Common skin lesions
- Ageing skin
- Epidemiology of non-melanoma skin cancer
- Squamous cell carcinoma
- Basal cell carcinoma CME
- Benign melanocytic lesions
- Nonmelanocytic congenital naevi
- Benign keratinocytic and adnexal lesions
- Dermal and subcutaneous tumours
- Introduction to skin surgery
- Processing skin biopsies
- Surgical procedures
- Non-surgical physical treatments
- Topical treatment of photodamage
Originally developed for the University of Auckland Goodfellow Unit in 2007. The course and several interactive quizzes are available on CD – from the Goodfellow Unit. You may download the order form for the CD-ROM (PDF file).
Author: Hon A/Prof Amanda Oakley, Dermatologist, Hamilton, New Zealand, 2008.
Images have been sourced from the following:
- Hon Assoc Prof Amanda Oakley
- The Department of Dermatology, Waikato Hospital
- MoleMap New Zealand (with permission)
Dermal and subcutaneous lesionsNext Previous
- Describe clinical features and management of dermal and subcutaneous tumours of vascular, neural, fibrous, metastatic or other origin.
Angiokeratoma is a scaly vascular papule due to epidermal proliferation encircling dilated vessels. Angiokeratoma may be solitary or diffuse. Diffuse lesions may be genital (Fordyce), acral (Mibelli) or rarely, generalised (Fabry disease: deficiency of ceramide trihexosidase resulting in deposition of glycosphingolipids).
Pyogenic granulomas are formed of granulation tissue (vascular proliferation with inflammatory infiltrate). There is a characteristic collarette of skin around a juicy or friable red nodule that bleeds easily. Pyogenic granulomas may be due to minor trauma plus Staphylococcal infection. They are particularly common on lips and fingers, and during pregnancy and childhood.
Cherry angiomas are extremely common benign red, blue, purple or almost black lesions occurring in middle age on the trunk. They can readily be distinguished from melanocytic lesions by dermoscopy, which shows red, blue or purple lacunes. Occasionally they become thrombosed and may fall off or persist as a firm bluish papule.
Glomus tumor presents most often as a painful subungual papule.
Malignant vascular lesions
Angiosarcoma usually arises on the head and neck, or arise in areas of chronic lymphoedema. It presents as an advancing area of purpura and ecchymosis, usually in an elderly person. Prognosis is poor as the tumour is often multifocal so difficult to excise, and only partially sensitive to radiation.
Kaposi sarcoma (KS) is a low grade vascular malignancy related to human herpesvirus 8. There are four types.
- Classic KS
- African endemic KS
- KS in iatrogenically immunocompromised patients
- AIDS-related KS
Acquired telangiectasia is common and affects vessels of various size. Some examples are illustrated.
Acquired telangiectatic naevus
Systemic sclerosis (CRST syndrome)
Hereditary telangiectasia (Osler-Rendu-Weber)
Benign hereditary telangiectasia
Telangiectasia eruptiva macularis perstans (mastocytosis)
Oestrogen-induced telangiectasia (pregnancy)
Telangiectasia due to potent topical steroids
Thread veins / venulectasia (venous disease)
Basal cell carcinoma
Telangiectasia of unknown origin
Acquired lymphangiectasia usually follows lymph node dissection, or traumatic injury interrupting lymphatic drainage, usually in the axilla or genital area. Frogspawn-like clear or haemorrhagic papules develop some time later and tend to cause distressing ooze.
Neurofibromas are spindle cell tumours and present as soft to firm, single or multiple dermal nodules that may be pedunculated. Sometimes it is possible to invaginate the lesions because there is a defect in the dermis. There are diffuse, pigmented and plexiform variants. Plexiform neurofibroma is pathognomonic of NF1 neurofibromatosis; these may rarely undergo malignant transformation. Neurofibromatosis may also present with café au lait macules (>6), which are present at birth; axillary freckling; and other types of cutaneous neurofibroma, which arise later in childhood and adult life.
Other neural tumours include neurilemmoma, neuroma, granular cell tumour and neurofibrosarcoma (malignant schwannoma).
Merkel cell carcinoma
Merkel cell carcinoma (primary neuroendocrine carcinoma of the skin) is rare. It presents as a rapidly growing violaceous nodule that can ulcerate. It frequently recurs after excision; distant metastases develop in about 40% and 30% die of their disease within 5 years.
Dermatofibromas (histiocytomas) are common firm dermal papules caused by a proliferation of fibroblasts. They often follow insect bites, so most frequently arise on lower legs. They dimple on lateral compression.
Keloids are scars with excessive bands of collagen.
A solitary angiofibroma may also be called fibrous papule or perifollicular fibroma. These are very common the nose and look like intradermal naevi. They can be removed by shave excision or electrodessication. Multiple angiofibromas around the nose and cheeks are associated with tuberous sclerosis, which appear during childhood and become increasingly prominent. These patients may also have periungual fibromas.
Skin tags are pedunculated papillomas filled with loose collagen.
Other fibrous lesions include:
- Acquired digital fibrokeratoma
- Infantile digital fibromatosis
- Giant cell tumour
- Dermatofibrosarcoma protuberans
- Malignant fibrous histocytoma
- Atypical fibroxanthoma
- Epithelioid sarcoma
Cutaneous lesions due to distant primaries are most often due to:
- Metastatic squamous cell carcinoma
- Metastatic adenocarcinoma
- Metastatic breast carcinoma
- Metastatic small cell (oat-cell) carcinoma of lung
Lipomas are very common. They are due to a proliferation of adipose tissue and present as solitary or multiple asymptomatic soft subcutaneous nodules. Multiple lesions are seen in association with various syndromes and may be familial.
Leiomyoma includes multiple piloleiomyomas, genital leiomyoma and angioleiomyoma. They usually present in young adults and may be painful.
Uncommon skin tumours include:
- Osteoma cutis
- Cutaneous endometriosis
- Accessory tragus
Look for the skin lesions described in this section in the next twenty or so patients you see.