Other cases - ix Flashcards

1
Q

Cataracts ix

A
  • Clouding of lens
  • Slit lamp examination of the anterior chamber – cataract visible (lens appears brown or white)
  • Reduced red reflex
  • Glare vision test - reduced visual acuity under the conditions of glare stress
  • Normal eye examination apart from opacity in the crystalline lens
  • Dilated fundus examination – fundus + optic nerve are normal
  • Measurement of intra-ocular pressure – normal
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2
Q

Glaucoma ix

A
  • Gonioscopy – measurement of the angle between the cornea and the iris to determine whether glaucoma is open-angle or close-angle
  • Corneal thickness measurement/Pachymetry – influence IOP reading

• Tonometry
o Normal range: 10-21 mmHg
o Glaucoma if intra-ocular pressure >21mmHg

• Fundoscopy
o Optic disc cupping (normal cup:disc ratio is 0.3-0.7) – rim gets thinner and thinner as the disease progresses until there is no rim left (i.e. cup:disc ratio increases)
o Flame haemorrhages in late disease

• Slit-lamp biomicroscopy
o Most frequent method used
o Assessment of cornea, anterior chamber, drainage angle
o Measurement of intra-ocular pressure

• Ocular coherence tomography
o Produces visual records + provides quantification of exact cup:disc ratio + areas of neuroretinal thinning

• Visual field testing
o Scotomas indicating loss of the nerve fibre layer

Closed angle oedema also shows
• Shallow anterior chamber

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3
Q

Uveitis ix

A

• Clinical diagnosis

• Slit lamp findings in anterior uveitis
o White cells in anterior chamber
o Hypopyon
o Keratic precipitates

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4
Q

Conjuctivitis ix

A
  • Clinical diagnosis
  • Rapid adenovirus immunoassays
  • Cell culture
  • Gram stain
  • PCR
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5
Q

Closed angle glaucoma diagnostic criteria

A

• Based on at least two of these symptoms
o Ocular pain
o N/V
o Hx of intermittent blurring of vision

•	And at least 3 of the following signs
o	IOP >21mmHg
o	Corneal epithelial oedema
o	Mid-dilated non-reactive pupil
o	Shallow chamber in the presence of occlusion 
o	Conjunctival hyperaemia
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6
Q

rheumatic fever ix/dx

A

Hx of streptococcal infection (increased anti-streptolysin O titre, anti-DNAse, anti-hyaluronidase etc or throat culture showing growth of GABHS)
+ 2 major criteria or 1 major + 2 minor

J<3NES PEACE
Joints (polyarthirits, hot/swollen joints, restricted movement)
Heart (carditis (can be pericarditis, myocardtis or endocarditis), valve damage)
Nodules
Erythema marginatum
Sythenham chorea

Previous rhuematic fever (increased anti-streptolysin O titre, anti-DNAse, anti-hyaluronidase etc or throat culture showing growth of GABHS)*
ECG with PR prolongation** (does not count if carditis present)
Arthralgia (does not count arthritis present)
CRP + ESR elevated
Elevated temperature

  • Positive serology is the most important means of demonstrating antecedent infection
    • ECG might also show features of pericarditis (saddle shaped ST elevation + PR segment depression)

• Echo
o Morphological changes to the mitral valves
o Severity of regurgitation (mitral>aortic>tricuspid)
o Pericardial effusion if pericarditis if present
o Myocardial thickening or dysfunction
o Valvular dysfunction

• Throat culture
o Growth of β-haemolytic group A streptococci (GAS)
o However, group A streptococci have usually been eradicated before onset of the disease

• Rapid antigen test for group A strep – positive

• *Anti-streptococcal serology – above normal range (demonstrates previous infection)
o Anti-streptolyisin O titre
o Anti-DNAse B titre
o Anti-hyaluronidase titre
o Positive serology is the most important means of demonstrating antecedent infection

GABHS = group A β-haemolytic streptococcus

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7
Q

HSV ix

A
  • Viral culture
  • HSV PCR
  • Glycoprotein G-based type-specific serology (gG1, gG2) – positive antibody to HSV-1 or HSV-2
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8
Q

VZV ix

A

• Clinical dx – based on the way skin lesions appear

  • PCR – viral DNA
  • Viral culture – positive varicella zoster virus in culture
  • Direct fluorescent antibody testing (DFA) – positive for varicella-zoster virus antigen
  • Tzanck test - multinucleated giant cells in the fluid of the vesicles

• Latex agglutination
• ELISA
o These two tests are not used in acute disease, but can be useful in determining seroconversion after vaccination or documenting immune status
o Result – positive for IgG for varicella

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9
Q

EBV infectious mononucleosis glandular fever ix

A

• FBC
o Lymphocytosis (highest in week 2-3)
o Atypical lymphocytosis

• Heterophile antibodies - Monospot test, Paul Bunnell test
o Non-specific for EBV infection
o IgM antibodies produced form infected B cells agglutinate RBC from other species (sheep, horse, goat, bovine)
o May be negative in the early course of EBV IM
• Adults – repeat
• In children <4 (B cells do not produce heterophile antibodies) – EBV ab
o Patients who remain heterophile-negative after 6 weeks with a mononucleosis illness are considered to be heterophile-negative IM + should be tested for EBV-specific antibodies

• EBV-specific antibodies
o Indicated if pt has infectious mononucleosis symptoms but negative heterophile antibodies
- Early primary infection - VCA IgM
- Acute primary infection - VCA-IgM, VCA-IgG
- Past infection - VCA-IgG, IgG EBV EBNA

  • Real-time PCR – EBV DNA detection
  • If splenic rupture is suspected (but pt is haemodynamically stable) – CT abdo
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10
Q

HIV ix

A

• False negatives during the window period
o Serum HIV ELISA
o Serum HIV rapid test
o Serum Western blot – used as a confirmatory test following a positive ELISA or rapid test

• Testing during the window period/ acute infection
o Serum p24 antigen – present during high viral replication [detectable in the blood during acute infection + again during late stages of infection]
o HIV DNA PCR in peripheral blood mononuclear cells – infants

• CD4 count
o Indicates immune status + assists in the staging process
o CD4 count <200 cells/microlitre – defines AIDS and places the patient at high risk of most opportunistic infections

• Serum viral load (HIV RNA)
o Establishing a baseline viral load before therapy
o Monitoring response to antiretroviral therapy
o quantitative viral RNA in plasma – used to confirm acute HIV

• FBC – may be normal or show anaemia, thrombocytopenia, lymphocytopenia, reduced CD4 cell count

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11
Q

Tonsilitis ix

A

• Throat culture
o Standard test for the definitive dx of bacterial tonsillitis

  • Suspected rheumatic fever = group A β-haemolytic streptococci throat infection – serological testing for streptococci – rapid streptococcal antigen test
  • Suspected infectious mononucleosis – heterophile antibodies
  • Not recommended – throat swabs, rapid antigen tests
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12
Q

Alcohol withdrawal ix

A

Questionnaires
• Screen the patient for alcohol-use disorder using a formal assessment tool (AUDIT-C, FAST, PAT)
o Number of alcohol units = % ABV x Volume (L)
• Identify patients who have tested positive for alcohol misuse + are at risk of alcohol withdrawal by assessing their level of alcohol dependence
o CAGE questionnaire – considered positive if score >2
• Severity of withdrawal
o CIWA-Ar scale (clinical institute withdrawal assessment from alcohol revised scale)

  • O/E – signs of alcohol abuse (e.g. chronic liver disease)
  • Obs – tachycardia, temperature

• VBG
o Respiratory alkalosis – pt with delirium tremens, hyperventilation
o Hypochloraemic metabolic acidosis – vomiting
o Metabolic acidosis with a high anion gap – alcohol ketoacidosis

• Blood glucose
o Hypoglycaemia is common – secondary to poor nutrition or heavy alcohol use

• FBC
o Macrocytic anaemia
o Thrombocytopenia – splenomegaly, folate deficiency, toxic effect of alcohol on platelets

• U+E
o Low Mg2+, K+, PO43-
• ECG – always performed on pt with electrolyte deficiencies – they can cause life-threatening cardiac arrhythmias

• LFT – elevated
o AST>ALT
o raised GGT

• Bone profile
o Hypocalcaemia 2y to hypomagnesaemia suppressing PTH
o Low Vitamin D – poor intake, lack of exposure to sunlight, toxic effects of alcohol, malabsorption

  • Coagulation studies – prolonged INR + PT in chronic liver disease
  • CT head – in patients with a) alcohol related seizure, b) altered cognition – more likely to bleed heavily due to deranged clotting + thrombocytopenia, subdural haemorrhage
  • Ammonia – consider in all patients with an altered level of consciousness + signs of liver disease – may indicate liver failure
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13
Q

Anaphylaxis ix

A

• Clinical dx

• Mast cell tryptase
o Normally undetectable in serum
o Elevated in anaphylaxis

• Histamine levels

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14
Q

Aspirin overdose ix

A

• ABG
o Initially – respiratory alkalosis
o Later – high anion gap metabolic acidosis

• Serum salicylate level
o Salicylate intoxication - >350 mg/L (2.5 mmol/L)

• Ketones – positive particularly in children
• Glucose – hyper or hypoglycaemia
• U+E - Low K, Ca, Mg
• LFTs
o Direct hepatotoxicity can occur
o Most patients develop asymptomatic elevation of transaminases
• PT, APTT, INR
o Coagulopathy may be present
o Platelet dysfunction, low F 7, hypoprothrombinaemia

• CXR – non-cardiogenic pulmonary oedema may be present
• ECG
o Commonly sinus tachycardia
o Prolonged QT or ventricular dysrhythmias may occur - life threatening

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15
Q

Paracetamol ix

A

• Serum paracetamol level 4h after overdose - to determine which patients would benefit from N-acetylcysteine

• Serum AST + ALT
o May be normal
o May rise to ALT >1000 IU/L – hepatotoxicity

  • FBC
  • Glucose
  • Coagulation screen - Serum PT + INR – used to monitor the severity of hepatotoxicity
  • Arterial pH + lactate level – acidosis, raised lactate
  • U+Es or renal function tests
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16
Q

Opiate overdose ix

A

• Therapeutic trial of naloxone
o In pt who present with altered mental status, bradypnea, miosis

  • ECG – look for myocardial ischaemia
  • CXR – ARDS (non cardiogenic pulmonary oedema)
17
Q

Skin cancer ix

A
  • SCC – Excisional biopsy – to determine depth of spread
  • BCC – when non-surgical treatments are used, an incisional biopsy must be sent before treatment for confirmation of the dx

• Malignant melanoma – biopsy to determine invasion by clark level/breslow thickness
Thickness –> Breslow classification
Depth of invasion into the skin layers –> Clark’s classification

If there is local invasion – Invasive tumours extend beyond the BM, penetrate into the dermis, may invade deeper structure

  • Dermatoscope
  • CT/MRI/PET/CXR/FBC – is suspecting metastases
18
Q

Psoriasis ix

A
  • Clinical diagnosis
  • Skin biopsy when in doubt
  • Guttate psoriasis – anti-streptolysin O titre, throat swab
19
Q

Cellulitis + erysipelas ix

A
  • History + examination
  • FBC - raised WCC
  • raised CRP
  • Blood culture or swab MCS – identifies pathogen + susceptibility (e.g. MRSA, staph aureus, strep pyogenes)
  • If cellulitis is associated with, or adjacent to, a wound or pustular focus - purulent focus culture and molecular dx procedures - growth of typical pathogen (e.g. Staph aueus)

• CT/MRI – if orbital cellulitis to identify posterior spread of infection

20
Q

Erythema nodosum ix

A

• Investigate for underlying causes

• FBC - increased WCC
• Anti-streptolysin-O titre - raised in streptococcal infection
• CXR
o Bilateral hilar adenopathy - sarcoidosis
o Unilateral hilar adenopathy - TB, malignancy, histoplasmosis, coccidioidomycosis, brucellosis
• Calcium + ACE - in sarcoidosis
• Purified protein derivative skin testing - positive in TB
• Stool examination – Yersinia enterocolitica, Salmonella, Campylobacter
• Microscopy of the lesions - septal panniculitis without vasculitis, septal infiltration of neutrophils, oedema, haemorrhage

21
Q

Erythema multiforme ix

A

• Investigate for underlying causes

  • HSV serology [most common cause]
  • Serum PCR – to differentiate Herpes zoster (varicella) for HSV
  • Cold-hemagglutination serology – dx of M pneumoniae [most common cause]
  • M pneumoniae titre – dx of M pneumoniae
  • CXR – dx of M pneumoniae [bronchial thickening with areas of interstitial infiltration, subsegmental atelectasis involving a lower lobe]
22
Q

Molluscum contgiosum ix

A

• Clinical dx

• Haematoxylin + eosin staining
o To provide definitive dx
o Performed on biopsy specimens
o Henderson-Patterson bodies

If many lesions on adults (>60) - may suggest immunocompromise - test for HIV

23
Q

Breast - triple assessment of solid lumps

A
  1. Clinical examination
  2. Radiological examination
    <35 US
    >35 mammogram
  3. FNA or core biopsy
    FNA - will provide info on types of cells + whether they are dysplastic or not
    Core biopsy - will additionally provide information on the local architecture (e.g. invasion of surrounding structures)
24
Q

Breast cancer on mammogram

A

Increased density
Irregular margins
Speculation (like shards of glass)
Accompanying clustered irregular microcalcifications

25
Q

Breast abscess ix

A
  • Breast US
  • FNA + drainage
  • CYTOLOGY of nipple discharge/sample from FNA
  • Milk/aspirate/discharge/biopsy tissue CULTURE for sensitivity
26
Q

Which grading system is used in breast cancer?

A

Nottingham grading system

27
Q

Where does breast cancer commonly metastasise?

Breast cancer staging ix

A
Breast cancer commonly metastasises to
Bones
Brain
Liver 
Lungs
Staging 
Bone scan
CT scan (brain/chest)
Liver US
CXR
Bloods
FBC
U+Es
LFTs
ESR
Caclium
Bone profile
28
Q

Vitamin A deficiency ix

A

• Serum retinol-binding protein

  • Zinc level – zinc deficiency interferes with the production of retinol binding protein
  • Iron studies – iron deficiency can affect the metabolism of Vitamin A
29
Q

Vitamin B deficiency ix

A

B1 (thiamine)
• Best dx test – good clinical response to administration of thiamine IV
• Thiamine loading test – load pt with thiamine, in deficient patients the urine excretion of thiamine + thiamine pyrophosphate is lower than normal
• Blood thiamine level
• Wernicke’s – CSF is normal if untreated blood pyruvate + blood transketolase will rise

B2 (riboflavin)
• Riboflavin

B3 (niacin)
• After niacin has been processed it can be excreted in the urine
• Products in urine – nicotinic acid, niacin oxide, 2-pyridone, 2-methyl nicotinamide

B9 (folate)
• MCV, Hct, Hb, blood film – macrocytic megaloblastic anaemia

B12 (cobalamine)
• Clinical dx
• MCV, Hct, Hb, blood film – macrocytic megaloblastic anaemia

30
Q

Vitamin C deficiency ix

A

• Ascorbic acid replacement therapy

31
Q

Vitamin D deficiency ix

A
  • Secondary hyperparathyroidism - low/N Ca,low PO43-, high PTH
  • low Vitamin D
32
Q

Vitamin E deficiency ix

A

• Clinical dx

33
Q

Vitamin K deficiency ix

A
  • Prolonged bleeding time, PT, APTT
  • Plasma vitamin K
  • Antibody test for high level des-gamma-carboxy prothrombin protein in vitamin K absence (DCP-PIVKA) – most sensitive marker
34
Q

Necrotising fasciitis ix

A
  • No definitive test – surgery is required to confirm/rule out NF
  • FBC – high WBC w L shift

• U+Es
o Increased U + Cr
o Low Na (non specific finding that may be seen in any systemic infection or circulatory collapse)

• High CK
o Non specific finding suggestive of systemic infection or circulatory collapse
o If spreading soft-tissue infection is present (e.g. cellulitis), then necrotising fasciitis should be suspected

  • High lactate
  • High CRP

• Microbiology
o Blood and tissue cultures – to make a definitive bacteriological dx
o Wound swab
o Gram stain + culture of affected tissues
o Fungal culture important in immunocompromised + trauma patients

• Radiology
o XR/CT/US – Soft tissue gas
o MRI – show extent of tissue involvement

• Surgical exploration – should be obtained in all patients