2012
DOI: 10.4084/mjhid.2012.023
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Multiple bone and joint disease in a sickle cell anaemia patient: a case report

Abstract: This case highlights the fact that bone involvement is the commonest clinical manifestation of Sickle Cell Disease (SCD) both in the acute settings such as painful vaso-occlusive crisis (VOC) and as a source of chronic, progressive debility such as avascular necrosis (AVN), chronic osteomyelitis and fixed flexion deformity of joints.Protracted multiple bone involvement i.e. bilateral femoral and left humeral chronic osteomyelitis, Left elbow, Left knee and right humeral septic arthritis together with avascular… Show more

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Cited by 4 publications
(5 citation statements)
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“…It occurs mostly in children from rural setting. Sickle cell anemia and malnutrition (which is common is rural population in our country) certainly explain chronic anemia responsible for decreased immunity, leading to multifocal bone involvement [6] [7] [8] [10].…”
Section: Discussionmentioning
confidence: 99%
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“…It occurs mostly in children from rural setting. Sickle cell anemia and malnutrition (which is common is rural population in our country) certainly explain chronic anemia responsible for decreased immunity, leading to multifocal bone involvement [6] [7] [8] [10].…”
Section: Discussionmentioning
confidence: 99%
“…Management of SCMO is a challenge for the medical team. Due to the complexity of the disease, care must be multidisciplinary, involving clinicians, radiologists and biologists [6]. Indeed, faced with an SCMO, several problems must be taken into account.…”
Section: Samplesmentioning
confidence: 99%
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“…The bilateral forms are extremely rare [1]. Olaniyi in Nigeria [2] brought back a case with multiple osseous localizations with a bilateral femoral attack. A bilateral tibial attack due to Pantoea agglomerans was reported by Bachmeyer [3] at a SS homozygote drepanocytosis patient.…”
Section: Commentsmentioning
confidence: 99%