IDIOPATHIC CHONDROLYSIS

FRANK CUCE, D.O., Orthopaedic Surgery Resident

KIRK W. DABNEY, M.D., Attending Pediatric Orthopaedic Surgeon

February 13, 1996

CLINICAL CASE PRESENTATION

ORTHOPAEDIC DEPARTMENT

THE ALFRED I. DUPONT INSTITUTE

WILMINGTON, DELAWARE

CASE HISTORY

This is a 12 year old Asian female with insidious onset of left hip pain 4 months in duration. At one point, her pain was so severe she could not bear weight and had to be picked up from school. She denies trauma to the hip. She could not participate in sports secondary to pain and also developed a limp with apparent leg length discrepancy secondary to pelvic obliquity and local muscle spasm. She complains of no other joint symptomatology. Her previous medical history is negative.

PHYSICAL EXAM

She was afebrile on presentation to the Alfred I. dupont Institute. Physical examination demonstrated the following positive findings:

XRAYS

A CT scan in August showed joint effusion which was aspirated and evaluated. The aspirate was negative for infection or other pathology.

An arthrogram performed was also negative. Both studies done at outside facilities.

Recent radiographic findings revealed the following: Bone scan with increased uptake left hip on both sides of joint. Joint space narrowing left hip to 2 mm.

LAB VALUES
IDIOPATHIC CHRONDOLYSIS

Chondrolysis represents a process characterized by progressive destruction of articular cartilage resulting in secondary joint space narrowing and stiffness.

Types: May follow infection, trauma, prolonged immobilization and severe burns about the lower extremities. Also, it may be a complication of slipped capital femoral epiphysis.

Another type is idiopathic, characterized by an acute form of rapidly progressive chondrolysis occurring most frequently during adolescence with isolated involvement of the hip joint, but without a demonstrable cause.

HISTORY

Jones in 1971 described chondrolysis not associated with SCFE in black adolescent girls. Since that time, reports of idiopathic scoliosis have been recorded. As of 1989, after Daluga and Millar's study, 42 hips have been recorded. The female to male ratio is 6:1 and 52% of these patients are Caucasian.

ETIOLOGY

Etiology is unknown. Proposed theories include nutritional abnormalities, mechanical injury, ischemia, abnormal intracapsular pressure, and an inherent abnormal chondrocyte metabolism within the articular cartilage. The most accepted theory is that proposed by Golding in 1973, which postulated articular cartilage resorption to be secondary to an autoimmune response in genetically susceptible individuals.

INCIDENCE

This remains unreported in the literature, although 42 have been reported up to 1989. (Incidence of chondrolysis in SCFE is 8.2%).

CLINICAL PRESENTATION
LABORATORY

CBC, UA, RF, ANA, HCA-B27, Blood culture, and TB (PPD) are WNL.

ESR can be slightly elevated and rarely over 30.

XRAYS
RADIOGRAPHIC TESTS INCLUDE
PATHOLOGY
DIFFERENTIAL DIAGNOSIS
TREATMENT
REFERENCES
  1. Bleck EE. Idiopathic chondrolysis of the hip. JBJS (AM) 1983;65:1266.
  2. Daluga DJ, Millar EA. Idiopathic chondrolysis of the hip. JPO 1989;9:405.
  3. Duncan JW, Nasca R, Schrantz J. Idiopathic chondrolysis of the hip. JBJS (Am) 1979;61:1024.
  4. Duncan JW, Schrantz JL, Nasca RJ. The bizarre stiff hip-possible idiopathic chondrolysis. JAMA 1975;231:382.
  5. Kozlowski K, Scougall J. Idiopathic chondrolysis-diagnostic difficulties. Pediatr Radiol 1984;14:314.
  6. Lovell and Winter. Idiopathic chondrolysis of the hip. Pediatric Orthopedics 1037-1045.