MSK Flashcards

1
Q

Classification of arthropathies

A
Degenerative (OA)
- Primary
- Secondary (post-insult, neuropathic, other arthropathy)
- Erosive OA
Inflammatory / autoimmune
- RA
- Seronegative (psoriatic, ank spond, enteropathic, reactive)
- SLE
- Scleroderma
Infectious
- Typical bugs (rapid destruction)
- Atypical bugs (Mycobaterial / fungal / lyme)
Depositional
- Crystalline (gout, CPPD / hemochromatosis, HADD)
- Amyloid
- Hemophilic
- Sarcoid
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2
Q

Monoarticular process

A
Arthropathy
- Infectious arthritis
- Gout
- Secondary OA (e.g. post-traumatic)
- Early undifferentiated arthropathy
Intra-articular mass (see dedicated ddx)
Mimic = epiphyseal process
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3
Q

Polyarticular process

A

Likely an arthropathy. Thus, focus on degen vs inflammatory vs depositional

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4
Q

Intra-articular mass

A
Synovial proliferation
- Synovial osteochondromatosis
- PVNS
- Rice bodies (RA, atypical infection)
- Lipoma arborescens
Depositional diseases (gout, amyloid)
Vascular malformation (synovial hemangioma, AVM)
Neoplasm (chondroma, synovial chondrosarcoma or synovial sarcoma, synovial met)
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5
Q

Lumpy bumpy arthritides

A
Gout
Amyloid (does give vascular calcification and dense deposits, but not erosions)
Hypercholesterolemia (xanthomas)
Multicentric reticulohistiocytosis
Sarcoid
Cystic RA
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6
Q

Arthropathy – joint spaces preserved

A

Gout
Jaccoud’s arthropathy / SLE
Juvenile idiopathic arthritis

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7
Q

Chondrocalcinosis

A

CPPD
Hemochromatosis
Hyperparathyroidism

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8
Q

Arthritis in a kid

A

Juvenile idiopathic arthritis
Septic
Hemophilia
Neuropathic (e.g. congenital insensitivity to pain)

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9
Q

Thick, nonmarginal vertebral bony bridging

A

OA
DISH
Psoriatic
Reactive

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10
Q

The 5 D’s of neuropathic joint

A
Dislocation
Destruction
Disorganization
Debris
Density (increased)
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11
Q

Causes of neuropathic joint

A
Peripheral
- Diabetes
- Alcoholic neuropathy
- Congenital insensitivity to pain
- Leprosy / syphilis
Central
- Trauma / paralysis
- Syrinx / cord mass
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12
Q

Atlantoaxial instability / dens pannus

A

RA

Depositional arthropathies

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13
Q

Big overgrown epiphyses

A

Juvenile idiopathic arthritis
Hemophilia
CP / neuromuscular disorders
Other causes of hyperemia

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14
Q

Sacroiliitis

A
Unilateral (septic, OA, RA)
Bilateral asymmetric (reactive, psoriatic)
Bilateral symmetric (ank spond, enteropathic)
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15
Q

Periarticular osteopenia

A

Complex regional pain syndrome / Reflex sympathetic dystrophy
Inflammatory arthropathy
Disuse osteopenia

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16
Q

Preserved joint space

A

Gout
PVNS
TB
Complex regional pain syndrome / reflex sympathetic dystrophy

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17
Q

T2 fluid bright soft tissue mass without internal enhancement

A

Collection
Cyst (ganglion, synovial, epidermal inclusion)
Bursa

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18
Q

T2 fluid bright soft tissue mass with internal enhancement

A

Myxoma
PNST
Sarcoma (myxoid, synovial)
Necrotic tumor

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19
Q

Fat containing soft tissue mass

A
No calcs
- Lipoma
- Atypical lipomatous tumor / Liposarcoma
Calcs
- Hemangioma
- Heterotopic ossification
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20
Q

T1 bright soft tissue mass, but not fat

A

Blood (Hematoma +/- tumor)
Protein (ganglion, abscess)
Melanin (melanoma)

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21
Q

T2 dark soft tissue mass

A
Calcification (dystrophic, gouty tophus)
Blood (PVNS, GCT of tendon sheath, hematoma, hemorrhagic tumor)
Fibrous tissue (fibroma / fibrosarcoma, desmoid, scar, leiomyoma)
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22
Q

Soft tissue mass without flow on US

A

Neoplasm (benign or malignant)
Collection (abscess / hematoma)
Depositional

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23
Q

Indeterminate soft tissue mass

A
Neoplastic
- Benign (PNST, desmoid, rhabdomyoma)
- Malignant (sarcoma, mets / lymphoma)
Foreign body reaction / granuloma
Deposition (tophus, amyloid)
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24
Q

Aggressive soft tissue mass young adult

A

Synovial sarcoma
Rhabdomyosarcoma
Desmoid
Alveolar soft part sarcoma

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25
Soft tissue calcification
Dystrophic = MC (if ossified, it’s heterotopic ossification) - Trauma - Infection (esp. parasitic) - Dermatomyositis / polymyositis / scleroderma - Venous insufficiency (phleboliths) Other causes (remember, 3 sound like cancer even though only one is): - CPPD / HADD - Metastatic calcification - Tumoural calcinosis, calcinosis of chronic renal failure - Sarcoma (synovial, osteosarc)
26
Olecranon bursitis
Unilateral (trauma, infection) | Bilateral (gout, RA)
27
Muscle edema
``` Supply problem (denervation, ischemia) Primary myopathy Direct insult (trauma, infection, radiation) ```
28
Lesion in posterior elements of the spine
``` Benign - Osteoblastoma / osteoid osteoma - Aneurysmal bone cyst - Giant cell tumour Malignant - Myeloma - Metastasis - Chondrosarcoma ```
29
Lesion in vertebral body
``` Chordoma Giant cell tumour Langerhans cell histiocytosis Ewing sarcoma Lymphoma Metastasis Myeloma ```
30
Lesion in rib (FAMMEE)
``` Fibrous dysplasia ABC Mets Myeloma Enchondroma Eosinophilic granuloma ```
31
Sclerotic mets (6BLP)
``` Bone (osteosarcoma) Breast Brain (medulloblastoma) Bronchus (carcinoid) Bladder (TCC) Bowel (mucinous) Lymphoma Prostate ```
32
Mixed lytic and sclerotic lesions
Mets: breast, lung, cervix, testicular, prostate, ganglioneuroblastoma Brown tumour POEMS
33
Aggressive bone lesions (adult)
Mets / myeloma / lymphoma Sarcoma Osteomyelitis Brown tumour (sometimes)
34
Aggressive bone lesions (peds)
Met from childhood malignancy / Ewings / lymphoma / leukemia Sarcoma Osteomyelitis LCH
35
Nonaggressive metaphyseal / diaphyseal bone lesions
``` Medullary - Fibrous dysplasia - ABC / UBC - Enchondroma Cortical - Fibroxanthoma (FCD and NOF) - Osteoblastoma / osteoid osteoma Either - Brown tumour - Chondromyxoid fibroma ```
36
Epiphyseal lesions (adult)
``` Neoplasm - Giant cell tumour - Clear cell chondrosarcoma - Mets / myeloma / lymphoma Osteomyelitis (Brodie's abscess) Other lesions (geode, subchondral lesion, AVN) ```
37
Epiphyseal lesions (peds)
Chondroblastoma LCH Osteomyelitis / Brodie's abscess
38
Polyostotic adult
Mets / myeloma / lymphoma Brown tumors / HPT Fibrous dysplasia
39
Expansile lesion, fluid-fluid levels
``` ABC - Primary - Secondary (GCT, osteoblastoma, chondroblastoma) Telangiectatic osteosarcoma Expansile met Pseudotumor from hemophilia ```
40
Cancers that met to cortex
``` Bronchogenic (cookie bite sign) Breast Melanoma RCC Epidermoid ```
41
Focal periosteal rx’n / marrow edema
``` Stress fracture / reaction Trauma / contusion Osteomyelitis Infiltrative neoplasm Radiation ```
42
Polyostotic periostitis
``` Hypertrophic osteoarthropathy - Secondary (lung malignancy, CF, endocarditis, IBD, etc.) - Primary (pachydermo-periostitis) Venous insufficiency Thyroid acropachy ```
43
Acro-osteolysis (PINCHFO)
``` Psoriasis Injury: thermal burn, frostbite Neuropathy: diabetes, leprosy Collagen vascular disease: scleroderma, Raynaud, mixed CTD Hyperparathyroidism Familial: Hajdu Cheney Other: PVC exposure ```
44
Acro-osteolysis - terminal tuft
``` Scleroderma / Raynauld’s (look at soft tissues of fingertips and for calcs) Psoriatic / Reactive arthritis Thermal injury Hyperparathyroidism Drugs (phenytoin / ergot poisoning) ```
45
Acro-osteolysis - midshaft / band-like
Hyperparathyroidism PVC exposure Primary acro-osteolysis (Hajdu-Cheney)
46
Acro-osteolysis - single digit
Epidermal inclusion cyst Glomus tumour Subungual mets (lung, GU, breast) Trauma
47
Causes of AVN
``` Idiopathic Drugs (steroids, chemo, NSAIDs, alcohol) Traumatic Inflammatory (vasculitis, SLE, CTD, pancreatitis) Deposition disease Caisson disease Pregnancy ```
48
Ivory vertebrae
Mets / lymphoma / sarcoma / chordoma Hemangioma Paget's TB
49
Vertebra plana
``` Young - LCH - Neuroblastoma metastasis - Leukemia / lymphoma - Infection: bacterial, TB - Trauma - Ewing Old - Mets / myeloma / lymphoma - Trauma, osteoporotic compression #, Kummel's osteonecrosis (if intervertebral vacuum phenomenon) - Infection ```
50
Bone-in-bone
Focal (post-trauma, post-infectious) | Diffuse (osteopetrosis)
51
Vertebral body sclerotic changes
``` Rugger jersey spine: - Renal osteodystrophy / HPT Sandwich vertebrae (denser and more sharply defined): - Osteopetrosis Picture frame vertebral body: - Paget ```
52
H-shaped vertebral body
Sickle cell anemia | Gaucher
53
Lucent metaphyseal bands (LINE P)
``` Leukemia / lymphoma Infection (TORCH) Neuroblastoma mets Endocrine: rickets, scurvy, hypervitaminosis D (Prematurity, hospitalization) ```
54
Dense metaphyseal bands
``` Growth arrest lines Healing rickets Lead poisoning Scurvy Bisphosphonate therapy (zebra stripe sign) Normal variant (look for normal fibula) ```
55
Syndromes with multiple bone lesions
Osteochondromas: Multiple hereditary exostoses Enchondromas: Ollier’s, Maffucci’s (soft tissue hemangiomas) Fibroxanthomas: Jaffe-Campanacci Fibrous dysplasia: McCune-Albright (café au lait spots, precocious puberty), Mazabraud (intramuscular myxomas) Osteomas: Gardner’s (polyposis, desmoids) LCH: Hans-Schuller-Christian (diabetes insipidus, exophthalmos), Letterer-Siwe (visceral involvement poor prognosis) Angiomas: Cystic angiomatosis, lymphangiomatosis
56
Diffuse osseous sclerosis
``` Sclerotic mets / lymphoma/ POEMS Myelofibrosis and mastocytosis Renal osteodystrophy Fluorosis Mild osteopetrosis ```
57
Diffuse demineralization
``` Osteoporosis Osteomalacia (vit D / calcium / phosphate deficiency) Osteogenesis imperfecta Hyperparathyroidism Diffuse tumor (most often myeloma) ```
58
Osteoporosis (AMEDICAL)
``` Age Meds (steroids, heparin, Dilantin, etc.) Endocrine (menopause, amenorrhea, Cushing’s hypogonadism) Diet (poor calcium intake, anorexia) Anemia (sickle cell, thalassemia) Liver disease ```
59
Undertubulated bones (peds)
``` Anemia (thalassemia, sickle cell) Gaucher Niemann-Pick Leukemia Polyostotic fibrous dysplasia Multiple hereditary exostosis ```
60
Erlenmeyer flask deformity (CHONG)
``` Craniometaphyseal dysplasias Hemoglobinopathies (sickle cell, thalassemia) Osteopetrosis Niemann-Pick Gaucher’s ```
61
Short metacarpals (BIC Pen)
``` Basal cell nevus syndrome Idiopathic Chromosomal (Turners) Pseudo and pseudopseudohypoparathyroidism Noonan syndrome ```
62
Localized gigantism
Macrodystrophia lipomatosa Vascular lesions Klippel-Trenaunay-Weber syndrome Neurofibromatosis
63
Wormian bones (PORKCHOPS)
``` Pyknodysostosis Osteogenesis imperfecta Rickets Kinky-hair syndrome Cleidocranial dysostosis Hypothyroidism / hypophosphatasia Otopalatodigital syndrome Primary acro-osteolysis / Primary HOA (pachydermoperiostitis) / progeria Syndrome of Downs ```
64
Rhizomelic skeletal dysplasia
Achondroplasia | Thanatophoric dysplasia
65
Mesomelic skeletal dysplasia
Leri-Weill dyschondrosteosis (Acro)Mesomelic dysplasia (different types, may be mesomelic or acromesomelic) Ellis-van Crevald (acromesomelic)
66
Acromelic skeletal dysplasia
Jeune syndrome / asphyxiating thoracic dystrophy | Peripheral dysostosis
67
``` Marrow replacement (Replaced marrow is lower in signal on T1WI than discs/skeletal muscle & does NOT drop out of signal on OOP imaging) ```
``` Benign - Myelodysplastic syndrome - Myelofibrosis - Mastocytosis - Gaucher disease Malignant - Mets / myeloma / lymphoma / leukemia - Waldenstrom macroglobulinemia - Sarcoma (e.g. dense osteoid) ```
68
Red marrow reconversion (Red marrow is lower in signal on T1WI than yellow marrow, but NOT lower than discs/skeletal muscle Red marrow drops out of signal on OOP imaging)
Physiologic (athletes, living at altitude) Hypoxemia (smoking, anemia) Hematopoietic stimulation (drugs, obesity)
69
Serous bone marrow atrophy (aka gelatinous transformation) T1: mildly low signal intensity STIR: high signal intensity
Anorexia / cachexia / malnutrition (including alcoholism) - look for loss of subq fat Malignancy Heart failure Other severe systemic illness
70
Post-arthroplasty complications
``` Periprosthetic fracture Malalignment Loosening Infection Particle disease ```
71
Manifestations of loosening
Motion > 2 mm periprosthetic lucency New / enlarging periprosthetic lucency
72
Causes of loosening
Aseptic (micromotion) Infection Particle disease
73
Distal clavicular osteolysis (SHIRT)
``` Scleroderma Hyperparathyroidism Infection Rheumatoid arthritis Trauma ```