Musculoskeletal Disorders

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  • No man’s land in flexor tendon → Zone 2
  • Infertility workupWHO grade 2 is most common
  • BE FAN VEIN
  • Patellar clunk syndrome

HLA associations

HLAs
Diseases
DQ1
• Pemphigus Vulgaris
DQ7
• BP variant
DQ2 / DQ8
• Celiac disease
Seal with DQ ()
DR2
• Good Pasteur’s (GBS)
• Narcolepsy (DQB1:06:02)
• Multiple sclerosis
(B16, DR2)
2nd - Good doctor () - have MS () - always sleeps ()
DR3
Chronic active hepatitis
Dermatitis herpetiformis
SLE
Sjogren’s
T 1 DM
DR4
Rheumatoid arthritis
Pemphigus vulgaris (DQ1, DR4)
DR5
• Hashimoto’s thyroiditis (DR3, DR5)
B27
Ankylosing spondylitis
Reactive arthritis
Psoriatic arthritis
B35
De Quervain's thyroiditis
B47
• CAH
B51
Behcet’s disease
B57
Abacavir hypersensitivity (B*57:01)
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Osteoarthritis (OA)

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  • 51 (HLA B51) yr old Nolan (Anti enolase) on a Bus (behcets)
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Synovial fluid
Synovial fluid
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  • Most Common Joint Disease
    • Cause: Degeneration of cartilage.

Clinical Features

  • Inflammatory Changes: 
    • Absent or unnoticed.
  • Involvement: 
    • Usually affects knee and hip joints.
    • 1st CarpoMetacarpal joint involvement → Specific of OA
  • Symptoms:
    • Pain.
    • Decreased range of motion leading to muscle wasting (e.g., vastus medialis).
    • Crepitations (cracking or popping sounds in joints).
    • Deformity or swelling.

Loose Bodies in joints

  • M/c/c in adults: Osteoarthritis
  • M/c/c in children: Osteochondritis dissecans
  • O/c: RA, Charcots arthritis, FBs

X-ray Features (Chronological Progression)

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  • Mnemonic: LOSS
      1. Loss Joint Space
          • Earliest finding due to cartilage destruction.
      1. Osteophytes
          • Regenerating bone break off
            • form loose bodies (joint mice),
            • common in elderly.
      1. Subchondral Sclerosis
        1. Increased bone density below cartilage.
      1. Subchondral Cysts
        1. Fluid-filled sacs beneath cartilage.

Knee Osteoarthritis

  • Median compartment is affected commonly
    • Bilateral Genu Varum (bow-legged).
  • Muscle affected ⇒
    • Quadriceps
      • Vastus medialis
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Heberden's Nodes: 

  • High, involving DIP (Distal Interphalangeal) joints.
  • Mnemonic: HD and BP
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  • Mnemonic: High for DIP.

Bouchard's Nodes: 

  • Low, involving PIP (Proximal Interphalangeal) joints.
  • Mnemonic: Bouchard → Below for PiP.

Joints Involved in OA

Affected Joints:

  • Distal Interphalangeal (DIP).
  • Proximal Interphalangeal (PIP).
  • First Carpometacarpal (CMC).

Spared Joints:

  • Wrist.
  • Metacarpophalangeal (MCP).
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Rheumatoid Arthritis (RA)

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  • 51 (HLA B51) yr old Nolan (Anti enolase) on a Bus (behcets)
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  • JIA is similar to Rheumatoid arthritis → Difference:
    • JIA Uveitis, < 16 years
    • RA Scleritis, Episcleritis, Keratoconjuctivitis Sicca
  • Kaplan Syndrome
    • CWP + rheumatoid arthritis.
  • Note: Felty syndrome
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  • X ray
    • Upper lobes opacities
  • We Felt (Felty syndrome) pain fo RA () ENT pg → We gave him a cap (Caplan)
  • NOTE:
    • Erasmus syndrome: CWP + Systemic sclerosis
    • Erase & Cap → CWP syndromes
    • EraSS → Systemic sclerosis

Synovial Disease

  • Type: Most common inflammatory arthritis.

General Features

  • Rheumatoid factor: IgM Against Fc part of IgG (MRF → M against G)
  • Prevalence: Female > Male.
  • Characteristic: 
    • Erosive arthritis (destroys joints),
    • unlike SLE → non-erosive.
  • Nature: Chronic autoimmune multisystem disease.
  • Symptoms:
    • Involvement can be bilateral.
    • Initial presentation:
      • Only wrist joint may show redness/inflammation.
      • PIP inflammation may not be noticed.
    • Morning stiffness.
    • Symmetrical peripheral joint involvement.
  • Prominent periarticular osteopenia.

Joints Involved

  • Atlanto axial dislocationSpecific
  • Upper Limb: 
    • MCP > Wrist > PIP
  • Lower Limb: 
    • Knee and Hip.
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Diagnosis

  • Elevated CRP and ESR
  • Rheumatoid Factor/RA factor
    • Most sensitive marker.
    • IgM class antibody,
    • 5% false positive,
    • can be positive in sore throat
  • Anti-CCP (Cyclic Citrullinated Peptide): 
    • Most specific marker.
    • positive → erosive arthritis

Monitoring:

  • Follow up for next 6 weeks.

X-ray Findings

  1. Narrowed Joint Space.
  1. Osteopenia
  1. Juxta-articular Osteoporosis
      • Generalized bone thinning near joints.
  1. Marginal Erosions.
  1. Absence of Sclerosis/Osteophytes
      • differentiates from OA

Deformities in RA

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  • Involves small joints of hand:
    • MCP > wrist joint > PIP
    • Note: Rheumatic fever involves large joints (ankle, knee).
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1. Boutonniere's Deformity

  • Flexion at PIP joint.
  • Hyper extension at DIP joint.
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2. Swan-neck Deformity: 

  • Flexion at DIP joint.
  • Hyper extension at PIP joint.
  • SFD (Street food of delhi) → Swan neck → Flexion at distal
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3. Z thumb Deformity: 

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  • Fingers deviated to ulnar side;
  • metacarpals deviated to radial side.
  • Z-thumb deformity/Hitch Hiker thumb deformity.
  • Different from Z-line deformity (ulnar deviation).
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NOTE:

  • Mallet finger:
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    • Flexion at DIP, no deformation at PIP.
    • Seen in wicket-keepers (injury to extensor tendon, not part of RA).
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4. Windswept Deformity: 

  • Both knees face the same side.
 
  • Windswept deformity
    • (valgus on one side, varus on the other).
      • Children/Overall:
        • Rickets (m/c).
      • Adults:
        • Rheumatoid Arthritis (m/c)
      • Mnemonic: Kaatadichapo kunjnugal rocket (ricket children) pole poi, Adult Room adachitt (RA)
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5. Hallux Valgus: 

  • Lateral deviation of the great toe.
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6. Hammer Toes: 

  • Deformity of the
      1. second,
      1. third, or
      1. fourth toe,
      1. where the toe is bent at the middle joint.

7. Bilateral Genu Valgum (knock-knees).

Management (erosive arthritis):

  • Aggressive treatment.
  • NSAIDs
  • Triple therapy:
    • Start with Methotrexate (MTX).
      • If good response
        • continue.
      • If no response,
        • add Hydroxychloroquine and Sulfasalazine.

Extra-Articular Manifestations

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  • Rheumatoid Nodules:
    • Most common extra-articular manifestation.
    • Extensor distribution (olecranon process, occiput, spine tips, dorsum of hand).
  • Eye Manifestations:
    • Keratoconjunctivitis sicca.
  • Spinal Risk:
    • Avoid yoga/spinal movements/sports (neck rotation, headstand).
      • Risk of atlantoaxial subluxation
    • Cause spinal cord compression and quadriplegia.
  • Cardiovascular Manifestations:
    • Rheumatoid nodules in heart
      • between SA and AV node, causing 1st-degree heart block
    • Damage to myocardium.
    • Accelerated atherosclerosis
      • important cause of death
    • Note: Aschoff nodules in rheumatic fever.
  • Respiratory Manifestations:
    • Rheumatoid nodules in lungs.
    • Pleuritis/pleural effusion (exudative).
    • Light’s criteria for exudative effusion:
        1. Pleural fluid protein/serum protein >0.5
        1. Pleural fluid LDH/serum LDH >0.6
        1. Pleural fluid LDH >2/3rd upper reference limit of normal for serum.
  • Hematological:
    • Anemia of chronic disease (normocytic normochromic & microcytic hypochromic).
  • Peripheral Nervous System:
    • Mononeuritis multiplex (multiple peripheral nerves involved).

Morning stiffness d/ds:

  • 2 conditions
      1. Severe in RA
          • difficulty brushing teeth,
          • getting late for office
      1. Ankylosing spondylitis
          • stiffness reduces with activity

Chylothorax

  • L subclavian vein catheterization
  • Lymphatic leaks
  • Triglyceride > 110 mg/dl
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Pseudo chylothorax

  • Seen in RA
  • Normal TGCholesterol crystals +

Scleromalacia Perforans

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  • Description:
    • Anterior necrotising scleritis without inflammation.
  • Presentation:
    • No redness/pain,
    • progressive atrophy → leading to scleral perforation.
  • Most common in:
    • Women with rheumatoid arthritis.
  • If no h/o RAStaphyloma


Treatment of RA

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  • For B cell ⛔R/o hep B
  • For TNF α ⛔R/o TB
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  • NSAIDs and Steroids
    • ↓ Pain and Inflammation
    • No effect on disease Progression
    • Fast acting
  • DMARDs or SAARDs
    • Slow down the disease progression
    • Slow acting
    • Used now
        1. Methotrexate (DOC)
        1. Sulfasalazine
        1. Leflunomide
        1. Hydroxychloroquine
    • Mnemonic - sulfikkar () met () and left () gave water with chlorine ()
  • Biological agents
    • TNF alpha inhibitors
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Spondyloarthropathies (Sero-negative)

  • General Characteristics
    • Type: Inflammatory arthritis affecting the spine and other joints.
    • Rheumatoid FactorNegative.
    • General Features:
      • Young males > Females.
      • HLA-B27: Positive.
      • Extra-articular symptoms: Uveitis (inflammation of the eye).
  • Conditions Involved
      1. Ankylosing Spondylitis (m/c): 
        1. Most common.
      1. Enteropathic Arthritis
        1. Associated with inflammatory bowel disease.
      1. Psoriatic Arthritis
        1. Associated with psoriasis.
      1. Reactive Arthritis
        1. Triggered by infections (e.g., Shigella, Chlamydia).
    • Note: Rheumatoid arthritis
      • is a/w scleritis,
      • not uveitis.

Reactive Arthritis (Reiter's Disease)

Q. A 4-year-old girl presented with pain in the left knee and ankle along with some swelling and restriction of movements. There is a history of fever and blood in stools 4 weeks ago. What is the probable diagnosis?
  • HLA Association: HLA-B27 and B51

Definition

  • *Joint inflammation caused by sterile inflammation reaction
    • following a recent entropathic or urogenital infection**.

Triggered by:

  • GI infection,
  • non-gonococcal urethritis (sexually acquired reactive arthritis),
  • HIV patients

Triad of Features

Keratoderma Blennorrhagicum
Keratoderma Blennorrhagicum
Circinate Balanitis
Circinate Balanitis

Mnemonic:

  • Cant see
    • Conjunctivitis (non-gonococcal, esp. Chlamydia)
  • cant pee
    • Urethritis
    • Circinate Balanitis:
      • Superficial erosions on glans/penis
  • cant climb a tree
    • Polyarthritis:
      • >1 month,
      • non-suppurative,
      • lower limbs (post GI/urethritis infection)
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    • Keratoderma Blennorrhagicum:
      • Hyperkeratotic papules on palms and soles

Treatment

  • Physical therapy and rehabilitation.
  • NSAIDs.
  • Intra-articular steroid injection in severe cases.

Ankylosing Spondylitis (AS)

Uveitis A/w HLA B27 - associated arthritis = JRAP

  • Ankylosing Spondylitis
  • Psoriatic arthritis
  • Reiter's syndrome/Reactive arthritis.
  • JIA

Also Known As:

  • Marie-Strümpell Disease.
  • Bechterew's Disease.
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ANS
Ochronosis ??

CARROT STICK #

  • ANKYLOSING SPONDYLITIS
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Schober test:

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  • 2 marks
    • 1st → mark at posterior superior iliac spine +
    • 2nd → 10cm above
  • Reveals spine involvement (flexion not possible).
  • Normal person:
    • Spine flexible,
      • gap increases to 15cm on bending
  • In patient:
    • Flexion limited
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Antibody:

  • Targets cytosolic 5' nucleotidase.

Pathology: 

  • Enthesopathy
    • inflammation where tendons or ligaments attach to bone
      • Cause enthesitis affecting Achilles tendon
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Presentation

  • Young male with low backache.
    • Morning Stiffness: 
      • Improves with activity (distinguishes from RA).
    • When he stands or puts his foot on the ground, there is pain in the foot or sole.
    • Decreased Lumbar Spine Movement.
    • Sacroiliitis:
      • Juxta-articular erosion.
      • Blurring of margins.
      • Sclerosis leading to joint fusion.
  • Involvement: Axial > Peripheral joints.
    • Most commonly affects Sacro-iliac (SI) joint (m/c).
    • Also affects spine and hip.
    • Starts in sacro-iliac joint.
    • Spine fused by syndesmophytes anteriorly and posteriorly.
  • History of red eye (anterior uveitis - extra-articular manifestation).

X-ray

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  • It shows sacroiliitis.
  • If the disease is progressive, it shows a large number of osteophytes present.
  • Calcification present in paravertebral ligaments.
    • Causes bamboo spine.

Bamboo Spine

  • Fusion and squaring of the spine due to:
    • Calcification between vertebrae, restricting movement.
    • Inflammation → syndesmophyte formation
      • (vertical/bridging syndesmophytes)
    • → fusion anteriorly and posteriorly
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Dagger Sign

  • Calcification of only the interspinous ligament.
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Trolley Track Sign

  • Calcification of paraspinal ligaments and interspinous ligaments.

Enthesopathy

  • Tendons like the Achilles tendon involved → tendinitis
    • complaints of heel pain.

Cardiovascular Manifestation

  • Valvular aortic regurgitation.

Lung Manifestations

  • Stiffness of costochondral joint.
  • Extra parenchymal restrictive lung disease.
    • No proper exhalation
    • So residual volume is increased.
  • In contrast, in parenchymal restrictive lung disease, there is fibrosis of the lung.

HLAB27 Test = JRAP

  • Positive.
  • HLAB27 is also Positive in:
    • Juvenile rheumatoid arthritis.
    • Ulcerative colitis.
    • Reiter syndrome/Reactive arthritis.

MRI:

  • Most sensitive.
    • Bone marrow edema is seen first.
    • STIR-MRI identifies bone marrow edema.

Clinical Tests

  • Decreased Chest Movements.

For Testing Lumbar Spine Motility:

  • Schober Test/Modified Schober Test:
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    • Measures distance between two points on the spine
    • from standing to full flexion;
    • in AS,
      • distance does not increase due to fusion.
  • Note on Non-Erosive Arthritis (e.g., SLE): 
    • Joint inflammation occurs,
    • no loss of articular cartilage or destruction of subchondral bone.

For Sacroiliitis:

  • Gaenslen's Test.
  • FABER Test (Flexion, Abduction, External Rotation) / Figure-of-4 Test.
  • Pump Handle Test.

Treatment

  • NO ROLE OF DMARDS
  • Infliximab.
  • NSAIDs → Biologicals
  • Monoclonal antibody TNF α agonist. Reactive arthritis.

Psoriatic arthritis

  • Pencil-in-cup deformity.
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Crystal Deposition Arthropathies

Gout

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Gout as a Disease

  • Precipitates crystals in the joint space of the patient.
  • local erosive lesion
    • 1st metatarsal phalangeal joint in the patient.
  • Because of recurrent flare up of acute gout.

Pathogenesis

  • Metabolism: 
    • Abnormality in purine metabolism.
  • Uric Acid (UA): 
    • Increased uric acid production (normal values: 3.5 to 6.5 mg/dL).
  • Mechanism: 
    • Sudden change in UA levels
    • Deposition of crystals in cold peripheral joints
    • Local inflammatory reaction
    • Collateral damage and pain.

Clinical Features

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  • Most Common Joint: 
    • First MTP joint of the big toe.
  • Preponderance:
    • Middle-aged, male > female.
    • Associated with consumption of alcohol, red meat, and chemotherapy.
  • Symptoms:
    • Acute gouty pain,
    • often forming tophi (urate crystal deposits).

Joint Aspiration

  • IOC (Investigation of Choice) for acute gouty attack.
  • Fluid-Turbid.

Characteristics of Crystals:

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  • Monosodium Urate (MSU).
  • Needle-shaped.
  • Negatively birefringent on polarizing light microscopy
    • crystals appear yellow when parallel to the filter
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Pseudo gout

  • Positive birefringence crystals in polarised microscopy are seen in
    • Rhomboid shaped
    • Ca pyrophosphate
  • That involves knee joint.
  • Chondrocalcinosis Calcification of meniscus
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  • Mnemonic: Miss U → Needles (needle-shaped), Negatively birefringent, Yellow (when parallel).

X-ray Findings:

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  • 1st MTP.
    • Podagra.
  • On X-ray foot:
    • Overhanging/Martel's Sign/Rat bite erosions
      • Erosions with overhanging edges
    • Punched-out Lesions.
  • Joint Destruction.
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  • In the skull, vertebra, and pelvis are usually present in multiple myeloma.

DECT (dual energy)

  • Helps identify uric acid deposits.

Tests Done Are

  • Serum uric acid: Elevated.
    • In both overproducer & in under excreter.
  • 24 hours urinary uric acid value is used to differentiate b/w
    • Overproducer &
    • Under excreter

Management

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Acute Gout Attack:


1. NSAIDs

  • DOC: Indomethacin
  • Mnemonic: Indian Goat
  • DO NOT USE aspirin and paracetamol
  • Avoid Aspirin (→ ↑↑ UA levels/crystallization → ⛔ tubular secretion of UA in low doses)

2. Steroids:

  • If NSAIDs do not work OR
  • Indomethacin (COX-1 inhibitor) allergy

3. Colchicine

  • Most effective drug
  • MOA:
    • Inhibits phagocytosis /granulocyte migration
      • ⛔ microtubules → ↓↓ chemotaxis → ⛔ migration of leukocytes
        ↓↓ IL-1 release from neutrophils
  • S/E:
    • Can cause myopathy and diarrhoea
    • Bone marrow suppression
    • Alopecia

Chronic Gout:

Drugs decreasing production of uric acid


  • Inhibit xanthine oxidase
    • Allopurinol
      • DOC for chronic gout
      • Not used in acute gout
      • If kidney function is normal
    • Febuxostat
      • Avoid in MI
  • For Overproducer
  • Avoid a nonvegetarian diet.
  • Certain vegetarian food should also be avoided.

Drugs increasing excretion of uric acid (Uricosuric agents)


  • For under excreter
  • Probenecid, Sulfinpyrazone, Lesinurad
    • Aspirin ⛔ Uricosuric action of Probenecid
    • ↑↑ Action of Penicillin
  • Plenty of fluids should be taken
  • Mnemonic: Goat (Gout, lerinurAaadu) pee cheyyan Probe () cheyyum
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  • S/E:
    • ↑ urate stones
    • ↑ calcium stones
    • Precipitate acute gout

  • Probenecid:
    • ⛔penicillin secretionProlong action
  • Aspirin
    • Uricosuric action of Probenecid

Drugs increasing metabolism of uric acid


Feature
Rasburicase
Pegloticase
Source
Recombinant urate oxidase (uricase)
PEGylated recombinant urate oxidase
Main Use
Prevention & treatment of TLS
Refractory chronic gout
fastest urate lowering agents
Long acting uricase
Route
IV
IV (every 2 weeks)
Contraindication
G6PD deficiency
G6PD deficiency
Adverse Effects
Hemolysis, methemoglobinemia, hypersensitivity
Infusion reactions, anaphylaxis, antibodies
  • Converts uric acid → allantoin (more soluble, easily excreted).
  • Mnemonic: Goat food (to ↑ metabolism) → Rasberry Pie (Rasburicase, pegloticase) in a case ()
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Allopurinol

  • DOC:
    • Chronic gout
    • Tumor Lysis Syndrome
    • Lesch-Nyhan Syndrome
      • Defective purine metabolism
    • Organ transplant
  • Side effects:
    • Hypersensitivity (severe):
      • Stevens-Johnson Syndrome (associated with HLA-B*5801)
    • Orotate decarboxylase inhibition:
      • Causes orotic aciduria
    • DRESS syndrome
    • Mnemonic: Allu (Allopurinol) arjun → Johnson (SJS) powder → Dress up () and Oridath irunn (Orotic aciduria) muthram ozhich
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Pseudo-Gout

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X-ray: 

  • Chondrocalcinosis 
    • calcification of articular cartilage

General Features

  • Prevalence: Most common in elderly patients.
  • Gender: Female > Male.
  • Association: Associated with hypothyroidism.
  • Involvement: Most commonly affects the knee joint (large joints).

Investigations

  • Synovial Fluid Aspirate:
    • Crystals: Calcium Pyrophosphate Dihydrate (CPPD) crystals.
    • Shape: Polygonal.
    • Birefringence: Positive birefringence (crystals appear blue when parallel to the filter).
    • Mnemonic: PseudoGout: Positive, Polygonal, Blue (when parallel).

Charcot's Arthropathy

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  • Associated with neuropathic joint.
  • Sensations are lost.
  • m/c - Long standing diabetes
  • M/c bone affected - Tarsal
  • Painless, progressive swelling
  • Ankle commonly affected
  • Rocker bottom feet deformity
  • X-ray:
    • Joint destruction
    • New bone formation
    • Loose bodies
  • 6 D's:
    • Distension of joint
    • Destruction
    • Debris
    • Dislocation
    • Deformity
    • Normal/ Increased bone density

Loose Bodies in joints

  • M/c/c in adults: Osteoarthritis
  • M/c/c in children: Osteochondritis dissecans
  • O/c: RA, Charcots arthritis, FBs

Licked candy appearance

  • also seen in leprosy.
    • Mnemonic: Charcot → Chocobar → Lick cheyth
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  • 51 (HLA B51) yr old Nolan (Anti enolase) on a Bus (behcets)
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