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Article: Perthes’ disease and femoroacetabular impingement in a child with proximal femoral focal deficiency

TitlePerthes’ disease and femoroacetabular impingement in a child with proximal femoral focal deficiency
Authors
Issue Date2012
PublisherBMJ Group. The Journal's web site is located at http://casereports.bmj.com
Citation
BMJ Case Reports, 2012, v. 2012 Nov. 11 How to Cite?
AbstractThis report is of a 44-year-old immunocompetent woman with septic arthritis of the right hand. Scedosporium apiospermum was isolated from the hand. The patient was treated with radical debridement and arthrodesis of the wrist. Itraconazole was given postoperatively as long-term therapy. A girl with known proximal femoral focal deficiency presented with Perthes’ disease at 5 years of age. Her treatment involved a Salter osteotomy. This in conjunction with articular incongruence, due to deformity of the femoral head, resulted in mixed type femoroacetabular impingement when she was 10 years old. Surgical hip dislocation and femoral neck osteochondroplasty successfully relieved her symptoms of impingement. This is the first reported case of Perthes’ disease in a patient with proximal femoral focal deficiency. The case highlights the importance of thoroughly investigating pain in patients with proximal femoral focal deficiency, a condition which is normally painless. Timely diagnosis of Perthes’ disease and containment procedures can prevent collapse of the femoral head and the resultant sequelae. Acetabular over-coverage should be avoided in pelvic osteotomy to prevent the development of femoroacetabular impingement.
Persistent Identifierhttp://hdl.handle.net/10722/222451
ISSN
2020 SCImago Journal Rankings: 0.231
PubMed Central ID

 

DC FieldValueLanguage
dc.contributor.authorPun, T-
dc.contributor.authorStokes, OM-
dc.contributor.authorChow, W-
dc.contributor.authorTo, MKT-
dc.date.accessioned2016-01-18T07:40:33Z-
dc.date.available2016-01-18T07:40:33Z-
dc.date.issued2012-
dc.identifier.citationBMJ Case Reports, 2012, v. 2012 Nov. 11-
dc.identifier.issn1757-790X-
dc.identifier.urihttp://hdl.handle.net/10722/222451-
dc.description.abstractThis report is of a 44-year-old immunocompetent woman with septic arthritis of the right hand. Scedosporium apiospermum was isolated from the hand. The patient was treated with radical debridement and arthrodesis of the wrist. Itraconazole was given postoperatively as long-term therapy. A girl with known proximal femoral focal deficiency presented with Perthes’ disease at 5 years of age. Her treatment involved a Salter osteotomy. This in conjunction with articular incongruence, due to deformity of the femoral head, resulted in mixed type femoroacetabular impingement when she was 10 years old. Surgical hip dislocation and femoral neck osteochondroplasty successfully relieved her symptoms of impingement. This is the first reported case of Perthes’ disease in a patient with proximal femoral focal deficiency. The case highlights the importance of thoroughly investigating pain in patients with proximal femoral focal deficiency, a condition which is normally painless. Timely diagnosis of Perthes’ disease and containment procedures can prevent collapse of the femoral head and the resultant sequelae. Acetabular over-coverage should be avoided in pelvic osteotomy to prevent the development of femoroacetabular impingement.-
dc.languageeng-
dc.publisherBMJ Group. The Journal's web site is located at http://casereports.bmj.com-
dc.relation.ispartofBMJ Case Reports-
dc.rightsBMJ Case Reports. Copyright © BMJ Group.-
dc.titlePerthes’ disease and femoroacetabular impingement in a child with proximal femoral focal deficiency-
dc.typeArticle-
dc.identifier.emailChow, W: wchowa@hkucc.hku.hk-
dc.identifier.emailTo, MKT: mikektto@hku.hk-
dc.identifier.authorityTo, MKT=rp00302-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1136/bcr-2012-006748-
dc.identifier.pmid23148394-
dc.identifier.pmcidPMC4544581-
dc.identifier.scopuseid_2-s2.0-84892543663-
dc.identifier.hkuros256753-
dc.identifier.volume2012-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl1757-790X-

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