Oxford questions Flashcards
Wells Score
If <2, perform a D-dimer test – if negative, DVT is excluded. Consider alternative diagnoses.
If ≥2, or if the D-dimer is positive, proceed to Doppler and compression ultrasound examination of the venous system.
Which patients with a DVT should undergo investigations for an underlying cause
Those aged >55yrs with unprovoked DVT, and those with recurrent unprovoked DVT or DVT at an unusual site
Ann Arbor classification
The Ann Arbor classification is used for lymphoma staging, based on distribution of diseased tissue:
Stage I involves only one lymph node area
II involves 2 or more on one side of the diaphragm
III involves 2 or more on both sides of the diaphragm
IV involves any extra-lymphatic tissue (including bone marrow)
The presence of ‘B symptoms’ is denoted by adding B as a suffix
Classic complications of CLL
Autoimmune haemolytic anaemia
Hypogammaglobulinaemia
Two groups of patients diagnosed with Myasthenia Gravis
Young women (20-35)
Tend to present with a generalised, and often acute condition
Older men (60-75)
Who tend to present with prominent oculobulbar involvement
Classic presentation of Myasthenia Gravis
Patients usually present with fatigueable weakness
Progressively weakness over the course of the day is classic. The weakness improves with rest
Ocular and bulbar involvement is also possible, leading to ptosis, swallowing difficulties and speech disturbance
Most common antibodies in Myasthenia Gravis
Anti-AChR antibodies
Anti-MUSK antibodies
Most important investigation for Myasthenia Gravis
Forced vital capacity (FVC) is the key initial investigation in first presentation or flare
If this is low (<1.5l) then make sure ITU are at least aware of the patient, as they can rapidly deteriorate and require intubation and ventilation
Measure this at least 4-hourly in patients with acute/relapsed MG at presentation
Genetic disorders associated with colorectal cancer
Hereditary non-polyposis colorectal cancer (HNPCC)
Autosomal dominant, due to mutations in various mismatch repair genes and responsible for 3% of colorectal cancers
Familial adenomatous polyposis (FAP)
Autosomal dominant defect in APC gene
MUTYH-associated polyposis
An autosomal recessive condition which may cause polyposis and confers increased colorectal cancer risk
How does Hep B present
Hep B often presents with a subclinical or flu-like illness but can present with:
Acute hepatitis
Hepatomegaly
Jaundice (only 30-50%)
Dark urine/pale stools due to intrahepatic cholestasis
Serum-sickness-like syndrome
Rash, polyarthritis, fever
Rarely, arteritis or immune-complex-mediated renal failure
Chronic liver disease
Hep B medication
Pegylated interferon
Good:
No resistance
Finite duration of therapy
Bad:
Less well tolerated due to side-effect profile
Only moderate antiviral activity
Nucleoside (Lamivudine, Entecavir) and Nucleotide (Tenofovir) analogues
Good:
Potent antiviral effects
Few side-effects
Bad:
Risk of resistance to some drugs
Where in the spinal column does the spinal cord end?
L1
For a spinal cord compression why is an MRI of only the spinal cord inadequate
Clinical signs are poor at localising the site of the lesion
Metastases are present at more than one site in the spinal canal in 33% of patients with malignant cord compression
Surgical fixation requires good bone texture either side of a lesion, so this area must be imaged too
Most malignant causes of spinal cord compression
Lung cancer (25%)
Prostate cancer (16%)
Myeloma (11%)
Non-Hodgkin lymphoma (8%)
Breast cancer (7%)
Key features to address in a dementia history?
Try to establish:
Patient’s (and collateral) view of memory decline
Biographical history
Objective view of memory decline (e.g. knowledge of current affairs)
Impact of memory decline on day-to-day living and hobbies
Social history, including safety and driving
General medical history (especially medications)
Micro and Macro pathological of UC
Macro:
Inflammation extends proximally from the rectum
Hence inflammation can be classified as proctitis (limited to rectum), left-sided colitis (extending to sigmoid and descending colon), or pan-colitis (when entire colon involved)
Mucosa is reddened, inflamed, and bleeds easily.
Extensive ulceration, with islands of normal mucosa
Micro:
Superficial inflammation of mucosa (cf. Crohn’s, which is full-thickness)
Chronic inflammatory cell infiltrate in lamina propria (part of mucosa just under epithelium)
Crypt abcesses
Goblet (mucus-making) cell depletion
How to classify acute presentation of UC
Truelove and Witts’ criteria
Extra intestinal manifestations of UC
Mouth ulcers (strictly part of the GI tract but often considered separately)
Erythema nodosum
Uveitis/episcleritis
Arthropathy
Pyoderma granulosum
Primary sclerosing cholangitis (75% of this is seen in ulcerative colitis patients)
UC complications
Acute
Toxic megacolon
Mortality approx. 20%
Primary sclerosing cholangitis
Colorectal carcinoma
Risk increased 10-20 times once patients have had UC for 20 years
5-asa treatment probably reduces risk
Do colonoscopy starting at 10 years
Mucosal dysplasia on rectal biopsy is associated with cancer elsewhere in the bowel.
Then repeat at 1,3,or 5-year intervals depending on risk
Pouchitis after colectomy (with relapsing-remitting course)
Osteoporosis from steroid therapy
Bisphosphonates to over 65s on steroids and DEXA
Then bisphosphonates if T<1.5
How does Crohn’s disease present with
Extra intestinal manifestations of Crohn’s
Micro/Macro for Crohn’s
Crohn’s complications
What’s the differential diagnosis of heart murmurs?