Pathology Flashcards
(35 cards)
Thymoma
Pemphigus
Thymomas are the most common tumour of the thymus. Approximately 40% are malignant. Paraneoplastic syndromes can result in pemphigus. Paraneoplastic pemphigus has erythematous, scaly plaques in a lupus-like butterfly distribution on the face as well as involving the scalp, back, chest, and intertriginous areas.
Hepatocellular carcinoma
Icterus
Hepatocellular carcinoma can produce jaundice (icterus) by either obstruction of the hepatic ducts or by hepatocellualr failure.
Lymphoma
Erythema multiforme
There are many aetiological causes of erythema multiforme including
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Infection (bacterial, fungal, parasitic and viral)
Drugs (penicillins, cephalosporins, anticonvulsants, etc)
Immunological disorders collagen diseases, vasculitides, leukaemia, multiple myeloma, myeloid metaplasia, polycythemia and non-Hodgkin lymphoma.
Gastric carcinoma
Acanthosis nigricans is most commonly associated with intra-abdominal neoplasms. Although acanthosis nigricans can also occur without an associated malignancy, the new appearance of extensive acanthosis nigricans in an older patient should prompt additional investigation for an internal cancer.
Areas of necrotic mucosa with an off-white slough covering most of the sigmoid colon and rectum.
Pseudomembranous colitis
Pseudomembranous colitis is a specific form of infective colitis associated with hospital patients receiving antibiotics. The pseudomembrane is produced from necrotic mucosa and exudates.
Generalised continuous epithelial oedema with a fine granular appearance. There are patches of erythema, contact bleeding and frank ulceration.
Ulcerative colitis
In ulcerative colitis the earliest changes noted at colonoscopy are a loss of the vascular pattern due to oedema obscuring the submucosal vessels. The oedema also produces the granular appearance as described.
As the condition becomes more severe erythema, contact bleeding and ulceration result. Recurrent attacks followed by repair produce mucosal regeneration nodules or pseudopolyps. Pseudopolyps represent tags of mucosa that have partially detached during healing and remain as projections.
Areas of normal appearing mucosa with interdispersed areas of oedematous mucosa penetrated by deep fissuring ulceration.
Crohns colitis
Small aphthous ulcers are the early feature of Crohn’s disease, in contrast to the erythema and loss of the vascular pattern in ulcerative colitis.
In more severe disease the oedematous mucosa is penetrated by deep fissuring ulceration to give a cobblestone appearance. Multiple biopsies should be taken, as the presence of granulomata will confirm the diagnosis.
This cancer is autosomal dominant and affects the eye.
Retinoblastoma
Patients who suffer from retinoblastoma are found to have the autosomal dominant tumour suppressor gene RB1.
Commonest intra-abdominal childhood malignancy of primitive renal tubules and mesenchymal cells.
Wilms’ tumour
Wilms’ tumour occurs in children alone. It is treated well by surgery and chemotherapy.
Tumour suppressor genes affected in this familial cancer include MLH1 and MSH2.
Hereditary non-polyposis colonic carcinoma (HNPCC)
MLH1 and MSH2 are found in patients who are suffering from hereditary non-polyposis colon cancer, and also some cases of endometrial cancer.
The tumour suppressor gene involved in this autosomal dominant syndrome is associated with multiple colonic polyps.
Familial adenomatous polyposis
Familial adenomatous polyposis sufferers have the APC tumour suppressor gene. FAP affects the colon.
Associated with a defect in DNA gyrase.
Xeroderma pigmentosa
Xeroderma pigmentosum affects the skin, and having the XP gene increases the chances of developing skin cancer by over a 1000 times.
Bronchial carcinoma with a couple of peribronchial and ipsilateral hilar lymph nodes involved but no evidence of metastases.
T2, N1, M0
The TNM system is used to describe the extent of oncogenesis from a cancer.
T denotes the tumour size, N denotes the nodal involvement, and M denotes whether metastasis is found.
TX is used to show that positive cytology was found, however the location of the tumour is unknown or is too small to show on CT or MRI.
A large bronchial carcinoma with widespread nodal involvement and bony metastases.
T4, N3, M1
Weight loss in a smoker with normal chest x ray but positive sputum cytology for carcinomatous cells.
TX, N0, M0
The following conditions all can cause a pleural effusion.
Which of the following would typically cause a transudate (
Nephrotic syndrome
All inflammatory and malignant causes of pleural effusions are exudates (>30 mg/L protein).
Nephrotic syndrome, liver cirrhosis and heart failure would be examples of a transudate.
Shortly after birth a newborn baby is noted to be drooling excessively.
A diagnosis of oesophageal atresia is made.
Which of the following is not associated with oesophageal atresia?
(Please select 1 option)
Aspiration pneumonia
Cyanosis during feeding
Empty stomach on USS
Oligohydramnios
Tracheo-oesophageal fistula
Oligohydramnios
Infants with oesophageal atresia are often diagnosed before birth by a finding of polyhydramnios (due to their inability to swallow amniotic fluid).
Eighty five per cent of patients with oesophageal atresia have a tracheo-oesophageal fistula which causes cyanosis during attempted feeding and aspiration pneumonia.
On USS the stomach would be expected to be empty.
A 9-year-old boy is admitted with acute onset of abdominal pain that has localised to the right iliac fossa. He is found to be pyrexial with localised peritonism in the right iliac fossa. What is the main cell type involved at a cellular level in this child's condition? (Please select 1 option) Eosinophils Erythrocytes Macrophages Monocytes Neutrophils
Neutrophils This is the correct answerThis is the correct answer
This child is most likely to have appendicitis.
Neutrophils are the main cell type involved in acute inflammation.
Eosinophils are predominantly involved in hypersensitivity.
Erythrocytes are red blood cells and macrophages are the main effector cells in chronic inflammation and only play a minor component in acute inflammation.
Macrophages are derived from monocytes in the circulation.
A 37-year-old dog breeder is bitten by one of his dogs. He does not seek medical attention until four days later when the wound has become red, swollen and is discharging a mucopurulent fluid. Which of the following organisms is most likely to be causing the infection? (Please select 1 option) Pasteurella multocida Staphylococcus aureus Streptococcus milleri Streptococcus pneumoniae Streptococcus pyogenes
Pasteurella multocida
Pasteurella multocida is commonly found in dog bites and cat scratches.
Staphylococcus aureus is a common cause of cellulites and infected ulcers.
Streptococcus milleri is a common cause of infection following human bite.
Streptococcus pyogenes is a common cause of necrotising fasciitis.
A 24-year-old lady who is four weeks post partum presents complaining of a hot painful lump in the right breast.
Examination reveals cellulitis overlying a fluctuant tender lump. Aspiration is performed and 10 ml of pus are obtained, which are sent for culture.
What is the most likely causative organism?
(Please select 1 option)
Escherichia coli
Staphylococcus aureus
Staphylococcus epidermidis
Streptococcus pyogenes
Streptococcus milleri
Staphylococcus aureus
This lady has a lactational abscess.
The most common causative organism is Staphylococcus aureus which is thought to be acquired from the infant’s oropharynx, since 50% of infants are colonised with Staphylococcus aureus by the second day of life.
Non-lactational abscess are often also caused by Staphylococcus aureus, but anaerobic infection is also common.
A 37-year-old lady who has had low back pain radiating to her calf for six weeks, presents to the emergency department. She reports severe abdominal pain and in the last 12 hours she has been unable to micturate.
Rectal examination reveals an empty rectum and altered peri-anal sensation. Neurological examination of her limbs reveals weakness in both legs but upper limbs are normal.
What is the most likely diagnosis from the following list?
(Please select 1 option)
Central disc prolapse at C6/7
Central disc prolapse at L4/5
Constipation
Lateral disc prolapse at C6/7
Multiple sclerosis
Central disc prolapse at L4/5
This lady has symptoms and signs of a cauda equina compression - she cannot micturate, has weak legs and altered peri-anal sensation.
Lateral disc prolapse would cause severe pain in the affected limb.
Multiple sclerosis can cause neurological symptoms but given this lady’s previous back pain, a disc problem is much more likely.
Constipation would not cause neurological signs.
A problem at the cervical level would cause symptoms in the upper limbs.
A 58-year-old woman presents to the neurosurgical clinic having been investigated for new onset epilepsy, accompanied with severe headaches.
CT and MRI have shown a space occupying lesion in the frontal lobe that has an enhancing ring around an area of necrosis.
What is the most likely diagnosis from the list below?
(Please select 1 option)
Astrocytoma
Ependymoma
Glioblastoma
Meningioma
Oligodendroglioma
Glioblastoma
The site of the tumour excludes a menigioma as it is reported to be in the frontal lobe and as such is intrinsic.
Ependymomas arise from an ependymal surface usually the fourth ventricle.
Glioblastomas are the most common intrinsic brain tumour accounting for between 30-50% of brain tumours in adults, with a peak incidence between 55-65 years of age. The CT and MRI findings are also typical of a glioblastoma.
Astrocytomas account for about 10% of primary brain tumours in adults, but are more common in children.
Oligodendroglioma account for 3%.
A 59-year-old lifelong smoker presents to her GP complaining of increasing shortness of breath and has noticed ptosis and constriction of her pupil. She is referred by her GP for a chest x ray that is reported as showing an apical mass. Biopsy confirms a malignant tumour. What is the eponymous diagnosis? (Please select 1 option) Horner's syndrome Pancoast's tumour Peyronie's disease Pott's cancer Wilms' tumour
Pancoast’s tumour
This lady has almost certainly got a Pancoast’s tumour (first described by Henry Pancoast, an American radiologist, in 1924). It is a neoplasm of the apex of the lung that typically invades the chest wall and brachial plexus.
The ptosis and constriction of her pupil is suggestive of a Horner’s syndrome but this is a consequence of her Pancoast’s tumour (ususally a non-small cell carcinoma).
Other structures an apical tumour (superior sulcus tumour) may locally invade or compress are:
phrenic nerve
vagus nerve
suclavian vein and artery
brachiocepalic vein (superior vena caval syndrome), and
brachial plexus.
Peyronie’s disease is hardening of the corpora cavernosa of the penis caused by scar tissue.
Pott’s cancer is a scrotal cancer (of historical interest) caused by coal tar exposure.
A Wilms’ tumour is a malignant tumour of the kidney that usually occurs in childhood.
A 67-year-old smoker presents to the haematuria clinic with a two week history of frank haematuria. He has no previous urological history. He is a lifelong smoker.
Examination is unremarkable. USS of his pelvis demonstrates a filling defect on the wall of the bladder.
From the following list what is the most likely diagnosis?
(Please select 1 option)
Bladder adenocarcinoma
Bladder diverticulum
Bladder stone
Bladder squamous cell carcinoma
Bladder transitional cell carcinoma
Bladder transitional cell carcinoma This is the correct answerThis is the correct answer
The filling defect on the bladder wall in conjunction with haematuria is suggestive of a bladder tumour of which the most common is transitional cell carcinoma.
Bladder diverticula do not usually cause haematuria.
Bladder stones usually present with a mobile defect in the bladder.