2. The lymphatic system is an important component of the circulatory system
Lymph constitutes the excess of tissue fluid, which is derived from blood
plasma and removed from the interstitial tissue via the lymphatic system.
Lymph contains nutrients, hormones, fatty acids, toxins, and cellular waste
products.
Most of the lymphatic system consists of a network of small vessels; hence
it is difficult to image it and especially to introduce contrast media into
these small lymphatic ducts. However, in the last few years, the lymphatic
imaging has been advanced by combining soft tissue contrast and
resolution offered by MR imaging, supplemented by the injection of
contrast media via a lymph node.
INTRODUCTION
4. The lymphatic system consists of ,
A) Small terminal lymphatic ducts that be divided into 3 types depending on
their origin,
Soft tissue -Lower concentration of proteins in the peripheral lymph (17%–
30%of the blood level)
Liver - Contains the highest concentration of proteins of all lymph (80%–
90% of the blood level)
Intestinal lymphatic ducts {higher concentration of lipids and proteins
(60% of the blood level)}-CHYLE
ANATOMY OF THE LYMPHATIC SYSTEM
5. B) Lymph nodes- Regulate the composition of lymph and mount an immune
response if pathogens are detected.
7. METHODS OF IMAGING THE LYMPHATIC SYSTEM
Modalities of lymphatic imaging include ,
A) Lymphoscintigraphy
• Lymphoscintigraphy is performed by injection of radioactive tracers
intracutaneously or subcutaneously into the feet or hands. The tracers are
rapidly absorbed into terminal lymphatic ducts.
• Lympho-scintigraphy provides dynamic information but lacks spatial
resolution and anatomic details.
• Lymphoscintigraphy is often used to identify the sentinel lymph node, or
the first node to receive the lymph drainage from a tumor
8.
9. B) Fluoroscopic Peripheral and central Lymphangiography
It is performed through cannulation of peripheral lymphatic ducts on the
dorsum of feet or hands, interstitial injection into interdigital web spaces,
or cannulation of lymph nodes in the groins and injection of iodized oil-
based contrast media(Lipiodol)
Advantages: Excellent spatial resolution
Disadvantages:
Exposure to ionizing radiation
Longer examination time than DCMRL
Limited dynamic information due to slow movement of viscous contrast
media
Paradoxical embolization
12. C) Peripheral Magnetic Resonance Lymphangiography
• Lymphatic ducts in the lower and upper extremities can be imaged by MR
imaging using T2-weighted images or with injection of GBCM into the
dermal plane in the feet and hands on T1-weighted images
• Effectively plan treatments such as lympho-venous bypass in cases of
lymphedema
17. • The patient is placed supine on a detachable MR imaging table, outside the
scanning room, with posterior elements of the torso coil underneath the
patient before the start of cannulation. Anterior elements of the coil are
placed when the patient is taken into the scanner, after the lymph node
cannulation.
Positioning
18. • Both inguinal regions are prepared and draped under sterile conditions.
Under ultrasound guidance, a 22- to 25-gauge needle is placed in the
medulla of an inguinal lymph node on each side.
Lymph Node Cannulation
19.
20. • Endotracheal intubation was considered essential in all patients
because of age or coexisting morbidities that resulted in an
inability to perform repeated breath-hold sequences for 20–
30seconds, which are required for the dynamic T1-weighted
high-resolution imaging with volumetric excitation
(THRIVE)sequence.
21. • Any routinely used GBCM can be used for DCMRL.
• Dose : 0.1 mmol/kg used for routine intravenous injection. 0.2 mmol/kg
can be used occasionally in larger patients.
• Dilution: Diluted with normal saline 1:1 for older children and adults and
1:2 or 1:3 for younger children to reduce T2 effects of concentrated
gadolinium causing darkening from paramagnetic effects of undiluted
gadolinium.
• The total volume is divided and half of the amount is injected on each
side. The entire tubing is primed with contrast containing solution. A
syringe with normal saline is also attached to the 3-way stopcock on each
side to flush the system and push the contrast remaining in the tube.
Contrast Media
22. • FOV: Mid-neck to the lesser trochanter
• The 16-channel torso phased arraycoil, with a 55-cm area of coverage by
the MR coil was preferred,
• The 2 main components of central MR lymphangiography include T2-
weighted imaging and postcontrast dynamic T1-weighted imaging
(DCMRL), both acquired with fat suppression.
MR Imaging Examination
23.
24. T2-weighted images
Advantages:
• T2-weighted images help to localize areas of lymphedema, which may
remain undetected by DCMRL.
• They also provide anatomic information of the cisterna chyli and
thoracic duct that can be complementary to DCMRL in cases where the
contrast does not propagate into the thoracic duct due to distal
obstruction or lymph leak.
• Static, noncontrast T2-weighted MR lymphangiography can be useful in
procedural planning for DCMRL and potential intervention. There are
no data on frequency of visualization of cisterna chyli and thoracic duct
on heavily T2-weighted images.
25.
26. Limitations:
• Difficulty to visualize smaller lymphatic ducts because of insufficient
signal from small amounts of fluid within them and difficulty to
differentiate lymphatic ducts from other overlapping fluid-containing
structures and veins.
• It is a static imaging technique that lacks dynamic information,
which is important when it comes to demonstrating lymphatic reflux
or leakage
31. • PB is a potentially fatal condition involving airway obstruction caused by
casts that can lead to significant asphyxia.
• It is characterized by expectoration of branching bronchial casts that are
formed by exudation of proteinaceous material and sometimes cells in the
airway. PB can occur in patients,
• After single-ventricle palliation, cystic fibrosis, sickle cell anaemia, asthma,
and lymphangiomatosis.
• Fontan patients(prevalence 4%)
• Lymphatic plastic bronchitis
1) PLASTIC BRONCHITIS
38. Chylothorax and chyloperitoneum can be congenital and isolated or
associated with lymphatic dysplasia. They can occur secondary to trauma,
surgery, severe infection such as tuberculosis or fungal infestations, as well
as malignancy
2) CHYLOTHORAX AND CHYLOPERITONEUM
42. • Protein losing enteropathy (PLE) is characterized by rapid loss of serum
proteins into the gut lumen. The resulting hypoproteinemia can lead to
edema, ascites, pleural, and pericardial effusions due to an imbalance
between oncotic and hydrostatic pressures.
• PLE is either caused by lymphatic abnormalities or chronic mucosal injury
as occurs in inflammatory bowel disease or neoplasm.
• elevated CVP
• Abnormal lymphatic flow /lymphangectasia
3) PROTEIN LOOSING ENTEROPATHY
43.
44.
45. • Biko and colleagues have reported intrahepatic DCMRL that involves
injection of GBCA directly in the liver lymphatics and tracking the
passage of contrast using T1-weighted MR images
• Liver lymphangiography is performed by inserting a 25- gauge needle in
the periportal space. This technique facilitates the diagnosis of protein-
loosing enteropathy and chylous ascites.
57. • DCMRL is a novel technique to image CCLs performed by injecting GBCA
into groin lymph nodes and following the passage of contrast through
the lymphatic system using T1-weighted MR images. To date, it has been
successfully applied to image and guide treatment of the lymphatic
abnormalities associated with Fontan procedure such as plastic
bronchitis. It is also useful in the assessment of chylothorax and
chyloperitoneum and their potential treatment planning. Its role in other
areas such as intestinal lymphangiectasia and lymphatic anomalies is
likely to increase.
Summary
58. References
Magnetic Resonance Lymphangiography -Govind B. Chavhan,
MD, DABR,*, Christopher Z. Lam, MD, Mary-Louise C. Greer, MD,
Michael Temple, MD, Joao Amaral, MD, Lars Grosse-Wortmann, MD
Chavhan GB, Amaral JG, Temple M, et al. MR lymph-angiography in
children: technique and potential applications. Radio graphics
2017;37(6):1775–90.
Betterman KL, Harvey NL. The lymphatic vasculature: development and
role in shaping immunity. Immunol Rev 2016;271(1):276–92.
Dori Y, Zviman MM, Itkin M. Dynamic contrast-enhanced MR
lymphangiography: feasibility study in swine. Radiology
2014;273(2):410–6.
which result from accumulation of tissue fluids due to impaired lymphatic drainage.
These advances have focused on the visualization of the central conducting lymphatics (CCLs) such as the cisterna chyli and thoracic duct by dynamic contrast-enhanced magnetic resonance lymph-angiography (DCMRL) as well as in the imaging of the extremity’s lymphatic system. This review discuss the anatomy of the lymphatic system and various methods of imaging of the lymphatic system and focus on the DCMRL technique along with its current and potential clinical applications.
The right lymphatic duct is short (approximately 1.25 cm)
The thoracic duct is a long channel, measuring approximately 38 to 45 cm in adults.
The cisterna chyli measures approximately 5 to 20 mm in width and 5 to 7 cm in craniocaudal dimension in adults
The anatomy of the thoracic duct is variable. Similarly, the cisterna chyli can have variable shape including an inverted Y or V and a string of pearls.
The thoracic duct transports approximately 1.5 to 2.5 L of lymph/chyle daily.
Over the years, imaging of the lymphatic system has evolved from direct lymphangiography through cannulation of peripheral lymphatic ducts on the dorsum of feet and hands and interstitial in-jection of contrast media into interdigital web spaces to injection of contrast media directly into lymph nodes.1
Tc-99 sulphur colloid-45min- static/dynamic
Melanoma
Gamma camera
Spect ct
35-year-old man with left chylothorax after lung biopsy using video-assisted thoracoscopy.
A. Axial CT scan obtained one week prior to LG shows large amount of left pleural effusion (chylothorax). B. Isolated lymphatic of dorsum of right foot was cannulated using 30-G LG needle and both needle and lymphatic were firmly tied (arrow). C. Radiographic image obtained 5 minutes following Lipiodol injection shows Lipiodol extravasation (arrows) at calf level. D Radiographic images obtained 15 minutes following Lipiodol injection show good opacification of inguinal and pelvic lymph nodes as well as ascending lymphatics. F, G. Radiographic anteroposterior and lateral images obtained one hour following Lipiodol injection show pseudoaneurysm-like leakage (arrows) of Lipiodol at 9th thoracic spine level. H. CT reconstructed image obtained 5 hours following LG shows leakage site (arrow) adjacent to descending thoracic aorta and prominent Lipiodol leakage to left lung. Left chest tube draining 700 mL per day was eliminated three days after LG. LG = lymphangiography
21-year-old woman with bilateral primary lymphoedema. Angled three-dimensional (3D) spoiled gradient echo magnetic resonance lymphography (MRL) maximum intensity projection (MIP) image, obtained 45 min after Gadoteridol injection, clearly depicts a reticular network of enlarged lymphatic vessels in both lower legs (small arrows). Furthermore, areas of dermal backflow are revealed bilaterally, indicating delayed lymphatic flow with neovascularization due to obstruction (asterisks). Note the concomitantly enhanced veins in both lower legs (arrowheads).
A small volume of saline is gently injected to confirm the needle is appropriately located within the medulla and to ensure there is no extravasation. Injection of saline increases the size of the node
The needle is then connected to long 21-inch tubing with a 3-way stopcock on the end and taped in place
Syringes with contrast media (dilute gadolinium) and saline flush are connected to the 3-way stopcock
The patient is then transferred to the MR imaging scanner.
Groin lymph node cannulation for MR lymphangiography in an 8-month-old baby. Longitudinal ultra-sound image of the left groin (A, B) shows a lymph node (arrowheads) with a needle (arrow) within the central echogenic medulla. The lymph node size increases with injection of saline (B).
The patient is placed on the detachable MR table in the preparatory room, just outside the imaging room, with the posterior elements of a 16-channel torso phased-array coil in place. Both inguinal regions are prepared and draped. Each angiographic catheter is connected in sequence to a short T-connector, a proximal three-way stopcock, 21-inch tubing, and a distal three-way stopcock. The distal three-way stopcock is connected tosyringes that are prefilled with the mixture of gadolinium-based contrast material and normal saline. A, The configuration of the connections. B, A plastic shield is placed over the abdomen and pelvis to protect the sterile field to avoid dislodgement of the intranodal cannula and to lift the weight of the anterior coil off of the patient. C, The anterior component of the coil is placed over the shield. This setup provides a large field of view from the lower neck to the inguinal regions.
A precontrast mask is acquired that is used for subtraction. The images are acquired every minute from the start of intranodal injection of contrast until it reaches the venous angle between left subclavian and left internal jugular veins.
The dynamic images are reformatted using maximum intensity projection.
Variable morphology of cisterna chyli. (A) Coronal T2-weighted image of the abdomen in a 17-year-old boy with nonspecific abdominal pain shows a usual slightly bulbous cisterna chyli (arrow). (B) Coronal T2-weighted MRCP image in a 10-year-old child with history of choledochal cyst resection demonstrates an irregular cisterna chyli (arrow) joined by lumbar trunks. (C) Coronal T2-weighted MRCP image in another 15-year-old child with choledocholithiasis demonstrates a thin tubular cisterna chyli (arrow).
It demonstrates normal central con-ducting lymphatics. Coronal 3D T1-weighted images at 4 minutes (A), 5 minutes (B), 6 minutes (C), 7 minutes (D), and 8 minutes (E) after injection of contrast demonstrate progressive passage of the contrast (arrows) up to the venous angle (arrowhead).
A–E, Selective thick-slab maximum intensity
projections at different time-points after intranodal contrast material injection. contrast material appears in the retroperitoneal lymphatics within 2 minutes (arrow in B)and in the thoracic duct (thick white arrow in C and D) and venous angle within 4–8 minutes (thin white arrow in D). Depending on the volume of injection, contrast material washes out of the CCL in 15–20 minutes. Transient stasis or pooling of contrast material proximal to the venous angle insertion (thin white arrow in C and D)is considered a normal finding related to bolus injection of contrast material in the CCL. There is progressive accumulation of contrast material in the renal collecting system on the delayed images consistent with venous entry of contrast material.
DCMRL therefore playsan important role in planning of the embolization treatment in these patients. Elevated CVP in TCPC results in increased lymph production, mainly by the liver as well as increased impedance to lymphatic drainage. This causes congestion in the central lymphatic system, and in the presence of PLPS, it can result in overflow of lymph into the lung parenchyma and/or into the airways, resulting in protein leakage into the airways. This may be mediated by a potential inflammatory component, as evidenced by presence of fibrin and inflammatory cells in bronchial casts of Fontan patients with plastic bronchitis.
Chest plain radiograph demonstrate consolidation and atelectasis at the right lobe.
Chest CT shows multifocal consolidation, atelectasis, airway stenosisand mucus plug.
The MRI scan demonstrated the presence of a dilated right-sided peribronchial lymphatic network supplied by retrograde lymphatic flow through a large collateral lymphatic vessel originating from the thoracic duct.
Selective embolisation
Plastic bronchitis in a 4-year-old child with Fontan surgery. Coronal 3D T1-weighted images with thin maximum intensity projection (MIP) reconstruction at 8 minutes (A), 10 minutes (B), and 16 minutes (C) after injection of contrast demonstrate an abnormal ectatic lymphatic duct extending from retroperitoneum to the left side of superior mediastinum (arrows), lymphangiectasia in retroperitoneum (arrowheads) and mediastinum (arrowheads),and extensive and progressive chylolymphatic reflux into left supraclavicular and axillary lymph nodes. There is also chylolymphatic reflux into the lungs (dashed arrows).
Time lapse DCMRL in plastic bronchitis
Congenital left chylothorax in a 7-week-old baby. Coronal 3D T1-weighted images precontrast (A) and18 minutes after injection of contrast (B) demonstrate left pleural effusion with opacification on postcontrast image suggesting lymphatic leak (dashed arrows). A thin MIP reconstruction image (C) shows abnormal tortuous CCL (arrowheads) without a single normal looking thoracic duct and chylolymphatic reflux into left pleural cavity(arrows).
Congenital chyloperitoneum in an 8-week-old baby from chyle leak. Coronal T2-weighted (A), and post nodal injection coronal 3D T1-weighted images at 3 minutes (B) and 15 minutes (C) after injection of contrast
demonstrate contrast leakage from retroperitoneal lymphatic channel (arrow on B) with progressive opacification of ascites on left side of the abdomen.
Chylolymphatic reflux and pulmonary lymphangiectasia in a 13-year-old girl with recurrent chylopericardium and chylothorax. A, B, Rapid opacification of normal pelvic and retroperitoneal lymphatics. C, D, The cisterna chyli and thoracic duct appear at 7–8 minutes; there is apparent narrowing at the junction
of the middle and superior thirds of the thoracic duct (arrow), but no obstruction to transit of contrast material. At 8–9 minutes, there is chylolymphatic reflux (arrows in F, G, I, K) from the thoracic duct into dysplastic lymphatic channels in the mediastinum, left lower lobe, and pleura, which progresses over the next 10 minutes(E–L). M, Delayed 40-minute image shows pooling of contrast material within the pericardial (thick arrow) and pleural (thin arrow in L and M) spaces with washout of contrast material from the CCL.
Protein losing enteropathy (PLE) in a 23-month-old child. Axial T2-weighted images of the abdomen (A,B) demonstrate mild ascites, mesenteric edema, and diffuse bowel wall thickening in keeping with PLE. This child
had normal CCL as demonstrated
14-year-old male with ahistory of hypoplastic left heartsyndrome post Fontan palliation who presents with protein-losingenteropathy (PLE). a Coronalplane of T2-weighted imaging ofthe abdomen and chest in a patient b with PLE showing the duodenum(arrow) with minimal fluid and no significant T2 signal. b In a coronalplane at the same location , a high-resolution contrast-enhancedT1 sequence shows enhancement of the duodenum(arrow) consistent with PLE
22-year-old female with a history of hypoplastic left heart syndromepost Fontan palliation who presents with protein-losing enteropathy(PLE). a–f Time series of intrahepatic dynamic contrast magneticresonance lymphangiography (IH-DCMRL) showing coronal maximum intensity projections of the abdomen and chest. a At the time of the start of injection (t = 0) showing the site of injection (arrow). b At 2 min afteri njection demonstrating contrast moving along the hepatic lymphatic system(arrow) and exiting into the hepatic hilum (arrowhead). c At 3 minafter injection showing contrast beginning to leak into the duodenum(arrow) and opacifying the thoracic duct (TD) (arrowhead). d At4.5 min after injection demonstrating further filling of the duodenumand hilar lymphatic channels (arrow). e At 8.5 min after injection where there is complete filling of the first portion of the duodenum (arrow) aswell as hepatic, hilar, retroperitoneal lymphatics, and the TD. f A more
delayed coronal image obtained 12 min after injection shows enhancementof the duodenal wall (arrowhead) and filling of the duodenal lumenwith contrast. h Confirmation of the MRI findings was demonstrated by intrahepatic injection of blue dye with endoscopy showing a leak into the duodenal lumen
Magnetic resonance enterography image showing a thickened lymphangiectatic duodenal loop (arrow) corresponding to loss of lymph throughout the duodenal loop.
Selective intranodal magnetic resonance lymphangiogram recorded prior to embolization showing enhanced contrast medium uptake by the lymphatic system and retrograde flow into the intestinal lymphatics from the intestinal lymphatic trunk, confirming a duodenal obstruction.
Selective glue embolization of the refluxing and leaking intestinal lymphatic trunk with n-butyl-2-cyanoacrylate (n-BCA) liquid embolic system (Trufill; Cordis Neurovascular, Miami Lakes, FL, USA) resulted in rapid reversal of the PLE over just a few weeks after the procedure
Gastrointestinal endoscopy image showing chylous lymphangiectasia localized to the duodenal loop (A, B) and complete resolution after the procedure (C, D).
MRI lymphangiography. (A) Unenhanced coronal T2 MRI sequence of the abdomen demonstrates multiple large T2 hyperintense lymphatic masses (black stars). (B) Coronal MR sequence following injection of contrast through bilateral inguinal lymph nodes demonstrates only partial opacification of these masses (black stars). her diarrhea
Fluoroscopic image of n-BCA glue injection into the periduodenal mass (white arrowhead) through 25 G needle (black arrow). Note the contrast in the duodenum (black stars).cessation of her diarrhea, and two days after the procedure she was discharged to home. Two weeks later, she reported near complete resolution of soft tissue edema, relief of abdominal pressure and return of regular bowel movements. Her weight decreased from 135 lbs. to 116 lbs. and her albumin increased from 1.7 g/dL to 2.7 g/dL.
Retroperitoneal lymphangiectasia in a 29-year-old woman with chronic lymphedema of the left lower extremity, with multiple large cysts in the inguinal region and retroperitoneum, after repeated surgical excisions of lymphatic cysts and sclerotherapy .Because of progression of the cystic collections and lower extremity edema, dynamic MR lymphangiographic imaging was performed to evaluate the integrity of the CCL and to determine if lymphatic dysplasia, rather than lymphatic malformation, was the origin of the cystic collections. A, There is severe left lower extremity edema with soft-tissue overgrowth. B, C, D, Short t inversion recovery images demonstrate large cystic collections in the inguinal
region that extend into the left retroperitoneum (arrow in B) and subcutaneous edema of the left lower extremity (C) and lateral abdominal wall (D),which may be collateral pathways for lymphatic flow from the lower extremities. E, F, After a right-sided inguinal nodal injection, there is reflux of contrast material from the right-sided retroperitoneal channels into aneurysmal dysplastic lymphatic channels in the left side of the retroperitoneum and pelvis (arrows in E, F). The thoracic duct was not visible, even on delayed images, because of pooling of injected contrast material within the dysplastic lymphatics and resultant poor antegrade transit of contrast material.
DCRML imaging of the patient with GLA and bilateral pleural effusion demonstrates normal size TD (white arrow) and abnormal pulmonary lymphatic perfusion that originates in the left retroperitoneum and extends into the mediastinum and left pleural cavity (black arrowheads).
DCRML imaging of the patient with GLA, and progressive deterioration of pulmonary function and hemoptysis demonstrated dilated TD (white arrow) and abnormal pulmonary lymphatic perfusion that originates in the distal TD toward lung parenchyma (white arrowheads).