Rare Diseases Symptoms Automatic Extraction

A rare case of lymphangiomyomatosis treated with leuprolide acetate: five-years follow-up.

[lymphangioleiomyomatosis]

Lymphangiomyomatosis (LAM) is a rare and systemic disease that is characterized by the abnormal proliferation of smooth muscle-like cells in the lungs and along the axial lymphatic system. The authors herein present a rare case of LAM that was treated with long-term use of leuprolide acetate, a gonadotropin-releasing hormone analogue (GnRHa).

Diseases presenting "long-term use" symptom

  • cushing syndrome
  • cystinuria
  • lamellar ichthyosis
  • lymphangioleiomyomatosis
  • megacystis-microcolon-intestinal hypoperistalsis syndrome

You can validate or delete this automatically detected symptom