Background: Histologic delineation of the events involved in the development of long bones and the developmental age at which these events occur is needed to elucidate the genetic and molecular mechanisms associated with these events. This report describes the sequence of histologic events involved in the formation of long bones and their epiphyses in the New Zealand White rabbit.
Methods: Prenatal studies were performed on twelve, fourteen, fifteen, sixteen, eighteen, twenty-one, twenty-four, and twenty-seven-day-old rabbit embryos, and postnatal studies were performed on newborn rabbits and on three-to-four-day-old; one, two, four, and six-week-old; and two, three, four, six, and eight-month-old rabbits. Histologic specimens from embryos were embedded in plastic and stained with toluidine blue or safranin O-fast green, and specimens from postnatal rabbits were embedded in paraffin and stained with hematoxylin and eosin or safranin O-fast green.
Results: Studies of twelve-day-old embryos demonstrated upper and lower limb buds filled with undifferentiated mesenchymal cells, and studies of fourteen-day-old embryos showed mesenchymal condensation and beginning cartilage formation outlining major long bones. Long-bone and epiphyseal development progressed through sixteen structural stages, and the developmental age at which these stages occurred was determined. These stages included limb-bud formation with uniform distribution of mesenchymal cells and formation of an apical ectodermal ridge (stage 1); mesenchymal condensation (stage 2); cartilage differentiation (stage 3); formation of a primary center of ossification (stage 4a); epiphyseal cartilage vascularization with formation of cartilage canals (stage 7); vascular invasion of the developing secondary ossification center (stage 9); bone formation and marrow cavitation in the secondary ossification center with formation of hematopoietic marrow (stage 10); fullest relative extent of secondary-ossification-center development in epiphyseal cartilage (stage 14); thinning of the physis (stage 15); and resorption of the physis with establishment of continuity between epiphyseal and metaphyseal circulations (stage 16).
Clinical Relevance: The detailed classification system presented here will allow for correlations between genetic and molecular mechanisms and histologic events in normal and abnormal development of long bones and their epiphyses. Many of the nonosseous structures formed during long-bone and epiphyseal development in the fetus, infant, and child are amenable to assessment with sonography and magnetic resonance imaging. An understanding of the histopathological features of developmental abnormalities of the long bones and their epiphyses revealed with newer imaging techniques should greatly improve management by allowing earlier diagnosis.
Roberto Rivas, MD; Centro Nacional de Rehabilitación, Mexico City, Mexico
Frederic Shapiro, MD; Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Children’s Hospital, 300 Longwood Avenue, Enders-11, Boston, MA 02115. Please address requests for reprints to Dr. Shapiro.