
S: Common sites are skin, eyes and anus. Worrying features include:
- Asymmetry
- Border irregularity
- Colour variation
- Diameter > 6mm
- Evolving (enlarging/changing).
D: If melanoma is suspected then the lesion should be surgically excised with a 2-3mm margin. The biopsy should then be sent for histological diagnosis and staging.
T: Surgical excision with our without chemotherapy or radiotherapy.
Prognosis related to Breslow thickness (depth of tumour in mm) and Clark’s level (useful if 4mm but 95-100% if
Seborrheic keratosis
A: Appear with advancing age
S: Painless, raised lesions with “stuck on” appearance
D: Skin biopsy can confirm if diagnosis is in doubt
T: If needed, can be removed by cryotherapy or curettage