Diaphragm — Openings with Vertebral Levels, Nerve Supply, Development and Diaphragmatic Hernias

Written & medically reviewed by the Kinase Medical Team · Last reviewed

Quick Answer

The diaphragm has three major openings: the caval opening at T8 (inferior vena cava, right phrenic branches), the oesophageal hiatus at T10 (oesophagus, both vagal trunks) and the aortic hiatus at T12 (aorta, thoracic duct, azygos vein). Motor supply is the phrenic nerve (C3 to C5). It develops from four components; failure causes a congenital diaphragmatic hernia.

What is the diaphragm and what does it do?

The thoracic diaphragm is a dome-shaped fibromuscular sheet that separates the thorax from the abdomen. Its convex upper surface forms the floor of the thoracic cavity and its concave under-surface forms the roof of the abdominal cavity. It is the primary muscle of inspiration: on contraction it pulls the central tendon down, increases the vertical diameter of the thorax and lowers intrathoracic pressure so that air is drawn in. It is slightly asymmetric — the left dome sits a little lower than the right.

Beyond breathing, the diaphragm helps the anterior abdominal muscles raise intra-abdominal pressure during micturition, defecation and parturition, and during the Valsalva manoeuvre. It also acts as a thoraco-abdominal pump: descent of the diaphragm compresses the inferior vena cava and abdominal lymphatics and helps push blood and lymph upward toward the heart and the thoracic duct.

  • Shape: two domes (right and left hemidiaphragm) joined at a central tendon.
  • Insertion: all muscle fibres converge on the central tendon, whose upper surface is partly fused to the fibrous pericardium.
  • Main action: muscle of quiet inspiration; assists abdominal straining and venous and lymphatic return.
  • Landmark role: the oesophagus, vagus and phrenic nerves, descending aorta and inferior vena cava all cross between chest and abdomen through it.
Diaphragm - Definition, Function, Muscle & Anatomy | KenhubShort anatomy tutorial on the diaphragm — origin, openings, innervation and function.Video: Kenhub - Learn Human Anatomy · 4:33 · Watch on YouTube · Loads from YouTube (privacy-enhanced mode) only when you press play.

What are the openings of the diaphragm and their vertebral levels?

StatPearls describes three major and five minor openings. The three major ones, together with their levels and contents, are the most repeated anatomy question on this topic.

Major openings of the diaphragm
OpeningLevelPositionStructures passing through
Caval opening (vena caval trunk)T8In the central tendonInferior vena cava; some branches of the right phrenic nerve
Oesophageal hiatusT10Within a sling of fibres from the right crus, to the left of the median planeOesophagus; right and left vagal trunks; oesophageal branches of the left gastric vessels; lymphatics
Aortic hiatusT12In front of the body of T12, between the cruraAorta; thoracic duct; azygos vein
Minor openings and gaps
OpeningContents
Lesser aperture of the right crusGreater and lesser splanchnic nerves
Lesser aperture of the left crusHemiazygos vein; greater and lesser splanchnic nerves
Behind the medial lumbocostal archSympathetic trunk
Foramen of Morgagni — between the sternal and costal partsSuperior epigastric branch of the internal thoracic artery and lymphatics of the abdominal wall
Medial and lateral lumbocostal archesAreolar tissue that, when present, separates the kidney from the pleura
Gray's Anatomy illustration of the diaphragm seen from below. The pink muscle fans out from the ribs and lumbar vertebrae toward a pale central tendon. The round caval foramen lies in the right half of the tendon, the oesophageal opening lies to its left, and the aortic opening lies between the two crura in front of the lumbar spine.
The diaphragm from below: caval foramen in the central tendon (T8), oesophageal opening (T10) in the muscle of the right crus, and the aortic opening (T12) between the two crura, with the opening for the lesser splanchnic nerve at the side.Image: Henry Vandyke Carter (Gray's Anatomy, 1918), Public domain

Where does the diaphragm arise — sternal, costal and lumbar parts?

The peripheral muscle arises from the circumference of the lower thoracic aperture in three groups and converges on the central tendon.

Origin of the diaphragm
PartOrigin
SternalTwo fleshy slips from the back of the xiphoid process
CostalInner surfaces of the cartilages of the lower six ribs on each side, interdigitating with transversus abdominis
Lumbar — archesMedial lumbocostal arch (fascia over psoas major, attached to the side of L1 and the front of its transverse process) and lateral lumbocostal arch (fascia over quadratus lumborum, from the transverse process of L1 to the lower border of the 12th rib)
Lumbar — right crusAnterolateral surfaces of the bodies of the upper three lumbar vertebrae and the intervening discs
Lumbar — left crusCorresponding parts of the upper two lumbar vertebrae

The medial margins of the two crura form a tendinous arch in front of the aorta called the median arcuate ligament. Muscle fibres of the right crus pass up and to the left to encircle the oesophageal opening like a sling. These fibres act as a physiological sphincter that helps prevent regurgitation of gastric contents into the thoracic oesophagus.

What is the nerve and blood supply of the diaphragm?

Nerve supply of the diaphragm
TypeSupplyNotes
MotorRight and left phrenic nerves (C3 to C5)The only motor supply — the whole muscle is paralysed if the phrenic nerve is interrupted
Sensory — central partPhrenic nerveSupplies the parietal pleura and peritoneum over the central surfaces
Sensory — peripheryLower six intercostal nervesSupplies the margins of the muscle
  • Arteries: musculophrenic artery (from the internal thoracic), superior phrenic artery (from the aorta), the lower five intercostal arteries with the subcostal artery, and the inferior phrenic artery.
  • Veins and lymphatics follow the arteries; the thoraco-abdominal pump compresses abdominal lymph vessels on descent and helps drive lymph up the thoracic duct.
  • Phrenic nerve injury: a paralysed hemidiaphragm is pulled up into the chest by negative intrathoracic pressure and shows as an elevated hemidiaphragm on X-ray; unilateral weakness is commoner than bilateral. Compression by a thoracic mass, including lung cancer, is one cause. The right dome normally sits about one intercostal space higher than the left.
  • Valsalva link: a held deep breath makes the diaphragm and abdominal muscles raise intra-abdominal pressure, a manoeuvre used to separate right- from left-sided murmurs.

How does the diaphragm develop in the embryo?

The adult diaphragm forms from four embryonic components: the septum transversum, the pleuroperitoneal membranes, the dorsal mesentery of the oesophagus and the mesoderm of the body wall. StatPearls gives the same four parts under diaphragm formation; each contributes a different region.

Embryonic contributions
ComponentForms (as described in the source)
Septum transversumThe anterior central tendon
Pleuroperitoneal membranes / foldsThe posterolateral parts of the diaphragm, where Bochdalek hernias occur
Mesentery of the oesophagusContributes to the diaphragm; the pleuroperitoneal folds must fuse with it (and with the septum transversum) by about week 10
Body wall mesodermContributes to the diaphragm (listed as the fourth component)

Closure of the pleuroperitoneal canals is the critical event. A congenital diaphragmatic hernia (CDH) arises from failed closure or fusion of the pleuroperitoneal membranes and other muscular components between 8 and 12 weeks of gestation. A Bochdalek hernia results when the pleuroperitoneal folds fail to fuse with the septum transversum and the dorsal mesentery of the oesophagus by about the 10th week.

What is a congenital diaphragmatic hernia and what are its types?

CDH is a defect that lets abdominal viscera (stomach, spleen, liver, bowel) enter the chest. The herniated organs compress the developing lung, leading to pulmonary hypoplasia (bilateral but worse on the side of the defect), abnormal remodelling of the pulmonary arterioles and pulmonary hypertension. The incidence is about 1 to 4 per 10,000 live births.

Types of congenital diaphragmatic hernia
TypeSiteFrequency / features
BochdalekPosterolateral (pleuroperitoneal fold)70–85% of CDH; about 80% are left-sided; intrapleural, so it compresses the lung and causes pulmonary hypoplasia
MorgagniAnterior, parasternal (anteromedial)About 2–5% of cases; a mediastinal hernia that typically does not cause pulmonary hypoplasia
Central tendon defectCentralRare; arises from the septum transversum
Hiatal hernia and eventrationOesophageal hiatus / thin muscle sheetListed with the six anatomical types of CDH
  • Associations: about 10–15% have a chromosomal anomaly (for example trisomy 13, 18 or 21), and 30–40% have other congenital anomalies, mainly cardiac or central nervous system.
  • Right-sided and bilateral defects are less common and carry a worse prognosis.
  • Poor prognostic sign: herniation of the liver into the chest.
What Is Congenital Diaphragmatic Hernia: IllustratedShort illustrated explainer of congenital diaphragmatic hernia from a children's hospital.Video: The Children's Hospital of Philadelphia · 3:16 · Watch on YouTube · Loads from YouTube (privacy-enhanced mode) only when you press play.

How is a diaphragmatic hernia diagnosed and managed?

With modern obstetric imaging, roughly 60–70% of CDH cases are diagnosed before birth, usually at the routine 18–24 week anatomy scan. Ultrasound may show abdominal organs in the chest, mediastinal shift, polyhydramnios or an absent stomach bubble in the abdomen. Fetal MRI measures lung volume more accurately.

Practical points on CDH care
StepPoint to remember
AntenatalSerial ultrasound and Doppler; delivery planned at a tertiary centre with neonatal surgery and ECMO; prognosis refined by observed-to-expected lung-to-head ratio and liver herniation
Neonatal stabilisationGentle ventilation is the cornerstone: preductal saturation 85–95%, peak inspiratory pressure below 25 cm H2O, PEEP 3–5 cm H2O, permissive hypercapnia (PaCO2 45–60 mmHg)
Pulmonary hypertensionSuspect with hypoxaemia and a difference between preductal and postductal saturation (right-to-left ductal shunt); echocardiography within 48 hours
SurgeryNo longer an emergency: repair is usually done 48–72 hours after birth, once the infant is stable; defect closed with sutures or a patch

What are the high-yield exam points on the diaphragm?

  • Levels: IVC T8, oesophagus T10, aorta T12 — the single most repeated fact.
  • Vagal trunks go through the oesophageal hiatus; thoracic duct and azygos go through the aortic hiatus; right phrenic branches go with the IVC.
  • Phrenic nerve C3–C5 is the sole motor supply; periphery is sensory via lower six intercostal nerves.
  • Right crus (L1–L3) forms the oesophageal sling; the median arcuate ligament crosses the aorta at the level of the crura.
  • Bochdalek = posterolateral, most common (70–85%), usually left; Morgagni = anterior, rare, no lung hypoplasia.
  • Septum transversum forms the central tendon; pleuroperitoneal folds the posterolateral part.
  • The foramen of Morgagni transmits the superior epigastric vessels.

Frequently asked questions

What are the vertebral levels of the diaphragmatic openings?
The caval opening lies at T8 and transmits the inferior vena cava and some right phrenic nerve branches. The oesophageal hiatus lies at T10 and carries the oesophagus and both vagal trunks. The aortic hiatus lies at T12 and carries the aorta, thoracic duct and azygos vein. Remember the mnemonic I 8, 10 EGGS, AT 12.
Which structures pass through the oesophageal hiatus?
The oesophagus, the right and left vagal trunks, the oesophageal branches of the left gastric vessels and some lymphatic vessels pass through the hiatus at T10. It lies within a sling of muscle fibres derived from the right crus, to the left of the median plane, which acts as a physiological sphincter against reflux.
What is the nerve supply of the diaphragm?
Motor supply is exclusively from the right and left phrenic nerves, arising from C3 to C5. The phrenic nerve also carries sensation from the central parts, including the parietal pleura and peritoneum over them, while the periphery of the diaphragm is supplied by the lower six intercostal nerves.
From which embryonic structures does the diaphragm develop?
It forms from four components: the septum transversum, the pleuroperitoneal membranes, the dorsal mesentery of the oesophagus and the mesoderm of the body wall. The septum transversum gives the central tendon, and the pleuroperitoneal folds contribute the posterolateral parts, where Bochdalek hernias occur if they fail to fuse.
What is the difference between Bochdalek and Morgagni hernia?
Bochdalek hernia is posterolateral, accounts for 70 to 85 percent of congenital diaphragmatic hernias and is left-sided in about 80 percent. It compresses the lung and causes pulmonary hypoplasia. Morgagni hernia is anterior and parasternal, forms only 2 to 5 percent of cases and typically does not cause pulmonary hypoplasia.
When does a congenital diaphragmatic hernia occur in fetal life?
It arises from failed closure or fusion of the pleuroperitoneal membranes or other muscular components between 8 and 12 weeks of gestation. A Bochdalek hernia occurs if the pleuroperitoneal folds do not fuse with the septum transversum and the dorsal oesophageal mesentery by about the tenth week.
Why is a diaphragmatic hernia repaired after stabilisation and not immediately?
Outcome depends mainly on pulmonary hypoplasia and pulmonary hypertension. Early emergency repair was associated with high mortality from pulmonary hypertension, so repair is now usually delayed to 48 to 72 hours after birth to allow stabilisation with gentle ventilation. Repair uses permanent sutures or a prosthetic patch.

Sources

  1. StatPearls — Anatomy, Thorax: Diaphragm (NCBI Bookshelf)
  2. StatPearls — Congenital Diaphragmatic Hernia (NCBI Bookshelf)
  3. StatPearls — Diaphragm Disorders (NCBI Bookshelf)

For exam preparation and education only — not a substitute for clinical judgement or local guidelines. How we write and review these pages: editorial policy.

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