Author/Authors :
Franz، Alois نويسنده Department of Orthopedics, Trauma and Hand Surgery, St.
Marien Hospital, Siegen, Germany , , Abusafieh، Mohammed نويسنده Department of Orthopedics, Trauma and Hand Surgery, St.
Marien Hospital, Siegen, Germany ,
Abstract :
Introduction: Alkaptonuria (AKU) is a very rare disease and occurs
due to the deficiency of the enzyme homogentisate1, 2-dioxygenase (HGD)
which results in ochronosis, a term used to describe the dark
pigmentation of the tissues. Alkaptonuria affects mostly the knee joint
followed by the hip as major weight bearing joints, where the life
quality of such patients is severely affected. Case Presentation: We
present a case of Caucasian male who was suffering from severe
osteoarthritis of the knee. Initially he underwent an arthroscopic
partial meniscectomy in a nearby hospital. Fourteen months later we
performed a total knee replacement using the Journey II CR prosthesis.
We found a dark pigmentation of the inside of the knee (synovial tissue
and cartilage). A positive urine test and a pathological specimen
examination revealed the diagnosis of AKU. The patient had no
complications after the surgery and underwent a standard rehabilitation
program. Conclusions: Osteoarthritis could be the first manifestation of
patients with AKU and the onset of the joint disease could be late and
rapid.