Pathology- Musculoskeletal Disorders Flashcards

1
Q

Osteitis Deformans aka ?

A

Paget’s

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Increased alkaline phosphatase 40 times normal limit indicates?

A

Osetitis Deformans aka Paget’s

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Signs and symptoms of Paget’s are?

A

Older Male
bone deformities,
osteoporosis circumscripta (skull)
bowing tibia,
pseudofractures,
cortical thickening,
osteoblastic-osteoclastic activity,
saber shin,
deafness, IVORY WHITE VERTEBRA (leads to osteosarcoma, less than 1%)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Neurfibromatosis is aka?

A

VON RECKLINGHAUSEN’S disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

This condition causes tumors to form in the brain, spinal cord, and nerves. It is genetically inherited, autosomal dominant, and affects chromosome 17

A

Neurofibromatosis aka Von Recklinghausen’s disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Neurofibromas can do what and cause what?

A

Can compress nerves
Cause Cafe-au-lait spots

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

bone thinning, lesions/growths in bones, one bone =monostotic, many bones =polyostotic. What is this condition called?

A

Fibrous Dysplasia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

This fibrous dysplasia condition affects young girls, has several bones involved, is endocrine related, precocious (early puberty)

A

McCune-Albright’s Syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Most common benign bone tumor of the vertebra. Has a jail-bar or corduroy appearance

A

Hemangioma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

This is the most common benign bone tumor of the body. Is described as sessile & pedunculated.

A

Osteochondroma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Brittle bones disease -Genetic, abnormal collagen, fractures, blue sclera

A

Osteogenesis imperfecta

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Overgrowth & sclerosis bone, however, weak & fractures

A

Osteopetrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

common in post-menopausal females, increase in fractures, decrease in bone density, Dowenger’ Hump

A

Osteoporosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

This is a staph infection in bone

A

Osteomyelitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Staph attacks bones, what does Strep attack?

A

The kidneys, then the heart

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

TB of spine, spreads lungs →thoracics→ eats joint→ vertebra collapses → increased kyphoses = Gibbus deformity

A

Pott’s Disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Temporary loss of blood flow to the femoral head causing it to collapse and become irritated , most common in 4 to 8-year-old

A

Legg Calve Perthes (LCP)

18
Q

Narrowing joint spaces, subchondral sclerosis & osteoblastic activity. Weight bearing joints, Asymmetrical Labs are normal

A

Osteoarthritis
aka DJD (Degenerative Joint Disease)

19
Q

Increased occurrence in females 20-40. SYMMETRICAL wear, pannus formation, ulnar deviation, inflammation of synovium, affects limbs & cervicals, morning stiffness

A

Rheumatoid Arthritis

20
Q

RA + Pneumonia is called?

A

CAPLAN’S

21
Q

LONG standing RA (Hepatomeagaly, Splenomegaly) is called?

A

Felty’s syndrome

22
Q

Juvenille RA is called?

23
Q

Aka Reactive Arthritis, STD Reactive arthritis. More common in adult men, Chlamydia, feet and spine, CONJUNCTIVITIS, urethritis, & arthritis. “Lover’s Heel”

Hint: Can’t see, Can’t pee, Can’t dance with me

A

Reiter’s

24
Q

Affects joints (debris, dysfunction, deformity, dislocation, destructive, distention, disease). You can’t feel the joint and you are doing damage without knowing

A

Charcot Joint aka Neurogenic Joint

25
Pencil-in-cup deformity in phalanx, destroys joints. "Pitted nails" "SILVER SCALES" "ray sign" on Xray.
Psoriatic arthritis 70% skin, 30% arthritis
26
Tophi, podagra, destruction around joint, purine metabolism problem. Uric acid crystals
GOUT
27
Calcium pyrophosphate crystals settling in joint, typically knee
Pseudogout aka CPPD
28
Symmetrical, starts in SI joints, young males, poker or bamboo spine. HLA - B27, breathing difficulties, trolley track & dagger sign, shiny corner sign on Xray
Ankylosing Spondylitis aka MARIE STRUMPELL
29
Males over 50-years-old, ALL calcification, cervical pain, stiffness & decreased ROM. Affects the cervicals and is associated with DM. Hint: toss a dish into the forrest
DISH (Diffuse Idiopathic Skeletal Hyperostosis) aka FORESTIER'S Disease
30
0-12 years old boys, autosomal recessive, severe - FATAL, pseudohypertrophy of calf muscles, increased CPK 30 times "X-linked", mother to son, pelvis & legs
Erb-Duchenne's Muscular Dystrophy
31
10-70 year old, autosomal recessive, mild, less severe than Duchenne's, slower, affects pelvis & legs
Becker Muscular Dystrophy
32
10-20 year old, autosomal dominant, mild, affects face & shoulders
Facioscapulohumeral Dystrophy
33
Adults, autosomal dominant, slow progression, affects face, tongue & extremities
Myotonic Dystrophy
34
Acute polyneuropathy, polyradiculitis, following surgery or immunization, Rapidly ASCENDING paralysis. Can last for hours, days, or months. Etiology unknown
Guillain-Barré aka Acute Demyelinating Polyneuritis aka Landry's Paralysis
35
Female, myoneural junction, decrease acetylcholine receptors, especially the cranial nerves, ptosis, diplopia, eyes effected 1st. This is a type II hypersensitivity.
Myasthenia Gravis aka Erb-Goldflam's
36
Muscle weakness, fatigue, and pain. Reduced reflexes and weakness in the muscles of the eyes. common with small cell carcinoma (lung), increased contractions with repeated stimuli. Autoimmune disorder.
Lambert-Eaton
37
Autosomal dominant, onset in childhood, calf muscle atrophy, demyelination, pain. Loss of muscle bulk in legs, high arches, hammer toes. Hint: She bit her calf
Charcot-Marie-Tooth
38
Autosomal dominant, hyperextensible skin & joints due to malformed collagen, LARGE ARTERY FRAGILITY
Ehlers-Danlos Syndrome
39
30-40 year old, myalgia, early fatigue, painful cramps, weakness of exercising muscles, burgundy colored urine (mypglobinuria).
McArdle's
40