Rare Diseases Symptoms Automatic Extraction

Prospective analysis of hip arthroscopy with 2-year follow-up.

[focal myositis]

Numerous indications, but little outcome data, have been reported for hip arthroscopy. The purpose of this prospective study is to report the 2-year results of hip arthroscopy performed on a consecutive series of patients for a variety of disorders.Case series.There were 38 procedures performed on 35 patients who have achieved 2-year follow-up. All patients were assessed with a modified Harris hip score (pain and function) preoperatively and postoperatively at 1, 3, 6, 12, and 24 months or until a subsequent procedure was performed. Variables studied included age, sex, diagnosis, duration of symptoms, onset of symptoms, center-edge angle, Workers' Compensation, and pending litigation.Follow-up was obtained on all patients. The median score improved from 57 to 85 points. This included 10 cases (9 patients) who underwent a subsequent procedure at an average of 10 months (6 total hip arthroplasty, 1 core decompression, 3 second arthroscopy) with an index score of 54 compared with 52 at the time of the second procedure. The median improvement for the following diagnoses was: loose body (34), labral lesion (27), synovitis (26), chondral injury (18), arthritis (14), and avascular necrosis (-11). Of the variables studied, the most statistically significant finding was that older men with longer duration of symptoms did worse. Two complications occurred in 1 patient: partial neuropraxia of the lateral femoral cutaneous nerve and focal myositis ossificans along the anterior portal tract.Hip arthroscopy can be performed for a variety of conditions (except end-stage avascular necrosis) with reasonable expectations of success and an acceptable complication rate. This is the first report to quantitate the results of hip arthroscopy for a heterogeneous population.

Diseases presenting "arthritis" symptom

  • acute rheumatic fever
  • child syndrome
  • congenital adrenal hyperplasia
  • cystinuria
  • familial hypocalciuric hypercalcemia
  • familial mediterranean fever
  • focal myositis
  • harlequin ichthyosis
  • homocystinuria without methylmalonic aciduria
  • inclusion body myositis
  • lamellar ichthyosis
  • malignant atrophic papulosis
  • pyomyositis
  • sneddon syndrome
  • trochlear dysplasia
  • typhoid
  • wiskott-aldrich syndrome

This symptom has already been validated