Complications of Fractures of Proximal Humerus

Complications in fractures of proximal humerus are more likely after surgical than after nonoperative fracture care. Therefore a careful postoperative follow-up is necessary to note the complication at the earliest and intervene at the right time

Most common complications associated with fractures of proximal humerus are- [Read more...]

Pigmented Villonodular Synovitis

In this disease, the synovial membrane proliferates and its surface develops nodules and villi. It also turns into brown colour.

The cause of the condition is unknown. It is thought to be an inflammatory process. It occurs most commonly in young adult.

Two primary forms are described

  • Diffuse form that affects the entire synovial lining
  • Localized form.

The diffuse form is most common and  involves the large joints, while the localized form typically occurs around the small joints of the hands and feet. [Read more...]

Popliteal Cysts – Diagnosis and Treatment

Diagnosis of politeal cyst is usually evident on clinical examination. Conventional radiography in the anteroposterior, lateral, and oblique projections is done to check fluid density and to rule any other lesion that might give rise to poplliteal swelling.

Ultrasonography helps in assessing th swelling and  can distinguish between fluid and solid mass.Popliteal cysts are best shown by sagittal ultrasound image projection. Ultrsound can also be used o rule vascular tumours by looking at arterial pulsations. [Read more...]

Synovial Chondromatosis

Synovial chondromatosis is a condition characterized by the formation of  multiple foci of cartilage in the  synovial membrane of a joint. It also occurs in bursae and tendon sheaths.

When the cartilage is ossified, the condition is called  synovial osteochondromatosis.

This is  a benign condition and is very rare in occurrence. It usually occurs in persons over 40 years of age and occasionally in adolescents. It is twice as common in the males [Read more...]

Recurrent Momentary Lateral Subluxation of the Tibiofemoral Joint

This entity was first reported by Beals in 1978. In this condition there is  painful, spontaneous, audible popping  of one or both knees. This occurs in infants and children and the causative factor is lateral displacement of the tibiofemoral joint.

It appears to be caused by an isolated contraction of the biceps femoris muscle in association with capsular laxity.

Radiograms in the anteroposterior projection will show lateral subluxation of the tibiofemoral joint.

The proximal tibiofibular articulation is normal.

Treatment

Part-time splinting of the knee in extension will provide symptomatic relief of the painful, irritable knee. A conservative, nonsurgical approach to management should be followed

As the child gets older and the joint capsular hyperlaxity diminishes, the episodes of involuntary subluxation cease.

Treatment of Discoid Meniscus

The menisci in the knee joint are required for

  • Compensation of incongruity between the femur and tibia
  • In the distribution of joint pressure
  • Shock absorber, for stabilization of the knee, in provision of rotation, in spreading of synovial fluid, and in nutrition of articular cartilage.

An intact meniscus transmits 70 to 90 percent of the total load across the knee joint. Therefore, it is desirable to preserve the meniscus whenever possible.

A conservative nonoperative method of management is recommended In the treatment of discoid meniscus  if pain and functional disability are minimal.

SIlent discoid menisci  require no treatment. however, they should be kept under observation.

Conservative measures

  • Immobilization of the knee
  • Restriction of physical activity
  • Progressive exercises for the quadriceps.

Operative Measures

If the knee locking persists their is functional disability or pain partial or complete excision of the discoid meniscus is indicated.

Diagnostic arthroscopy is carried out to know the pathologic changes and the type of discoid meniscus.

Partial resection of the discoid meniscus is preferred when it is of the complete or incomplete type with minimal tearing and slight degeneration

Excision of the entire meniscus is performed when it is of the Wrisberg type  or when it is torn and there is marked degenerations.

Nonsurgical Management in Osteochondritis Dissecans

Treatment of  Osteochondritis Dissecans in children under 12 years of age is nonoperative. Arthroscopy is reserved for the cases in which the fragment has become detached.

If the lesion is in a non-weight bearing area or it involved only a portion of the weight-bearing area of a joint it is observed with serial radiograms made every six to eight weeks to determine its natural course.

Protection from weight-bearing is not required unless the lesion begins to separate and symptoms persist.

In case the weight bearing is prohibited, it is resumed gradually with aid of crutches providing partial support.

Generally, a period of three months is required for healing of the lesion.

In case of suspected seapration of fragment, bone imaging with technetium-99m and computed tomographic studies should be carried out.

If osteochondritis dissecans in a child fails to respond to nonsurgical management, arthroscopic examination and drilling of the osteochondritic lesion are recommended.

Indications of arthroscopy

Arthroscopy  directly visualizes the involved area and determines its exact location and size, and the degree of articular cartilage separation.

Arthroscopy is indicated in osteochondritis dissecans in patients 12 years of age and older in whom the weight-bearing area is involved with a lesion over 1 cm. in diameter.

Arthroscopic examination is also indicated in case of late diagnosis.

In children under 12 years of age arthroscopy should be done when, there is no radiographic or clinical evidence of improvement after a reasonable period of non operative treatment, or if the lesion becomes partially or completely detached.

Neuropathic Joint Disease or Charcot Joint in Children

This condition was described by Charcot, in 1868. He described it as a bizarre destruction of the knee joints with indolent swelling and instability in patients of tabes dorsalis> He proposed that the disease resulted from traumatization of a joint deprived of sensation.

Later Steindler classified the condition into the condition into the destructive, atrophic and hypertrophic proliferative forms.

Charcot-like changes in joints are seen in patients who have absence or depression of pain and proprioceptive sensation and who take part in extended continuous physical activity.

As a consequence their joints sustain repeated trauma. [Read more...]

Meningomyelocele

In this condition the normally developed spinal cord or cauda equina may be protruded along with the meninges and these structures may be adherent to the posterior aspect of the sac.

Clinical Features

  1. Though myelocele is the most common type of spina bifida (many cases are still born), yet meningomyelocele is the commonest variety of spina bifida in the living children.
  2. The bony defect may usually extend over 3 or more segments.
  3. At the summit of the swelling skin may be absent or atrophic, so here the meninges are exposed. That is why complications like infection and rupture are not uncommon.
  4. In transillumination test the nerves may be seen within the sac (cf. meningocele), though it is a translucent swelling.
  5. Neurological manifestations are almost always present. There may be sensory disturbances alongwith trophic changes in the lower extremities. There may be motor disturbances and in advanced cases one may find extensive paralysis of the legs. Bilateral talipes is quite common in this condition, as also urinary incontinence.
  6. X-ray will show the bony defect. There may be other abnormalities of the vertebrae, like scoliosis or kyphosis or even haemivertebra.

Complications

  1. Infection
  2. Rupture
  3. Urinary obstruction, hydronephrosis and urinary tract infection

Treatment

Operation must be performed as early as possible. Child’s condition should also be considered, as it should withstand operation.

Delay in operation may cause

  1. Infection within the sac and postoperative problems.
  2. The sac may rupture and will make operation extremely difficult with infection spreading throughout the subarachnoid space.
  3. There will be more adhesion of nerves with the wall of the sac, which will be difficult to separate.
  4. Gradually extensive paralysis of the legs and incontinence may occur, so that surgical intervention may become contraindicated.

Steps of Operation

  1. The sac is opened and the redundant membrana is excised. Meticulous care must be taken to separate all the nerve fibres which are adherent to the posterior wall of the sac and then they are replaced into the vertebral canal.
  2. The membranes are sutured in the midline deep to the bony defect.
  3. Adjacent erector spinae muscles and the overlying fasciae are brought in the midline and sutured. Two lateral release incisions are made to minimize tension on the suture line of the muscles. The skin is closed without tension. If difficulty is encountered to bring the skin in the midline, a rotation flap may be used.
  4. Further care of these children may be necessary. Repeated orthopaedic and urological surgery may be necessary to rectify orthopaedic defects and urinary incontinence. C.S.F. shunts may be necessary for hydrocephalus.

Meningocele

In this condition protrusion of meninges occurs through the defect in the neural arch. Such protrusion contains only cerebrospinal fluid. So it gives rise to a cystic swelling.

Usually the duramater stops at the margin of the defect and usually the pia and arachnoid protrude. The overlying skin remains intact.

It is common in the lumbosacral region. Meningocele also occurs in the skull, where it is more common in the occipital region or at the root of the nose.

Clinical Features

  1. It is present since birth
  2. It is a cystic swelling, that means fluctuation test is positive
  3. It is a highly translucent swelling
  4. It is compressible
  5. Expansile impulse is present when the child cries or coughs
  6. The overlying skin is normal and free
  7. On careful palpation the edge of the bony defect is palpable
  8. Neurological manifestations are usually absent (cf. meningo-myelocele, where neurological manifestations are usually present).
  9. This condition may be associated with hydrocephalus and this combination is known as Arnold-Chiari syndrome.
  10. X-ray is confirmatory and will show the bony defect

Complication

  1. Infection
  2. Rupture

Treatment

Operation should be performed as early as possible, but child’s condition and strength should be sufficient to withstand operation. This operation is often performed within a few days of birth. If the operation is delayed are:

  1. The skin and the sac are opened with incisions perpendicular to each other. This will minimize the chance of postoperative C.S.F. leakage.
  2. The redundant part of the sac is excised
  3. The margins of the excised sac are sutured together in the midline
  4. To strengthen the bony gap, the adjacent erector spinae muscle and the overlying fasciae are approximated over the gap with the help of lateral release incisions (to minimize tension in the suture line).
  5. The skin is closed.