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Ochronotic arthropathy of bilateral hip joints:A case report
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作者 Nicolas Yap San Min Urba Rafi +2 位作者 Juan Wang Bin He Lei Fan 《World Journal of Clinical Cases》 SCIE 2023年第1期210-217,共8页
BACKGROUND Ochronosis,also known as alkaptonuria,is a rare autosomal recessive selfmetabolic disease arising from deficiency of homogentisate 1,2 dioxygenase enzyme.It affects several organs and muscoskeletal structur... BACKGROUND Ochronosis,also known as alkaptonuria,is a rare autosomal recessive selfmetabolic disease arising from deficiency of homogentisate 1,2 dioxygenase enzyme.It affects several organs and muscoskeletal structures.We herein report a case of a patient who presented with severe hip arthropathy complicated with late stage ochronosis.CASE SUMMARY A 56-year-old male patient was admitted in our department in 2019 with complaints of chronic low backache and left hip pain.After the required investigations were done,lumbar disc herniation and severe hip arthritis were the initial diagnosis.A total left hip arthroplasty was performed.Ochronotic osteoarthritis was only obtained post-surgery as confirmatory diagnosis.He was again admitted mid 2022 with the same complaints on the right hip.Subsequently,he underwent a total right hip arthroplasty.Post-operative recovery and follow-ups were deemed very satisfactory.CONCLUSION Ochronosis is an unusual diagnosis for a patient who presents with typical hip arthritis.Thus,unless meticulous history taking and advanced laboratory tests,the diagnosis can easily be missed by surgeons. 展开更多
关键词 ALKAPTONURIA Metabolic disease ochronotic osteoarthropathy Hip arthritis Bilateral hip arthroplasty Case report
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One-stage revision arthroplasty in a patient with ochronotic arthropathy accompanied by joint infection:A case report
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作者 Xiao-Chao Wang Xiao-Min Zhang +6 位作者 Wan-Ling Cai Zhen Li Chao Ma Yi-Hai Liu Qi-Lian He Tian-Sheng Yan Xue-Wei Cao 《World Journal of Clinical Cases》 SCIE 2022年第25期9036-9043,共8页
BACKGROUND Ochronotic arthropathy(OcA)is a rare disease,which is caused by the accumulation of homogentisic acid in the joint.Patients with OcA have obvious joint pain and the disease progresses rapidly,eventually res... BACKGROUND Ochronotic arthropathy(OcA)is a rare disease,which is caused by the accumulation of homogentisic acid in the joint.Patients with OcA have obvious joint pain and the disease progresses rapidly,eventually resulting in disability.Arthroplasty is an efficacious treatment in patients with OcA.However,when OcA patients have joint infection,is joint replacement an option?In the present report,we performed total knee arthroplasty in a patient with OcA and knee infection under the guidance of one-stage revision theory.CASE SUMMARY A 64-year-old male was referred to our hospital due to severe left knee pain with limited mobility for 2 years.On physical examination,the patient was found to have dark brown pigmentation of the sclera and auricle.Laboratory test results showed elevations in C-reactive protein level(65.79 mg/L)and erythrocyte sedimentation rate(90.00 mm/h).The patient underwent debridement of the left knee joint,during which the cartilage surface of the knee joint was found to be black-brown in color.Bacterial culture of synovial fluid revealed Achromobacter xylosoxidans.We then carried out arthroplasty under the guidance of the theory of one-stage revision.After surgery,the patient’s left knee joint pain disappeared and function recovered without joint infection.CONCLUSION OcA accompanied by joint infection is rare.One-stage revision arthroplasty may be a treatment option for this disease. 展开更多
关键词 ochronotic arthropathy Arthroplasty One-stage revision ALKAPTONURIA Homogentisic acid Case report
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Multiple Arthroplasty in a Patient with Alkaptonuric Arthritis
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作者 Chen-Yi Ye De-Ting Xue Xi Chen Rong-Xin He 《Chinese Medical Journal》 SCIE CAS CSCD 2015年第17期2404-2405,共2页
Alkaptonuria (AKU) is an extremely rare autosomal recessive metabolic disorder characterized by a triad of homogentisic aciduria, arthritis, and ochronosis, affecting only 2 5 in a million individuals. The managemen... Alkaptonuria (AKU) is an extremely rare autosomal recessive metabolic disorder characterized by a triad of homogentisic aciduria, arthritis, and ochronosis, affecting only 2 5 in a million individuals. The management of AKU is usually symptomatic. However, surgical intervention necessitates in cases of signiticant arthritis, Here, we presented a 64-year-old female who underwent bilateral total hip and right total knee arthroplasties achieving a successful clinical outcome throughout the 3 years of follow-up. 展开更多
关键词 ALKAPTONURIA OCHRONOSIS ochronotic Arthritis Total Hip Replacement
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