Rare case of Sporadic hypophosphatemic osteomalacia combined with psoriasis reported

Written by Dr Supreeth D R Published On 2023-03-05T20:00:38+05:30 | Updated On 5 March 2023 2:31 PM GMT

Rare case of Sporadic hypophosphatemic osteomalacia combined with psoriasis reported

Hypophosphatemic osteomalacia (HO) is an unusual metabolic disease characterized by low concentrations of serum phosphate levels, which leads to reduced mineralization of the bone matrix. Typically, HO consists of 4 common types: X-linked dominant hypophosphatemia (XLH), autosomal dominant hypophosphatemic rickets (ADHR), tumor-induced osteomalacia (TIO), and sporadic HO.The...

The clinical manifestations include gradually increased bone pain, deformities, fractures, limited mobility, short stature, and muscle weakness. Bone mineral density scan shows moderate-to-severe osteoporosis. Psoriasis is considered as a multisystem chronic inflammatory disorder on the basis of its hereditary background. Psoriatic arthritis (PsA) is an inflammatory condition of joints and is usually associated with the development of plaque psoriasis. According to the classification criteria for psoriatic arthritis (CASPAR), the case presented here fully met the criteria of PsA, but was finally confirmed as HO accompanied by psoriasis.

Yuan Li et al reported the case of a 48-year-old man in “International Journal of Rheumatic Diseases.” The patient developed multiple joint and bone pain and muscle weakness over 5 months with a 23-year history of psoriasis. He was diagnosed with psoriatic arthritis by primary hospitals but was unresponsive to etanercept and adalimumab treatments. After referral to the authors’ hospital, the patient was diagnosed with HOs combined with psoriasis.

On physical examination - A few scaly erythema and plaques were scattered on his head, trunk, and limbs. The Psoriasis Area and Severity Index score was 6.4. No joint swelling, deformation, or tenderness was noted. The power of the lower limbs was grade 4, while the upper limbs were normal.

Blood tests showed high serum alkaline phosphatase (ALP) level of 313 U/L (normal 40–150 U/L). The erythrocyte sedimentation rate, C-reactive protein, liver transaminases, urea, and creatinine were normal. The immune indices, including anti-nuclear antibody, anti-extractable nuclear antigen autoantibody profiles, rheumatoid factor and HLA-B27, were performed, and all were negative. Magnetic resonance imaging (MRI) and computed tomography(CT) of lumbar and lower extremities, which were done in primary hospitals, illustrated bone edema and osteoarthritis with effusion.

The patient was treated with oral phosphate solution, calcium, and active vitamin D, and the symptoms of bone and joint pain and muscle weakness gradually relieved. Since TIO accounts for the majority of adult-onset HO, positron emission tomography – computed tomography or octreotide imaging examinations had been done yearly to locate any underlying tumor in the patient, with negative findings in the 4-year follow-up.

The authors concluded that – “Diagnosis of HO remains a challenge to rheumatologists, and especially to dermatologists when accompanied by psoriasis. After excluding the inherited HO and with negative tumor, this report may be the first male case of sporadic HO combined with psoriasis.”

MBBS, Dip. Ortho, DNB ortho, MNAMS

Dr Supreeth D R (MBBS, Dip. Ortho, DNB ortho, MNAMS) is a practicing orthopedician with interest in medical research and publishing articles. He completed MBBS from mysore medical college, dip ortho from Trivandrum medical college and sec. DNB from Manipal Hospital, Bengaluru. He has expirence of 7years in the field of orthopedics. He has presented scientific papers & posters in various state, national and international conferences. His interest in writing articles lead the way to join medical dialogues. He can be contacted at editorial@medicaldialogues.in.