Septic arthritis/bone tumor Flashcards

1
Q

Septic Arthritis

general

A

An infection of the joint due to direct inoculation, contiguous extension, or hematogenous spread of infectious organisms into the joint space

Surgical emergency: irreversible damage to tissue after 24 hours

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2
Q

septic arthritis

etiology

A

Etiology: majority of septicarthritisinfections are monomicrobial
Staphylococci:
Staphylococcus aureus(most common), S. epidermidis
Streptococci:
Streptococcuspyogenes, S. pneumoniae, S. agalactiae

Gram-negative bacteria:
Pseudomonas aeruginosa
Escherichia coli
Kingella kingae
Neisseria gonorrhoeae → Young, sexually active patient
Haemophilusinfluenzae
Salmonellaspecies → Sickle cell anemia

gonorrhea usualy multiple joints

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3
Q

septic arthritis

RF of infants and kids

A

Infants and children:
Prematurity
Hemophilia (due to hemarthroses)

Immunosuppression:
Chemotherapy
HIV
Sickle cell anemia
Diabetes

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4
Q

septic arthritis

Adult RF

A

Age > 80 years
Chronic disease/immunosuppression:
Diabetes
HIV

Joint disease:
Rheumatoid arthritis
Osteoarthritis
Gout

Joint procedures:
Surgery
Intra-articular injections
Joint prosthesis
Skininfectionsor ulcers

IV drug use

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5
Q

septic arthritis

Invasion of the joint occurs through:

Previously damaged joints

A

Hematogenous seeding(most common)
Direct inoculation of organisms into the joint
Extensionfrom an adjacent infection

Previously damaged joints are particularly susceptible to infection by way of:
Neovascularization
Dysfunctional cellular defenses
Absentbasement membraneon thesynovial membrane

know how you can end up w infection

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6
Q

septic rthritis

Progression of the disease:

A

Bacterial invasion → inflammation →release ofcytokines andproteases
This response, plus bacterial toxins → destruction of:
Articularcartilage
Synovium
Subchondralbone

If a large effusion develops → impairment of the blood supply → aseptic necrosis

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7
Q

septic arthitis

Clin man

A

Constitutional symptoms:
Fever
Fatigue
Tachycardia

Signs and symptoms:
Moderate-to-severejoint painand effusion
Erythema and warmth
Tenderness to palpation
Limited active and passiverange of movement
Usually monoarticular, but may be oligo- or polyarticular

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8
Q

septic arthritis

commonly affected joints

A

Knee (> 50% of cases)
Wrist
Ankle
Hip
Elbow
Axialjoints (in IV drug users):
Sacroiliac
Sternoclavicular joint

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9
Q

septic arthritis

Dx

A

Arthrocentesis
Diagnosisis made withsynovial fluid analysis
Should be attempted before antibiotics are given
A positiveGram stain and/or culture confirms the diagnosis

A purulent aspirate gives a presumptive diagnosis:
WBC count > 50,000 cells/μL
Neutrophil predominance
Nucleic acid amplification testing may be performed ifN. gonorrhoeaeis suspected

Include an analysis for crystals to rule outgout

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10
Q

septic arthritis

A
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11
Q

septic arthritis

lab tests (4)

A

Lab tests
Used to support the diagnosis:
↑Erythrocyte sedimentation rate (ESR)
↑ CRP
Can be used to monitor response to therapy
↑ WBC count
Bloodcultures

Cervical,urethra, rectal, or oropharyngeal swabs fornucleic acid amplification testifN. gonorrhoeaeis suspected

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12
Q

septic arthritis

imaging

A

Plain-film radiograph:
Joint-space narrowing or widening
Subchondral bony changes,osteopenia
Periarticularsoft tissueswelling
Normal studies do not rule out septicarthritis

Ultrasound:
Identificationof a joint effusion
Can assist with aspiration of the effusion

MRI:
Sensitive for earlyidentificationof joint effusion
Evaluates the extent ofboneand soft-tissue abnormalities
Assesses for associated osteomyelitis

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13
Q

septic arthritis

Abx

A

Antibiotic therapy
Antibioticselectionis based on the initialGram stainand tailored based on culture data

Empiric regimen ifGram stainis negative:
Vancomycin plus 3rd- or 4th-generation cephalosporin
Duration of therapy depends on additional factors:

With negative bloodcultures:
2 weeks of parenteral antibiotics
Additional 1–2 weeks of oral antibiotics

With positive bloodcultures:
4 weeks of parenteral antibiotics

P. aeruginosa infection: 4–6 weeks

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14
Q

septic arthritis

P. aeruginosa infection length of Tx

A

4–6 weeks

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15
Q

septic arthritis

Surgical interventions

A

Joint drainage – open or arthoscopic drainage; needle aspiration
Surgical debridement in patients with prosthesis

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16
Q
A
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17
Q

Bone Tumors

General

children vs adults

A

Develops when bone cells divide uncontrollably
Benign or malignant
Malignant can be primary or metastatic
Primary arise from bone cells
Metastatic spread to bone from other tissues

In children…
Most are benign
Malignant tumors – osteosarcoma, Ewing sarcoma

In adults…
Metastatic tumors are 100x more common than primary malignant tumors
Metastasis from breast, lung, thyroid, prostate, or renal cancer

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18
Q

bone tumor

A
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19
Q

bone tumor

Proto-oncogenes

A

Genes that promote normal cell growth
With mutations, proto-oncogenes become oncogenes → overstimulate the cell growth

20
Q

bone tumor

Tumor suppressor genes

A

Help to balance cell growth by promoting apoptosis of mutated cells

21
Q

bone tumor

Oncogenes and/or mutated tumor suppressor genes

A

allow cells to keep growing uncontrollably resulting in tumors

22
Q

Bone Cancer

S/Sx

A

Symptoms
Pain
Unexplained, progressive
Occurs without weight bearing
Particularly painful at night
Increased pain with mechanical stress
Swelling
Fatigue

Signs 
Tenderness over the involved bone
Palpable painful bone mass
Limping (children)

23
Q

bone tumor

Dx/imaging

A

Plain film x-rays
MRI with contrast
Whole body bone scan if multicentric or metastatic tumors are suspected

Biopsy
Exceptions
Imaging studies clearly show benign characteristics
Multiple bone lesions in a patient with a confirmed primary cancer

24
Q
A
25
Q

Osteosarcoma

general
Arise from what cell

A

Also referred to as osteogenic sarcoma
Most common malignant bone tumor in children and young adults (10-25 years)
Highly malignant
Arise from osteoblasts

Approximately 90% of osteosarcomas occur in the extremities

Most common site of involvement
Metaphyseal sites of the most rapidly growing bones are more commonly involved
Around the knee (distal femurorproximal tibia) - ~50% of cases
Proximal humerus

Most cases are sporadic and have no identified cause
Osteosarcoma produces malignant osteoid (immature bone) from tumor bone cells

26
Q

osteosarcoma

RF

A

Risk factors
Prior treatment with radiation therapy
Other bone disorders: Paget’s disease
Hereditaryretinoblastoma (mutation of the pRB protein – seen in both cancers)

27
Q

osteosarcoma

Dx & labs

A

↑ alkaline phosphatase…Why?

Plain film x-rays followed by CT scan or MRI
“Hair on end” or “sunburst appearance” due to tumor spicules of calcified bone on plain films

Codman’s triangle due to lifting of the periosteum

Definitive diagnosis requires biopsy

28
Q

osteosarcoma

Tx

A

Combination of chemotherapy and surgery
Chemotherapy initiated prior to resection

Surgery: limb-sparing or amputation

29
Q

Ewing sarcoma

General
Mutation

A

Round-cell bone tumor resulting from a translocation between chromosomes 11 and 22

Second most common malignant bone tumor in children (10-25 years)

Most common site of involvement
Diaphyseal region of long bones
Femur
Sacrum
Tibia
Fibula

30
Q

ewing sarcoma

Dx

A

Plain film x-rays followed by CT scan or MRI

Moth-eaten destruction in a permeative pattern without clear borders

Multiple layers of subperiosteal reactive new bone formation in an onion-skin appearance

Definitive diagnosis requires biopsy

31
Q

ewing sarcoma

Tx

A

Combination of surgery, chemotherapy and radiation therapy

32
Q

Multiple Myeloma

general
Originate from what cells? That produce?

A

Most common primary malignancy of the skeleton
Malignancy derived from antibody producing plasma cells
Arises in the bone marrow with production of large amounts of monoclonal immunoglobulin (IgG or IgA)

33
Q

multiple myeloma

Clin man

A

Lytic lesions
Sharply circumscribed (punched-out lesions) on x-ray
Diffuse demineralization

Occurs mostly in older adults
Median age at diagnosis is 65 years

34
Q

multiple myeloma

Destruction of Bone
Affects on electrolytes?

A

Plasma cells activate osteoclasts, which promote bone destruction → lytic lesions

Bone destruction is accompanied by an increase of serum calcium → hypercalcemia

Back, hips, and ribs are the most common areas for pain

35
Q

multiple myeloma

Tx

A

Bisphosphonates
Stimulates osteoclast apoptosis
Prevent pathologic bone fractures and helps to lower serum calcium levels

36
Q
A
X-ray with multiple osteolytic lesions in the forearm with a pathologic fracture of the distal third of the ulna
37
Q

Chondrosarcoma

general
Arise from what cell

A

Malignant tumor of cartilage
Arises from chondrocytes
Occurs most commonly in people aged 40-75 years

Tends to grow slowly
Can have a soft tissue component involving surrounding soft tissues

38
Q

Chondrosarcoma

Most common site of involvement

A

Flat bones (pelvis and scapula)
Long bones (proximal femur, proximal humerus)

39
Q

Chondrosarcoma

Dx
What will you see?

A

Plain film x-rays followed by CT scan or MRI

Punctate or ring and arc calcifications
Cortical bone destruction

Biopsy
Required for definitive diagnosis
Determine the tumor grade

Low-grade: indolent, slow growing
High-grade: excruciating pain, fast growing

40
Q

Chondrosarcoma

Tx

A

Wide surgical resection for nonmetastatic disease
Chemotherapy (advanced disease)

41
Q

Osteochondroma

general

A

Cartilage-capped bony overgrowth arising on the external surface of a bone

Most common benign bone tumor

Often occur in people < 25 years

May be single or multiple

Single tumors will develop into a secondary malignant chondrosarcoma in 1% of patients

Multiple tumors tend to run in families

42
Q

osteochondroma

Most commonly arise from the appendicular skeleton in the metaphysis of long bones

A

Femur
Proximal tibia
Proximal humerus

43
Q

Osteochondroma

Imaging

A

Imaging studies
Bony prominence with a cartilage cap (usually <2 cm) off the surface of the bone
MRI will reveal that the medullary canal is in continuity with the base of the exostosis

44
Q

Osteochondroma

Tx

A

Observation if asymptomatic

Excision if the tumor is causing pain, compressing a large nerve or vessel, disturbs growth, or has a destructive appearance (transformation into malignant chondrosarcoma)

45
Q

Osteoma

general
Where are they found? What do they produce? Describe it

A

Benign

Also known as osteoid osteomas
Areas of uniformly dense bone that produces high levels of prostaglandins

Most common in the skull, mandible, femur, spine
Painful most often at night

Pain relief within 30-60 minutes of administration of NSAIDs…why?

Diagnosed incidentally on imaging studies
Do not require biopsy and can be followed periodically with plain films

46
Q

Bone Tumors

Key Points

A

In children, most bone tumors are benign

In adults, especially those age > 40, metastatic tumors (breast, lung, prostate, or renal cancer) are about 100x more common than primary malignant tumors

Have a high suspicion for bone tumors in patients who have unexplained bone pain, particular pain at night or at rest

Assessment begins with plain film x-rays, but typically requires MRI and biopsy for definitive diagnosis

Treatment of malignant tumors often involves a combination of surgery, chemotherapy, and radiation therapy