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PSIQUIATRIA INFANTIL

In document AREA TEMATICA - PROFESION- ESPECIALIDAD (página 95-109)

This is a chronic inflammatory disease of the spine and sacroiliac joints. There is predominance in young males and the condition is associated with HLA B27 (positive in 95%).

Causes

The exact cause and pathophysiology of this condition are not known. However, it is thought to be associated with HLA B27.

Signs and symptoms

Question mark posture.

Bamboo spine: due to calcification of ligaments.

Pain and stiffness: symptoms improve with exercise.

Investigations

Bloods: seronegative for rheumatoid factor.

Radiology: CXR and MRI scan assess changes in the spine.

Treatment

Conservative: patient education. Refer to physiotherapy.

Medical: analgesia (NSAIDs) and DMARDs, e.g. sulphasalzine (first line).

Surgery: corrective spinal surgery.

Complications

Osteoprosis.

Spinal fractures.

Increased risk of cardiovascular disease, e.g. stroke and myocardial infarction.

MAP 10.3 Spondyloarthropathies (Continued )

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Musculoskeletal System

Map 10.3 Spondyloarthropathies PSORIATIC ARTHRITIS

What is psoriatic arthritis?

This is an inflammatory arthritis that is associated with the skin condition psoriasis. It is associated with HLA B27. The signs and symptoms also depend on how and where the joints are affected. Accordingly, psoriatic arthritis may be split into 5 subtypes:

1 Asymmetrical oligoarthritis (distal and proximal interphalangeal joints). 2 Symmetrical rheumatoid-like arthropathy.

3 Ankylosing spondylitis variant. 4 Polyarteritis with skin and nail changes. 5 Arthritis mutilans.

Causes

The exact cause is unknown. It is thought to be due to an inflammatory process coupled with genetic involvement of the HLA B27 gene. The greatest risk factor is a family history of psoriasis.

Signs and symptoms

Psoriasis: well-demarcated salmon-pink plaques with evidence of scaling. These plaques are usually present on the extensor surfaces (chronic plaque psoriasis) but sometimes smaller plaques may occur in a raindrop pattern over the torso. This is called guttate psoriasis and is often preceded by an upper respiratory tract infection/sore throat that is caused by Streptococcus.

Joint pain and stiffness.

Swelling of affected joints.

Nail changes: there are 4 nail changes noted in psoriasis: yellowing of the nail, onycholysis, pitting and subungual hyperkeratosis.

Investigations

Psoriasis is a clinical diagnosis.

Bloods: seronegative for rheumatoid factor.

Radiology: ‘Pencil-in-cup’ deformity on hand X-ray. X-ray of affected joints to assess severity.

Treatment

Conservative: patient education. Refer to physiotherapy. Explain to patients that psoriasis does not have a cure and control of the disease is more realistic.

Medical: analgesia (nonsteroidal anti-inflammatory drugs [NSAIDs]) and disease modifying antirheumatic drugs (DMARDs), e.g. methotrexate (first line). Manage psoriasis.

Surgery: rarely joint replacement.

Complications

Neurological manifestations if atlanto–axial joint involvement.

Joint destruction.

ENTEROPATHIC ARTHROPATHIES

What are enteropathic arthropathies?

This is an arthritis that develops in association with inflammatory bowel disease (IBD). It is indistinguishable from reactive arthritis.

Causes

The exact cause and pathophysiology of this condition are not known. However, it is thought to be associated with HLA B27.

Signs and symptoms

Those of IBD, see page 40.

Spondylitis.

Sacroiliitis.

Peripheral arthritis: usually of large joints.

Investigations

Those for IBD, see page 40.

Radiology: X-ray of affected joint. Assess severity.

Treatment

Analgesia (NSAIDs).

Treatment of IBD, see page 40.

Complications

Severely decreased mobility with axial involvement.

ANKYLOSING SPONDYLITIS What is ankylosing spondylitis?

This is a chronic inflammatory disease of the spine and sacroiliac joints. There is predominance in young males and the condition is associated with HLA B27 (positive in 95%).

Causes

The exact cause and pathophysiology of this condition are not known. However, it is thought to be associated with HLA B27.

Signs and symptoms

Question mark posture.

Bamboo spine: due to calcification of ligaments.

Pain and stiffness: symptoms improve with exercise.

Investigations

Bloods: seronegative for rheumatoid factor.

Radiology: CXR and MRI scan assess changes in the spine.

Treatment

Conservative: patient education. Refer to physiotherapy.

Medical: analgesia (NSAIDs) and DMARDs, e.g. sulphasalzine (first line).

Surgery: corrective spinal surgery.

Complications

Osteoprosis.

Spinal fractures.

Increased risk of cardiovascular disease, e.g. stroke and myocardial infarction.

MAP 10.3 Spondyloarthropathies (Continued )

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162 Map 10.4 Gout

What is gout?

Gout is an inflammatory crystal monoarthropathy caused by the deposition of urate crystals. These monosodium urate crystals often

precipitate in the metatarsophalangeal joint (MTPJ). Gout involving the big toe is known as a podagra.

Causes

There are many causes of gout but essentially anything that increases urate levels may be the underlying cause. Some examples include,

HorrificDELAY:

Hyperuricaemia, Hereditary.

Diuretics (thiazides).

Ethanol.

Leukaemia.

renAl impairment.

associated with Lesch–NYhan syndrome.

Signs and symptoms

Calor, dolor, rubor and tumour (heat, pain, redness and swelling) of the affected joint, which is usually the MTPJ in 50% of patients.

Tophi (urate deposits) may be present on tendon surfaces, e.g. the elbow, or visible on the ear.

Patients may have symptoms of renal calculi.

Investigations

Bloods: serum urate levels, FBC, WCC, U&Es, creatinine, ESR, CRP.

GFR: assess kidney function.

Synovial fluid analysis: positive if birefringent monosodium urate crystals seen.

Characteristic Pseudogout Gout

Joints affected Larger proximal Classically 1st MTPJ Crystal type Calcium

pyrophosphate crystals

Sodium urate crystals

Crystal shape Rhomboid Needle Light microscopy Negative

birefringence

Strongly positive birefringence

Pseudogout vs. gout Complications

Joint damage.

Renal calculi.

Tophi formation.

Treatment

Conservative: patient education. Lifestyle advice, e.g. encourage alcohol reduction and a low purine diet. Review medications that the patient is taking and stop causative agents, e.g. thiazide diuretics, if possible.

Medical:

Analgesia.

Acute: colchicine and steroids.

Chronic: allopurinol. Febuxostat may be used if allopurinol is not tolerated by the patient.

MAP 10.4 Gout

163

Musculoskeletal System

Map 10.4 Gout What is gout?

Gout is an inflammatory crystal monoarthropathy caused by the deposition of urate crystals. These monosodium urate crystals often

precipitate in the metatarsophalangeal joint (MTPJ). Gout involving the big toe is known as a podagra.

Causes

There are many causes of gout but essentially anything that increases urate levels may be the underlying cause. Some examples include,

HorrificDELAY:

Hyperuricaemia, Hereditary.

Diuretics (thiazides).

Ethanol.

Leukaemia.

renAl impairment.

associated with Lesch–NYhan syndrome.

Signs and symptoms

Calor, dolor, rubor and tumour (heat, pain, redness and swelling) of the affected joint, which is usually the MTPJ in 50% of patients.

Tophi (urate deposits) may be present on tendon surfaces, e.g. the elbow, or visible on the ear.

Patients may have symptoms of renal calculi.

Investigations

Bloods: serum urate levels, FBC, WCC, U&Es, creatinine, ESR, CRP.

GFR: assess kidney function.

Synovial fluid analysis: positive if birefringent monosodium urate crystals seen.

Characteristic Pseudogout Gout

Joints affected Larger proximal Classically 1st MTPJ Crystal type Calcium

pyrophosphate crystals

Sodium urate crystals

Crystal shape Rhomboid Needle Light microscopy Negative

birefringence

Strongly positive birefringence

Pseudogout vs. gout Complications

Joint damage.

Renal calculi.

Tophi formation.

Treatment

Conservative: patient education. Lifestyle advice, e.g. encourage alcohol reduction and a low purine diet. Review medications that the patient is taking and stop causative agents, e.g. thiazide diuretics, if possible.

Medical:

Analgesia.

Acute: colchicine and steroids.

Chronic: allopurinol. Febuxostat may be used if allopurinol is not tolerated by the patient.

MAP 10.4 Gout

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Musculoskeletal System

164

Osteoma

Location: skull.

Associated with Gardner’s syndrome (this syndrome is associated with the APC gene on chromosome 5).

Giant cell tumour

Location: epiphysis (long bones).

Soap bubble appearance.

Ewing’s sarcoma

Location: diaphysis (long bones), pelvis, scapula, ribs.

Onion skin appearance.

Very aggressive.

Predominance in children.

Osteoblastoma

Location: vertebrae.

Similar to osteoid osteoma.

Benign Malignant

Enchondroma

Location: intramedullary bone.

Cartilaginous neoplasm.

Seen in phalanges.

Osteochondroma

Location: metaphysis (long bones).

Most common benign bone lesion.

Chondrosarcoma

Location: medullary cavity of femur, humerus, tibia, pelvis, scapula, spine, skull and craniofacial area.

Osteoid osteoma

Location: femur and tibia, phalanges and vertebrae.

Intracortical lesion best differentiated on CT.

Nidus.

Osteosarcoma

Location: metaphysis (long bones).

Risk factors: Paget’s disease, radiation, familial retinoblastoma.

Predominance in children.

Bimodal: 75% <20 years; increases >60 years.

In document AREA TEMATICA - PROFESION- ESPECIALIDAD (página 95-109)

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