1.Pathological Fracture of Femoral Neck Leading to a Diagnosis of Wilson's Disease: A Case Report and Review of Literature.
Nishit BHATNAGAR ; Purushotham LINGAIAH ; Jeetendra Singh LODHI ; Yugal KARKHUR
Journal of Bone Metabolism 2017;24(2):135-139
Wilson's disease (WD) is a rare inherited disorder of copper metabolism. It chiefly has hepatic, neurological and ophthalmic manifestations. Although osteoporosis, rickets and early arthritis are common features of WD, they are under-recognized. Musculoskeletal manifestations very rarely lead to diagnosis of the disease. Here we present a case of a 12-year-old girl who presented with a 3-month-old pathological fracture of neck of femur. WD was diagnosed on investigating the cause of the pathological fracture, which was managed by performing a conventional McMurray's intertrochanteric osteotomy. At 6 months follow up, fracture had united and patient was able to ambulate with support. WD can be a rare cause of pathological fracture. A high index of suspicion must be maintained in patients of pathological fracture presenting with associated neuropsychiatric or hepatic manifestations.
Arthritis
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Child
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Copper
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Diagnosis*
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Female
;
Femur
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Femur Neck*
;
Follow-Up Studies
;
Fractures, Spontaneous*
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Hepatolenticular Degeneration*
;
Humans
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Infant
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Metabolism
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Neck
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Osteoporosis
;
Osteotomy
;
Rickets
2.Acromioclavicular joint septic arthritis in an immunocompetent child: A case report.
Saurabh DUTT ; Jeetendra LODHI ; Vinod KUMAR ; Abhishek KASHYAP
Chinese Journal of Traumatology 2018;21(3):182-185
Septic arthritis of acromioclavicular (AC) joint is a rare entity. It is generally seen in patients who are immunocompromised. Only 15 cases have been reported till now, with only one case series of 6 patients. We report a case of septic arthritis of AC joint in an immunocompetent child. A 9 years old girl presented with history of pain in left shoulder for 4 days associated with fever. No history suggestive of any immunocompromised state was complained. On local examination, a swelling of around 3 cm in diameter was found over left AC joint region with raised local temperature, tenderness on palpation and positive response in fluctuation test. Total leukocyte count was 18.7 × 10/L with 80% of neutrophils. Erythrocyte sedimentation rate (ESR) was 28 mm/1 h. C-reactive protein (CRP) was 12 mg/L. X-ray showed enlarged left AC joint space. Ultrasound revealed hypoechoic collection in the AC joint and the surrounding area. The aspirate was thick and purulent in nature, revealing Gram positive cocci at staining. Arthrotomy and thorough lavage of AC joint was done. Culture of the aspirate showed Methicillin Resistant Staphylococcus Aureus (MRSA) after 48 hours that was sensitive to amikacin, gentamicin, erythromycin and teicoplanin. Patient was symptom-free at 2 months of follow-up with no signs of osteomyelitis on the radiographs. Thus this is the first case of AC joint septic arthritis in healthy individual. Being proximal to the shoulder joint, AC joint septic arthritis can be confused with the shoulder joint septic arthritis. Thus, high index of suspicion is required for accurate diagnosis.
Acromioclavicular Joint
;
Anti-Bacterial Agents
;
therapeutic use
;
Arthritis, Infectious
;
diagnosis
;
therapy
;
Child
;
Female
;
Humans
;
Immunocompetence