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Complications
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Local
• Wound sepsis, usually with Streptococcus pyo­genes or Pseudomonas aeruginosa.
Scarring.
Wound contractures.
General
Sepsis, particularly chest infection in inhalational injury, urinary tract infection resulting from cath­eterization and septicaemia directly from wound invasion.
Acute peptic ulceration (Curling’s ulcer).
Seizures in children, owing to electrolyte
imbalance.
Acute kidney injury, resulting from the initial
• hypovolaemia due to plasma loss, precipitation of haemoglobin or myoglobin, or nephrotoxic anti­microbial agents.
Psychological disturbance. Burn injuries are dis­proportionately sustained by children, the elderly and patients with mental health conditions. Patients with severe burns require assessment by a
Burns 85
psychiatric nurse or psychiatrist and often require psychological support and treatment.
Prognosis
The prognosis from a major burn is dependent upon the severity of the burn, total body surface area and physiological reserve of the patient. Young infants and the elderly carry a higher mortality than young adults. Refinements in the protocols used for severe burns, the organization of burn care to allow immedi­ate access to expert advice and early transfer to a major burns unit has resulted in improvements in the survivability of major burns in younger patients (<50 years of age). Very few deaths occur during resuscita­tion, with most deaths now occurring due to later complications, including sepsis.
Additional resources
Case 8: Burnt thorax Case 9: Burn treatment
1111
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The skin andits adnexae
Amer J. Durrani
Learning objectives
To understand the general functions of the skin.To understand the anatomy and embryology of the skin.To recognize the range of benign lesions and conditions that may
present in the skin.
To distinguish between melanoma and non- melanoma skin cancers,
and premalignant skin lesions, their presentation and management.
skin surface. The basal layer is the layer of origin of
General functions ofthe skin
The skin can be considered as the largest organ in the body (16% total body weight in adults). It has multiple protective functions: as a barrier to mechanical trauma, chemical and thermal injury, and entry of microorganisms. It has a metabolic function in regard to vitamin D synthesis and a critical role in thermoregulation.
Skin anatomy andembryology
The skin has an outer epidermis, which is in a con­tinuous state of regeneration. It is histologically divided into five layers (Figure 11.1). Cells mature from the basal layer to be shed as keratinocytes at the
Ellis and Calne’s Lecture Notes in General Surgery, Fourteenth Edition. Edited by Christopher Watson and Justin Davies. © 2023 John Wiley & Sons Ltd. Published 2023 by John Wiley & Sons Ltd. Companion website: www.wiley.com/go/Watson/GeneralSurgery14
most skin cancers.
Below the epidermis, the dermis is subdivided into a superficial layer (papillary dermis) and deep layer (reticular dermis). The skin appendages are located in the dermis and extend into subcutaneous fat. They are structures from which tumours and inflammatory skin conditions can arise (hair follicles, sebaceous, eccrine and apocrine sweat glands, pain, temperature and pressure receptors). The distinction between the two layers of the dermis is also of importance when considering burn injury and healing (Chapter10).
The dermis is a network of collagen that supports the neurovascular supply to the skin and dermal appendages. Elastin within the dermis provides stretch and elastic recoil, and loss of these fibres con­tributes to the ageing process seen in the skin. Hyaluronic acid and proteoglycans provide a gel to facilitate metabolite diffusion in the dermis.
The hypodermis is the layer beneath the skin and contains adipocytes, which provide insulation and can act as an energy source.
The epidermis is derived from ectoderm and der­mis from mesoderm. Merkel cells and melanocytes originate from the neural crest (see later for malig­nant tumours derived from these cell types), and Langerhans cells are of mesenchymal origin (involved in cellular immunity).
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Stratum corneum
Stratum lucidum
Stratum granulosum Epidermis
Stratum spinosum
Stratum basale
Papillary dermis
Hair
follicle
Figure11.1 Layers of the skin with adnexal structures.
Sebaceous
glands
Sweat gland
Epidermoid cyst
An epidermoid cyst (commonly referred to incorrectly as a sebaceous cyst) is a benign cyst that develops from the upper portion of a hair follicle. They are especially common on the scalp (pilar cyst), face, scrotum and vulva, and on the lobe of the ear. The cyst is fluctuant and cannot be moved separately from the overlying skin. There may be a typical central punctum (usually absent from a pilar cyst), and the contents are ‘cheesy’ with an unpleasant smell (keratin and cellular debris). The lining membrane consists of epidermis- like epithelium.
Epidermoid cysts may also result from traumatic implantation of epidermis into the subcutaneous tissue (inclusion cyst, sometimes referred to as an implanta­tion dermoid cyst). Typically, these are on the pulps of fingers; there may be a healed scar overlying them.
Reticular dermis
Dermis
Subcutaneous adipose tissue
Complications
• Infection.
• Calcification, producing a hard subcutaneous tumour misnamed a ‘benign calcifying epithelioma’.
• Ulceration, which may then resemble a fungating carcinoma (‘Cock’s peculiar tumour’
1
).
Treatment
An uninfected sebaceous cyst can be considered for removal in order to prevent possible complications, particularly the risk of infection. A small elliptical skin incision is made around the punctum of the cyst under local anaesthetic; the capsule is identified and
1
Edward Cock (1805–1892), Surgeon, Guy’s Hospital,
London, UK.
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the cyst removed intact. Failure to remove the cyst in its entirety may lead to recurrence.
If the cyst is acutely inflamed and infected, incision and drainage may be required and the wound allowed to heal by secondary intention, with a course of oral antibiotics. This may be followed later by subsequent excision of the capsule wall if the cyst recurs.
Dermoid cyst
This is a congenital subcutaneous cystic swelling resulting from an embryological nest of epithelial cells along a line of fusion. The common sites are over the external angular process of the frontal bone (the external angular dermoid at the upper outer margin of the orbit), the root of the nose (internal angular dermoid) and in the midline. When in rela­tion to the skull, the underlying bone is usually hol­lowed out around it. The possibility of communication with an intracranial dermoid or the meninges should be excluded by ultrasound and, if indicated, mag­netic resonance imaging (MRI) scan prior to excision.
Plantar warts
Otherwise known as verrucas, these occur on the weight-
bearing areas of the foot. Pressure forces the wart into the deeper tissues, producing intense local pain on walking. They may occur in epidemics in schools and other such places where the hygiene of the communal bath or changing room is not of a high standard. They should be treated by topical podophyllin or curettage.
Ganglion
A ganglion presents as a cystic, subcutaneous swell­ing that transilluminates brilliantly. It most com­monly occurs around the wrist and dorsum of the foot (joint capsule origin), or along the flexor aspect of the fingers and on the peroneal tendons (tendon sheath origin). Although ganglia are among the most com­mon surgical lumps, their origin is uncertain. They may represent a benign myxoma of joint capsule or tendon sheath, a hamartoma or myxomatous degen­eration due to trauma. They are thin­a synovial lining and contain clear colourless material with a jelly-
like consistency.
walled cysts with
Verruca vulgaris (wart)
This is a well- localized horny projection that is com­mon on the fingers, hands, feet and knees, particu­larly of children and young adults. Crops of warts may occur on the genitalia and perianal region, in many cases spread by sexual contact. Warts are often multi­ple and are due to a number of different strains of human papilloma virus.
Microscopically, there is a local hyperplasia of the prickle cell layer (stratum spinosum) of the skin (acanthosis) with marked surface cornification.
Treatment
Untreated, warts usually vanish spontaneously within 2 years, hence the apparent efficacy of folklore ‘wart cures’. Often, reassurance that these lesions will disappear is all that is required, but if treatment is demanded, they can be treated with topical applica­tion of silver nitrate, podophyllin, frozen with liquid nitrogen or curetted under local or general anaesthesia.
Treatment
The patient may complain of discomfort or of the cos­metic appearance; if so, the cyst should be excised under a general anaesthetic using a bloodless field produced by a tourniquet. The old­ment of hitting the ganglion with the family bible rup­tures the cyst, but recurrence usually occurs after some time. Unfortunately, recurrence is also com­mon after surgical excision.
fashioned treat-
Pilonidal sinus
The majority of pilonidal sinuses occur in the skin of the natal cleft. They may be solitary or appear as a row in the midline. Frequently, tufts of hair are found lying free within the sinus (Latin pilus, hair; nidus, nest).
Usually, young adults are affected, males more than females, and more often dark- haired individu­als; the sinuses are rarely seen in children and do not present until adolescence. They are an uncommon
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occupational disease of hairdressers, in whom sinuses may occur in the clefts between the fingers. They are very occasionally found in the axilla, at the umbilicus, in the perineum and on the sole of the foot as well as on amputation stumps.
Aetiology
The occurrence of pilonidal sinuses remote from the natal cleft, and on the hands and feet of people working with cattle, where the contained hair is clearly of ani­mal origin, supports the hypothesis that these sinuses occur by implantation of hair into the skin; these set up a foreign body reaction and produce a chronic infected sinus. It may be that, in some cases, postanal pits act as traps for loose hairs, thus combining both the congeni­tal and acquired theories of skin follicles from its distal end and works its way in due to tapered lateral hair extensions angled proxi­mally, rather as a grass seed migrates up one’s sleeve.
origin. The hair enters the
Clinical features
The pilonidal sinus is asymptomatic until it becomes infected; there is then a typical history of recurrent abscesses, which either require drainage or discharge spontaneously.
Treatment
1 Acute abscess. This is drained and allowed to heal
by secondary intention.
Quiescent sinus. The track is excised, treated with
2
injection of fibrin glue, or simply laid open and allowed to heal by secondary intention. Recurrence is diminished by keeping all incisions away from the midline and keeping the surrounding skin free from hair by shaving or the use of depilatory creams. Laser treatment can be effective in reduc­ing hair growth in the area. Following excision of the sinus, particularly if it recurs after previous sur­gery, a local flap may be required with layered wound closure, to reduce the risk of recurrence.
Hidradenitis suppurativa
Hidradenitis suppurativa is a chronic inflammatory skin condition that affects apocrine gland- bearing skin in the axillae, groin, and under the breasts.
Typically, patients present with persistent or recur­rent abscesses, some of which may result in chroni­cally discharging sinuses. Recurrent infections are common, as is the resultant scarring. It is more com­mon in women, usually starting during puberty; there may be a family history (30–40% of patients) and it is associated with obesity and cigarette smoking.
Treatment
Management of hidradenitis suppurativa should include smoking cessation, weight control, wound care and pain management. Topical therapies may be effective in mild disease. Systemic antibiotics are frequently used for the control of acute infective episodes, often in conjunction with surgical incision and drainage. Medical therapy with biological agents may be of benefit.
Conditions affecting thenails
The nails are the site of some common and important surgical conditions.
Paronychia
Paronychia denotes bacterial infection of the lateral nail fold, usually of the finger, but it may complicate an ingrowing toenail (see later in this chapter). An acute paronychia is diagnosed when the nail fold is red, swollen and tender, and pus may be visible beneath the skin.
Treatment
If seen before pus has formed, while the nail fold is cellulitic, purulent infection may be aborted by a course of flucloxacillin or other appropriate anti­staphylococcal antibiotic together with immobiliza­tion by a splint to the finger and elevation of the arm in a sling. If pus is present, drainage is performed through an incision carried proximally through the nail fold, combined with removal of the base of the nail if pus has tracked beneath it.
Chronic paronychia is seen in those whose occupa­tion requires constant soaking of the hands in water, but it may also occur as a result of fungal infection (Candida) of the nails and where the peripheral circulation is defi­cient, as in Raynaud’s phenomenon (Chapter12).
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Ingrowing toenail
This is nearly always confined to the hallux and is usually due to a combination of tight shoes (particularly trainers) and the habit of paring the nail downwards into the lateral nail fold, rather than transversely; the sharp edge of the nail then grows into the side of the nail bed, producing ulceration and infection.
Treatment
If seen before infection has occurred, advice is given on correct cutting of the nails; advice is also given to avoid nylon socks and trainers. A small wick of cot­ton wool tucked daily into the side of the nail bed, after preliminary soaking of the feet in hot water to soften the nails, enables the nail to grow up out of the fold.
If an acute paronychia is present, drainage will be required by means of removal of the side of the nail or avulsion of the whole nail. For recurrent cases when the infection has settled, the affected side may be excised together with the nail root (wedge excision), or the entire nail may be oblite­rated completely by excision of the nail root
2
(Zadik’s liquefied phenol, or a combination of the two techniques.
operation) or by treating the nail bed with
Onychogryphosis
The nail is coiled like a ‘ram’s horn’. It may affect any of the toes, although the hallux is the most common site. It may follow trauma to the nail bed and is usually found in elderly subjects.
Treatment
Relatively mild examples can be kept under control by trimming the nail with bone- cutting forceps. Merely avulsing the nail is invariably followed by recurrence, and the only adequate treatment is exci­sion of the nail bed.
Subungual haematoma
As a result of crush injury to the terminal phalanx, with or without fracture of the underlying bone, a tense, pain­ful haematoma may develop beneath the nail. Relief is afforded by evacuating the clot through a hole made by either a dental drill or a red­cedures are painless. Occasionally, a small haematoma may develop after a trivial or forgotten injury and clini­cally may closely simulate a subungual melanoma.
hot sterile needle; both pro-
Subungual exostosis
This is nearly always confined to the hallux and is especially found in adolescents and young adults. It appears as a reddish­which is tender on pressure. The exostosis may ulcer­ate through the overlying nail, producing an infected granulating mass. The diagnosis is confirmed by X- ray of the toe, and treatment is to remove the nail and excise the underlying exostosis.
brown area under the nail,
Subungual melanoma
The nail bed is a common site for malignant melanoma (see later in this chapter). There is a long history of slow growth and often a misleading history of trauma. The lesion should be confirmed by removal of the nail plate and excision biopsy followed by mul­tidisciplinary team discussion and management with the likely recommendation for wide local excision (which may involve amputation of the digit) with sen­tinel node biopsy.
Glomus tumour
The nail beds of the fingers and toes are a common site of this extremely painful lesion, which is a benign tumour arising in a subcutaneous glomus body (highly innervated arteriovenous anastomoses in dermis responsible for temperature regulation). It is considered later in this chapter.
Lesions ofthe nail bed
It is convenient to list a number of relatively common conditions that affect the nail bed.
2
Frank Raphael Zadik (1914–1995), Orthopaedic Surgeon,
Leigh and Wigan, UK.
Tumours ofthe skin and subcutaneous tissues
Classication
1 Epidermal.
a Benign: skin tag, keratoacanthoma and sebor-
rhoeic keratosis.
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b Premalignant: Actinic keratosis, Bowen’s dis-
ease and squamous cell carcinoma in situ.
Non- melanoma skin cancer: squamous cell
c
carcinoma, basal cell carcinoma and Marjolin’s ulcer.
d
Secondary cutaneous deposits, e.g. from carci-
noma of breast, lung, kidney, leukaemia and Hodgkin’s disease.
2
Pigmented skin lesions and malignant melanoma. Tumours of sebaceous and sweat glands.
3 4
Dermal tumours from blood vessels, lymphatics,
nerves, fibrous tissue or fat.
Epidermal tumours
Skin tag (acrochordon)
This is a common, benign, pedunculated tumour, often pigmented with melanin. Microscopically, it comprises a keratinized papillary tumour of squa­mous epithelium.
Keratoacanthoma (molluscum sebaceum)
This is a lesion that occurs in elderly patients, most commonly men, in sun- exposed areas such as the face and nose (75%), although it may occur on any skin surface. It appears as a rapidly growing nodule, which may reach 3cm or more in diameter in a few weeks, with a characteristic central crater filled by a keratin plug. It closely resembles a squamous carci­noma or rodent ulcer in appearance, and it is only the history of very rapid growth that helps differentiate it from the latter.
Histologically, it consists of a central crater filled with keratin surrounded by hypertrophied squamous stratified epithelium. There is no invasion of the sur­rounding tissues.
If left untreated, the lesion disappears over a period of 4–5months, leaving a faint white scar. It appears to be of hair follicle origin and may be associated with a minor injury.
Treatment
It is safest to remove the lesion to establish histologi­cal proof of the diagnosis.
Seborrhoeic keratosis (basal cell papilloma)
This is a common tumour occurring after the age of 40 years. It appears as a yellowish or brown raised lesion on the face, arms or trunk, and is often multiple.
Table11.1 Fitzpatrick skin types
Skin type Typical appearance
I Pale white skin, blue
eyes, red or blond hair
II Fair skin, blue eyes Burns easily, does
III Darker white skin Tans, after initial
IV Light-
V Brown skin Rarely burns, tans
VI Dark brown or black
It often appears greasy, and its surface is by a network of crypts.
Microscopically, there is hyperkeratosis,
of the basal cell layer and melanin pigmentation.
The lesion is entirely benign, but if there is diagnostic doubt on clinical examination and with a dermatoscope, the exclusion of skin cancer can only be made with certainty by incision or excision biopsy and histological examination.
brown skin Burns minimally,
skin
Response to sun exposure
Always burns, does not tan
not tan
burn
tans easily
darkly easily
Never burns, always tans
characterized
proliferation
Solar (actinic) keratosis
This is a small, hard, brown, scaly tumour on sun­exposed areas of skin (e.g. the forehead, ears and backs of hands) of the elderly. Keratoses are more common in individuals with fair skin (Fitzpatrick skin types I and II prolonged exposure to ultraviolet light.
Microscopically, hyperkeratosis is present, often with atypical dividing cells in the basal layer of the epidermis.
The lesions may be treated with liquid nitrogen cryotherapy or curettage; large areas may require top­ical chemotherapy (e.g. 5­has also been used, and acts as an immune modifier, stimulating an immune response with resolution of the lesions.
3
omas Fitzpatrick (1919–2003), Dermatologist, Massachusetts General Hospital, Boston. e Fitzpatrick scale is a 6- point scale describing how dierent skin types respond to sun exposure.
3
; Table 11.1) usually associated with
fluorouracil). Imiquimod
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The importance of this lesion is that it may undergo
change into a squamous cell carcinoma.
Bowen’s disease
Also known as intra- epidermal squamous cell carci­noma, this appears as a very slowly growing, red, scaly plaque, and represents squamous carcinoma in situ. It may be mistaken for a psoriatic plaque. Human papillomavirus (HPV) DNA (particularly HPV16, but also HPV2) has been found in some lesions.
Microscopically, atypical keratinocytes with vacuoli­zation, mitoses and multinucleated giant cells are prominent in the epidermis, but the basal layer is intact.
Treatment is excision; if left untreated, eventually a squamous cell carcinoma will supervene.
4
Cutaneous squamous cell carcinoma
This is the commonest form of skin cancer after basal cell carcinoma, occurring on skin in areas exposed to sunshine, such as the face and backs of the hands. Like solar keratoses, it is relatively common in white subjects (Fitzpatrick skin type I), with cumulative lifetime sun exposure as the most significant risk factor. Incidence increases after the age of 40 years and the male:female ratio is 3:1.
Predisposing factors
These include the following.
Solar keratosis.
• Bowen’s disease.
• Exposure to sunshine or ultraviolet irradiation.
Exposure to ionizing irradiation.
• Infection with human papilloma virus subtypes
6and 11.
• Carcinogens, e.g. pitch, tar, soot and mineral oils.
• Chronic ulceration, particularly in burns scars
(Marjolin’s ulcer– see below).
• Immunosuppressive drugs, e.g. azathioprine and
ciclosporin.
Pathology
Macroscopically, it presents as a typical malignant ulcer with indurated, raised, everted edges and a central scab.
Microscopically, there are solid columns of epithe­lial cells growing into the dermis with epithelial pearls of central keratin surrounded by prickle cells. Occasionally, anaplastic tumours are seen, in which these pearls are absent.
Spread occurs by local infiltration and then via lym­phatics. Blood­advanced cases.
borne spread occurs only in very
Treatment
A tissue diagnosis with either an incision or excision biopsy is mandatory. Subsequent treatment may con­sist of a wider excision, which may necessitate a reconstruction (skin graft and local flap) depending on the site and size of the lesion. Adjuvant radiother­apy may be required based on the histological charac­teristics of the primary tumour. If the regional lymph nodes are involved, block dissection is indicated.
Marjolin’s ulcer
This is the name applied to malignant change in a scar, ulcer or sinus, for example, a chronic venous ulcer, an unhealed burn or the sinus of chronic osteo­myelitis. It has the following characteristics:
slow growth, because the lesion is relatively
avascular;
painless, because the scar tissue does not contain
cutaneous nerve fibres;
lymphatic spread is late, because the scar tissue
produces lymphatic obliteration.
Once the tumour reaches the normal tissues beyond the diseased area, rapid growth, pain and lymphatic involvement take place.
5
Basal cell carcinoma (rodentulcer)
This is the most common form of skin cancer in white people (80% of non­occurs usually in elderly subjects, in males twice as commonly as in females. Ninety percent are found on the face above a line joining the angle of the mouth to the external auditory meatus, particularly around the eye, the nasolabial folds and the hairline of the scalp. The tumour may, however, arise on any part of the
melanoma skin cancers). It
4
John Templeton Bowen (1857–1941), Dermatologist,
Harvard Medical School, Boston, MA, USA.
5
Jean Nicholas Marjolin (1780–1850), Surgeon, Hôpital
Sainte- Eugénie, Paris, France.
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skin, including the anal margin. Predisposing factors are exposure to sunlight or irradiation.
Pathology
Macroscopically and on examination with a dermato­scope, the tumour has raised, rolled but not everted edges. It consists of pearly nodules over which fine blood vessels can be seen to course (telangiectasia). Starting as a small nodule, the tumour very slowly grows over the years with central ulceration and scabbing.
Microscopically, solid sheets of uniform, darkly staining cells arising from the basal layer of the skin are seen. Prickle cells and epithelial pearls are both absent.
Spread is by local infiltration, with slow but steady destruction of surrounding tissues; in advanced cases, the underlying skull may be eroded, or the face, nose and eye may be destroyed, hence the name ‘rodent’. Lymphatic and blood- borne spread occur with extreme rarity.
Treatment
Treatment is by surgical excision, with an adequate measured margin, with reconstruction if required (skin graft or local flap). At anatomical sites where this may prove challenging, i.e. for high risk tumours at high risk sites (e.g. eyelid, periorbital and nasal areas),
6
Mohs
micrographic surgery offers the lowest risk of tumour recurrence. It is also indicated in late cases where the tumour has recurred after irradiation or has invaded the underlying bone or cartilage.
Adjuvant radiotherapy may be required or used as a primary treatment depending on patient and tumour factors following a multidisciplinary discussion.
Pigmented skin lesions andmalignant melanoma
Benign pigmented skin lesions
• Intradermal melanoma or naevus (the common
mole).
6
Frederic Edward Mohs (1910–2002), Surgeon, University of Wisconsin. Pioneered the concept of rapid histological examination at the time of tumour excision to ensure complete tumour excision while allowing maximal preservation of healthy tissue.
• Junctional melanoma or naevus. Compound melanoma or naevus.
Spitz naevus.
Malignant melanoma.
Nearly everyone possesses one or more moles; some have hundreds, although they may not become apparent until after puberty. Those moles that are entirely within the dermis remain benign, but a small percentage of the junctional naevi, so called because they are seen in the basal layer of the epidermis at its junction with the dermis, may undergo malignant change (Figure11.2).
Intradermal melanoma or naevus
This is the most common variety of mole. The naevus may be light or dark in colour and may be flat or raised, hairy or hairless. A hairy mole is nearly always intradermal. They may be found in any place in the body except the palm of the hand, the sole of the foot or the scrotal skin.
Histologically, there is a nest of melanocytes situ­ated entirely within the dermis where the cells form
encapsulated masses. They never undergo
non­malignant change, and need no treatment unless the diagnosis is uncertain.
Junctional melanoma or naevus
The junctional naevus is pigmented to a variable shade from light brown to almost black. It is nearly always flat, smooth and hairless. It may occur any­where on the body and, unlike the intradermal nae­vus, may be found on the palm of the hand, sole of the foot and the genitalia.
Histologically, naevus cells are seen in the basal layers of the epidermis from which the cells may spread to the surface.
Only a small percentage of junctional naevi undergo malignant change, but it is from this group that the vast majority of malignant melanomas arise.
Compound melanoma or naevus
Clinically, this is indistinguishable from the intradermal naevus, but histologically, it has junc­tional elements that make it potentially malig­nant. It may be darker and palpable due to a raised border.
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(a) Normal (b) Intradermal melanoma
(c) Junctional melanoma (d) Malignant melanoma
Figure11.2 (a) The normal skin contains melanocytes (shown as cells) and melanin pigment shown as dots. The
pigment increases in sunburn and freckles. (b) A benign intradermal naevus; the melanocytes are clumped together in the dermis to form a localized benign tumour. (c) A junctional naevus with melanocytes clumping together in the basal layer of the epidermis. (d) These are usually benign but may occasionally give rise to an invasive malignant melanoma.
Spitz naevus
Spitz naevus is an uncommon type of mole (melanocytic naevus) that usually affects young people and children, hence it used to be known as a juvenile melanoma. It is a benign skin tumour, but it may resemble a malignant melanoma clinically and microscopically, so Spitz naevi are often excised as a precaution.
7
Sophie Spitz (1910–1956), Pathologist, Memorial Sloan
Kettering Cancer Centre, NewYork, NY, USA.
7
Malignant melanoma
Malignant melanomas develop from melanocytes, which are situated in the basal layer of the epidermis and originate from the neuroectoderm of the embry­onic neural crest. Some melanomas contain no visi­ble pigment (amelanotic melanoma). While most melanomas arise in the skin, they may also occur at other sites to which neural crest cells migrate, in par­ticular the pigmented choroid layer of the eye.
Malignant melanomas can arise de novo or in pre­existing naevi, either junctional naevi or compound naevi where there is a junctional component. They mainly occur in fair- skinned people on light- exposed
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