joints, skeletal muscle Flashcards
Pannus
- Exuberant inflamed synovium
- Chronic infl w/ T cells (CD4+), B cells, plasma cells, Macs
- Granulation tissue w/ hemosiderin
- Erodes articular cartilage and bone
Rheumatoid factor
AutoAb against Fc portion or IgG
Classic picture of RA
- Radial deviation of wrist
- Ulnar deviation of fingers
- flexion-hyperextension of fingers (swan neck; boutonniere)
- Synovial cysts - Baker cyst (back of knee)
Rheumatoid nodules
Fibrinoid necrosis surrounded by Macs
found in areas subject to pressure: ulnar aspect of forearm, elbows, occiput, lumbosacral
Criteria for rheumatoid Arthritis
- AM stiffness
- > 2 joints
- typical hand joint inv
- symmetric
- rheumatoid nodules
- serum RF
- Typical radiologic changes
Seronegative spondyloarthropathies
ligamentous attachments
- immune mediated, no specific AutoAb
- HLA B27 positive
- RF negative
Triad of Reiter syndrome
Arthritis
Urethritis/Cervicitis (nongonococcal)
Conjunctivitis
risk factors for primary gout
> 30 yrs genetic heavy drinking obesity drugs eg thiazides pb toxicity
Myopathy
disorder of muscle
muscular dystrophy
inherited disorder
progressive muscle weakness and wasting
segmental muscle necrosis
destruction of a portion of the myocyte length
muscle regeneration
satellite cells reconstitute destroyed muscle
fiber hypertrophy
response to inc in load
myotonia
tonic spasm of one or more muscles
also a condition characterized by such spasms
hypotonia
deficient tone or tension
arthrogryposis
fixation joints in an extended or flexed position
creatine (phospho)kinase (CK;CPK)
Enzyme highly concentrated in muscle and brain
Gower’s sign
indicates weakness of the proximal muscles
- use hands and arms to walk up from a squatting position
Type 1 fiber
sustained endurance, standing red oxidative scant glycogen abundant lipid many mitochondria
Type 2 fiber
sudden short bursts, purposeful motion white oxidative and/or anaerobic abundant glycogen scant lipid few mitochondria
fiber type grouping
neuron/axon drop out leads to larger motor units (muscle fibers per neuron)
Grouped atrophy
loss of motor neuron leads to atrophy of associated muscle
Denervation atrophy
disorder of motor neurons
breakdown of myosin and actin
resorption of myofibrils
Exophthalmic ophthalmoplegia
thyrotoxic myopathy
protrusion of eyeballs
diplopia due to orbital edema and contracture of ocular muscles
soft tissue tumors: benign > malignant or Benign
benign outnumbers malignant
most common cause of soft tissue tumor is
unknown
Ewing sarcoma and primitive neuroectodermal tumor
t(11;22)
EWS-FLI1 fusion
Liposarcoma-myxoid and round cell type
t(12;16)
FUS-DDIT3 fusion
Synovial sarcoma
t(X;18)
SS18-SSX fusion gene
Rhabdomyosarcoma-alveolar type
t(2;13)
PAX3-FOX01 fusion
Extraskeletal myxoid chondrosarcoma
t(9;22)
EWS-CHN fusion
Prognosis: soft tissue tumor
Stage
location and size
superficial vs deep
size
metastasis
etc
Prognosis: soft tissue tumor
Grade
Cell pleomorphism
Necrosis
Mitotic rate