7.4 & 7.5
7.4 The Thoracic Cage
Learning Objectives:
Discuss the components that make up the thoracic cage
Identify the parts of the sternum and define the sternal angle
Discuss the parts of a rib and rib classifications
Definition:
The thoracic cage, also known as the rib cage, forms the thorax (chest) portion of the body. It consists of:
12 pairs of ribs with their costal cartilages
The sternum
The ribs are anchored posteriorly to the 12 thoracic vertebrae (T1–T12).
The thoracic cage protects vital organs such as the heart and lungs.
Components of the Thoracic Cage:
Figure Reference: Figure 7.32 shows the thoracic cage including the sternum and ribs.
Ribs Classification:
Ribs are classified into:
True ribs (1–7) - Attaching directly to the sternum
False ribs (8–12) - Do not attach directly to the sternum.
Floating ribs (11–12) - Last two pairs of false ribs that do not attach to the sternum at all.
Sternum
Definition:
The sternum is the elongated bony structure that anchors the anterior thoracic cage. It has three parts:
Manubrium - The wider, superior portion of the sternum.
Jugular notch - A shallow, U-shaped border at the top of the manubrium, felt at the anterior base of the neck.
Clavicular notch - Shallow depression on either side of the superior-lateral margins; site of the sternoclavicular joint between the sternum and clavicle.
The first ribs attach to the manubrium.
Body - The elongated central portion of the sternum.
Sternal angle - The joint between the manubrium and body, forming a slight bend where the second rib also attaches; vital for identifying and counting ribs as the second rib is the highest palpable rib.
Ribs 3–7 attach to the body.
Xiphoid process - The inferior tip of the sternum; cartilaginous early in life, ossifying during middle age.
Ribs
Definition of Ribs:
Each rib is a curved, flattened bone contributing to the wall of the thorax.
Attachment:
Ribs articulate posteriorly with thoracic vertebrae T1–T12, and most attach anteriorly via costal cartilages to the sternum.
Parts of a Typical Rib:
Head of the rib - Posterior end articulating with costal facets of corresponding thoracic vertebra.
Neck of the rib - Narrowed portion lateral to the head.
Tubercle of the rib - A small bump on the posterior surface of the rib, articulating with the facet on the transverse process of the corresponding vertebra.
Body/Shaft of the rib - Extends from the tubercle to the anterior end.
Angle of the rib - The point where the rib has the greatest curvature, aligning with the medial border of the scapula in anatomical position.
Costal groove - Shallow groove along the inferior margin of each rib for passage of blood vessels and nerves.
Rib Classifications
Classification based on Relationship to the Sternum:
True ribs (vertebrosternal ribs) 1–7:
Costal cartilage attaches directly to the sternum.
False ribs (vertebrochondral ribs) 8–12:
Do not attach directly to the sternum; connections via cartilage.
Ribs 8–10 attach to rib 7's cartilage indirectly.
Floating ribs (vertebral ribs) 11–12:
Short ribs that do not connect to the sternum or any other rib; terminate in the abdominal wall musculature.
7.5 Embryonic Development of the Axial Skeleton
Learning Objectives:
Discuss the two types of embryonic bone development within the skull
Describe the development of the vertebral column and thoracic cage
Development Overview:
The axial skeleton begins to form during early embryonic development, with growth, remodeling, and ossification continuing for several decades post-birth.
Understanding these processes is vital for recognizing abnormalities in skeletal structures.
Development of the Skull
Notochord Formation:
During the third week of embryonic development, a rod-like structure known as the notochord develops dorsal along the embryo's length.
Tissue over the notochord enlarges to form the neural tube, giving rise to the brain and spinal cord.
Somite Formation:
By the fourth week, mesoderm tissue thickens and separates into somites (block-like tissue structures); the most medial part is called the sclerotome.
Sclerotomes consist of mesenchyme, forming fibrous connective tissues, cartilages, and bones.
Skull Bone Development Mechanisms:
First Mechanism:
Forms the top and sides of the braincase via intramembranous ossification.
Mesenchymal cells localize, differentiate into bone-producing cells, forming skull bones.
Areas between growing braincase bones are called fontanelles (soft spots) that allow shape alteration during birth and continued skull growth post-birth.
The largest fontanelle is at the junction of the frontal and parietal bones, reducing in size to disappear by age 2.
Second Mechanism:
Develops facial bones and braincase floor through endochondral ossification.
Mesenchymal cells differentiate into cartilage cells, forming cartilage models that gradually convert to bone.
The skull is disproportionately larger at birth compared to the jaws and lower face due to the underdevelopment of the maxilla and mandible, and small paranasal sinuses.
Growth occurs during early childhood with significant enlargement of the face and jaws as teeth appear.
Development of the Vertebral Column and Thoracic Cage
Vertebrae Development:
Begins with mesenchyme cells from the sclerotome around the notochord differentiating into a hyaline cartilage model for each vertebra which ossifies via endochondral ossification.
The notochord largely disappears during vertebra growth, leaving remnants for intervertebral discs.
Ribs and Sternum Development:
Ribs develop as part of the cartilaginous model of vertebrae, separating from vertebrae by the eighth week.
Rib cartilage model ossifies except for the anterior portion, which remains as costal cartilage.
The sternum forms as paired hyaline cartilage models along the midline beginning in the fifth week, which fuse and ossify into bone.
The manubrium and body ossify first, with the xiphoid process remaining cartilage until late life.
Craniosynostosis
Definition:
The premature closure of a suture line in the skull, leading to abnormal skull growth and head deformation.
Caused by ossification defects or improper brain enlargement.
Affects about 1 in 2000 births, more common in males.
Types:
Primary craniosynostosis: Early fusion of one suture, restricting subsequent growth in that area.
Complex craniosynostosis: Involves premature fusion of multiple sutures, leading to more significant deformity and potentially impacting brain development.
Characteristics:
Compensatory growth in non-affected areas leads to abnormal head shapes (e.g., scaphocephaly: long, narrow wedge-shaped head).
Brain growth typically remains adequate despite skull deformities.
Treatment:
Usually surgical; involves opening the skull along the fused suture to allow for growth.
Some cases may require removal of skull parts and replacement with artificial plates.
Earlier surgery correlates with better outcomes, with most children developing normally thereafter without neurological issues.