OE EMQs Flashcards
Ocular signs associated with systemic diseases
- Reiter’s syndrome
- Syphilis
- Myasthenia gravis
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- Uveitis
- Argyll-Robertson pupil, where there is miosis and the pupil accommodates but does not react to light
- Ptosis
Common skin infections
- A 60-year-old obese patient with diabetes presents with a red, itchy, pustular rash in the sub-mammary folds, axillae and groin.
- An elderly man presents with severe pain in the left thigh and inability to walk. Multiple vesicles in a linear configuration are seen over the anterior thigh.
- A 30-year-old man presents with severe generalised itching which is worse at night. Both his wife and little baby are also scratching themselves.
- A mother presents to the surgery with her three children. All three children have flesh coloured umbilicated nodules on their faces.
- A 40-year-old man presents to his GP with a red, hot, swollen and painful leg. He admits to wounding the leg whilst gardening the previous day.
- Candidal intertrigo favours warm, moist surfaces and is common in the obese as well as diabetics.
- Herpes zoster is more common in the elderly and immunosuppressed. Severe pain limiting function may be the presenting complaint.
- Scabies causes a generalised itch which is severe when the body is warm. It is transmitted by close contact and other members of the family have to be treated simultaneously. Papules, nodules, burrows and excoriations are found and areas most affected are the backs of the hands, genitalia and soles or palms in infants.
- Molluscum contagiosum is a common viral infection transmitted by direct skin to skin contact, and therefore common in children and families. Lesions disappear spontaneously or after trauma, therefore scratching and picking result in resolution. In adults, multiple molluscum or genital molluscum are associated with HIV infection.
- Cellulitis is a common skin infection and usually follows a discernible wound, for example, minor trauma or tinea pedis.
Common Alcohol problems
- hepatic encephalopathy
- delirium tremen
- intoxication
Night blindness and beriberi are caused by what deficiency?
Vit A and thiamine
Night blindness and beriberi are diseases that usually affect people in developing countries; they are caused by vitamin A and thiamine deficiency respectively. Dry beriberi can to progress to Wernicke-Korsakoff, but in developed countries the syndrome is associated with alcoholism.
classic presentation of PMR
Weight loss, fatigue and headaches
Reactive arthritis (Reiter’s syndrome) is associated with…
urethritis, arthritis and iritis/uveitis. It is typically associated with a prior history of either urethritis or diarrhoeal illness. The disease typically affects young males.
Patients who have fibromyalgia tend to be middle-aged women who have a history of
depression
Sclerodactyly describes…
the tight skin over the fingers. As well as being a feature of diabetes, it is also seen in scleroderma.
- An autosomal dominant anaemia that is caused by a red cell membrane defect.
- An autosomal recessive anaemia affects the haemoglobin, causing it to polymerise at low oxygen saturations, leading to severe muscle pain from blood vessel occlusion.
- This acquired haemolytic anaemia can be classified into ‘warm’ and ‘cold’ sub-classes.
- This mechanical haemolytic anaemia can occur in malignant hypertension or eclampsia.
- This X linked recessive anaemia occurs with a defect in pentose phosphate pathway.
- Hereditary spherocytosis
- Sickle cell anaemia usually affects people of black African descent. The polymerisation of the haemoglobin causes occlusion of the blood vessels leading to the symptoms.
- Autoimmune haemolytic anaemias can be sub-typed into ‘warm’ and ‘cold’. Warm and cold describe at what temperatures the antibodies against the RBCs best work.
- Microangiopathic haemolytic anaemia.
- Glucose-6-phosphate dehydrogenase deficiency
Complications of Chronic Renal Failure
- pruritus. Can be treated by UV phototherapy.
- Anaemia, Due to erythropoietin deficiency.
- encephalopathy, Associated with a flapping tremor.
- Osteodystropy, Associated with failure of 1 alpha-hydroxylation of cholecalciferol.
- Dialysis dementia, Associated with accumulation of aluminium.
- dyslipidaemia is common in CRF and is due to impaired lipoprotein lipase activity with combined hyperlipidaemia.
- Gout is a common problem in patients with chronic renal failure.
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Dressler’s syndrome
This is a pericarditis that develops two to 10 weeks after a myocardial infarction or heart surgery.
XO genotype is associated with
Turner’s syndrome
- Short stature
- Failure of pubertal development
- Wide carrying angle
- Web neck
- Possible cardiac defects, such as coarctation.
Klinefelter’s syndrome is
one of the commonest causes of elevated LH/FSH with low testosterone. There is absence/paucity of secondary sexual characteristics, the patient is often tall, has small testes and there is often reduction in IQ.
Associated with a 47 XXY karyotype.
A congenital condition in which obesity is associated with mental retardation.
Prader-Willi syndrome
Obesity associated with hypogonadotrophic hypogonadism and mental retardation.
Hypothalamic gonadotrophin releasing hormone deficiency with anosmia.
Kallmann’s syndrome
Kallmann’s syndrome is a common cause of hypogonadotrophic hypogonadism associated with failure of development of the olfactory bulbs hence anosmia.
the two commonest causes of acute pancreatitis
Alcohol and gallstones
Acute cholecystitis is distinguished from biliary colic in that there is …
no acute inflammation associated with the latter and so there is no pyrexia or peritonism and no elevated WBC/CRP.
Charcot’s triad
jaundice, pain and fever
Theme:Head and neck swellings
A Branchial cyst
B Carotid body tumour
C Cystic hygroma
D Lymphoma
E Parotid adenolymphoma
F Parotid pleomorphic adenoma
G Submandibular duct calculus
H Submandibular tumour
I Thoracic outlet syndrome
J Thyroglossal cyst
commonest parotid tumours (75%)
A 63-year-old woman is referred with a longstanding and slow growing painless swelling overlying her left mandible. On palpation the lesion is firm and non-tender, and there is no facial nerve damage evident.
Pleomorphic adenomas
They typically have a smooth edge and irregular surface. They should be excised carefully taking care not to rupture the tumour as it can seed and regrow. Pleomorphic adenomas have a small risk of malignant transformation if left long term.
Carotid body tumours usually present as
painless masses but occasionally may compress the vagus or hypoglossal nerves causing dysphagia, hoarseness, stridor, or weakness of the tongue. They are more common in people living at high altitude.
A 76-year-old man is seen with multiple non-tender masses on both sides of his neck. He also reports weight loss, lethargy and night sweats. The lesions have a rubbery consistency and vary between 2 and 4 cm in diameter.
Patients with lymphadenopathy and constitutional symptoms must be regarded as having a lymphoma until proven otherwise. All head and neck lymphadenopathy must undergo FNA to exclude a squamous carcinoma prior to excision. However, FNA is often inadequate for diagnosis of lymphoma and an excision biopsy is required for characterisation of lymphoma and planning of chemotherapy.
A 68-year-old male hypertensive smoker presents with sudden painless loss of vision in one eye. Fundoscopy reveals a pale retina with a cherry red spot at the macula.
Central retinal artery occlusion causes pallor of disc and retina, the macular is spared as it receives branches from the post ciliary artery. The occlusion is commonly atherothrombotic embolus. There is dramatic loss of vision within seconds`
A 83-year-old female with a past medical history of angina, presents with sudden painless loss of vision in one eye. Fundoscopy reveals a hyperaemic retina with engorged veins accompanied by multiple haemorrhages
Central retinal vein occlusion is commoner than central retinal artery occlusion. Its causes include chronic simple glaucoma, arteriosclerosis, hypertension and polycythaemia. There is sudden loss of vision and the fundus looks like a stormy sunset.
A 71-year-old male presents to his GP complaining of a gradual deterioration in his vision. In particular he has noticed that buildings do not appear straight. On fundoscopy there is pigment, exudate and bleeding at macula
Age related macular degeneration (ARMD) is the commonest cause of blindness in the United Kingdom. There is degeneration of central vision. The presence of drusen precedes the ARMD fundoscopic appearance.
A 20-year-old male presents with difficulty night driving. Examination of his fundus reveals pigmentation at the periphery.
Retinitis pigmentosa is the most prevalent inherited retinal degeneration condition. There are many forms of the disease. Most are sporadic but may be inherited autosomal dominantly, autosomal recessively or X linked. Autosomal dominant forms have the best prognosis and X linked the worst. The onset is gradual and insidious and the most common complaint is difficulty with night vision although the presentation varies. It has associations with:
Usher syndrome (retinal dystrophy and hearing loss)
Congenital renal diseases such as renal-retinal dysplasia and Alport disease
Neuronal diseases
Enzyme deficiencies
Mitrochondrial disorders.
The only carcinoma provided here that is associated with clubbing is
bronchial carcinoma.
A 69-year-old male presents with a six month history of 10 kg weight loss. He is a smoker of 10 cigarettes/d and has a history of hypertension. On examination, he is thin and has a palpable left supraclavicular lymph node.
This man has an enlarged Virchow’s node and hence Troisier’s sign - suggestive of gastric carcinoma
Courvoisier’s law
- the presence of an enlarged gallbladder which is nontender and accompanied with mild jaundice, the cause is unlikely to be gallstones. Usually, the term is used to describe the physical examination finding of the right-upper quadrant of the abdomen. This sign implicated possible malignancy of the gall bladder or pancreas and the swelling is unlikely due to gallstones.[1][2]
Prehn’s sign
Negative Prehn’s sign indicates no pain relief with lifting the affected testicle, which points towards testicular torsion which is a surgical emergency and must be relieved within 6 hours.
Positive Prehn’s sign indicates there is pain relief with lifting the affected testicle, which points towards epididymitis.
Virchow’s node
Troisier’s sign
The finding of an enlarged, hard node (also referred to as Troisier’s sign) has long been regarded as strongly indicative of the presence of cancer in the abdomen, specifically gastric cancer, that has spread through the lymph vessels.
A flapping tremor/asterixis is caused by the three failures:
Liver
Lungs
Kidneys.
A 79-year-old man has a six month history of rapidly progressive memory impairment. He has also had bradykinesia and rigidity, which was not responsive to co-beneldopa (Madopar) and has recently become very aggressive to his wife.
Lewy body dementia
This patient has Lewy body dementia hallmarked by the presence of Lewy bodies within the brain stem and neocortex. There are features of parkinsonism which fail to respond to therapy and fluctuating cognitive loss.
Left-sided colon cancer is more likely to present with
obstructive symptoms. Examination may be normal in early disease or reveal:
Cachexia
Abdominal tenderness
Hepatomegaly
Distension
Ascities
Rectal mass
Blood in late disease.
Bronchiectasis is due to
abnormal dilation of the proximal and medium sized bronchi. There are many causes:
Infection
Obstruction
Cystic fibrosis
Ciliary dyskinesia
Young syndrome
Allergic aspergillosis
Alpha1-antitrypsin deficiency
Autoimmune diseases such as
Rheumatic arthritis
Ulcerative colitis.
It classically presents as cough with large amounts of mucopurulent sputum, sometimes blood streaked. Haemoptysis may be present. Patients often have clubbing and cyanosis with crackles and wheezing may be heard on auscultation. Antibiotics and physiotherapy are the mainstay of treatment.
A 35-year-old international aid worker complained of feeling generally unwell with right sided abdominal pain, shivering and night sweats. He has a high swinging temperature and is tender in the right upper quadrant. A single mass is palpated in the right liver lobe, revealed to be cystic in nature on ultrasound scanning. His white cell count is elevated but liver function tests are normal.
An amoebic liver abscess is the most likely cause of a swinging temperature and a cystic liver mass. There is no history of diarrhoea in a half of cases. Liver function tests may be normal or show a cholestatic picture.
An asymptomatic 55-year-old woman is investigated for a persistently raised alkaline phosphatase level. Her AST and ALT are only mildly elevated. On examination she has tendon xanthomata, and a smooth liver edge is palpable 3 cm below the costal margin. Her IgM is raised; results from auto-antibody screening are awaited.
Primary biliary cirrhosis is often asymptomatic and diagnosed after finding a raised alkaline phosphatase on routine testing. Xanthomata, hepatomegaly and a raised IgM are features of this autoimmune disorder. Antimitochondrial antibodies are usually positive.
Tietze’s syndrome is a
benign condition of unknown aetiology consisting of non-specific inflammation and swelling of one or more costal cartilages. The resulting discomfort may be similar to pleuritic pain but local tenderness is elicited on palpation of the lump. Treatment is conservative, with local corticosteroid injection if necessary.
A 57-year-old woman presents to her GP with a continuous ache on the right side of her chest. She also admits to weight loss and haemoptysis and volunteers that her right eyelid has recently begun to droop.
This lady has a right apical bronchogenic carcinoma (Pancoast’s tumour). Horner’s syndrome (ptosis, meiosis, anhydrosis and enophthalmos) has occurred as a result of neoplastic infiltration of the sympathetic outflow.
A 17-year-old student presents in the Emergency department with increasing shortness of breath on exertion. On examination he is very thin and has signs consistent with a large right pleural effusion. Abdominal examination reveals 5 cm hepatomegaly and a hard irregular mass in the left side of the scrotum.
This young man has signs consistent with a left testicular carcinoma with distal metastases in the liver and lungs. Urogential tumours (that is, renal, gynaecological and testicular) classically cause multiple large pulmonary metastases known as ‘cannonball metastases’.
A 19-year-old man presents to his GP with a two day history of shortness of breath on exertion and a non-productive cough. He has felt non-specifically unwell with a headache for several days. Clinical examination is normal but a chest x ray shows patchy shadowing of both lower lobes.
Mycoplasma pneumoniae is one of the principal causes of atypical pneumonia.
Non-specific symptoms, such as headache, diarrhoea and fatigue, tend to precede chest symptoms and at presentation chest x ray often shows consolidation before auscultatory signs become apparent. M. pneumoniae is notable for causing a wide range of extra-pulmonary conditions, including erythema multiforme and cold agglutinin production leading to haemolytic anaemia.
There is also a strong association with Guillain-Barré syndrome.
A 64-year-old man with a six month history of weight loss, constipation and rectal bleeding presents to his GP with shortness of breath and pleuritic chest pain which came on suddenly during a meal. Chest examination was normal.
This man has a history suggestive of colorectal tumour. He is therefore at risk of developing deep venous thrombosis, both as a result of direct venous compression by the tumour and also because of the pre-coagulant effect associated with carcinomatosis.
The diagnosis of sarcoidosis is based on
the non-specific symptoms of weight loss and malaise coupled with a history of polyuria which is suggestive of hypercalcaemia, a common feature of active sarcoid. A maculopapular or vesicular rash on the face occurs frequently and if it becomes chronic and granulomatous, is termed ‘lupus pernio’.
Sarcoidosis is a multi-system granulomatous disease and in cases of insidious onset the presentation may therefore reflect involvement of any organ. More commonly however, the onset is acute and is characterised by erythema nodosum and bilateral hilar lymphadenopathy on chest x ray which is often associated with varying degrees of dyspnoea and non productive cough.
Cryptogenic fibrosing alveolitis (known as idiopathic pulmonary fibrosis in the USA) generally presents in t
he sixth decade of life. Respiratory symptoms, other than progressive dyspnoea and dry cough, are uncommon. The classic examination findings are digital clubbing and fine end-inspiratory bibasal crackles.
One major side effect of metformin is
lactic acidosis. This may be severe in situations of tissue hypoxia and in conditions such as renal impairment, alcohol abuse, liver disease and heart failure.
Fluoxetine when given in combination with xxx increases the risk of xxx
sulphonylureas
hypoglycaemia
A 26-year-old female presents with a two month history of severe headaches that appears to be relieved by standing. On examination, it is noted that she is obese. She has no neurological abnormalities or visual disturbances.
Benign intracranial hypertension is a problem that more commonly is seen in young obese women. The patients may also have papilloedema.
A 67-year-old lady presents with a three week history of intermittent facial pain. She says that the pain starts just in front of the right ear and spreads down toward the mouth. It is a sharp, stabbing pain that comes on intermittently - especially when she is out in the cold. There are no obvious signs on examination.
Trigeminal neuralgia is a relatively common problem that is mostly seen in patients aged over 60. It is characterised by sharp facial pain that comes on suddenly and the pain is in the distribution of the trigeminal nerve. The pain is usually brought on by a trigger such as cold air/chewing/cleaning teeth. The treatment is usually with pain relief and surgery.
A 52-year-old male presents with a one month history of episodic headache. The pain is left sided and is described as “boring in one eye”; it can then spread to his forehead. He usually gets these episodes at night, a few hours after going to sleep. There are no obvious abnormal signs on examination.
Cluster headache is characterised by an intense pain that is concentrated around one eye. The attacks are more common at night and most commonly affect males aged over 40 years.
The risk factors for developing pulmonary embolisms include
Possible features include
Increased age
Obesity
Malignancy
Pregnancy
Treatment with HRT or the OCP
Immobility.
Shortness of breath
Pleuritic chest pain
Haemoptysis
Hypotension
Tachycardia
Dyspnoea
A raised JVP.
A sign that is often linked to vitamin D deficiency is
the ‘waddling gait’. The insufficient vitamin D leads to an initial hypocalcaemia. Over a longer period of time the deficiency can cause secondary hyperparathyroidism.
A 55-year-old female presents with a two month history of fatigue and itchy skin. On examination, it is observed that she has yellow sclera and hepatomegaly. A blood test shows raised bilirubin and raised alkaline phosphatase.
what antibody would be present?
Antimitochondrial antibodies
Primary biliary cirrhosis is an autoimmune disorder of the bile ducts with in the liver. Over 90% of patients with primary biliary cirrhosis have antimitochondrial antibodies.
A 30-year-old female who is 28 weeks pregnant presents with hyperpigmentation around the cheeks, eyes and forehead, giving a ‘mask-like’ appearance.`
Melasma
This is also termed the ‘mask of pregnancy’. Most pregnant women develop increased pigmentation of the skin, which improves spontaneously after pregnancy. Melasma is also associated with the combined OCP.
A 62-year-old female presents with severe, sharp and episodic pain during swallowing.
Involved cranial nerve
Glossopharyngeal
This story is typical of glossopharyngeal neuralgia, a similar condition to trigeminal neuralgia but affecting the IX nerve. The episodic lancinating pain may be produced by swallowing.
A 58-year-old female presents with weight loss despite an increase in her appetite. She also describes overwhelming heat intolerance. On examination she has a tremor and is very agitated.
Initail treatment
Carbimazole
The symptoms point towards hyperthyroidism and thus the treatment is carbimazole.
A 50-year-old woman presents with increased weight gain and bruising on her skin. On examination her limb muscles are wasted, her skin is very thin and she has unusual facial hair.
Treatment?
Surgery
Symptoms point towards a diagnosis of Cushing’s which is treated by removal of the cause, often a pituitary tumour.