MSK path 1 Flashcards

(70 cards)

1
Q

Granulomatous / destruction of internal elastic membrane; Aorta & major branches
large arteries

A
Giant Cell (temporal) arteritis 
(GCA)
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2
Q

Granulomatous of aorta, females <50 y/o
PULSELESS disease
Ischemic bowel disease, pulmonary, coronary, renal arteries also affected
large arteris

A

Takayasu

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3
Q

Fibrinoid necrosis
NO GLOMERULONEPHRITS  BUT it does affect the kidneys (renal involvement  severe HTN (RBCs in urine , NOT CASTS)
NO ANCA (RATHER, IMMUNE COMPLEXES!  30% a/w Hepatitis B
NO PULMONARY INVOLVEMENT
Many stages evident in biopsy
Wrist and Foot drop due to ulnar & common fib involvement

A
Polyarteritis Nodosa
(PAN)
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4
Q

Mucucutaneous lymph node syndrome
Coronary artery involvement
Children (tx: IgG and AsA)

A

Kawasaki Diseasea

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5
Q

Limited – only respiratory
Systemic – involves renal arteries (glomerulonephritis – focal segmental)
c-ANCA

A

Wegeners aka

Ganulomatosus w/ polyangiitis (GPA)

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6
Q

Eosinophilic granulomatosus, respiratory tract
Asthma, Eosinophilia
P-ANCA

A

Churg-Strauss

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7
Q

Fibrinoid necrosis but w/ NO GRANULOMAS
Hypersensitivity vasculitis
p-ANCA more than -ANCA , can have immune complexes (mistake on Pandout)
glomerulonephritis (75%) + pulmonary hemorrhage
also has neuropathy: wrist/ foot drop
All lesions about the same stage

A

Microscopic Polyangiitis

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8
Q

IgA deposits in small vessels

Palpable purpura – legs to buttocks/ arthritis, abdominal pain, glomerulonephritis

A

Henoch-Scholein purpura

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9
Q

HS rxn to tobacco component in heavy smokers

Can involve nerves and veins  severe pain & chronic ulcerations (stop smoking before progression to frank gangrene)

A

Thromboangiits Obliterans (Burger’s disease)

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10
Q

Rotator Cuff Tendinitis - primary cause of pain

A

tendonitis

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11
Q

Extensor radialis brevis

Pain w/ supination and wrist extension

A

Laterial epicondylitis

Tennis elbow

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12
Q

Flexor carpi radialis

Pain w/ pronation & wrist flexion

A

Medial epiconylitis

Golfer/ pitchers elbow

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13
Q

Flexor tenosynovitis (flexor digitorum, superficialis)

A

Trigger Fingers

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14
Q

Inflammation of the sheaths of the extensor pollicis brevis & abductor pollicis brevis

A

De Quervain’s Tenosynovitis

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15
Q

Burning or tingling in hand usually at night
Median nerve compression in carpal tunnel
*median nerve may also be compressed at the pronator teres)
Thenar atrophy, Tinel’s sign, Phalen test

A

Carpal Tunnel Syndrome

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16
Q
Does communicate with the joint 
Point tenderness over greater trochanter, worsened w/ external rotation and abduction
Worsen when lying on same side 
Difference in leg length can cause this
Lateral thigh pain above the knee
A

Trochanteric Bursitis

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17
Q

Lateral femoral cutaneous nerve (L2-L3) entrapment  diffuse lateral thigh pain (sites of compression = inguinal ligament, insertion of psoas

A

Meralgia paresthetica

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18
Q

40% communicate with the knee; may rupture  medial ankle ecchymosis
seen from behind the patient

A

Popliteal cyst (Baker’s cyst)

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19
Q

Superficial to kneecap swelling

Always consider sepsis

A

Prepatellar Bursitis

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20
Q

may rupture  Thompson sign

A

Achilles Tendinitis

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21
Q

Women in high heeled shoes! Pain in 3rd/4rth toes due to entrapment of interdigital plantar nerves

A

Morton’s neuroma

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22
Q

Prominence of metatarsal head on either side of the foot

A

Bunionette

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23
Q

Excessive proliferation of skin & bones at distal extremities – excessive collagen desposition
Full syndrome – periostitis of long bones
Chest malignancy & lung infections

A

Hypertrophic Osteoarthopathy

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24
Q

Younger patients, outer membrane IA inactivates compliment
Tenosynovitis of wrists, ankles, fingers, toes – migratory arthralgia
Often follows menstruation
Better to culture GU or pharynx where bug originally came from
Staph aureus #1
GAS #2
Salmonella in Sickle cell pts

A

N gonorrhea

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25
Most common viral arthritis
Parvovirus (B19)
26
Catcher Crouch Syndrome – lumbar radiculoneuropathy
Rubella
27
Arthritis-urticaria syndrome | Explosive arthritic of the knee
Hepatitis B
28
Cryoglobulinemia vasculitis, palpable purpura over lower legs Type II and III
Hepatitic C
29
Large effusions, little pain – occurs months/ years after the tick bite! Over-diagnosed in south – more likely STARI Most often the knee or TMJ Larger joints
Lyme Disease
30
Articular Syndrome - <24 hours, severe pain in all joints of the body Reactive arthritis – spondyloarthritis (could be a presenting sign of HIV) Psoriatic arthritis
HIV arthralgia
31
Only seen in HIV pts | Salivary gland enlargement, CD*+ lymphocytosis, sicca, parotid gland
Diffuse Infiltrative Lymphocytosis Syndrome (DILS)
32
Fetty Syndrome
from long-standing RA - enlarged spleen – a/w deforming nodules in joints
33
Non-neoplastic reactive proliferation (fibroblastic – can develop several weeks after trauma) Mesenchymal reaction to injury May appear anywhere – most common on the flexor forearms Or the trunk
Nodular Fasciitis
34
Deep tissue Bizzarre cells filled with lipid vacuoles Usually painless, located in deep soft tissue  can reach a large size before it is detected
Liposarcoma
35
Reactive bone formation in the muscle as a result of injury – bone women in granulation tissue
Myositis Ossificans
36
Children- infrabdominal Young adult – abdominal wall (during/after pregnancy) = desmoid (a/w Gardner syndrome & familial adenomatous polyposis Adult – extra-abdominal Bland spindle proliferation – no mitotic figures, no necrosis
Fibromatosis | desmoid tumor
37
Soft tissue – painless mass It often arises in the soft tissues of the thigh and the posterior knee. It is generally a large, painless mass deep to fascia and has an ill-defined margin. Bone – painful – arises in metaphysis of femur or tibia
Fibrosarcoma
38
typical spindle cells arranged in a “storiform” (woven mat) pattern are seen; to the right are the typical bizarre giant cells. By 1977, MFH was considered the most common soft tissue sarcoma of adult life. Despite the frequency of diagnosis, MFH has remained an enigma. No true cell of origin has ever been identified. May occur following radiation tx of another sarcoma
Malignant Fibrous Histiocytoma
39
White fish flesh appearance Almost two-thirds of RMS cases develop in children under the age of 10 Mark w/ antibody to vimentin (intermediate cytoplasmic filament)
Rhabdomyosarcoma
40
10% of adult sarcromas – found in a joint or deep soft tissue Arises from mesenchymal cells, not the synovium Most have t(X;18) translocation Biphasic pattern of spindle cells and epithelial cells – within soft tissue
Synovial Sarcoma
41
Benign localized developmental arrest in the diaphysis | Monostotic or polystotic (risk for osteosarcroma – though this would arise in a different location – metaphysis!)
Fibrous Dysplasia
42
(a/w café au lait skin spots, endocrinopathies Can involve the facial bones Benign localized developmental arrest in the diaphysis
McCune Albright syndrome
43
Fibrous Cortical Defect > 5-6 cm: Few or no symptoms except pain Usually found incidentally on radiography Fractures can occur through the thinned cortex Eccentric Sharply delimited -scooped out -Storiform/ woven pattern/ fibroblast cell origin
nonossifying fibroma
44
very bloody, cystic lesions. They appear like a “sponge filled with blood.” These too, may contribute to pathologic fracture and can be an operative challenge if not expected because of excessive bleeding.
Aneurysmal bone cysts
45
Bone-forming tumor - osteoma Round tumors that project from sub- or endosteal surfaces of cortex Usually solitary; multiple seen in ....
Gardner's syndrome
46
Half involve the tibia and fibula. Usually they are cortical rather than medullary lesions. A prime characteristic of osteoid osteomas is that they are painful. They produce prostaglandin E2 and interestingly have a characteristic pattern of pain. They are more commonly painful at night and they are relieved by aspirin. Intake of alcohol causes a massive increase in pain
Osteoid osteoma
47
benign cartilage capped tumors attached to the underlying skeletal system by a stalk displacement of growth plate in endochondral bones There is a condition of multiple hereditary exostosis which is autosomal dominant and may give rise to chondrosarcomas
Osteochondroma =Exotosis *metaphysis
48
arise inside medullary cavities, typically in the hand and the feet, those tubular bones.
Chondroma | *diaphysis
49
nonhereditary syndrome of multiple enchondromas
Ollier
50
multiple enchondromas form as well as soft tissue hemangiomas.
Maffucci syndrome
51
``` Multinucleated osteoclast type giant cells • Benign but uncommon • Locally aggressive • 20’s to 40’s • Cystic degeneration • Arise around knee > wrist Epiphysis ```
Giant Cell Tumor of Bone
52
Prominent bone formation extends into soft tissue Lifted periosteum forms triangular shell of reactive bone: CODMAN TRIANGLE (arrow) Characteristic but not pathognomonic
Osteosarcoma
53
Common sites include metaphysis around the knee in younger people. There is an association with retinoblastoma.
Osteosarcoma
54
2nd most common primary malignant bone tumor | Surgery, insensitive to chemotherapy
Chondrosarcoma
55
round blue cell tumor so known because of its characteristic, very high nuclear cytoplasmic ration, mostly nucleus 85% of these have genetic signatures which relate them to peripheral neuroectodermal tumors They arise in the medulla of the bone, primarily in diaphysis of long bones
Ewing’s sarcoma (peripheral primitive neuroectodermal tumor) *diaphysis
56
anticipation with increased repeat expansions and more severe phenotypes in younger generations. Percussion and grip myotonia : Increased CGT repeats of DNA on chromosome 19,
Myotonic dystrophy
57
muscle phosphorylase deficiency from which glycogen can not break down during exercise to produce ATP
McArdle’s Disease
58
Anti-Jo-1/ Anti-Synthetase Syndrome
“Jo is the f-a-mily mechanic” | Mechanics hands
59
Proximal and distal muscle weakness Poor response to steroid tx + neurological symptoms Basophilic w/ Gomori Trichome stain
Inclusion body myositis
60
CD8 cells invade muscle w/ increased MHC I expression
Polymyositis
61
20-50 y/o, CD4 & B cell activation  RF and aCCPs, symmatric Granulation tissue  pannus  joint erosion  fibrosis
RA
62
Reduction in chondrocytes at growth plate • Most common cause of inherited dwarfism; autosomal dominant • Short extremities, normal trunk, large head, normal mentation
ACHONDROPLASIA
63
Unbalanced and excessive osteoclast and osteoblast function; increased bone turnover • Osteolytic, mixed osteolytic-osteoblastic,
Paget dz
64
Failure of the bone to mineralize properly in an adult
OSTEOMALACIA
65
Increased bone activity + peritrabecular fibrosis + cystic brown tumors primary hyperparathyroidism
osteitis fibrosa cystica
66
More lung disease than any other autoimmune | connective tissue disease
Scleroderma
67
the most common | pleuropulmonary manifestation of lupus
pleuritis
68
one of the most unpredictable and potentially serious adverse effects of methotrexate treatment
Pneumonitis
69
myositis + arthritis + lung disease (20% of all)
Can be part of anti-synthetase syndrome
70
NSIP 1. It has lymphoid follicles (germinal centers) [shown in panel A] 2. It is bronchiolocentric [shown in both panel A and panel B] 3. It has more lymphocytes [shown in both panel A and panel B] 4. It has macrophages and multinucleated giant cells [shown in panel B]
Sjogren's disease of lung