Long Answer Questions
Q.1 Describe supracondylar fracture humerus in children under clinical features, management and complications.
+A. CLINICAL FEATURES
1. History
Typically caused by a fall on an outstretched hand. Child presents with pain, swelling, deformity, and inability to move the elbow.
2. Examination
Early presentation:
- Posterior prominence of olecranon due to distal fragment tilt.
- Three-point bony relationship is maintained.
Late presentation:
- Swelling may obscure deformity.
- Assess for vascular injury – absent radial/ulnar pulses, signs of ischemia (5 P’s).
- Check for nerve injuries:
- Median nerve – pointing index.
- Radial nerve – wrist drop.
3. Radiological Features
- Anteroposterior (AP) view: Proximal shift, medial/lateral tilt, rotation of distal fragment.
- Lateral view: Posterior displacement/tilt and rotation of distal fragment.
B. MANAGEMENT
1. Undisplaced Fractures
Immobilization with above-elbow slab at 90° flexion.
2. Displaced Fractures
Require hospital admission due to risk of early complications.
a) Closed Reduction and Percutaneous K-wire Fixation
- Most common method for displaced fractures.
- Reduction done with 30-40° elbow flexion and supinated forearm.
- K-wires inserted percutaneously under image guidance.
- Posterior slab applied for 3 weeks.
- Follow-up X-rays at 48 hours and 1 week.
b) Open Reduction and K-wire Fixation
- Indicated when closed reduction fails or fracture redisplaces.
- Also used for open fractures or brachial artery exploration.
c) Continuous Traction
- Used in late presentation with swelling or open wounds.
- Methods: Smith’s traction (K-wire through olecranon), Dunlop’s traction (skin traction).
- Rarely used in modern practice.
C. COMPLICATIONS
1. Immediate Complications
- Brachial artery injury: Compression or transection may lead to ischemia or gangrene. Requires vascular repair.
- Nerve injury: Median nerve most commonly affected. Usually recovers spontaneously.
2. Early Complications
Volkmann’s Ischemia:
- Ischemia of forearm flexors due to brachial artery occlusion.
- Symptoms: Severe pain, stretch pain, inability to move fingers, tender forearm.
- Treatment:
- Remove tight bandages.
- Elevate limb, encourage finger movement.
- Fasciotomy if no improvement in 2 hours.
3. Late Complications
- Malunion: Results in cubitus varus (gunstock deformity). Treatment: Corrective supracondylar osteotomy if severe.
- Myositis Ossificans: Ectopic bone formation from aggressive physiotherapy or massage. Treatment: Rest and gentle mobilization; late cases may need excision.
- Volkmann’s Ischemic Contracture (VIC): Fibrosis of forearm muscles causing wrist/finger deformity.
- Mild: Passive stretching and Volkmann’s splint.
- Moderate: Maxpage operation (soft tissue release).
- Severe: Bone surgery like carpal excision or forearm shortening.
Q.2 Describe Pott's spine and its management.
+A. Pott's Spine
Pott’s spine, or tuberculosis of the spine, is the most common form of skeletal tuberculosis. The dorso-lumbar region is most frequently affected.
B. PATHOPHYSIOLOGY
Tuberculosis of the spine is always secondary. Bacilli reach the vertebral column via the haematogenous route from a primary focus (lungs or lymph nodes), primarily through Batson’s plexus — a valveless venous network connected to the abdominal visceral plexus.
Types of Vertebral Tuberculosis
- Paradiscal (most common): Involves adjacent vertebrae and the intervening disc.
- Central: Affects a single vertebral body; leads to collapse and wedging deformity.
- Anterior: Infection remains in the anterior body and spreads under the anterior longitudinal ligament.
- Posterior: Involves posterior structures—pedicle, lamina, spinous and transverse processes.
Mechanism of Destruction
- Granulomatous inflammation leads to erosion of vertebral margins and disc degeneration.
- Vertebral collapse causes angular kyphosis or gibbus, especially in the dorsal spine.
- Children show faster and more severe destruction due to weaker bones.
Cold Abscess Formation
- Collection of tubercular pus without classical inflammation.
- Tracks posteriorly (spinal canal), anteriorly (prevertebral), or laterally (paravertebral).
- May follow musculo-fascial planes to cause remote swellings.
Healing
Lytic lesions are replaced by new bone and vertebral fusion. Resultant spinal deformities are permanent.
C. MANAGEMENT
Goals: (i) Disease healing, (ii) Prevention and management of complications like paraplegia.
1. Anti-Tubercular Chemotherapy (ATT)
Mainstay of treatment — even effective with abscess or paraplegia.
2. Spine Care
Rest:
- Short-term bed rest for pain relief in early stages.
- Prolonged immobilisation if severe destruction is present.
- Supports: Minerva jacket or collar for cervical spine.
Mobilisation:
- Begins after symptom improvement.
- Supports:
- Cervical collar – cervical spine.
- ASH brace – dorso-lumbar spine.
- Brace discontinued after bony fusion. Strenuous activities avoided for 2 years.
3. Treatment of Cold Abscess
- Small abscesses: Resolve with ATT alone.
- Superficial abscesses:
- Aspiration: Thick needle via anti-gravity zig-zag tract to prevent sinus formation.
- Evacuation: Drainage, curettage of walls, and primary closure. Psoas abscess via extraperitoneal kidney incision.
4. Surgical Intervention
- Progressive neurological deficit.
- Severe spinal deformity.
- Non-responding abscesses.
5. MRC Trial Recommendations (1973–74)
- Bed rest not mandatory.
- Streptomycin not essential.
- POP jacket not beneficial.
- Debridement not routinely helpful.
Short Answer Questions
Q.1 VIC
+Volkmann’s Ischaemic Contracture (VIC)
Definition
VIC is the late sequel of Volkmann’s ischaemia.
The ischaemic muscles in the forearm undergo necrosis and are gradually replaced by fibrous tissue.
This fibrous tissue contracts, pulling the wrist and fingers into a fixed flexion deformity.
If peripheral nerves are also involved, sensory impairment and motor paralysis of the forearm and hand occur.
Clinical Features
1. Appearance
Atrophy of the forearm musculature.
Flexion deformity at the wrist and fingers.
Skin is dry, scaly, and atrophic.
Nails show atrophic changes.
2. Volkmann’s Sign
Helps differentiate the cause of finger flexion deformity.
The patient can extend the fingers fully at the interphalangeal joints only when the wrist is flexed.
On attempting wrist extension, the fingers automatically flex at the interphalangeal joints.
Reason: When the wrist is extended, the already shortened flexor muscle-tendon unit is further stretched, pulling the fingers into flexion.
3. Neurological Signs
Hypoaesthesia or anaesthesia of the hand may be present due to nerve involvement.
Treatment
1. Mild deformities
Passive stretching of contracted muscles.
Use of a turn-buckle splint (Volkmann’s splint) to gradually correct the deformity.
2. Moderate deformities
Soft tissue sliding operations:
Flexor muscles are released from their origin at the medial epicondyle and ulna.
Common procedure: Maxpage operation.
3. Severe deformities
Bony procedures may be required:
Shortening of forearm bones.
Excision of selected carpal bones to reduce deformity.
Q.2 Osteosarcoma (Osteogenic Sarcoma)
+Definition
Second most common primary malignant bone tumour (after multiple myeloma).
A malignant tumour of mesenchymal cells, characterised by the formation of osteoid or bone by tumour cells.
Highly aggressive and rapidly metastasising.
Classification
1. Based on clinical setting
Primary osteosarcoma:
- Commoner type, seen in 15–25 years.
- No pre-malignant conditions associated.
- More malignant than secondary.
Secondary osteosarcoma:
- Occurs in older age (>45 years).
- Develops in association with Paget’s disease, fibrous dysplasia, multiple enchondromatosis, multiple osteochondromas, post-irradiation bone changes, etc.
2. Based on dominant histo-morphology
- Osteoblastic – excessive bone formation.
- Chondroblastic – cartilage cell predominance.
- Fibroblastic – fibroblast predominance.
- Telangiectatic / Osteolytic – lytic, vascular type; most malignant.
General Characteristics
- All osteosarcomas are aggressive and metastasise rapidly via blood, usually to the lungs.
- Lymph node involvement is rare.
- Osteolytic type has worse prognosis than osteoblastic.
- Rarely crosses the epiphyseal plate.
Common Features
Age: 15–25 years (most common primary bone tumour in this age).
Sites: Metaphyseal region, especially lower end of femur, upper end of tibia, upper end of humerus.
Gross pathology:
- Osteoblastic → grey-white, hard, gritty.
- Chondroblastic → bluish-grey, opalescent.
- Fibroblastic → soft, “fish-flesh” sarcoma.
- Telangiectatic → necrosis, blood-filled cavities.
Histology: Anaplastic mesenchymal cells producing osteoid (pathognomonic).
Clinical Features
- Pain – constant, boring, worsening with time.
- Swelling – usually metaphyseal, firm, irregular, warm, and tender.
- Shiny skin with dilated veins over swelling.
- Restricted joint movements due to bulk.
- Pathological fracture may be presenting feature.
- Compression of neurovascular structures may occur.
- Lymph nodes: usually reactive.
Radiological Features
- Irregular metaphyseal destruction with new bone formation.
- Cortical erosion.
- Periosteal reactions: irregular, spiculated.
- Codman’s triangle: sub-periosteal new bone at tumour margins.
- Sun-ray (sunburst) appearance: tumour spicules radiating outward.
Investigations
- Serum alkaline phosphatase (SAP): often raised; useful for follow-up.
- Chest X-ray / CT: to detect pulmonary metastasis.
- Bone scan / MRI / CT: to detect local and skip lesions.
- Biopsy: open, core needle, or FNAC. Osteoid production confirms diagnosis.
Treatment
- Confirm diagnosis – Histology + radiology correlation.
- Assess tumour spread – chest imaging, bone scan, CT/MRI.
- Control of tumour:
- Local control (Surgery)
- Amputation: still mainstay in advanced or inoperable cases.
- Limb-salvage surgery: possible with early detection + wide excision, reconstruction with bone graft/prosthesis.
- Radiotherapy – Limited role; used for inoperable or inaccessible lesions.
- Chemotherapy
- Cornerstone of modern treatment.
- Pre- or post-operative to control micro-metastases.
- Drugs: High-dose methotrexate, citrovorum factor, cyclophosphamide (Endoxan), cisplatin, etc.
- Given in specialised centres due to toxicity.
- Immunotherapy – Experimental: transfer of sensitised lymphocytes.
- Local control (Surgery)
Prognosis
- Without treatment → death within 2 years (often <6 months with metastasis).
- Surgery alone → 5-year survival ~20%.
- Surgery + chemotherapy → survival up to 70% disease-free at 5 years.
- Telangiectatic/osteolytic type → worst prognosis.
Very Short Answer Questions
Q.1 Pump handle test
+Pump-handle test: With the patient lying supine, the examiner flexes his hip and knee completely, and forces the affected knee across the chest, so as to bring it close to the opposite shoulder. This will cause pain on the affected side.
Q. Garre’s osteomyelitis
+This is a sclerosing, non-suppurative chronic osteomyelitis. It may begin with acute local pain, pyrexia and swelling. Pyrexia and pain subside but the fusiform osseous enlargement persists. There is tenderness on deep palpation. There is no discharging sinus. Shafts of the femur or tibia are the most commonly affected.
Importance: Lies in differentiating it from bone tumours, which commonly present with similar features, e.g., Ewing’s tumour or osteosarcoma.
Treatment: Guarded. Acute symptoms subside with rest and broad-spectrum antibiotics. Sometimes, making a gutter or holes in the bone brings relief in pain.
Q.3 Trigger finger/thumb
+This condition results from constriction of the fibrous digital sheath, preventing free gliding of the contained flexor tendon.
Clinical Features
- Initially: pain at the base of the affected finger, especially on passive extension.
- As the sheath thickens: tendon swells proximal to it.
- Locking of finger: swollen tendon cannot enter the sheath when straightening from flexion.
- Locking may be overcome by:
- Strong effort → finger extends with a snap (like a trigger).
- Passive extension with the other hand.
Treatment
- Early stage → local ultrasonic therapy.
- Persistent pain → local hydrocortisone injection.
- Long-standing cases → surgical splitting of tight tendon sheath.
Q.4 Volkmann’s sign
+Volkmann’s sign helps in determining the cause of flexion deformity of the fingers.
Description
- Full extension of fingers at the interphalangeal joints is possible only when the wrist is flexed.
- On extending the wrist, the fingers automatically flex at the interphalangeal joints.
Reason
When the wrist is extended, the shortened flexor muscle–tendon unit is further stretched over the front of the wrist, which pulls the fingers into flexion.
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