Clin Med 2 Flashcards
(96 cards)
STS epidemiology
peak onset at 15yo, male > female, rhabdomyosarcoma > osteosarcoma > Ewing’s sarcoma
is there screening for STS?
NO
STS ddx part 1
enchondroma (benign but can turn to chondrosarc), osteoid osteoma (prox femur –> NSAID), myositis ossificans (post traumatic)
STS ddx part 2
bone cyst, gout, brown tumors of hyperparathyroid (primary –> parathyroid adenoma, secondary –> chronic renal dz), osteomyelitis (Brodie’s abscess - hematogenous spread), Paget’s (endo dz)
STS risk factors
prior rad therapy, genetic ca syndromes
genetic ca syndromes: li fraumeni syndrome
germline mutation in TP53 tumor suppressor gene –> STS, osteosarc, RMS, fibrosarc, UPS; get whole body MRI
genetic ca syndromes: familial adenomatous polyposis (FAP)
auto dom colorectal ca syndrome, germline mutation in APC gene on chrm 5q21 –> adenomatous colon polyps –> CRC by 35-40yo
genetic ca syndromes: Gardner syndrome
variant of FAP w/ extracolonic manifestations like osteomas, skin cysts, hypertrophy of retinal epith, desmoid tumors/fibromatosis
genetic ca syndromes: Carney-Stratakis syndrome vs Hereditary retinoblastoma vs neurofibromatosis
auto dom –> GISTS, paragangliomas vs germline mutation in retinoblastoma tumor suppressor gene RB1 vs mutation in neurofibrin 1/2 gene (NF1/2) –> malig peripheral nerve sheath tumors
STS anatomic sites
extremities > visceral > retroperitoneum > trunk > head and neck
where are osteosarcs vs Ewing’s sarcs?
metaphyseal vs diaphyseal
STS diagnostic imging
XR (esp in children to min rad), MRI (gold standard), CT (sm cortical lesion, lung windows/metastases), angiogram (for vasc, resectability)
STS diagnostic bx
pre-tx core needle bx before diagnosis and grading; bx needs to be along future resection axis w/ minimal dissection and careful attn to hemostasis –> don’t do it yourself –> call the surgeon who’ll be operating to do bx; DON’T do needle aspiration/FNA
STS general tx
multidiscip care; spare limbs –> need good margins, neoadjuvant chemo +/- XRT if primary resection = difficult; allograft/rotationplasty/reconstruction; external beam rad, intraoperative RT, proton beam therapy
STS specific tx: osteosarc vs Ewing’s sarc vs chondrosarc
radio resistant, chemo sensitive –> neoadjuvant/preop chemo before surgery; recurrence in lung vs radio and chemo sensitive vs radio and chemo resistant
presentation: osteosarc vs Ewing’s sarc vs chondrosarc
painful swelling around knee/humerus, night pain and limping, firm/soft mass fixed to underlying bone, high ALP vs pain and constitutional sxs like osteomyelitis/sarc, can metastasize vs pain at lesion/mass (shoulder), can become high grade or de-differentiate
radiology: osteosarc vs Ewing’s sarc vs chondrosarc
Codman’s triangle vs onion skinning vs mass w/ matrix appearance
pathology: osteosarc vs Ewing’s sarc vs chondrosarc
osteoblasts secreting osteoid, cotton candy vs round and blue, no osteoid –> no cotton candy vs chondrocytes secreting cartilage
how does liposarcoma occur?
from adipocytes and has fatty tissue around sacromatous elements (spindle shaped sarcoma cells), develop from well-differentiated tumors in retroperitoneum then limbs
when does angiosarcoma occur?
can appear after rad therapy, assoc w/ chronic lymphedema; not good if >5cm or metastatic
GIST. tx?
GI stromal tumor that can occur anywhere in the GI tract, metastasize to liver. cKIT, PDGF, VEGF = inhibited by sm molec tyrosine kinases; adjuvant therapy for 3 y
Describe elbow
Links forearm and upper arm in concert w/ shoulder; uni-axial hinge joint
elbow stabilizers: static vs dynamic
bony structures vs muscles, ligaments, capsules
3 joints in elbow: humeroulnar vs humeroradial vs proximal radioulnar
True elbow joint, modified hinge joint for fl/ex vs combined hinge and pivot joint, some fl/ex and more rotation of radial head on capitulum of elbow vs rotation for supination and pronation