Common presentations NOS Flashcards

1
Q

How do u assess pt p/w PR bleeding?

A
  • Sx: nature of bleeding (blood mixed in with stool often higher up, bright red fresh often lower down), quantity pt has noticed, WL, change in bowel habit (frequency + consistency), tenesmus (e.g. in fissures), anal sx (sore/pain in fissures, itch in haemorrhoids)
  • FH of bowel Ca/polyposis, PMH, DH e.g. aspirin
  • Examination: pallor, CV shock, obvious WL, abdo masses, hepatomegaly,
  • Stool: blood mixed with stool (darker, often left colon/transverse colon from cancer or IBD), shiny black/plum coloured (melaena, higher bleeding), bright red (suggests rectum/anus, if clearly separate from stool usually anal), blood on surface of stool (may be anal or may be rectum/DC lesion)
  • DRE: usually needed to confirm blood in rectum + exclude rectal masses, essential if referring to secondary care
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2
Q

Causes of PR bleeding

A
Common:
o	Diverticular disease inflammation
o	Colon polyps or carcinoma, or anal cancer
o	Haemorrhoids
o	Anal fissure, fistula-in-ano
o	IBD – CD, UC (younger)

Less common:
oAngiodysplasia (common in elderly, AV malformation)
o Infectious gastroenteritis
o Massive upper GI bleeding
o Radiation proctitis
o Ischaemic colitis – mesenteric vascular insufficiency
o Solitary rectal ulcer
o Dieulafoy’s lesion – submucosal bigger artery in GIT, brisk bleeding with little/no ulceration, most common in stomach but can be anywhere, pain uncommon
o Endometriosis
o Meckel’s diverticulum (children more common than adults)
o Rectal varices
o Trauma e.g. sexual abuse
o STI

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3
Q

What are haemorrhoids and what causes them?

A

Anal mucosal pads become enlarged + congested, can cause anal pain, pruritis ani + bright PR bleeding

May be related to constipation, prolonged straining, increased anal sphincter tone and obstructed venous flow (e.g. in pregnancy)

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4
Q

Types of haemorrhoid

A

Internal (usually painless, origin above dentate line)

External (origin below dentate line). Grade I no prolapse, grade II prolapse on defecation then reduce, grade III need manual reduction, grade IV can’t be reduced

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5
Q

Sx of haemorrhoids

A

bleeding after defecation (paper or in faeces or may be lots in pan), soiling, mucus discharge, pruritis ani, sometimes pain (e.g. thrombosis), rectal mass, tenesmus

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6
Q

Differentials for a pt with ‘haemorrhoids’

A

perianal haematoma (covered by skin, whereas haemorrhoids mucosal-covered), rectal prolapse, anal fissure, anal polyp, IBD, rectal Ca

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7
Q

Haemorrhoid infarction

A

cushions get engorged – severe pain, local swelling, looks black/blue, local oedema. Bed rest, analgesia, stool softeners. Most resolve with time

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8
Q

How are haemorrhoids managed?

A

dry + wash perineum after defecation, digital replacement to relieve sx, local anaesthetic creams, treatment to reduce spasm of internal sphincter (GTN ointment [unlicensed], botulinum toxin injection). Can also have some surgical management. Prevent with more fibre in diet or bulking agents

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9
Q

Features of bladder outflow obstruction

A

Voiding/obstructive sx: weak/intermittent stream, straining, hesitancy, terminal dribbling, incomplete emptying
Storage/irritative sx: urgency, frequency, urge incontinence, nocturia

Post-micturition sx: dribbling

Haematuria unusual but may be due to rupture of veins over an enlarged prostate, or obstructing bladder tumour

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10
Q

BPH

A

unusual before 50, transitional zone affected which compresses prostatic urethra.

Medical treatment if bothersome LUTS – alpha blocker (doxazosin, alfuzosin, tamsulosin, terazosin), or 5-alpha reductase inhibitor if high risk of progression/v big prostate (e.g. finasteride). Poss also anticholinergic if still storage issues

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11
Q

Prostate Cancer

A

RF are age, black African/Caribbean origin, FH, BRCA1/2 mutation, possible link to diet, smoking

CF: LUTS, urinary retention, haematuria/haematospermia, pain (back, perineal, testicular), constipation, anuria, uraemia, SUI, bone pain/#/hypercalculaemia/MSCC, lung mets, liver mets pain/jaundice, brain-fits, pelvic LN causing swollen legs/scrotal oedema

GP Ix are DRE, PSA, U+E (renal), LFT (raised LFTs – liver mets), bone profile

Ix that may be done at referral include MRI and TRUS with biopsy

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12
Q

Bladder neck dysfunction

A

younger men, bladder neck doesn’t open properly when voiding. Urodynamics diagnosis. Can try alpha blockers, or a cystoscopic bladder neck incision

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13
Q

Urethral strictures

A

leads to backflow. May be congenital, or acquired through catheterisation, radiotherapy, trauma, infective, neoplastic from prostate/TCC/SCC. Can do urethral dilatation, or an actual surgery

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14
Q

Blepharitis

A

Inflammation of lid margins +/- lashes/lash follicles. Can lead to styes or chalazions. May be meibomian gland dysfunction, seborrhoea or S aureus (i.e. usually not infectious but can be).

CF: asymptomatic, or itchy burning eyes due to unstable tear film. Crusty scaly deposits on lashes, may see meibomian glands plugged with secretions, or lid may swell if block. Pt often c/o eye feeling dry, but it may actually be watering

M: lid hygiene to reduce bacteria + unblock MGs (this involves clean warm compresses, lid massage, mixing baby shampoo with warm water and using cotton bud on lid margin). If chronic topical chloramphenicol/fusidic acid may be needed, or oral doxycycline if severe

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15
Q

Tinea capitis

A

Scalp ringworm

children > adults. Dermatophyte scalp infection. Can be spread through hairbrushes, clothing, towels.

Presentation – dry scaling, moth-eaten hair loss, black dots (hairs broken off at scalp surface), smooth areas of hair loss, kerion (very inflamed mass), favus (yellow crust, matted hair) or carrier state. May get swollen LNs

M: adv soften crusts with moistened dressings, discard/disinfect things like hairbrushes/scarves/pillows, don’t share towels, treat any pets. Give oral antifungal if there is positive skin + sample – usually griseofulvin for 4-8w. Consider also topical antifungal

Comps – secondary cellulitis or impetigo

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16
Q

Seborrheic dermatitis

A

chronic relapsing form of eczema affecting sebaceous glands, SD is when inflamed and dandruff is when non-inflamed. Due to proliferation of skin commensal Malassezia yeast, non-pathogenic form

Infantile <3m, cradle cap – diffuse greasy scaling, may spread to armpit + groins. Salmon-pink patches that may flake, not itchy baby usually ok

Adult form – may be a/w oily skin, FH of SD/psoriasis, immunosuppression, neuro disease, lack of sleep, stress. Affects scalp, face, behind ears, upper trunk. Often winter flares, minimal itch usually, oily + dry facial skin, ill-defined localised scaly patches/diffuse scale in scalp, often a/w blepharitis, may have rashes in seborrheic areas

M: keratolytics to remove scale e.g. salicylic acid, topical antifungal creams/shampoos, mild corticosteroids if inflamed, coal tar cream/shampoo

17
Q

Head lice

A

itch + scalp irritation at nape of neck + skin behind. Can usually see the nits (eggs) as adherent white grains on hair shaft. Red-brown spots on skin due to excreted digested blood. Scratching can cause crusting + scale

18
Q

hair dye allergy to PPD

A

mild dry itchy rash, more severe can cause blistering/swelling/marked erythema

19
Q

Scalp psoriasis

A

o Red scaly plaques, white-silver scale, thickened red skin, often back of head but may be widespread or in multiple discrete areas, may affect scalp alone or with other psoriasis, may extend into face. May have mild hair loss but not permanent balding
o Often causes severe ‘dandruff’ – pt embarrassed. May have no sx or may be very itchy. Tends to be chronic but often fluctuates

20
Q

Sebo-psoriasis

A

Mixture of SD + psoriasis with greasy yellow scale rather than silvery

M: coal tar or antifungal shampoos leave on for 5-10 mins then reapply. More severe may need leave on things like topical steroid and calcipotriol, salicylic acid or coal tar

21
Q

Scalp folliculitis

A

inflammation of follicles, v small itchy pustules on scalp often at hairline. May be a few or many, often become sore + crusted from itching

topical Abx e.g. fusidic acid gel, mild top steroid, oral antihistamines, oral Abx

22
Q

What is galactorrhoea?

A

Non-puerperal lactation

23
Q

Causes of galactorrhoea

A
  • Hyperprolactinaemia (i.e. serum prolactin elevated). Mildly elevated may be physiological but should repeat, if very elevated >5000 implies pituitary tumour.

Mechanical stimulation of breasts – neuroendocrine reflex prolactin secretion, most likely in women who have recently stopped breastfeeding

24
Q

CF of hyperprolactinaemia

A
  • Women: a/oligomenorrhoea, breast pain, breast enlargement, infertility, hirsutism, loss of libido
  • Men: impotence, loss of libido, reduced seminal fluid volume, gynaecomastia
25
Q

Pathological causes of hyperprolactinaemia

A

o Drugs – SSRIs, COCP (promote storage + synthesis of prolactin), TCAs, anti-emetics cos of dopamine blockade (e.g. prochlorperazine, metoclopramide), methyldopa
o Prolactinoma of pituitary
o Craniopharyngioma/other tumour – may compress pituitary stalk/hypothalamus, interrupting the hypothalamic dopaminergic inhibition of prolactin release
o Ectopic prolactin synthesis e.g. bronchial carcinoma
o Other rare causes like renal failure (reduced clearance of prolactin), acromegaly

26
Q

What is an abdominal wall hernia?

A

Protrusion of abdo contents through fascia of abdo wall, contain peritoneal sac, may also have viscera (usually SB + omentum). May become irreducible/incarcerated, or strangulated (contents trapped, compromises blood supply, causes swelling then infarction + bowel obstruction).

27
Q

Incisional hernia

A
  • A risk of any abdominal surgery, esp after open. Due to wound failing to heal, exacerbated by patient + technical factors
  • M: need repair with reinforcing mesh, recurrence common if overweight
28
Q

Epigastric hernia

A
  • Defect in midline above umbilicus in linea alba, may have multiple, usually no sx but may cause epigastric pain/N+V/bloating. Straining causes it to bulge
  • Differentiate from diastasis recti – widening of LA without fascial defect
  • M: need surgical repair as high risk of incarceration + strangulation
29
Q

Umbilical hernia

A
  • V common, may be congenital (omphalocele), infantile (a/w prematurity, usually resolve) or adult (majority acquired e.g. multiple pregnancies or ascites). Usually omentum +/- bowel, gradually enlarges, may cause pain on coughing/straining, an ache or dragging sensation
  • If <1cm nearly always closes by 5y, if >1.5cm or child >4y usually needs repair
30
Q

Femoral hernia

A
  • Less common than inguinal, more common in older women esp if parous. Risk of strangulation much higher than inguinal hernia
  • Causes lump in groin, lateral + inferior to pubic tubercle classically. Often appears on coughing/straining, may have cough impulse, may be able to reduce. Lower abdo pain in incarceration. Put finger over femoral canal (approx. a finger’s breadth medial to femoral artery) and ask to cough – femoral hernia should remain reduced while inguinal hernia will reappear…
  • Strangulation – red + tender, tense, irreducible, colicky abdo pain, distension, vomiting
  • All should be repaired as elective but ASAP, or obv emergency if incarcerated
31
Q

Inguinal hernia

A
  • Male>female, obesity, constipation, chronic cough, heavy lifting.
  • Infants: more common in boys + prematurity. Congenital ones need urgent referral for repiar
  • Causes groin swelling, can have sudden pain or appearance from heavy lifting, indirect more likely to cause pain/dragging sensation in scrotum, may get impulse on coughing, lump may be reducible. With time enlarges + more fibrous adhesions so harder to reduce
  • For children they usually repair quickly
  • For adults if small may just need reassurance but safety net about obstruction.\
32
Q

Type of inguinal hernia

A

Indirect: through internal inguinal ring through canal lateral to inferior epigastric vessels, more common form + esp in children. Due to failure of closure of PV

Direct: protrudes directly through weakness in posterior wall of inguinal canal, medial to IEVs, more common in elderly, rare in kids

33
Q

Acne rosacea - what is it>

A

Chronic rash central face, usually begins after age 30, common in Celtic complexions. May be transient, recurrent or persistent.

34
Q

CF of rosacea

A

• Frequent blushing/flushing, erythema, papules, pinpoint pustules, inflammation, telangiectasia. On nose, forehead, cheeks, chin (rarely upper limbs and trunk may be involved). Dry flaky facial skin. Sensitive skin (burning and stinging like in reaction to make up/sun cream). Rhinophyma (enlarged unshapely nose, prominent pores, fibrous thickening).

Peri-ocular skin often spared

May get persistent redness + swelling/oedema of upper face due to lymphatic obstruction (Morbihan disease). Yellow-brown papules/nodules due to granulomatous rosacea. Blepharophyma (firm swelling of eyelids).

Worse with sun + hot food/drink

35
Q

Management of rosacea

A
o	Advice: reduce triggers, avoid oil-based creams, never apply topical steroids (may get short term improvement but makes more severe over weeks), protect from sun with light oil-free sunscreens (e.g. ones esp for face), keep face cool to reduce flushing, reduce hot/spicy foods, reduce alcohol/showers/warm rooms
o	Topical (mild) – metronidazole cream/gel intermittent or long term for mild/with oral for more severe. Other topical options include azelaic acid, brimonidine or others for more complex types. Adv use for 2 months then r/v
o	Oral Abx – tetracyclines. Reduce redness, papules + pustules, and eye sx. For 6-12w dep on severity, often need further courses from time to time as doesn’t cure disorder. Usually use a low dose that doesn’t have antimicrobial effects, to reduce bacterial resistance
o	Sometimes oral isotretinoin is used in resistant cases
o	Some meds can help with flushing e.g. clonidine (alpha-2 agonist) or carvedilol (beta blocker) – reduce vascular dilatation, s/e may include hypotension/GI/dry eyes/blurred vision/bradycardia
36
Q

Mimickers of rosacea (more skin rashes yay)

A
  • SLE: malar erythema in 50% which may precede other sx. Skin warm + slightly oedematous, often recurs with sun exposure. More violaceous than red.
  • Dermatomyositis – heliotrope rash, papules, periungual telangiectasia in nail fold… weak muscles
  • Polymorphous light eruption – erythematous papules, vesicles and plaques on sun-exposed surfaces. Often hours after sun exposure (tho can be immediate), may have mild itching/burning sensation. Intermittent, recurrent. Abrupt onset + offset in a few days. May get flulike sx after sun exposure
  • Seborrheic dermatitis – chronic relapsing disease esp in sebum-rich areas. Comes and goes in severity, chronic, well-demarcated erythematous patches/papules/plaques. Greasy quality to the scales
  • Acne vulgaris – noninflammatory open/closed comedones and inflammatory papules/pustules/nodules
  • Topical steroid-induced acne – inflammatory papules, dry scaly eruption, perioral dermatitis. Looks like rosacea but resolves 1-2/12 after stopping steroids
  • Rare things – carcinoid syndrome (flushing is characteristic, due to neuroendocrine tumours), cutaneous lymphoma