Muscle Flashcards
1
Q
Cells of bone
- function
- formation
- other things needed to make bone
A
- osteoblasts (form bone)
- osteoclasts (multi nucleated macrophage tha breaks down bone)
- osteoprogenitor cells -> pre-osteoblasts -> osteoblasts -> osteocytes (comm in osteon)
- Ca, PO4, zinc, copper and Na
2
Q
Bone formation
- model: grows in length vs diameter
- perichondrium
- periosteum
- formation of bone collar
- formation of matrix calcification
- trabecular formation: who is involved
- secondary ossification
A
- hyaline cartilage -> grows in length by cartilage producing cells; diameter growth is in addition of ECM
- CT that covers cartilage produces periosteum
- CT that covers bone
- bony collar
- osteoblasts peel back periosteum and secrete osteoid on shaft of bone
- chondrocytes in primary ossification center secrete alkaline phosphatase causing matrix ossification -> will then produce VEGF and apoptose and matrix will deteriorate to form cavity
- VEGF causes angiogenesis in medullary cavity, blood vessels come from perichondrium moving up and down shaft of bone, also bring hematopoetic and osteoprogenitor stem cells into medullary cavity
- made with osteoblasts and osteoclasts
- secondary is at epiphyseal ends, connected to primary by growth plates, doesnt mature until after birth
3
Q
Fat embolism
- primary
- secondary
- what happens
- tx
A
- long bone fracture
- pancreatitis -> bc auto digestion of fatty organ
- lipid fat globule will escape from BM and will go into lungs illiciting immune response -> will end up causing decrease surfactant -> ARDS
- supportive care
4
Q
Osteon
- formed by
- haversion canal
- canaluculi
A
- made from osteoblasts, osteoclasts, and osteocytes
- have central neuro vasc bundle
- provide nutrition to osteon
5
Q
Histo of bone cells
- osteoblast
- osteoclast
A
- spherical nuc, prominent golgi (appears like clear zone around nuc)
- multi-nuc macrophage, adhere to bone via ruffle border
6
Q
How does maturation occur
- mononuc
- quiesent osteoclast
- active osteoclast
A
- RANKL binds to osteoclast precursor which turns it into mononuclear osteoclast
- RANK, IL1, IL6, MCSF
- RANK L, IL1
7
Q
Marrow
- red
- yellow
A
- contain hematopoeitic stem cells -> myeloid and lymphoid progenitors
- contain mesenchymal stem cells -> fat, cartilage, bone
8
Q
Where does erythropoesis occur?
A
- flat bones -> skull, sternum, ribs
9
Q
Ribs
- true
- false
- floating
- where do they break
A
- connect straight to sternum
- connect to cartilage that connect to sternum
- no connection to sternum
- mid-axillary line most commonly
10
Q
osteoporosis
- what is it
- involves
- fracture
- causes
- sxs
- dx osteopenia
- dx
- dx for severe
- tx: 1st line
- SERM: MOA, AE, specific for this dx
A
- bone resorption is higher than bone deposition
- trabecular bone
- dorsal lumbar vertebral bodies or femoral neck
- decrease estrogen (inhibit osteoclast activity), lack of activity (inhibits osteoclast activity), elevated cortisol (reduced bone apposition), calcium deficiency, hyperthyroidism (increase bone breakdown)
- asymptomatic until break
- 1-2.5 SD below reference
- > 2.5 SD below RR
- > 2.5 SD with hx of fragility fracture
- bisphosphonates -> prevent osteoclast from forming ruffled border
- estrogen agonist on osteoclasts and antagonist at breast; increased risk thromboembolism, increase risk endometrial CA; raloxifene
11
Q
Pagets Disease
- what is it
- sxs
- location
- labs
- xray
- tx
A
- increased osteoclast activity and then osteoblast activity -> formation of weak bone
- bone pain and deformity in affected area
- long bones, spine, pelvis
- elevated alk phos, normal level of Ca and phosphate
- xrays w/ sclerotic lesions and positive bone scans (increased activity at bone)
- bisphosphonates and calcitonin
12
Q
Fibrous dysplasia
- what is it
- sxs
- location
- McCune - Albright: genetics, sxs
- tx
A
- firbous tissue replace normal none
- bone beformation and patho fx
- mono or poly (w/ mccune-albright)
- GNAS gene -> codes for g-protein -> increased production -> increase cAMP; hypothyroid, pit dysfunction, cushing, cafe au-lait spots
- surgical debulking
13
Q
Pyogenic Osteomyelitis
- what is it
- MCC
- sickle cell
- IV drug MCC
- signs and sxs
- x-ray
- gold standard for imaging
- tx
A
- bacterial infection of bone
- S aureus
- S aureus, salmonella , e coli
- Pseduomonas
- bone pain w/ inflamm, hyperpig of skin, swelling of soft tissue
- periosteal elevation or thickening, osteolysis
- MRI
- surgical debridment, antibiotics (4-8 wks bc dont penetrate bone well)
14
Q
Bone Tumors
- osteochondroma: epi; location; x ray; tx
- giant cell: epi, location, xray, tx, prognosis, histo
- osteosarcoma: epi, location, labs, xray, tx
- ewings: epi, translocation, location, sxs, histo, tx, prognosis
A
- males, less than 25; benign; distal femur or prox tibia; looks like cauliflower; surgical excision
- 20-40 yrs; epiphyseal; benign; soap bubble; excise and radiation; tends to recur ; multinucleated giant cells, necrosis, hemmorrhage, hemosiderin
- 10-20 yrs, males; distal femur, prox tibia; alk phos increase; sunburst pattern; excision and radiation
- less than 15; 11:22; diaphysis and pelvis; sweling, erythema and pain; onion skinning, small round blue cells that are PAS+; chemo; early METS
15
Q
CT disorders
- RA: caused by; sxs; location; deformities; sequelae; labs; tx
- Lupus: caused by, epi, DOPAMINE RASH, labs
- Drug induced lupus
- Sjogrens syndrome: what is it, antibodies, HLA type, mgmnt
- Behcets Dx: what is it, sxs, tx
A
- autoimmune; symmetric inflamm arthritis that is worse in morning and can last for hours, subcu nodules; feet, knees, MCP, PIP; swan neck (DIP flexion and PIP hyperextension); anemia of chronic dx, effusion seruitis; RF (IgM anti - IgG) and anti-citrullinated peptides (mor specific); methotrexate w/ folate supplementation or TNF antagonists (need PDD), leflunomide (pyrimidine synthesis inhibitor
- systemic AI disorder; females; d: discoid lupus (circular erythematous macules w/ scales), oral ulcers, photosensitivity, arthritis, malar rash, immuno (anti DsDNA), neuro (psychosis, personality changes), elevated SED rate, renal dx, ANA, serusitis (pericarditis, pleuritis), heme (pancytopenia); anti-ANA, anti-DsDNA, anti-smith, falsely increased PTT, pancytopenia, anti-phodpholipid antibody, increased fetal loss\
- look for anti histone anti-bodies; stop offending agent and give NSAIDs, hydroxychloroquine (interferes with antiget processing), prednisone, cyclphosphamide ( alkylating agent); Methyldopa and hydralazine
- dry mouth, dry eyes and arthritis; HLA-DR3; anti-RO and anti-LA antibodies, ANA positive; steroids
- chronic vasc inflam dx; oral and genital ulcers, skin nodules, arthritis, uveitic, vascultisi; prednisone
16
Q
RA vs OA
- onset
- cause
- joints
- morning stiffness
- osteophytes
A
- RA is in younger, OA after 40
- AI vs biomechanical
- symmetric, small joints vs weight bearing joints
- lots of morning stiffness vs not very much
- osteophytes are absentvs present
17
Q
Seronegative Spondyloarthrpathies
- HLA type
- ankylosing spondylitis: sxs, cycle, dx
- reiters syndrome: also called, what is it, caused by, sxs, derm findings, tx
- psoriatic arthritis: what is it, MC finding, tx
A
- HLA B27
- sacrilitis, bamboo spine, uveitis, aortitis -> aortic regurg, costo vetebral and costo sternal junction issues -> resp problems; exacerbation and remissions; x-ray; NSAID and PT
- reactive arthritis; arthritis 1-6 weeks after infection; chlamydia, salmonella, shigella, campylobacter, yersinia; conjunctivits, urethritis, arthritis; circinate balanitis (inflammation and scaling around shaft and glans) and keratoderma blennorrhagica (thick crusty plaque on palm and sole); NSAID and antibiotics
- arthritis + psoriasis; nail pitting; UV light for skin, NSAIDs, MTX with resistant
18
Q
OA
- what is it
- sxs
- xray
- commonly affected
- tx
A
- non - inflamm degerative arthritis
- pain and crepitus, ROM decrease, DIP swelling and PIP swelling
- osteophytes and asymmetric joint spaces
- hips, knees, DIP and PIP
- NSAID, PT, surgery
19
Q
Scleroderma
- what is it
- diffuse
- limited/benign -> sxs
- dx
- TX
A
- systemic fibrosis of organs;
- progressive systemic sclerosis
- CREST; calcinosis, raynauds, esophogeal dysmotility, sclerodactyly, telangiectasia
- ANA+, anti-centromere, anti-Scl 70
- MTX for skin and then organ specific tx
20
Q
Sarcoidosis: epi, sxs, immuno pathogeneis, cardiac problems, CNS problems, visual; pulm; GI; renal; endocrine; heme; derm; DX; tx
A
- AA, 20-40 yrs
- hilar adenopathy, dry cough, noncaseating granuloma, ACE elevation
- TH2 cells produce IL2 -> activate CD8 and gamma IFN -> macrophages -> CD8 and macrophages form granulomas
- hyper Ca, elevated prolactin, increase CD4/CD8 ratio in the lavage
- heart block and arrythmias
- bells palsy
- uveitis
- restrictive pulm defects
- elevated LFT
- nephrolithiasis 2 to hyper Ca
- DI;
- pancytopenia; erythema nodosa; non caseating granulomas, increased ACE levels; prednisone
21
Q
Mixed CT disorder
- epi
- what is it
- antibodies
- tx
A
- women in 20s
- overlapping fx of scleroderma, SLE, inflam myopathy
- Anti U1 RNP antibody
- steroid, symptom dependent tx
22
Q
Pseudo gout
- caused by
- shape
- affects
A
- calcium pyrophosphate deposition
- rhomboid
- larger and more proximal joints
23
Q
Septic arthritis
- what is it
- caused by
- fluid findings
- tx
A
- monoarticular arthritis
- gonorrhea or s aureus
- no crystals; WBC greater than 50,000 is gonorrhea and less is s aureus
- antibiotics