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?

A

STILL’s

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
Q

Pencil-in-cup deformity in phalanx, destroys joints. “Pitted nails” “SILVER SCALES” “ray sign” on Xray.

A

Psoriatic arthritis

70% skin, 30% arthritis

26
Q

Tophi, podagra, destruction around joint, purine metabolism problem. Uric acid crystals

A

GOUT

27
Q

Calcium pyrophosphate crystals settling in joint, typically knee

A

Pseudogout aka CPPD

28
Q

Symmetrical, starts in SI joints, young males, poker or bamboo spine.

HLA - B27, breathing difficulties, trolley track & dagger sign, shiny corner sign on Xray

A

Ankylosing Spondylitis
aka MARIE STRUMPELL

29
Q

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

A

DISH (Diffuse Idiopathic Skeletal Hyperostosis)
aka FORESTIER’S Disease

30
Q

0-12 years old boys, autosomal recessive, severe - FATAL, pseudohypertrophy of calf muscles, increased CPK 30 times “X-linked”, mother to son, pelvis & legs

A

Erb-Duchenne’s Muscular Dystrophy

31
Q

10-70 year old, autosomal recessive, mild, less severe than Duchenne’s, slower, affects pelvis & legs

A

Becker Muscular Dystrophy

32
Q

10-20 year old, autosomal dominant, mild, affects face & shoulders

A

Facioscapulohumeral Dystrophy

33
Q

Adults, autosomal dominant, slow progression, affects face, tongue & extremities

A

Myotonic Dystrophy

34
Q

Acute polyneuropathy, polyradiculitis, following surgery or immunization, Rapidly ASCENDING paralysis. Can last for hours, days, or months. Etiology unknown

A

Guillain-Barré
aka Acute Demyelinating Polyneuritis
aka Landry’s Paralysis

35
Q

Female, myoneural junction, decrease acetylcholine receptors, especially the cranial nerves, ptosis, diplopia, eyes effected 1st. This is a type II hypersensitivity.

A

Myasthenia Gravis aka Erb-Goldflam’s

36
Q

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.

A

Lambert-Eaton

37
Q

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

A

Charcot-Marie-Tooth

38
Q

Autosomal dominant, hyperextensible skin & joints due to malformed collagen, LARGE ARTERY FRAGILITY

A

Ehlers-Danlos Syndrome

39
Q

30-40 year old, myalgia, early fatigue, painful cramps, weakness of exercising muscles, burgundy colored urine (mypglobinuria).

A

McArdle’s

40
Q
A