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☆
Rash
2Worrying features RR >30, sats <92%, wheeze, systolic BP
<00mmHg, confusion, tachy/ bradycardia, rapidly changing, painful, blistering, or non- blanchingrash.
Think about 2Life- threatening Meningococcal septicaemia (Fig.6.), nec-
rotizing fasciitis, TEN, SJS, urticaria (anaphylaxis), staphylococcal scalded skin syndrome; sles), shingles, erythema nodosum, erythema multiforme, vasculitis (eg Henoch– Schönlein purpura). tact), vasculitis, erythema ab igne, bullous disease (eg bullous pemphigoid and pemphigus vulgaris).
Ask aboutSpeed of onset, distribution of rash, pain, associated symptoms,
exacerbating and relieving factors, family history; joint/ GI disease, immunosuppression, weight loss; cation, vaccinations, previous drugs to treat skin disease; exposure to irritants, pets, exposure to others with illness/ skin disease.
Obs Temp, RR, BP, CRT, HR, O
Look at Hands and nails for pitting, Janeway lesions or Osler’s nodes, splinter
haemorrhages, and then examine aected area and fully expose rest of pa­tient. Try to form a description of the lesions based upon size, shape, colour, palpability, blisters, and associated features (E pp. 36–7). Also examine the scalp, genitals, and mouth. Other examination as dictated by history.
Investigations BldsIf suspect infection or systemic disease; FBC, CRP,
ESR, U+E; blood cultures. Further investigation— Table6.2. See also Table 6.3.
Table6.2 Investigating cutaneous eruptions
Test Use Example
Skin swab Viral PCR Herpes simplex
Blood test Autoantibodies Systemic lupus erythematosus
Nail clippings Fungal culture Onychomycosis
Patch testing Allergy testing Nickel allergy
Skin biopsy Culture Mycobacteria/ fungi
Skin scrapings Fungal culture Tinea
Skin swab Bacterial culture Impetigo
Wood’s light Fungal uorescence Erythrasma (skin folds)
Other acute Cellulitis, viral exanthem (eg chickenpox, mea-
Chronic Psoriasis, dermatitis (eg atopic, con-
PMH Previous skin disease,
DHAllergies, new medi-
SH Occupation,
sats.
2
Serology Guttate psoriasis
Histology TEN/ SJS
Immunouorescence Pemphigus/ pemphigoid
Microscopy Scabies
433RASH
434 CHAPTER6 Skin andeyes
Bacterial infections causingarash
Impetigo
$ Supercial epidermal infection typically seen around children’s faces.
SymptomsWeeping, spreading erythema, highly contagious. Signs Erythema with yellow crust, serous discharge; occasionally blisters. Investigations Skin swabsShow Staphylococcus aureus in >90% of cases, but
group Astreptococci (S.pyogenes) can befound.
Treatment Treatment of localized disease can be achieved with topical fusidic
acid/8h for wk. More extensive impetigo may require oral antibiotics, eg ucloxacillin g/ 6h PO (for staphylococci) and phenoxymethylpenicillin 500mg/ 6h PO (for streptococci). Ensure close contacts are examined and treated if ne­cessary; encourage good hand hygiene and avoidance of sharing towels.
Erysipelas
$ Epidermal streptococcal infection with cutaneous lymphatic involvement.
Results in painful, well- demarcated erythema (±lymphadenopathy); typ­ically seen on face orlegs.
Cellulitis
$ Non- necrotizing infection of the dermis.
Symptoms Hot, usually tender area of erythema, usually on leg
may be spreading; history of trauma to skin (insect bite, cannula site) or tinea pedis. May have systemic eects:fever, anorexia, N+V, diarrhoea.
Signs Warm spreading erythema (outline area with marker to observe re-
sponse to treatment), ±mild oedema, break in the skin, serous discharge, can develop blisters, lymphadenopathy in draining nodes, itemp, iHR,iRR.
Investigations blds iWCC and neutrophils, iCRP/ ESR; blood cul-
tures if pyrexial; D- dimer likely to be raised in infection so not useful in dierentiating cellulitis fromDVT; check multisite
MRSA swab; USS To exclude DVT (depending on Wells’
score E p. 508) or ruptured Baker’scyst.
TreatmentCheck local guidelines; likely organisms include S.aureus (may
be MRSA) or group Astreptococci (see also Box 6.):
• If patient is systemically well and has no other signicant
comorbidities, oral antibiotics (ucloxacillin g/ 6h PO; if MRSA suspected or proven doxycycline 200mg STAT then 00mg/ 24hPO)
• If signs of systemic upset (itemp, iHR, iRR) or coexisting disease
(DM, IHD, PVD), admit for IV antibiotics (ucloxacillin g/ 6h IV; if MRSA suspected or proven, vancomycin g/ 2hIV)
• 3Necrotizing fasciitis (E p. 435.) Very unwell, ‘out- of- proportion
skin pain’, rapidly spreading. Request senior help immediately
• 3Orbital cellulitis Painful or restricted eye movement, proptosis, or
visual disturbance.
K Box 6. Erythematous cannulasites
Cannulae should be dated and resited every 72h. If a cannula site is red and inamed or pus is present, remove cannula, and clean and dress the site. Give ucloxacillin g/ 6h PO or clarithromycin 500mg/ 2h PO (if penicillin allergic) for 5d. Discuss with microbiology if MRSA+ve.
Bilateral cellulitis is very rare; consider an alternative diagnosis in those with both legs aected.
TreatmentAs for cellulitis.
Skin swabs Not usually helpful, but
or face;
3Necrotizing fasciitis (E OHAM4p. 497.)
SymptomsRapidly spreading painful erythema (pain disproportionate to
rash) with features of sepsis, fever, unwell, dGCS; may occur at break in skin or operation site but often no apparent trauma.
Signs Rapidly spreading blanching erythema (outline with marker to ob-
serve spreading), blisters, ±oedema, lymphadenopathy in draining nodes, sometimes crepitus over tissues (late sign), itemp, iHR, iRR,dBP.
Investigations blds iWCC and neutrophils, iCRP/ ESR, ilactate; Blood cul-
tures and skin swabs/ tissue aspirationMay identify infective organism(s) but
do not withhold treatment to do tests if patient is systemically unwell;
X- rayMay reveal gas in subcutaneous tissues of aectedarea.
Treatment 3This is a surgical emergency.
• Seek senior help
immediately (the moment you suspect, not once you
have watched the fasciitis evolve and conrm your suspicions)
• Surgical debridement is the most important measure,
surgeon withoutdelay
consult senior
• Likely to need combination of IV benzylpenicillin, gentamicin,
clindamycin, and metronidazole. Seek urgent microbiology advice.
Pathogens These may be a mixture of aerobic and anaerobic organ-
isms seen following abdominal surgery or in diabetics (type ), a group AStreptococcus (type 2), or Clostridia (type 3— gas gangrene).
Outcome This depends upon speed of identication and initiation of
treatment, as well as comorbidity and the site aected. Extensive tissue loss from surgery and necrosis is common; overall mortality is720%.
3
Meningococcal septicaemia (E OHCM1p. 806.)
Symptoms Fever, non- blanching (purpuric) rash (note, early rash may
blanch), joint and muscle ache, malaise; meningitis frequently occurs, re­ected by headache, neck stiness, and photophobia.
Signs itemp, iHR, iRR, cap rell >2s, dBP, non- blanching petechial or pur-
puric rash;
Investigations blds iWCC and neutrophils, iCRP/ ESR, meningococcal
PCR, deranged clotting if severe sepsis(DIC); hold antibiotics before taking these if patient is unwell;
meningism/ photophobia if meningitis also present (Ep. 372).
Blood culturesDo not with-
CT headIdentify
any complications such as hydrocephalus or contraindications to LP;
LPWCC, Gram stain, MC+S, glucose, bacterial/viral PCR.
Treatment 3This is a medical emergency.
• Airway, Breathing (give O
• Seek help immediately— contact your seniors as soon as you suspect
), Circulation (obtain IV access)
2
• If patient is in shock (SBP <00mmHg), involve ICU team urgently
• 0.9% saline L STAT IV and goal- directed uid resuscitation (Ep. 485)
• Ceftriaxone 4g STAT IV withoutdelay
• Inform public health consultant once patient is stable.
Pathogen Neisseria meningitides, a Gram- negative diplococcus; since the
introduction of a vaccine for serogroup C, serogroup B accounts for the majority of infections seen in Europe and North America.
Outcome This depends upon speed of identication and initiation of
treatment. Mortality for meningococcal septicaemia is about 0% in the developed world. Complications in survivors include neurological decits (eg cognitive impairment, deafness), limb amputation, renal failure, and adrenal failure (Waterhouse– Friderichsen syndrome).
435BACTERIAL INFECTIONS CAUSING A RASH
436 CHAPTER6 Skin andeyes
Viral infections causingarash
Chickenpox (varicella zoster virus— VZV)(E OHCM1p. 400.)
Symptoms
Fever and malaise 4– 2d after exposure. Typical rash then develops: at lesions, evolving to itchy scabs. Older children and adults at risk of development of pneumonitis or encephalitis, manifesting as breathlessness or altered mental state.
Signs itemp, iHR, and presence of evolving rash; macules, papules,
vesicles, pustules, scabs, in centripetal distribution (spreading out from the trunk). iRR and dO ality, dGCS, or ataxia suggests CNS involvement. See Box 16.2.
Investigations
Serology
Viral antibody titres can be monitored but this is seldom necessary;
CXR
May show diuse consolidation in varicella pneumonitis;
other causes of neurology;
Treatment
Symptomatic: antipyretics and antihistamines. Antiviral therapy is usually given to patients ≥4yr (aciclovir 800mg/ 5h PO). In the immuno­compromised or those with complications (pneumonitis, encephalitis), use aciclovir 0mg/ kg/ 8h IV. Consider ICU admission for respiratory support.
Pregnancy
Primary VZV infection during the st 20wk of pregnancy is associ­ated with – 2% risk of foetal anomalies and spontaneous abortion; infection within 5days of delivery is also associated with a risk of neonatal VZV infec­tion. Women without a clear history of chickenpox should have viral specic IgG titres checked and if negative, should be oered VZV vaccination before becoming pregnant. The vaccine cannot be used in pregnancy, when primary infection may require zoster immune globulin (ZIG) to prevent the onset of disease, and oral aciclovir if the disease develops— discuss with microbiology.
K Box 6.2 Chickenpox
Uncommonly aects an individual more than once. Shingles Reactivation of chickenpox virus; the virus lies dormant in the dorsal root/ cranial nerve
Non- immune individualsCan catch chickenpox from patients who have
ganglia; either chickenpox or shingles; the infectious period runs from 48h prior to onset of the rash until all lesions crustover.
sats suggest respiratory involvement. Altered person-
2
Not usually undertaken but
LP
Lymphocytic pleocytosis in viral encephalitis.
vesicular uid
can be sent for viral
CT brain
PCR
Exclude
;
Shingles (herpes zoster)
Symptoms Initially focal pain, followed by classical blistering rash in
a dermatomal distribution (will not cross the midline), ±malaise. If multidermatomal, consider if patient immunocompromised.
Signs Erythematous papules, evolving into vesicles with pustules which crust
over after 77d. Usually thoracic or lumbar dermatome.
InvestigationsClinical diagnosis, but vesicular uid can be examined under
electron microscopy or sent for viral
TreatmentAntiviral therapy limits post- herpetic neuralgia and period of infect-
PCR.
ivity if started within 72h (valaciclovir g TDS 7days PO); parenteral antivirals can be considered in immunocompromised (aciclovir 0mg/ kg/ 8h IV). Treat pain with paracetamol, NSAIDs, and amitriptyline 25mg/ 24hPO.
•
Herpes zoster ophthalmicus Involvement of the ophthalmic branch of the
trigeminal nerve (CN Va); may lead to sight-threatening keratitis; apply 3% aciclovir ointment to eye/ 5h and
seek ophthalmic opinion
• Ramsay– Hunt syndrome (E OHCM1 p. 499.) Facial pain, vesicles in external
auditory canal and ipsilateral facial palsy; complete recovery in<50%.
Measles (rubeola)— notiable disease
Symptoms Prodrome of fever, coryza, and cough; rash spreading from
face and neck to trunk andlimbs.
Signs itemp, iHR, conjunctivitis, pathognomonic grey ‘Koplik’ spots
(rare to see!) on buccal mucosa seen 72d prior to maculopapularrash.
InvestigationsNone required routinely; measles serology in criticallyill. TreatmentSupportive care; vitamin Asupplements if malnourished; compli-
cations include pneumonitis, pneumonia, encephalitis; subacute sclerosing panencephalitis is a degenerative disease appearing 70yr post infection.
Rubella (German measles)— notiable disease
SymptomsRash with fever and coryza; adults may experience arthralgia. SignsDiscrete macular rash spreading from face to trunk and limbs; features
of concurrent illness/ infection (itemp, iHR, etc); tender lymphadenopathy.
InvestigationsNone routine; blds iviral specic IgM during infection. Treatment Supportive care; primary infection during st trimester of
pregnancy carries 790% foetal anomalies (eg deafness, cataracts).
Viral exanthema (the viralrash)
Symptoms Rash associated with prodromal symptoms of viral illness
(fever, myalgia, arthralgia, headache); may or may not beitchy.
Signs Widespread maculopapular rash; features of concurrent illness/
infection (itemp, iHR, pharyngitis, etc). Rash associated with numerous viruses (echovirus, parvovirus, EBV, measles) so not diagnostic.
InvestigationsNone required routinely; discuss with virology if unwell. TreatmentSimple analgesia; resolves over77d.
Fifth disease/ erythema infectiosum (‘slapped cheek’ fever)
SymptomsNon- itchy rash on cheeks, which feel burning hot; later spreads
to trunk and limbs; headache; otherwise well; usually in children.
Signs Erythematous rash on cheeks, and reticulate erythema (net- like
rash) on proximal limbs then trunk; caused by parvovirusB9.
InvestigationsNone required routinely. TreatmentRash will subside over 7– 0d; treat concurrent symptoms.
Herpes simplex virus (cold sore/ genital herpes)
SymptomsSmall painful vesicles usually around mouth or in genitalarea. SignsVesicles or pustules around mouth (usually HSV) or in genital area
(usually HSV2). Often resolve, but then return months or yearslater.
InvestigationsNot usually but vesicular uid can be sent for viralPCR. Treatment This consists of aciclovir 200mg/ 5h or 400mg/ 8h PO for pri-
mary HSV infections and painful genital infections. Treat facial and genital ‘cold sores’ with aciclovir 5% to aected area/ 4h topically.
Molluscum contagiosum
Symptoms Small, non- itchy spots, occurring on trunk and limbs in child-
hood (skin contact) and around groin in early adulthood (sexual trans­mission); highly contagious.
SignsSmall translucent papules (– 3mm), which look uid- lled, but are
actually solid, often with the central depression (punctum). Caused by a poxvirus, and usually resolve spontaneously after 6– 2mth.
InvestigationsNone routine; screen for other STDs in adults (Ep. 523). TreatmentNone required, 5% potassium hydroxide can be used in older
children or adults.
437VIRAL INFECTIONS CAUSING A RASH
438 CHAPTER6 Skin andeyes
Fungal infections causingarash
Dermatophytes $ Pathogenic fungi, which cause a range of diseases.
Tinea corporis‘Ringworm’,mildly itchy, asymmetrical rash which spreads
with a slightly raised, scaly edge, often leaving a clear centre.
Tinea facieiDermatophyte infection of theface. Tinea cruris Ringworm in the groin, though this lesion is often red and
more plaque- like with a well demarked border.
Tinea pedis‘Athlete’s foot’, is usually found in the webspaces of the toes, re-
sulting in itchy skin which is ssured and macerated. If found elsewhere on the foot it is often more diuse and scaly, but just as itchy. Pustules canoccur.
Treatment Treatment of small focal areas of tinea can be achieved with
topical antifungals (terbinane, clotrimazole, miconazole, etc); more widespread infections require oral therapy (terbinane, itraconazole).
Candida albicans $ Candida is a yeast, and thrives in warm moist areas, in
children’s nappies (nappy rash), in body folds (intertrigo), and also in inter­digital webspaces, mimicking tineapedis.
The rash is erythematous with a ragged, peeling edge which may con­tains small pustules. The mouth and genital tract can also be aected and present with small white plaques/ white discharge. Swab to conrm. Can herald immunosuppression: is further investigation required?
Treatment Remove predisposing factors (ensure skin remains clean and
dry) and topical antifungal creams (clotrimazole); use drops (eg nystatin) or pessaries (eg clotrimazole) for oral and genital tract infections re­spectively; resistant infections may require oral therapy (eg uconazole).
Infestations causingarash
Scabies $ This is an intensely itchy rash, often worse at night, caused
by the scabies mite, Sarcoptes scabiei.
Commoner in children and with social overcrowding (highly contagious). The rash is papular and found in the interdigital webspaces of the hands and feet, ankles, wrists, genitals, axillae, and umbilicus. Linear skin bur­rows are pathognomonic but not always present. Investigation: micro­scopic examination of skin scrapings/ dermoscopy looking formites.
Treatment Permethrin/ malathion:is only successful if the whole body is
treated, if all close contacts are treated and if bedding and clothing are washed. Itching may last up to 4wk after treatment. Severe infection may require PO treatment.
Lice These are blood- sucking parasites; Head lice(Pediculosis capitis) are
commonest in children, spread by direct contact and can result in scalp ex­coriation. The presence of eggs (‘nits’) in the hair conrms the diagnosis;
Body lice(Pediculosis corporis) are associated with poverty and not often seen
in the developed world; excoriations on the skin are often the onlysign;
(Phthiriasis pubis or ‘crabs’) are transmitted by sexual contact and com-
lice
monly aect coarse pubic hairs, but also leg, body, and facialhair.
Treatment Malathion/ permethrin (resistance common). Close contacts
should also be treated; clothing and bedding should be thoroughly washed on high temperatures.
Pubic
Chronic inflammatoryrashes (E OHCSpp. 444–7.)
Recalcitrant, severe eczema
Moderate to severe eczema
Mild to moderate eczema
Dry skin only
Step 4
Intensity of disease
Dermatitis (eczema) $ Found in 70% of the population in various forms:
• Atopic $ Onset usually in childhood; associated with asthma and allergies
•
Contact $ Type IV hypersensitivity (delayed); may blister
•
Venous eczema $ Seen in lower limbs of older patients with venousstasis
•
Seborrhoeic $ Greasy scaling of scalp/ central face, associated with
reaction to skinyeast.
Symptoms These include itchy, dry skin, or patches of infected skin. Signs Ill- dened erythematous patches with excoriations. Typically aect
the exures of the elbow, knees, and around the neck; vesicles and serous weeping (infected). Superimposed bacterial or viral infections are common. Chronic lichenication and hyperpigmentation can develop.
Treatment This is multifactorial and depends on underlying cause. Attempt iden-
tication and avoidance of known irritants/ allergens. In atopic eczema, triple therapy with topical steroids (E p. 76), topical emollients, and bath oil and soap substitutes form the mainstay; step 4 treatments such as UVB/ PUVA, ciclosporin, methotrexate, azathioprine may be prescribed by a dermatologist (Fig.6.2). Treat bacterial superinfection promptly, eg ucloxacillin g/ 6hPO.
Systemic therapy (eg ciclosporin)
Step 3
Step 2
Low-mid potency topical corticosteroids
Step 1
skin hydration, emollients, avoidance of irritants,
identication and addressing of specic trigger factors
Fig.6.2 Step- wise management of atopic eczema. † Calcineurin inhibitors include pimecrolimus (Elidel Reproduced from J Allergy Clin Immunol, 8, Akdis, C.A. etal., Diagnosis and treatment of atopic dermatitis in children and adults, 52– 69. © 2006, with per­mission from Elsevier. Available free at Mwww.jacionline.org
®
) and tacrolimus (Protopic®).
Psoriasis$ Inammation of the dermis, with epidermal hyperproliferation.
Occurs in 72% of the population, with peak incidences in the early 20s and 50s. Exacerbations can be precipitated by infections, drugs (eg lithium, β- blockers), UV light, alcohol, and stress.
Symptoms Itchy, dry patches of skin which can
bleed when scratched. Joint pain, swelling, and stiness (arthritis can precede skin involvement);
Signs Chronic plaque psoriasis
plaques, especially on the extensor surfaces of elbows and knees, lower back, and scalp; nail pitting; and soles; throat infection, causing numerous small pink papules/ plaques on the trunk;
Flexural psoriasis
Emollients, mild to moderate steroids, vitamin D analogues, and retinoids are common topical treatments. UVB/ PUVA, methotrexate, ciclosporin, anti- TNF/ other biologic therapies, especially if associated psoriatic arthritis (Ep. 514).
2
NICE clinical knowledge summary available at Mhttps://cks.nice.org.uk/topics/eczema-atopic/
3
NICE psoriasis guidelines available at Mguidance.nice.org.uk/ CG53
Pustular psoriasis can be generalized (emergency)
Guttate psoriasis
Occurs acutely, often 2– 3wk after a streptococcal
Tends to occur in later life, and forms in exures;
or UV therapy
Basic treatment
Well- dened pink/ red scaly
treatment
Continue topical
Continue basic treatment
Aects palms
Treatment
439CHRONIC INFLAMMATORYRASHES
2
3
440 CHAPTER6 Skin andeyes
Other causes ofrash
Urticaria (Hives or ‘nettle rash’.) Characterized by the formation of in-
tensely pruritic papules or plaques (‘weal’) which are pale initially but become erythematous with a surrounding rim of pale skin or erythema (‘are’). Acute (<6wk):common in response to certain topical chemicals (eg nettle sting) but also in response to systemic drugs (sometimes part of anaphylaxis), antigens (eg blood transfusion), or virus. Chronic (>6wk)— well patient, uctuating urticarial rash, cause often unknown. Treat with antihistamines.
Erythema nodosum Characterized by tender, erythematous nodules
or plaques, typically on the shins. Commoner causes: infections (strepto­coccal (commonest), Mycoplasma pneumoniae, TB, and EBV), sarcoidosis, inammatory bowel disease (IBD), autoimmune disorders, pregnancy, and drugs (sulfonamides and the oral contraceptive pill) (E OHCS1p. 451).
Erythema multiforme This is a hypersensitivity rash and has two sub-
types.
Erythema multiforme minor Produces ‘target’ lesions, with a red centre,
a clear circular area, and an outer redring. rash with involvement of one or more mucous membranes (classically the mouth). Often no precipitant is identied (750%) but associations are recog­nized with several infections (eg HSV, adenovirus, Mycoplasma pneumoniae) and drugs (eg sulfonamides, NSAIDs, penicillins) (E OHCS1p. 451).
SJS and 3TEN These represent dierent extents of severe, life-
threatening skin inammation that is usually drug induced. Widespread blisters, with skin shedding, erythematous macules, and mucosal erosions aect <0% body surface area (SJS) or >30% (TEN) with an overlap diag­nosis in between. Mortality is high. Dermatology review and senior help should be sought immediately, with close attention to skin care, uid re­placement, and prevention of superinfection (E OHCS1p. 451).
Pemphigus and pemphigoid These are rare primary blistering diseases.
Pemphigus causes supercial blisters and often involves the mucous mem­branes of the mouth; the blisters are delicate and burst easily, so areas of raw skin are often more noticeable than blisters. Pemphigoid causes tense blisters in older patients, and seldom aects the mouth. Both are autoimmune and require dermatology input. Can be life- threatening (E OHCS1p. 452).
Pyoderma gangrenosum This presents with painful nodules or pus-
tules which often ulcerate, leaving an undermined ulcer with a dusky purple edge. Associated with IBD, primary biliary cirrhosis, and rheuma­toid arthritis among others, the exact cause remains unclear. Needs urgent dermatology assessment (E OHCS1p. 452).
Henoch– Schönlein purpuraLargely self- limiting small vessel vascu-
litis typically seen following a simple upper respiratory tract infection in childhood. Petechiae and purpura develop on the legs and buttocks. May have associated abdominal pain, arthralgia, and oedema (E OHCS1 p. 241). Must check renal function and dipurine.
Granuloma annulareCommon, benign inammatory disorder of un-
clear aetiology, characterized by clusters of rm papules appearing on the hands, feet, or trunk which later merge into a ring. Associations include TDM, but most cases appear in well patients (E OHCS1p. 436).
Erythema multiforme majorA similar
Table6.3 Common skin manifestations insystemic disease
Diabetes mellitus (E pp. 342–4)
Coeliac disease (E p. 322)
IBD (E p. 323)
Rheumatoid arthritis (E p. 512)
SLE (E p. 515)
Hyperthyroidism (E p. 348)
Hypothyroidism (E p. 349)
Neoplasia Acanthosis nigricans (velvety, brown pigmented plaques,
Drug eruptions (E OHCS1 p. 451)
Vasculitis Palpable purpuric rash typically on shins; wide range of
HIV (E p. 494)
Candidiasis, necrobiosis lipoidica (yellow maculopapular lesions on the shins, can ulcerate), skin infections (cellulitis)
Dermatitis herpetiformis (intensely itchy papules and vesicles on knees, elbows, back, and buttocks)
Erythema nodosum, pyoderma gangrenosum
Rheumatoid nodules (rm nodules either loose or attached to deep structures over extensor surfaces, classically the elbows), vasculitis, pyoderma gangrenosum
Facial buttery rash, photosensitivity, red scaly rashes, diuse alopecia (hair loss)
Pre- tibial myxoedema (non- pitting plaques and nodules, classically on the shins), clubbing, alopecia
Sparse coarse hair, dry skin, asteatotic eczema (pruritic, dry, cracked skin)
often around the neck), dermatomyositis, ichthyosis (scaly skin), pruritus
Maculopapular rash (±fever and eosinophilia); urticaria; erythema multiforme, SJS/ TEN
other pathologies including telangiectasia, urticaria, ulcers (E p. 621 for autoantibodies in diagnosis)
Infections (oropharyngeal candida, facial/ genital molluscum contagiosum, herpes simplex, varicella zoster E p. 436); seborrhoeic dermatitis or psoriasis (Ep.439); Kaposi sarcoma (enlarging purple patches or plaques seen on feet, arms, legs, or oral mucosa)
441OTHER CAUSES OF RASH
442 CHAPTER6 Skin andeyes
Skinlumps
2Worrying features Weight loss, night sweats, hard irregular
lump,isize.
Think about 2Serious Skin cancer, sarcoma, lymphoma, TB;
CommonLipoma, epidermoid cyst, abscess, boil, carbuncle, ganglion, -
broma, lymph node, naevi, skin tags, keratoacanthoma, keloid scarring, tissued cannula (Box 6.5).
Ask aboutLocation, speed, and duration of onset, change with time,
pain, other lumps, trauma, bites, infections, skin changes, systemic symp­toms (eg weight loss, vomiting, fever); radiotherapy; immunosuppression; cupation;
FHSkin cancer.
Look for Site, size, shape, consistency (hard, rm, soft, uctuant), ten-
derness, temperature, surface, association with skin (moves with skin— intradermal, skin moves over it— subcutaneous), overlying skin (colour, punctum, ulcerated), edges, mobility/ tethering, pulsatility, transillumin­ation, relationship to nearby structures, lymphadenopathy, splenomegaly.
Investigations bldsConsider FBC, U+E, LFT, CRP,ESR; Imaging CXR,
USS, CT/ MRI;
BiopsyFNA, punch biopsy, excision biopsy.
Lipoma $ Common, benign tumour of mature fatcells.
Symptoms Single or multiple, non- painful, can cause pressure eects,
common on the trunk and neck, never found on palms/ soles offeet.
SignsSmooth, well- dened, soft, subcutaneous, mobile, no skin changes. ManagementLipoma can be surgically excised if causing distress.
Epidermoid cyst $ Proliferation of epidermal cells within dermis.
Symptoms Single or multiple, painful if infected, common on the trunk,
neck and face, almost never found on palms/ soles offeet.
Signs Firm, well- dened, intradermal, mobile; overlying punctum is
common; may discharge white/ cheesy material; can become inamed.
Management No treatment. Consider ucloxacillin 500mg/ 6h PO if in-
amed/ tender, may also require incision and drainage; surgical excision once non- inamed.
Ganglion cyst $ Cystic lesion of joint or synovial sheath of tendon.
SymptomsSingle, non- painful; 80% occur atwrist. SignsSmooth, well dened, subcutaneous, transilluminable. ManagementConservative; can be aspirated or excised, but 740%recur.
Fibroma $ Benign tumour of connective tissue; can occur in anyorgan.
Symptoms and signs These vary according to tissue aected, usually slow
growing with no overlying skin changes.
ManagementBiopsy/ imaging if any doubt; excision often possible.
Sarcoma $ Rare, but devastating malignant tumour of connective tissue.
SymptomsSingle, painful, progressive enlargement, weightloss. SignsFirm/ hard, tethered, regional lymphadenopathy. ManagementCombination of surgery, radiotherapy, and chemotherapy.
PMH Previous lumps, cancer,
SHForeign travel, sun exposure, oc-