xray imaging in non inflammatory arthritis

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By: DR. RAMAN SHINGADE 2 ND YR. RESIDENT GUIDE: DR. KANCHANA PACHCHIGAR TUTOR Greenspan Yochum and Rowe Radiopedia.org Learninradiology .com References: Xray Imaging in Non Inflammatory Arthritis

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thropathyHallmark radiographic features of non-inflammatory arthritis like osteoarthritis, connective tissue arthropathy and metabolic and endocrine ar

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Page 1: Xray imaging in non inflammatory arthritis

By: DR. RAMAN SHINGADE 2ND YR. RESIDENT

GUIDE: DR. KANCHANA PACHCHIGAR

TUTOR

• Greenspan• Yochum and Rowe• Radiopedia.org• Learninradiology.com

References:

Xray Imaging in Non Inflammatory Arthritis

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The constituent structures of a synovial/diarthrodial joint.

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Definition of Arthritis

•Disease that affects bones on both sides of the joint space and

•Narrows the space between them

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Narrowing of the joint space

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Radiographic features of arthritides

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Arthritis or not

Normal DJD

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Arthritis or not

Normal DJD

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Arthritis or not

Normal DJD

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Classification of Arthritides

•Inflammatory Arthritis

•Non-inflammatory Arthritis

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Non Inflammatory ArthritisDegenerative Arthritis (Osteoarthritis)

Primary

Secondary

Connective Tissue Arthropathy Scleroderma

MCTD

Metabolic & Endocrine Arthritis Acromegaly

Hemochromatosis

Haemophilia

Gout

Hyperparathyroidism

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2 forms of Osteoarthritis

Primary form • Idiopathic

Secondary form • Posttraumatic• Congenital disorders• Neuropathic Arthritis• Avascular Necrosis

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Primary Degenerative Arthritis

• Intrinsic degeneration of articular cartilage

• Excessive wear and tear• Most commonly weight bearing joints like knees and

hips• Less commonly non-weight bearing joints like knees

and hips

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•Hip

•Knee

• Spine

• Interphalangeal joints of the hand

Common Sites

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Hallmark radiographic features

• localized joint space narrowing

• subchondral sclerosis

• osteophytes

• cyst or pseudocyst

Osteoarthritis of Large joints

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narrow joint spacesubchondral sclerosis

osteophytes

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Right hip osteoarthritis

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Superolateral migration of femoral head with typical Eggers cyst in acetabulum.

Egger’s CystSuperolateralmigration

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Medial migration of the femoral head

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Postel coxarthropathy(aka rapidly destructive arthrosis)

• occurs predominantly in women

• characterized by rapid chondrolysis

• no/very little reparative changes

• mimics Charcot joint or infectious arthritis

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Right hip Postel Coxarthropathy

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Osteoarthritis of left knee

L L

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AP and lateral both knee radiographs bilateral knee osteoarthritis.

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Advanced osteoarthritis with loose bodies

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Narrowing of the femoropatellar joint compartment

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Patellar Tooth sign

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Patellar Tooth sign on AP projection

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•Not due to mechanical stress

• F:M = 10:1

•Most Often involves DIP joints• Sclerosis• Osteophyte formation

• 1st MCP joint of thumb

Osteoarthritis of Hand

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Hallmark radiographic features

• Heberden nodes

• Bouchard nodes

• joint space narrowing

• subchondral sclerosis

Osteoarthritis of Hand

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Heberden Nodes

Bouchard Nodes

Degenerative changes in the 1st carpometacarpal joint

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Osteoarthritis of bilateral first metatarsophalangeal joints

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hallmark radiographic features

• Facet narrowing and eburnation

• Foraminal stenosis

• Stenosis of spinal canal

• Narrowing of IVDS

Degenerative Disease of the Spine

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Osteoarthritis of the facet joints

Subchondral sclerosis

Narrowing of facet joints

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Bridging osteophytes

Bridging osteophyte

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Encroachment of the neural foramina by posterior osteophytes

Posterior osteophytes withNeural foraminal stenosis

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Vacuum disc phenomenon

Prominent osteophytes

Vacuum disc phenomenon

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Secondary Osteoarthritis

• Another process destroys articular cartilage

• Degenerative changes supervene

• How to recognize• Atypical age (e.g. DJD in 20 yrs age)• Atypical appearance (e.g. DJD in 1 hip only)• Atypical locations (e.g. DJD in shoulder)

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Secondary Osteoarthritiscauses

• Trauma (most common)• Avascular Necrosis• Neuropathic arthritis• Congenital Disorders• Haemophilia• RA

Bottom Line: Any arthritis can lead to 2° OA

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•most common cause of secondary/atypical osteoarthritis

• changes similar to those in primary osteoarthritis

• history of previous trauma

• younger age group

Posttraumatic Osteoarthritis

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Severe osteoarthritic changes due to previous dislocation

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Severe post-traumatic osteoarthritis following distal fibula fracture.

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Left knee Posttraumatic osteoarthritis.

L

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• destructive articular disease that occurs secondary to a loss or impairment in joint proprioception

• disturbance in sensations leads to multiple microfractures

• fragmentation of the bone and cartilage

Neuropathic Arthritis

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Causes

Shoulders • Syrinx• Spinal Tumor

Hips • Tertiary syphilis• Diabetes

Feet • Diabetes

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6 D’s of Neuropathic Arthritis

• Dense bones (subcondral sclerosis)

• Distension of joint

• Destruction of bone and cartilage

• Disorganization

• Debris (loose bodies)

• Dislocation

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Typical Neuropathic (Charcot) joint

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Typical charcot joint in man with syphilis

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Licked candy stick configuration

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• defined as death of the osseous cellular components and marrow due to inadequate blood supply

• definite anatomic predisposition for osteonecrosis at the epiphyseal centers

• usually escapes clinical detection and is diagnosed only with bony imaging

Avascular Necrosis(Ischemic or Osteonecrosis)

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• Spontaneous (idiopathic) • Trauma (fracture, dislocation)• Alcoholism• Corticosteroid therapy• Surgery • Hemoglobinopathy

Common causes -

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• Collapse of articular cortex• Fragmentation•Mottled trabecular pattern• Sclerosis (Snowcap sign)• Subchondral cysts • Crescent sign (Subchondral fracture)

Radiographic features

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Classical sites of Osteonecrosis

• head of femur

• neck of talus

• waist of scaphoid

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Snowcap and Crescent signs

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Collapsed Articular Cortex

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Epiphyseal Fragmentation

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Osteonecrosis of humeral head after sustaining fracture of the left humeral neck

Crescent sign

Increased bone density

Healed Fracture

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Pregnancy related Avascular necrosis.

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Osteonecrosis of right humeral head following chemotherapy

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•Developmental dysplasia of the hip

• Slipped capital femoral epiphysis

Secondary to Congenital Diseases

Includes

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•Putti's triad for developmental dysplasia of the hip include :

Superolateral displacement of proximal femur .

Increase in acetabular angle.

Small capital femoral epiphysis.

Developmental dysplasia of the hip

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Radiograph demonstrates Developmental Dysplasia of Hip in a 6 months old female baby.

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Developmental Dysplasia of Hip in a 12 years old female.

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• Loss of Capener triangle sign

• Decreased height of femoral epiphysis

• Absence of intersection of epiphysis by line tangent to lateral cortex of femoral neck

• Herndon hump

Slipped capital femoral epiphysis

Radiographic features:

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Radiograph demonstrates absence of Carpener triangle in left hip.

Carpener Triangle

Absence ofCarpener Triangle

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Absence of intersection of epiphysis by lateral femoral cortical line.

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Radiograph demonstrates Herndon hump and secondary osteoarthritis.

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Non Inflammatory Arthritis

Connective Tissue Arthropathy Scleroderma

MCTD

Metabolic & Endocrine Arthritis Acromegaly

Hemochromatosis

Gout

Haemophilia

Hyperparathyroidism

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Scleroderma

• generalized systemic inflammatory connective tissue disease of unknown cause

• strong female predilection (F:M 3:1)

• frequent involvement of the musculoskeletal system

• predominantly affects the fingers, wrists and ankles

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CREST syndrome

Calcinosis

Raynaud phenomenon

Esophageal dysmotility

Sclerodactyly

Telangiectasia

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• atrophy of the soft tissues at the tips of the fingers

• resorption of the distal phalanges

• subcutaneous and periarticular calcifications

• destructive changes of the small articulations

• flexion contractures

Radiographic features

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Atrophy of the soft tissues at the distal phalanges of the index, middle, and ring fingers

R

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Soft-tissue calcifications in the distal phalanges of the left hand, a typical feature of Scleroderma

L

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Acroosteolysis (arrow), soft tissue calcifications, and destructive changes of the distal interphalangeal joint of the middle finger.

R

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Subcutaneous calcifications alongwith destructive changes in distal IP joints

L

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Destructive changes in the distal interphalangeal joints, as well as soft-tissue calcifications

L

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Flexion contracture in scleroderma patient

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Mixed Connective Tissue Disease

• an example of Overlap syndrome

• combine the features of SLE, scleroderma, dermatomyositis, and rheumatoid arthritis

• antibody to the ribonucleoprotein (RNP)

• approx. 80% patients are female

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Radiographic features are combination of different conditions

• Tuft resorption and DIP erosions (Scleroderma)

• Erosive arthritis (Rheumatoid arthritis)

• Deforming, nonerosive arthritis (SLE)

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Abnormal tapering of the distal soft tissues and early surface erosion of the phalangeal condyle.

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Subtle surface erosions and Progressive erosions

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Terminal tuft resorption

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Subluxation of IP joint of the thumb and advanced ulnar deviation

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Juxta-articular demineralization and erosive articular disease

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Metabolic & Endocrine Arthritis

Acromegaly

Hemochromatosis

Gout

Haemophilia

Hyperparathyroidism

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Acromegaly

• result of excessive growth hormone (GH) production

• growth of intramembranous bone tissue and subcutaneous hypertrophy

• degenerative changes are the result of hypertrophy of articular cartilage

• it is not adequately nourished by synovial fluid because of its abnormal thickness

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Indices for Acromegaly

o Sesamoid Index • Product of height and width (in mm.) of sesamoid bone at MCP of thumb.

• Normal - <30 in females <40 in males

o Heel Pad Thickness • Distance from posteroinferior surface of calcaneum to nearest skin surface

• Normal <22 for 150 lb. individual

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• initially, widening of joint spaces in hand, particularly MCP joints

• later, thinning of the joint cartilages with osteophyte formation

• beak-like osteophytes

• Spade phalanx sign

Radiographic features

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Sesamoid Index and Heel Pad Thickness

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Spade phalanx sign

NORMAL ACROMEGALY

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Characteristic abnormalities in acromegalic hand

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Acromegalic osteoarthritis

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Hyperparathyroidism

• aka generalized osteitis fibrosa cystica or Recklinghausen disease of bone

• result of overactivity of the parathyroid glands

• leads to hypercalcemia

• 3 subtypes – primary, secondary and tertiary

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Radiographic features

• Osteopaenia

• Subperiosteal bone resorption

• Intracoritcal bone resorption

• Brown tumours (aka Osteitis Fibrosa Cystica)

• Soft tissue and cartilage calcifications

• Osteosclerosis

• Salt and pepper sign in skull

• Rugger-jersey spine

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Subperiosteal resorption is on the radial sides of proximal and middle phalanges

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Subchondral resorption resulted in widening of the sacroiliac joints.

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Brown tumor in distal radius

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Brown tumor in distal clavicle

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Chondrocalcinosis at the knee and the symphysis pubis

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Metastatic calcifications

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Typical hyperparathyroidism arthropathy at the distal interphalangeal joints of the index and middle fingers.

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Rugger-Jersey Spine

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Hemochromatosis

• characterized by iron deposition in various organs

•may be primary (endogenous or idiopathic) or secondary

• affects men 20-times more frequently than women

• 50% of patients with hemochromatosis will have a slowly progressing arthritis

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• features typical of osteoarthritis

• different pattern of joint involvement in hand

• second and third metacarpophalangeal joints

• hook-like osteophytes

• chondrocalcinosis

Radiographic features

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Osteoarthritic features in woman with hemochromatosis

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Magnified radiograph demonstrates involvement of the metacarpal heads

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Classical hook osteophytes

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Advanced Hemochromatosis arthropathy

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Hemophilia• group of disorders characterised by a tendency to bleed as a result

of deficient clotting factors

• deficiency of factor VIII (haemophilia A) or factor IX

• arthropathy is a consequence of recurrent bleeds into joints

• knees, elbows, hips and ankles are most commonly affected

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Radiographic features

• widened intercondylar femoral notch

• squared inferior margin of the patella

• haemophilic pseudotumours

• periarticular erosions

• features of osteoarthritis

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Widened intercondylar notch with joint effusion

L

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Haemophilic arthropathy with subtle haemarthrosis

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Advanced degenerative changes, with near-complete loss of joint space

L

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Haemophilic Pseudotumors

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Gout•metabolic disorder characterized by recurrent episodes of

arthritis

•monosodium urate monohydrate crystals in the synovial fluid leukocytes

• great toe is the most common site of involvement in gouty arthritis

•most patients are men (20:1)

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Radiographic features

• Articular erosion with preservation of part of joint

• Overhanging edge of erosion

• Lack of osteoporosis

• Periarticular swelling

• Tophi

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Periarticular erosions and soft tissue masses, representing tophi

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Multiple articular and periarticular erosions associated with large tophi.

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Typical involvement of the first MTP joint with “overhanging edge”.

Overhanging Edge

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Intraosseous tophi

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Tophus with dense calcifications adjacent to the olecranon process.

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Summary

Primary Osteoarthritis • Joint space narrowing• Osteophytes• No underlying cause

Posttraumatic Osteoarthritis

• Similar to 1° OA• Previous Trauma• Younger Age

OA 2° to DDH • Superolateral displacement of proximal femur .• Increase in acetabular angle

OA 2° to SCFE • Loss of Capener triangle sign• Absence of intersection of epiphysis

Neuropathic Arthritis • 6 D’s

Osteonecrosis • Radiolucent crescent • Preserved joint space

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SummaryScleroderma • Resorption of the distal phalanges

• Subcutaneous and periarticular calcifications

MCTD • Combination of different conditionsAcromegaly • beak-like osteophytes

• Spade phalanx sign

Hyperparathyroidism • Subperiosteal bone resorption• Brown tumours• Soft tissue and cartilage calcifications

Hemochromatosis • 2nd & 3rd MCP joints are characteristically affected

• Typical features of OAHaemophilia • Features of osteoarthritis

• Widened intercondylar notch

Gout • Tophi• Overhanging edge of erosions

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SPOTS

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SPOT 1

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SPOT 2

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SPOT 3

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SPOT 4

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SPOT 5

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Thank You