Hand Flashcards
Hand schpiel:
Today I examined ____.
He/she had evidence of a symmetrical/asymmetrical, deforming/non-deforming arthropathy involving x joints.
There was evidence/no evidence of disease activity and sparing/involvement of the DIPJ’s.
Extra-articular features included ____.
This leads me to a diagnosis of ____ but there are other differentials.
My findings in more detail are ____.
RA signs
- Ulnar deviation MCP/wrist
- Swan neck deformity
- Boutonnier’s deformity
- Z-deformity
OA signs
- Heberden’s nodes
- Bouchard’s nodes
- Squaring of the MCP joints
Psoriatic arthritis signs
- Sausage digits/dactylitis
Cases
- RA (29%)
- Limited Scleroderma/Scleroderma (19%)
- Psoriatic Arthropathy (10%)
- Ankylosing Spondlyitis (8%)
- Gout (3%)
- Haemochromotosis/SLE (2%)
Extra articular manifestations of RA:
- face (anaemia, dentition, eyes)
- chest (fibrosis, pleural effusions)
- heart (PHT, MR, AR)
- abdomen (splenomegaly, injection sites)
- pydoderma gangrenosusm
Seronegative arthropathy signs:
- face (anaemia)
- abdomen (stoma)
- spine (axial disease)
Gout areas:
- elbows & ears (tophi)
- other joints
- ? underlying cause
Scleroderma steps:
- diffuse vs limited
- blood pressure
- face (alopecia, anaemia, bird-life facies, oral diameter, telangiectasia)
- abdomen (hepatosplenomegaly)
- chest:
- skin
- pulmonary fibrosis
- signs of Pul HTN
- cardiac failure
Dermatomyositis
- Gottren’s sign (hands
- Mechanic hands
- Heliotrope rash (eyelids)
- Shawl sign (back and shoulders)
- Neuro upper and lower limb (power)
- Respiratory exam
Causes of deforming polyarthopathy (6):
- RA
- SLE
- Gout
- OA
- PsA
- Scleroderma
DIP involved (4):
- Gout
- PsA
- OA
- Scleroderma
DIP not involved (2):
- RA
- SLE
Where are Psoriatic plaques:
- Scalp
- Ears
- Elbows
- Umbilicus
- Genitalia
- Gluteal cleft
- Knees
- Finger nails and toe nails
Hand X-rays
- D emographics & DIPs
- S - oft tissue
- A - lignment
- B - one mineralisation & production
- C - artilage (joint space) & calcification
- D - istribution
- E - rosions
RA main findings on XR
- soft tissue swelling (swelling fusiform)
- juxta-articular osteopenia (becomes more generalised as the disease progresses
- initial joint space widening secondary to effusions; then become narrowed (concentric rather then eccentric)
- erosions initially at areas not covered by cartilage (intracapsular articular margins), then marginal erosions
PsA main findings on XR
- asymmetric destruction of the DIPs with bony ankylosis
- no or minimal juxta-articular osteopenia
- bone proliferation near joints and ligaments or tendon insertion sites (enthesis)
- bone erosions beginning in the periarticular region and progressing to more central areas
- soft tissue swelling (dactylitis)
- resorption of the terminal phalangeal tufts
- osteolysis of the bone with telescoping of the digit
Gout main findings on XR
- asymmetric soft tissue swelling
- juxta-articular erosions with sclerotic margin
- rat-bite appearance to erosions
Reporting back (hand):
- Intro - make the call, active vs non active, cx of disease, rx
- Look
- Feel
- Move
- Extra-articular
- Summary
- Relevant investigations (with likely results; straight forward stuff first)
- Keep talking!
RA extra-articular manifestations:
- MSK: examine other joints (shoulder, elbows, knees and feet).
- Cervical spine: atlantoaxial subluxation (cervical myelopathy).
- Eyes: episcleritis, scleritis, Sjogren’s
- Anaemia: conjunctival pallor
- Lungs: pleural effusion, pulmonary fibrosis, Caplan’s syndrome, bronchiectasis
- Heart: pericarditis, VHD
- Skin: pyoderma gangrenosum
- Abdomen: splenomegaly (Felty’s syndrome), hepato-splenomegaly (secondary amyloidosis)
- Kidney’s: nephrotic syndrome (oedema and proteinurina)
- Nervous system: mononeuritis multiplex, polyneuropathy
Causes for anaemia in RA
- Anaemia of chronic disease
- Fe-deficiency (GI loss secondary to NSAIDs)
- Folate deficiency secondary to MTx
- Pernicious anaemia (associated with AI disease)
- BM suppression (gold, sulphasalazine, MTX and penicillamine)
- Felty’s syndrome
- AI haemolytic anaemia
- Anaemia of renal disease
Organ systems involved in Scleroderma:
- Skin: RP, sclerodactyly; soft tissue atrophy, calcinosis, nail dystrophy, ulceration, grangrene, flexion deformities, oedema, telangiectasia, vitiligo, morphoea, pigmentation and pruritis.
- MSK: arthritis, myositis, myopathy, intra-articular calcification, osteopenia.
- GI: dysphagia, GORD, intestinal hypomotility –> bacterial overgrowth –> steatorrhoea and malabsorption, pneumatosis coli, colonic diverticulae, bowel obstruction, PBC.
- Renal: malignant HTN, GN, renal crises.
- Respiratory: ILD, restrictive lung defects, pleural effusions, atelectasis.
- CV: restrictive CM (myocardial fibrosis), pericarditis, pericardial effusions, pulmonary HTN, conduction defects.
Diagnostic criteria for scleroderma:
- Major: skin sclerosis affecting arms, face and/or neck
- Minor: sclerodactyly, flinger pulp atrophy, bilateral pulmonary fibrosis.
1 MAJOR or 2 MINOR criteria are required to make a diagnosis.
Nerve function in hands (3)
- Thumb up - median
- Finger abduction - ulnar
- Wrist extension - radial
DDx back exam (5)
- Ank Spond
- PsA with axial involvement
- Enteropathic - IBD-stoma
- Reactive
- DISH - diffuse idiopathic skeletal hyperostosis
- OA