Author/Authors :
Zabihiyeganeh، Mozhdeh نويسنده Bone and Joint Reconstruction Research Center, Shafa
Orthopedic Hospital, Iran University of Medical Sciences, Tehran, IR
Iran , , Chehrehgosha، Haleh نويسنده Department of Internal Medicine, Rasoul-e-Akram Hospital,
Iran University of Medical Sciences, Tehran, IR Iran , , Mirzaei، Alireza نويسنده Bone and Joint Reconstruction Research Center, Shafa
Orthopedic Hospital, Iran University of Medical Sciences, Tehran, IR
Iran ,
Abstract :
Introduction Ochronosis is a rare autosomal recessive disorder of
tyrosine metabolism, leading to deposition of elevated levels of
homogentisic acid in different parts of the body, especially in fibrous
and cartilaginous tissues. The current study presents a case with
delayed diagnosis and osteoporotic fracture in addition to severe
osteoarthritis and calcification. Case Presentation A 56-year-old female
with low back pain and painful knees and hips referred to the center.
Right hip arthroplasty was performed to manage her severe
osteoarthritis. Although characteristic features of ochronosis such as
urine darkening, subcutaneous pigmentation and degenerative ochronotic
arthropathy resembling osteoarthritis were observed in this patient,
surprisingly it remained unrecognized until the
5th decade. Bone mineral density showed that
osteoporosis and zoledronic acid had started. Conclusions Usually,
osteoarthritis is inversely correlated with the osteoporosis.
Considering ochronosis as an osteoarthritis predisposing factor, the
osteoporosis manifestation is not expected in such patients. However, in
the current case, simultaneous osteoarthritis and osteoporosis fracture
was observed, indicating unreliability of bone mineral density (BMD) in
such patients. Authors believe that ochronosis could reduce bone
quality, while its quantity might increase.