Literature DB >> 23658586

Tardive hip disease diagnosis in a young adult with sickle cell disease.

A A Bokolombe1, F Samato, T Lukinu, M B Ekila, M N Aloni.   

Abstract

BACKGROUND: Hip disease is a complication of Sickle Cell Disease most commonly occurs during adolescence and early adult life that constitutes from 3.3% to 26.7% % of cases in SCD patients. Damage to mature epiphysis may cause persistent symptoms requiring surgery which may need revision if it becomes loose with wear. CASE
PRESENTATION: We report a 27-year-old male who was diagnosed with hip disease following investigations for persistent pain in right hip associated with limp and painful limitation of movement. Avascular necrosis of the right femoral head was identified on a hip X-ray.
CONCLUSION: Further investigation will be necessary to identify risk factors in SCD Congolese patient and each SCD patient must be screened for predisposing factors.

Entities:  

Keywords:  Hip disease; Kinshasa; diagnosis; sickle cell anemia; young adult

Mesh:

Year:  2013        PMID: 23658586      PMCID: PMC3645092          DOI: 10.4314/ahs.v13i1.25

Source DB:  PubMed          Journal:  Afr Health Sci        ISSN: 1680-6905            Impact factor:   0.927


  10 in total

1.  Risk factors and impact of orthopaedic monitoring on the outcome of avascular necrosis of the femoral head in adults with sickle cell disease: 215 patients case study with control group.

Authors:  M Mukisi-Mukaza; C Saint Martin; M Etienne-Julan; M Donkerwolcke; M E Burny; F Burny
Journal:  Orthop Traumatol Surg Res       Date:  2011-11-11       Impact factor: 2.256

2.  Neonatal screening for sickle cell anaemia in the Democratic Republic of the Congo: experience from a pioneer project on 31 204 newborns.

Authors:  L Tshilolo; L M Aissi; D Lukusa; C Kinsiama; S Wembonyama; B Gulbis; F Vertongen
Journal:  J Clin Pathol       Date:  2009-01       Impact factor: 3.411

3.  Sickle-cell hip necrosis and intraosseous pressure.

Authors:  M M Mukisi; K Bashoun; F Burny
Journal:  Orthop Traumatol Surg Res       Date:  2009-03-13       Impact factor: 2.256

4.  The natural history of asymptomatic osteonecrosis of the femoral head in adults with sickle cell disease.

Authors:  Ph Hernigou; A Habibi; D Bachir; F Galacteros
Journal:  J Bone Joint Surg Am       Date:  2006-12       Impact factor: 5.284

Review 5.  The natural history of untreated asymptomatic osteonecrosis of the femoral head: a systematic literature review.

Authors:  Michael A Mont; Michael G Zywiel; David R Marker; Mike S McGrath; Ronald E Delanois
Journal:  J Bone Joint Surg Am       Date:  2010-09-15       Impact factor: 5.284

6.  Aseptic necrosis of the head of the femur among sickle cell anaemia patients in Uganda.

Authors:  C M Ndugwa
Journal:  East Afr Med J       Date:  1992-10

7.  Sickle cell disease as a cause of osteonecrosis of the femoral head.

Authors:  P F Milner; A P Kraus; J I Sebes; L A Sleeper; K A Dukes; S H Embury; R Bellevue; M Koshy; J W Moohr; J Smith
Journal:  N Engl J Med       Date:  1991-11-21       Impact factor: 91.245

8.  [Aseptic osteonecrosis of the femoral head in children with sickle-cell disease].

Authors:  Gamedzi Komlatsè Akakpo-Numado; Komla Gnassingbe; Kodjo Abossisso Sakiye; Missoki Azanlédji Boume; Abdoulatif Amadou; Hubert Tekou
Journal:  Sante       Date:  2008 Oct-Dec

9.  Risk factors for osteonecrosis of the femoral head in patients with sickle cell disease.

Authors:  A L Akinyoola; I A Adediran; C M Asaleye; A R Bolarinwa
Journal:  Int Orthop       Date:  2008-07-17       Impact factor: 3.075

10.  Idiopathic and secondary osteonecrosis of the femoral head show different thrombophilic changes and normal or higher levels of platelet growth factors.

Authors:  Elisabetta Cenni; Caterina Fotia; Enis Rustemi; Kimitachi Yuasa; Giuseppe Caltavuturo; Armando Giunti; Nicola Baldini
Journal:  Acta Orthop       Date:  2011-02-01       Impact factor: 3.717

  10 in total

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