Mixed II Flashcards
A 50-year-old woman presents with a five day history of right upper quadrant pain. The pain has become constant and associated with nausea. She has a pyrexia and tenderness in the right upper quadrant.
Acute cholecystitis
A 90-year-old patient develops acute distension of the abdomen. He has a dense hemiplegia from a stroke two weeks previously. He is confused. His abdomen is grossly distended and he has not passed stool or flatus for two days. A plain abdominal x ray shows dilated loops of large bowel.
Colonic pseudo-obstruction
Colonic pseudo-obstruction may follow acute medical events such as pneumonia, myocardial infarction or hypoxia. It is associated with electrolyte abnormalities that may accompany an acute illness.
Mechanical large bowel obstruction must be excluded by rectal examination, rigid sigmoidoscopy, plain x ray (there may be gas in the rectum) and CT scan.
Initial treatment is with fluids, correction of electrolyte abnormalities, avoidance of opiate analgesia and nasogastric aspiration (if there is also small bowel dilation). There may be a place for a rectal tube, enemas and an octreotide infusion.
If these measures fail, intravenous neostigmine may be effective. The next step is colonoscopic decompression. Surgery is the last resort.
A 35-year-old woman has an appendicectomy for perforated appendicitis. Ten days later she becomes unwell with a swinging fever and a high white blood cell count.
Pelvic abscess
Rectal examination may confirm the clinical diagnosis. Ultrasound and/or CT scan will establish the size of the abscess and whether any other collection is present. Drainage may be spontaneous, surgically per rectum or under radiological control.
Three days after a right hemicolectomy for carcinoma of the caecum, a 68-year-old patient begins vomiting and has abdominal distension. The abdomen is not tender and there are no bowel sounds. Passage of a nasogastric tube produces large volumes of aspirate.
Paralytic ileus
The management of post-operative ileus is primarily conservative. Normally an ileus resolves in three to four days. Small bowel motility returns in about 24 hours, then gastric motility after three to four days.
If the ileus persists, nasogastric aspiration is essential to prevent gastric dilatation and the risk of aspiration pneumonitis. The patient should have intravenous fluids and correction of any electrolyte imbalance plus minimal oral fluids.
Mechanical obstruction (abscess, haematoma, internal hernia, early adhesions) should be excluded by ultrasound or CT scan. A small bowel water soluble contrast examination may demonstrate a mechanical obstruction and may also relieve the ileus.
An 18-year-old motorcyclist is brought to the Emergency department after being hit by a car. He has a tachycardia and hypotension. Abdominal examination shows left upper quadrant tenderness. A diagnostic peritoneal lavage is performed. The aspirate is blood stained.
Ruptured spleen
The peritonitis results from irritation of the parietal peritoneum resulting in acute abdominal pain.
The quadrants of the abdomen represent close anatomical reference to the site of inflammation.
Referred pain can help identify sites of origin such as left shoulder tip pain in left subdiaphragmatic irritation.
These calculi develop in a quarter of all patients who develop gout. They have an acidic urine and the management involves reducing purine intake, alkalinising the urine and taking allopurinol.
Uric acid
Most uric acid stones are in patients who do not have gout. Other causes include
Myeloproliferative disorders
Chronic diarrhoea
Patients with an ileostomy
Excessive meat eating.
A 60-year-old lady presents with a renal colic. Her urinalysis and culture reveal an alkaline urine and Proteus mirabilis infection. An ultrasound scan and intravenous pyelogram reveal a staghorn calculus.
Triple phosphate
Urinary infection with urea splitting organisms, usually Proteus species, produces an alkaline urine. This increases the precipitation of calcium phosphate and magnesium ammonium phosphate.
A pathologist is sent a stone retrieved from the urine. It is laminated and has areas of black staining. Urinalysis reveals hypercalciuria.
Calcium oxylate
In many patients, investigation fails to find any disorder of calcium metabolism. If an abnormality is present it may be dietary, absorptive, resorptive or of tubular origin.
Only about 2-3% of patients with calcium stones have hyperparathyroidism.
The patient has the presence of lysine, arginine, ornithine and cystine in the urine. The disorder is autosomal recessive. The treatment includes urinary alkalinisation and penicillamine.
Cystine
In this condition there is a defect in the tubular reabsorption of cystine, orthinine, arginine and lysine (COAL). Stone formation is far more common in those who are homozygotes for the condition.
A 19-year-old patient attends her GP with a renal colic. She informs her GP that she has a hereditary disease and that her mother had this problem.
Cystine
Although an autosomal recessive condition the heterozygotes may still have an increased incidence of cystine stone formation. There are a number of phenotypes and the expression of the cystinuria gene is very variable.
Most patients have no underlying abnormality to account for stone formation.
The abnormalities that cause stones to form involve
Abnormal constituents in the urine
Stasis
Infection.
These lesions previously used to occur most commonly in Eastern Europeans. They are purple in colour and tend to be multiple. With the increase in AIDS they have been found increasingly on mucosal surfaces.
Kaposi’s sarcoma
Kaposi’s sarcoma used to be found more frequently in Eastern Europeans but are now recognised as an AIDS defining illness. They are purple papular lesions and can be found in the skin and on mucosal surfaces.
The lesions arise from skeletal muscle. They most commonly affect children and can be found in the head, neck, trunk and limbs.
Rhabdomyosarcoma
Rhabdomyosarcoma arises from skeletal muscle. It is the most common soft tissue sarcoma in children with a peak incidence between 2 and 5 years. About 70% of cases are under 10-years-old. There is smaller peak between12 and 18 years.
These lesions are very common and rarely become malignant. They are usually asymptomatic but may be multiple and painful.
Lipoma
Lipomas are characterised by soft rubbery tissue and can sometimes transilluminate. When multiple, familial (and often tender) the condition is Dercum’s disease/syndrome.
These are rare tumours which may be part of a genetic syndrome. They are composed of highly vascularised fibrous tissue and they are not malignant. Recurrence is common and most frequently found in the abdominal wall.
Desmoid tumours
These lumps arise following trauma. The cells regenerate in a disorganised manner. They are often found in amputation stumps and may produce pain.
Neuroma
When examining lumps, the site, size, consistency and colour are important to assess.
The regional lymph nodes must always be examined since malignant tumours may have spread along lymphatic drainage.
The risk of painful neuromas after amputation may be reduced by cutting (not tying) nerves as short as possible and keep the ends away from scar tissue.
A 44-year-old lady with a family history of multiple endocrine neoplasia type 2a develops a lump palpable in the thyroid gland. She has experienced diarrhoea and undergoes total thyroidectomy with ipsilateral modified block dissection of the neck.
Medullary
Medullary cancers arise from the parafollicular C cells and synthesise calcitonin.
A 75-year-old lady with a long history of Hashimoto’s thyroiditis develops a rapidly growing goitre.
Lymphoma
Lymphomas are rare, whilst squamous and sarcoma are even rarer with a poor prognosis.
A 45-year-old lady from an endemic goiterous region has a solitary tumour of the thyroid that has spread haematogenously to the lung and bone. Histological examination of the tumour reveals capsular invasion and vascular spread. No nodes are involved.
Follicular
Follicular carcinoma represents 15% of all thyroid malignancies but occurs in an older age group.