Musculoskeletal Manifestations of Sickle Cell Anaemia: A Pictorial Review
Author(s) -
A. Ganguly,
William D. Boswell,
Hifz Aniq
Publication year - 2011
Publication title -
anemia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.921
H-Index - 25
eISSN - 2090-1275
pISSN - 2090-1267
DOI - 10.1155/2011/794283
Subject(s) - medicine , medullary cavity , osteomyelitis , vascular occlusion , disease , bone marrow , pathology , avascular necrosis , infarction , ischemia , surgery , myocardial infarction , femoral head
Sickle cell anaemia is an autosomal recessive genetic condition producing abnormal haemoglobin HbS molecules that result in stiff and sticky red blood cells leading to unpredictable episodes of microvascular occlusions. The clinical and radiological manifestations of sickle cell anaemia result from small vessel occlusion, leading to tissue ischemia/infarction and progressive end-organ damage. In this paper we discuss and illustrate the various musculoskeletal manifestations of sickle cell disease focusing primarily on marrow hyperplasia, osteomyelitis and septic arthritis, medullary and epiphyseal bone infarcts, growth defects, and soft tissue changes.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom