oncology Flashcards
side effectsof bisphosphonates
osetonecrosis of jaw/hip: pain, fever
GI symptoms
side effects of prostate ca injections
Leuprolide is known to cause osteoporosis and flushing. It is known to cause generalised body pain
ovarian ca chemo
NICE recommends that if patients are of a good performance status then they should be offered combination carboplatin and paclitaxel chemotherapy as this offers approximately an 8% increased response from single agent carboplatin chemotherapy alone.
bladder ca causes
bladder cancer which is associated with smoking, occupational exposure to rubber and advancing age.
Cystoscopy and biopsy are required for diagnosis.
SVCO management
- The best initial treatment in SVCO is with high dose steroids.
2, radio/stent
opiods for bone mets
Boluses of IV opioids, morphine or fentanyl, will provide the best pain management strategy acutely
gatric ca and rash
acanthosis nigricans
hnpcc/lynch syndrome
colorectal ca, ovarian ca (psamomma bodies), renal pelvis, pancreatic, small bowel, liver and biliary tract, stomach, brain, breast
MSH
treatment of LEMS
The clinical description is typical of Lambert-Eaton myasthenic syndrome (LEMS) - a paraneoplastic disorder associated with small cell lung cancer.
As the syndrome is autoimmune, mediated treatments such as IV immunoglobulin, plasma exchange and high dose steroids may help, as well as treating the underlying small cell lung cancer, which is often very responsive to appropriate chemotherapy.
As LEMS is a non-metastatic phenomenon, whole brain radiotherapy would not be helpful.
FAP
APC
multiple colon polyps
small intestine, brain, bone, stomach, skin
FAP
APC
multiple colon polyps
small intestine, brain, bone, stomach, skin
Li fraumeni
Breast ca
Sarcoma, osteosarcoma, leukemia, brain, adrenal
TP53
Cowden syndrome
PTEN
Harmatomas and breast, thyroid, endometrial
Hereditary breast and ovarian ca
BRCA 1 and 2
Men - breast and prostate
management of pain and renal impairment in palliative care
Fentanyl is a synthetic opioid extensively metabolised by cytochrome P450 enzymes in the liver and gastrointestinal tract, thus it is unaffected by renal impairment. Due to its extensive first pass metabolism, it can only be given parenterally (that is, transmucosal, transdermal, intramuscular, intravenous or subcutaneous).