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The history 327
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14.1 Functions of the skin
Protection against physical injury and injurious substances, including
ultraviolet radiation
Anatomical barrier against pathogens
Immunological defence
Retention of moisture
Thermoregulation
Calorie reserve
Appreciation of sensation (touch, temperature, pain)
Vitamin D production
Absorption – particularly foetal and neonatal skin
Psychosexual and social interaction
The deep subcutis contains adipose and connective tissue.
Dermatoses (diseases of the skin) may affect all three layers and, to a greater or lesser extent, the various functions of the skin.
Hair
Hair plays a role in the protective, thermoregulatory and sensory functions of skin, and also in psychosexual and social in­teractions. There are two main types of hair in adults:
Vellus hair, which is short and ne and covers most of the
body surface.
Terminal hair, which is longer and thicker and is found on the
trunk and limbs, as well as the scalp, eyebrows, eyelashes, and pubic, axillary and beard areas.
Abnormalities in hair distribution can occur when there is transitioning between vellus and terminal hair types (e.g., hir­sutism in women) or vice versa (androgenic alopecia). Hairs undergo regular asynchronous cycles of growth and, thus, in
health, mass shedding of hair is unusual. Hair loss can occur as a result of disorders of hair cycling, conditions resulting in damage to hair follicles (such as scarring inammatory processes), or structural (fragile) hair disorders.
Nails
The nail is a plate of densely packed, hardened, keratinised cells produced by the nail matrix. It serves to protect the ngertip and aids grasp and ngertip sensitivity. The white lunula at the base of the nail is the visible distal aspect of the nail matrix (Fig. 14.2). Fingernail regrowth takes approximately 6 months, and toenail regrowth 12–18 months.
The history
The possible diagnoses in dermatological conditions are broad and some diseases have pathognomonic features. Thus, in order to ensure that your history-taking is focused and relevant, it may be appropriate to ask to glimpse the lesion or rash before embarking on detailed enquiry.
14
Common presenting symptom s
These include:
A rash: scaly, blistering or itchy
A lump or lesion
Pruritus (itch)
Hair loss or excess hair (hirsutism, hypertrichosis)
Nail changes
Ask:
When did the lesion appear, or the rash begin?
Where is the rash/lesion?
Lateral nail fold (paronychium)
Lunula
Cuticle
Eponychium
A
Fig. 14.2 Structure of the nail. A Dorsal view. B Cross-section.
Distal edge of nail plate
Nail plate
Hyponychium
B
Nail bed
Nail plate
Cuticle
Distal phalanx
Proximal nail fold (paronychium)
Matrix
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Has the rash spread, or the lesion changed, since its onset?
Is the lesion tender or painful? Is the rash itchy? Is the itch
intense enough to cause bleeding by scratching or to disturb sleep, as in atopic eczema and lichen simplex? Are there blisters?
Do the symptoms vary with time? For example, the pruritus of scabies is usually worse at night, and acne and atopic eczema may show a premenstrual exacerbation.
Were there any preceding symptoms, such as a sore throat in psoriasis, a severe illness in telogen efuvium, or a new oral medication in drug eruptions?
Are there any aggravating or relieving factors? For example, exercise or exposure to heat may precipitate cholinergic urticaria.
What, if any, has been the effect of topical or oral medi­cations? Self-medication wit h or al antihistamines may ameliorate urticaria, and topical glucocorticoids may help inammatory reactions.
Are there any associated constitutional symptoms, such as joint pain (psoriasis), muscle pain and weakness (dermato­myositis), fever, fatigue or weight loss?
Very importantly, what is the impact of the rash on the in­dividuals quality of life?
Past medical and drug history
Ask about general health and previous medical or skin conditions; a history of asthma, hay fever or childhood eczema suggests atopy. Coeliac disease is associated with dermatitis herpetiformis.
Take a full drug history, including any recent oral or topical prescribed or over-the-counter medications. Enquire about al­lergies not just to medicines but also to animals or foods.
Family and social history
14.2 Fitzpatrick scale of skin types
Type 1: always burns, never tans
Type 2: usually burns, tans minimally
Type 3: sometimes burns, usually tans
Type 4: always tans, occasionally burns
Type 5: tans easily, rarely burns
Type 6: never burns, permanent deep pigmentation
The physical examination
Proper assessment of the skin involves all the human senses, with the exception of taste. Once we have listened to the pa­tients history, we look at the rash or lesion, touch the skin, and occasionally use our sense of smell to diagnose infection and metabolic disorders such as trimethylaminuria (sh odour syn­drome). The increasing use of remote consultations (tele­dermatology) in clinical practice introduces the risk of certain aspects of patient assessment being compromised, limiting the ability to make a precise diagnosis.
Examination of the skin should be performed under conditions of privacy in an adequately lit, warm room with, when appro­priate, a chaperone present (p. 22). The patient should ideally be undressed to a degree that enables visualisation of all affected areas of the skin, but allowances should be made for modesty and religious practices. Routinely, the hair, nails and oral cavity (p. 213) should be examined, and the regional lymph nodes (p.
36) palpated. Assess skin type using the Fitzpatrick scale (see
Box 14.2 ).
In documenting the appearance of a lesion or rash, use the correct descriptive terminology (Box 14.3); doing so often helps crystallise the diagnostic thought processes.
Enquire about occupation and hobbies, as exposure to chem­icals may cause contact dermatitis. If a rash consistently im­proves when a patient is away from work, the possibility of industrial dermatitis should be considered. Ask about alcohol consumption and conrm smoking status.
Document foreign travel and sun exposure if actinic damage, tropical infections or photosensitive eruptions are being consid­ered. The risk of squamous cell and basal cell cancers increases with total lifetime sun exposure, and intense sun exposures leading to blistering burns are a risk factor for melanoma. The susceptibility of an individual to sun-induced damage can be determined by dening their skin type using the Fitzpatrick scale (Box 14.2).
Ask about a family history of atopy and skin conditions.
The history of a skin disorder alone rarely enables a denite diagnosis, with perhaps the occasional exception: an itchy eruption that resembles a nettle rash, the individual components of which last less than 24 hours, is very likely to be urticaria; and an intensely itchy eruption that affects all body areas except the head (in adults) and is worse in bed at night should be consid­ered to be scabies until proved otherwise.
Distribution of a rash
The distribution of dermatosis can be very informative. Is the eruption symmetrical? If so, it is likely to have a constitutional basis, and if not, it may well have an extrinsic cause. This golden rule has occasional exceptions (such as lichen simplex) but holds true in the majority of instances.
The pattern of a rash may immediately suggest a diagnosis: for example, the antecubital and popliteal fossae in atopic eczema (Fig. 14.3A); the extensor limb surfaces (see
Fig. 14.3B), scalp, nails (see Fig. 3.7A)andumbilicusinpso-
riasis; the exural aspects of the wrists and the oral mucous membranes in lichen planus (Fig. 14.4 ); the scalp, al ar grooves and nasolabial folds in seborrhoeic dermatitis; and the sparing of covered areas in photosensitive erupt ions. Does the rash follow a dermatome (as with shingles, see Fig. 7.9), or Lang­ers li nes of skin tension (as with pityriasis rosea), or Blaschko (developmental) lines (as with certai n genetic disorders)? The localisation of an eruption to fresh scars or tattoos may be a manifestation of sarcoidosis, a nd the anatomical location may provide a clue to diagnosis, such as the tendency of erythema
14.3 Descriptive terminology
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The physical examination 329
Term Denition
Abscess A collection of pus, often associated with signs and
Angioedema Deep swelling (oedema) of the dermis and subcutis
Annular Ring-like
Arcuate Curved
Atrophy Thinning of one or more layers of the skin
Blister A liquid-lled lesion (vesicles and bullae)
Bulla A large blister (>0.5 cm)
Burrow A track left by a burrowing scabies mite
Callus (callosity)
Circinate Circular
Comedo A blackhead
Crust (scab) A hard, adherent surface change caused by leakage and
Cyst A uid-lled papular lesion that uctuates and
Discoid Disc-like
Ecchymosis (bruise)
Erosion A supercial loss of skin, involving the epidermis; scarring
Erythema Redness of the skin that blanches on pressure
Erythroderma Any inammatory skin disease that affects >80% of the
Exanthem A rash
Excoriation A scratch mark
Fissure A split, usually extending from the skin surface through
Freckle An area of hyperpigmentation that increases in the
Furuncle A boil
Gyrate Wave-like
Haematoma A swelling caused by a collection of blood
Horn A hyperkeratotic projection from the skin surface
Hyperkeratosis Thickening of the stratum corneum
Ichthyosis Very dry skin
Keratosis A lesion characterised by hyperkeratosis
Lentigo An area of xed hyperpigmentation
Lichenication Thickening of the epidermis, resulting in accentuation of
symptoms of inammation (includes boils and carbuncles)
A thickened area of skin that is a response to repeated friction or pressure
drying of blood, serum or pus
transilluminates
A deep bleed in the skin
is not normally a result
body surface
the epidermis to the dermis
summer months and decreases during winter
skin markings; usually indicative of a chronic eczematous process
Term Denition
Macule A at (impalpable) colour change
Milium A keratin cyst Naevus A localised developmental defect (vascular, melanocytic,
epidermal or connective tissue)
Nodule A large papule (>0.5 cm)
Nummular Coin-shaped
Onycholysis Separation of the nail plate from the nail bed
Papilloma A benign growth projecting from the skin surface
Papule An elevated (palpable) lesion, arbitrarily <0.5 cm in
diameter
Patch A large macule
Pedunculated Having a stalk
Petechiae Pinhead-sized macular purpura
Pigmentation A change in skin colour
Plaque A papule or nodule that in cross-sectional prole is
plateau-shaped
Poikiloderma A combination of atrophy, hyperpigmentation and
telangiectasia
Purpura Non-blanchable redness (also called petechiae)
Pustule A papular lesion containing turbid purulent material (pus)
Reticulate Net-like
Scale A ake on the skin surface, composed of stratum
corneum cells (corneocytes), shed together rather than individually
Scar The brous tissue resulting from the healing of a wound,
ulcer or certain inammatory conditions
Serpiginous Snake-like
Stria(e) A stretch mark
Targetoid Target-like
Telangiectasia Dilated blood vessels
Ulcer A deep loss of skin, extending into the dermis or deeper;
usually results in scarring
Umbilication A depression at the centre of a lesion
Verrucous Wart-like
Vesicle A small blister (<0.5 cm)
Wheal A transient (<24 hours), itchy, elevated area of skin
resulting from dermal oedema that characterises urticaria
Xerosis Mild/moderate dryness of the skin
14
nodosum (see Fig. 5.7B), pretibial myxoedema (see
Fig. 10.2D) and necrobiosis lipoidica (Fig. 14.5)toinvolvethe
shins.
Morphology of a rash
The morphology (shape and pattern) of a rash is equally important. Violaceous, polygonal, at-topped papules, topped by a lacy
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A
A
B
B
Fig. 14.3 Distribution of rash. A Atopic eczema localising to the flexural
aspect of the knees.
patterning (Wickhams striae), are typical of lichen planus (see
Fig. 14.4). The Koebner (isomorphic) phenomenon, where a
dermatosis is induced by supercial epidermal injury, results in linear congurations (Fig. 14.6A), and occurs par excellence in psoriasis, lichen planus, viral warts and molluscum contagiosum. Linear or angular markings (erythema or scarring) raise the likelihood of artefactual (self-inicted) damage to the skin. The presence of blisters limits the diagnostic possibilities to a relatively small number of autoimmune (such as dermatitis herpetiformis, pemphigoid (see
Fig. 14.6B) and pemphigus), reactive (including erythema multi-
forme, Stevens–Johnson syndrome and toxic epidermal necrolysis), infective (such as bullous impetigo and herpes simplex infection) and inherited (for example, epidermolysis bullosa) disorders. An annular (ring-like) morphology may be seen in granuloma annulare (see Fig. 14.6C), sarcoidosis, subacute cutaneous lupus erythe­matosus, and fungal infections (ringworm). Deeply pigmented skin types are frequently associated with follicular accentuation of in­ammatory processes as well as an increased tendency to scarring compared to lighter skin types (Fig. 14.7AB).
B Psoriasis involving the extensor aspect of the elbow.
Colour
The vascular contribution to t he colour of a rash can be pivotal in diagnosis, particularly in light skin types, as redness can
C
Fig. 14.4 Lichen planus. A Discrete at-topped papules on the wrist. B
Wickhams striae, visible on close inspection. striae on the buccal mucosa.
Fig. 14.5 Necrobiosis lipoidica diabeticorum: peripheral erythema and
central yellow-coloured telangiectatic atrophic changes.
C A white lacy network of
A
A
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14
B
B
Fig. 14.7 A Follicular eczema in dark skin. B Keloids due to inammatory
change in dark skin.
remain wi thin blood vessels; non -blanchabl e redness (pur­pura) is the re sult of erythrocyte extravasation and en trapment in the collagen and elastic bres of the dermis. Erythematous and purpuric erupti ons usually have very different underlying causes.
The tint of the erythema may be helpful: a violaceous hue distinguishes lichen planus; a beefy-red or salmon-pink colour often typies psoriasis; and a heliotrope (pink – purple) colour is
C
Fig. 14.6 Rash morphology. A Koebner response in psoriasis. B
Tense bullae (blisters) in pemphigoid. annulare.
sometimes be difcult to assess in darker skin types. It is not sufcient to describe a rash as redor pink; it is essential to demonstrate whether or not a rash blanches on direct pres­sure or when the skin is stretched. Blanchable redness (ery­thema) indicates that the red blood cells causing the colour
C Annular lesions in granuloma
a feature of dermatomyositis, especially on the eyelids.
Macular purpura may be the result of thrombocytopenia or capillary fragility (see Fig. 10.10D), but palpable purpura (often painful) usually indicates vasculitis ( Fig. 14.8A) and necessi­tates exclusion of vasculitic inammation in other organs. Purpura elicitable by pinching the skin (pinch purpura)may be indicative of Amyloidosis light chain (AL) (see Fig. 14.8B).
In those individuals with skin pigmentation at the darker end of the spectrum, there is the added possibility of increased or decreased colour (hyper- or hypopigmentation) consequent to inammation (Figs 14.9 and 14.10). Disorders characterised by reduced pigmentation, such as vitiligo (see Fig. 3.10), are more obvious in dark skin.
A
A
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A
B
Fig. 14.8 Purpura. A Cutaneous vasculitis. B AL (light chain) amyloidosis.
B
Fig. 14.10 Pityriasis versicolor A in Caucasian skin (where affected skin is
lightly pigmented). hypopigmented).
on applying a shearing force in pemphigus (Nikolskys sign), and
B
Fig. 14.9 A Hyperpigmentation within antecubital fossa secondary to
atopic eczema. the cheek.
B Post-inammatory hypopigmentation in pityriasis alba on
the very earliest lesions of lichen planus glinting in reected light (see Fig. 14.11C).
Scratch marks (excoriations) indicate an itchy rash. In any pruritic eruption, it is prudent to look specically for the burrows of scabies (Fig. 14.12AB)onthehandsandfeet,aswellastotestforder­mographism and examine for lymphadenopathy (p. 34), as urticaria and lymphoma are also important causes of itch.
B in Afro-Caribbean skin (where affected skin is
Specic features
Morphology of lesions
There are also a number of subtle clinical signs that can be of great diagnostic help in common rashes, such as the distinctive silver-coloured scale that appears when psoriasis is scratched (Fig. 14.11AB), the urtication that develops when the pigmented lesions of urticaria pigmentosa (a form of cutaneous mastocy­tosis) are rubbed (Dariers sign), the separation of the epidermis
Lesions should be measured and described according to their anatomical location, colour, symmetry, surface texture, consis­tency, demarcation of margin, tenderness and whether they are freely mobile or attached to underlying tissue (p. 329). Remember to examine the regional lymph nodes.
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A
C
Fig. 14.11 Specic signs A Psoriasis before surface rubbing. B After surface rubbing. C Lichen planus showing light reection from small early lesions.
B
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A B
Fig. 14.12 Scabies burrows. A A tortuous burrow. B Through the dermatoscope, individual mites are visible as small, dark arrowheads.
A
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An irregularly roughened, jagged surface texture is often indica­tive of sunlight-induced damage (actinic keratosis), whereas the surface of a seborrhoeic keratosis (Fig. 14.13) has a smoother feel. The consistency of a lesion is often of diagnostic help: for example, the rm, button-like quality of a dermatobroma is very character­istic; neurobromas are rather soft (see Fig. 3.20); calcium deposits are hard; and cysts uctuate and transilluminate. Basal cell carci­noma, the most common malignant tumour, is usually smooth (but may ulcerate); on inspection, it exhibits a milky, pearlescent colour (which may glint) and irregular telangiectasia (Fig. 14.14).
It is reassuring to see hair growing out of a pigmented lesion, as this usually indicates a benign process such as a melanocytic naevus. However, the possibility that a pigmented lesion is a malignant melanoma (Fig. 14.15), a potentially life-threatening cutaneous malignancy, should always be considered. The acronym ABCDE refers to features in a skin lesion that might suggest a melanoma:
Asymmetry
Border irregularity
Colour variation
Diameter >6 mm, Dark or Different
Evolving or changing
Fig. 14.13 Seborrhoeic keratosis: multiple lesions over the temple
and zygomatic regions.
Fig 14.14 Basal cell carcinoma. A Viewed with the naked eye. B Dermatoscopy highlights distinctive telangiectasia.
Fig. 14.15 Malignant melanoma.
B
A
The physical examination 335
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Despite its origin from melanocytes, melanoma may occasion­ally lack pigment (amelanotic melanoma). The ugly duckling sign refers to pigmented lesions that immediately stand out as being different, and that therefore should be considered suspicious.
Mouth, hair and nail signs
General physical examination of the skin should always include the oral cavity, hair and nails.
Inspection of the oral mucous membranes may reveal diagnostic clues such as the lace-like patterning of lichen planus (Fig. 14.4C), or the erosions of pemphigus. Gum hy­giene may alert to the possibility of a nutritional deciency such as scurvy (see Fig 3.19A).
Is there excess hair, either in a male pattern distribution (hirsutism) or not (hypertrichosis), or hair loss (alopecia)? Hirsutism may be a marker for hyperandrogenism. Hyper­trichosis may be seen in malnutrition states, malignancy and porphyria cutanea tarda. Discrete, coin-sized areas of hair loss, with small exclamation mark’ hairs at the periphery, are char - acteristic of alopecia areata (Fig. 14.16), an autoimmune dis­order that may coexist with other autoimmune disorders. Diffuse, pronounced hair shedding (tel ogen efuvium) may be a physiological response t o severe illness, major surgical opera­tions, or chil dbirth and may be accompanied by transverse grooves on the fingernails, which gradually grow out normally (Beaus lines; see Fig. 3.7B).
Common abnormalities of the nails associated with underlying disease are covered on page 26 and in Box 3.3 and Fig. 3.7.
Some rare diseases produce specic nail appearances, such as the ragged cuticlesand abnormal capillary nail-bed loops associated with dermatomyositis (Fig. 14.17AB), and the pro­gressive thickening and opacication of nails in yellow nail syn­drome (Fig. 14.18).
14
Fig. 14.16 Alopecia areata.
Fig. 14.17 Nail appearances in systemic diseases. A The typical linear pattern of dermatomyositis with Gottrens papules on the dorsum of the hand. B
Nail-fold telangiectasia in dermatomyositis, viewed through the dermatoscope.
B
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Fig. 14.18 Yellow nail syndrome in a patient with lymphoedema and
pleural effusions.
Supplementary examination techniques
It is often necessary to complement naked-eye observation of the skin with assisted examination techniques, such as derma­toscopy, diascopy and Woods lamp.
Dermatoscopy
A dermatoscope consists of a powerful light source (polarised or non-polarised) and a magnifying lens, and enables considerably more cutaneous anatomical detail to be seen (Fig. 14.19).
Dermatoscopy is particularly useful in the assessment of pig­mented lesions but is also often of great help in assessing other skin tumours, hair disorders and certain infections (scabies, viral warts and molluscum contagiosum).
Diascopy
The pressure of a glass slide on the skin will compress the cutaneous blood vessels and blanch the area of contact. If blood is still visible through the glass, it is because red blood cells have extravasated (purpura). When granulomatous disorders (such as sarcoidosis or granuloma annulare) are diascoped, they typically manifest a green–brown (apple jelly) colour.
Fig. 14.19 Dermatoscope.
uoresce (such as erythrasma, pityriasis versicolor and some ringworm infections).
Investigations
After clinical examination, specic investigative techniques may be necessary in some cases to enable a precise diagnosis.
Skin biopsy
This involves a sample of skin being removed under local anaesthesia and subjected to histological or immunohisto­chemical examination in the laboratory. However, clinico­pathological correlation is usually necessary.
Mycology
A fungal infection can be conrmed (or refuted) by scraping scale from the surface of a rash with a scalpel blade, clipping samples of nail or plucking hair, and undertaking microscopic examination and culture.
Woods lamp
Examination of the skin using an ultraviolet light (Woods lamp) is useful in two clinical situations: it enhances the contrast between normal skin and under - or over-pigmented epidermis (making conditions such as vitiligo and melasma easier to see); and it can identify certain infections by inducing the causative organisms to
Patch testing
Patch testing (Fig. 14.20) is performed to establish whether a contact allergy is the cause of an individuals rash. It involves applying putative allergens to the patients skin, leaving the test patches undisturbed for 2 days, removing them and then reading the nal result after 4 days. A positive result is indicated by an inammatory reaction at the site of the patch.