mediastinummediastinum
Made by: Dr. Isha JaiswalMade by: Dr. Isha Jaiswal
Under guidance of: Prof M.L.B BhattUnder guidance of: Prof M.L.B Bhatt
Date:19Date:19thth
march 2014march 2014
IntroductionIntroduction
TheThe mediastinummediastinum isis the region in the chestthe region in the chest
between the pleural cavities that contain thebetween the pleural cavities that contain the
heart and other thoracic viscera except the lungsheart and other thoracic viscera except the lungs
BoundariesBoundaries
AnteriorAnterior - sternum- sternum
PosteriorPosterior - vertebral column and paravertebral- vertebral column and paravertebral
fasciafascia
SuperiorSuperior -thoracic inlet-thoracic inlet
InferiorInferior - diaphragm- diaphragm
LateralLateral - parietal pleura- parietal pleura
ThymusThymus
Located in anteriorLocated in anterior
mediastinum.mediastinum.
Develops from endoderm ofDevelops from endoderm of
33rdrd
pharyngeal pouchpharyngeal pouch
Present in childhood,Present in childhood,
involutes in adultsinvolutes in adults
Blood supplyBlood supply
Arterial :i nt. Mammary arteries
Venous: internal thoracic veins
Lymphatic drainage: lower cervical, int. Mammary and hilar nodes
Middle MediastinumMiddle Mediastinum
Contents:Contents:
HeartHeart enclosed in pericardiumenclosed in pericardium
Arteries:Arteries: Ascending Aorta,Ascending Aorta,
Pulmonary trunk with its Lt &Pulmonary trunk with its Lt &
Rt branchesRt branches
VeinsVeins: SVC,Pulmonary veins: SVC,Pulmonary veins
Nerves:Nerves: Phrenic, vagus nervePhrenic, vagus nerve
Bifurcation of Trachea withBifurcation of Trachea with
two principal bronchitwo principal bronchi
Tracheobronchial lymph nodesTracheobronchial lymph nodes
18
Posterior MediastinumPosterior Mediastinum
Boundaries:Boundaries:
Ant.Ant. Pericardium, Bifurcation of tracheaPericardium, Bifurcation of trachea
Post.Post. T5 to T12T5 to T12
sup.sup. Transverse thoracic planeTransverse thoracic plane
Inf.Inf. diaphragmdiaphragm
Sides:Sides: Mediastinal pleuraMediastinal pleura
19
LENGTH:10-15 cm
DIAMETER: 2cm in males &1.5
cm in females
Lined by ciliated columnar
epithelium
Lower level at T6 on
inspiration & T4 on expiration
Made of c shape rings
2 rings per cm
The rings make tube convex
anterolateraly
Posteriorly the gap is filled by
trachealis muscle.
NERVE SUPPLY:NERVE SUPPLY:
LYMPHATIC DRAINAGELYMPHATIC DRAINAGE
PretrachealPretracheal
paratracheal lymph nodeparatracheal lymph node
PARA SYMPHATHETIC:PARA SYMPHATHETIC:
vagus & recurrentvagus & recurrent
laryngeal nerves (laryngeal nerves (sensory &sensory &
secreto-motor to mucoussecreto-motor to mucous
membrane motor to trachealismembrane motor to trachealis
muscle)muscle)
SYMPHATHETIC: -middleSYMPHATHETIC: -middle
cervical ganglioncervical ganglion
(vasomotor)(vasomotor)
Blood supplyBlood supply
ARTERIAL SUPPLYARTERIAL SUPPLY
Upper tracheaUpper trachea
Inferior thyroid arteryInferior thyroid artery
Lower partLower part
Branches of the bronchialBranches of the bronchial
arteryartery
VENOUS DRAINAGEVENOUS DRAINAGE
Upper part :Upper part :
left brachiocephalic veinleft brachiocephalic vein
Lower part:Lower part:
Inferior thyroid veinInferior thyroid vein
Clues to locate mass toClues to locate mass to
mediastinummediastinum
Mediastinal masses : Masses in the lung
not contain air bronchograms
mediastinal mass will create obtuse
angles with the lung .
Mediastinal lines will be disrupted
– May contain air bronchograms
– A lung mass abutts the
mediastinal surface and creates
acute angles with the lung
LEFT: A lung mass abutts the mediastinal surface and creates acute angles
with the lung.
RIGHT: A mediastinal mass will sit under the surface of the mediastinum,
creating obtuse angles with the lung
Cervicothoracic signCervicothoracic sign
The anterior mediastinum ends at the level of theThe anterior mediastinum ends at the level of the
clavicles.clavicles.
The posterior mediastinum extends much higher.The posterior mediastinum extends much higher.
ThereforeTherefore
any mass that remains sharply outlined in the apex ofany mass that remains sharply outlined in the apex of
the thorax must be posterior and entirely within thethe thorax must be posterior and entirely within the
chest, andchest, and
any mass that disappears at the clavicles must beany mass that disappears at the clavicles must be
anterior and extends into neckanterior and extends into neck
See sharp
margin
above clavicle
Mass is in posterior mediastinum. because it remains sharply outlined in apex
of thorax, indicating that it is surrounded by lung.
This particular example is a ganglioneuroma
Thoracoabdominal signThoracoabdominal sign
A sharply marginated mediastinal mass seen throughA sharply marginated mediastinal mass seen through
the diaphragm must lie entirely within the chest.the diaphragm must lie entirely within the chest.
The posterior costophrenic sulcus extends far moreThe posterior costophrenic sulcus extends far more
caudally than the anterior aspect of the lungcaudally than the anterior aspect of the lung
ThereforeTherefore
Any mass that extends below the dome of the diaphragmAny mass that extends below the dome of the diaphragm
and remains sharply outlined must be in the posteriorand remains sharply outlined must be in the posterior
compartments and surrounded by lung, andcompartments and surrounded by lung, and
Any mass that terminates at dome of diaphragm must beAny mass that terminates at dome of diaphragm must be
anterioranterior
Can you
see the
outline of the
mass below
the diaphragm?
Margin of mass is apparent and below diaphragm, therefore this must
be in the middle or posterior compartments where it is surrounded by
lung
This example is a ‘Lipoma’
Hilum overlay signHilum overlay sign
Principle of hilum overlayPrinciple of hilum overlay
An anterior mediastinal mass will overlap the mainAn anterior mediastinal mass will overlap the main
pulmonary arteries, therefore they will be seen withinpulmonary arteries, therefore they will be seen within
the margins of the massthe margins of the mass
Hilum can
be seen
through
mass
this must be an anterior
mediastinal mass
because it overlaps rather
than “pushes out” the
main pulmonary arteries
This particular example is a thymoma
MEDIASTINALTUMORSMEDIASTINALTUMORS
EPIDEMOLOGYEPIDEMOLOGY
Mediastinal malignancies are heterogenous in natureMediastinal malignancies are heterogenous in nature..
most masses (> 60%) are:most masses (> 60%) are:
ThymomasThymomas
NeurogenicTumorsNeurogenicTumors
Benign CystsBenign Cysts
Lymphadenopathy (LAD)Lymphadenopathy (LAD)
In children the most common (> 80%) are:In children the most common (> 80%) are:
Neurogenic tumorsNeurogenic tumors
Germ cell tumorsGerm cell tumors
Foregut cystsForegut cysts
In adults the most common are:In adults the most common are:
LymphomasLymphomas
LADLAD
ThymomasThymomas
Thyroid massesThyroid masses
Mediastinal MassesMediastinal Masses
Compartment %
Malignant
Anterosuperior 59
Middle 29
Posterior 16
Mediastinal
division
Most common
tumors
Anterior-
superior
thymoma
middle lymphoma
posterior Neurogenic
tumors
ThymomaThymoma
PresentationPresentation
Most common primary anterior mediastinal tumorMost common primary anterior mediastinal tumor
M=F, most >40M=F, most >40
Most patients are asymptomaticMost patients are asymptomatic
Half of patients suffer have associated parathymicHalf of patients suffer have associated parathymic
syndromessyndromes
• myasthenia gravismyasthenia gravis
• hypogammaglobulinemiahypogammaglobulinemia
• pure red cell aplasiapure red cell aplasia
1/3 have chest pain, cough or dyspnea on presentation1/3 have chest pain, cough or dyspnea on presentation
Myasthenia gravis occurs in 30-50% of pts with thymoma.Myasthenia gravis occurs in 30-50% of pts with thymoma.
Hypogammaglobulinemia occurs in 10% of pts withHypogammaglobulinemia occurs in 10% of pts with
thymomathymoma
Pure red cell aplasia occurs in 5%, but thymoma occurs inPure red cell aplasia occurs in 5%, but thymoma occurs in
50% of pts with red cell aplasia50% of pts with red cell aplasia
Invasive thymomaInvasive thymoma
Encasement ofEncasement of
mediastinal structures,mediastinal structures,
infiltration of fatinfiltration of fat
planes, and an irregularplanes, and an irregular
interface between theinterface between the
mass and lungmass and lung
parenchyma, areparenchyma, are
highly suggestive ofhighly suggestive of
invasion.invasion.
Pleural thickening,Pleural thickening,
nodularity, or effusionnodularity, or effusion
generally indicatesgenerally indicates
pleural invasion by thepleural invasion by the
thymomathymoma
Thymic CarcinoidThymic Carcinoid
carcinoid tumors (neuroendocrine tumors) of the thymus are very rare,carcinoid tumors (neuroendocrine tumors) of the thymus are very rare,
accounting for <5% of all neoplasms of the anterior mediastinum.accounting for <5% of all neoplasms of the anterior mediastinum.
They originate from the normal thymic Kulchitsky cells, which belong to theThey originate from the normal thymic Kulchitsky cells, which belong to the
amine precursor uptake and decarboxylation (APUD) groupamine precursor uptake and decarboxylation (APUD) group
PresentationPresentation
men aged 30 to 50 yearsmen aged 30 to 50 years
(male/female ratio: 3:1)(male/female ratio: 3:1)
Rarely associated with carcinoid syndromeRarely associated with carcinoid syndrome
Associated endocrine abnormalities: Cushing’s syndrome due to ectopicAssociated endocrine abnormalities: Cushing’s syndrome due to ectopic
ACTH or MENACTH or MEN
73% have regional lymph node and/or distant osteoblastic bone mets73% have regional lymph node and/or distant osteoblastic bone mets
Thymic carcinoid tumor in a 22-year-old man with a 3-month history of a persistentThymic carcinoid tumor in a 22-year-old man with a 3-month history of a persistent
dry cough.dry cough.
Contrast-enhanced CT scan shows a heterogeneously enhancing thymic mass .Contrast-enhanced CT scan shows a heterogeneously enhancing thymic mass .
PET image shows intense FDG uptake by the massPET image shows intense FDG uptake by the mass
Thymic Carcinoma
Presentation
•M>F, 40s
•Thymic carcinomas are less common than thymomas, more aggressive
with a higher propensity for capsular invasion
•Early local invasion, widespread lymphatic and hematogenous
metastases
•Clinically, patients present initially with tussis, dyspnea, pleuritic chest
pain, phrenic nerve palsy, or superior vena cava syndrome
80% of patients with thymic carcinoma may have radiographic evidence
of invasion into adjacent structures in the mediastinum
40% may have evidence of mediastinal lymphadenopathy
•Distant metastases to regional lymphatics, bone, liver, kidney, and lung
are a common clinical feature
Thymic CarcinomaThymic Carcinoma
Thymic carcinomasThymic carcinomas
behave morebehave more
aggressively thanaggressively than
invasive thymomasinvasive thymomas
and are more likely toand are more likely to
metastasize to distantmetastasize to distant
sitessites
Thymic LymphomasThymic Lymphomas
Lymphoma is the mostLymphoma is the most
common cause of ancommon cause of an
anterior mediastinalanterior mediastinal
mass in children andmass in children and
the second mostthe second most
common cause of ancommon cause of an
anterior mediastinalanterior mediastinal
mass in adults.mass in adults.
cancers of the head and neck, abdomen, and pelvis can involve the thymus viacancers of the head and neck, abdomen, and pelvis can involve the thymus via
lymphatic pathwayslymphatic pathways
Metastatic disease toMetastatic disease to
the thymus in a 10-the thymus in a 10-
year-old boy 2 yearsyear-old boy 2 years
after diagnosis ofafter diagnosis of
alveolaralveolar
rhabdomyosarcomarhabdomyosarcoma
of the thigh.of the thigh.
Secondary Tumors of the Thymus
Primary Mediastinal LymphomaPrimary Mediastinal Lymphoma
5-10% of patients with lymphoma present with5-10% of patients with lymphoma present with
primary mediastinal lesionsprimary mediastinal lesions
Primary mediastinal lymphoma represents 10-Primary mediastinal lymphoma represents 10-
20% of primary mediastinal masses in adults and20% of primary mediastinal masses in adults and
are usually in the anterosuperior compartmentare usually in the anterosuperior compartment
Usually present with fever, weight loss and nightUsually present with fever, weight loss and night
sweatssweats
Pain, dyspnea, stridor, SVC syndrome due toPain, dyspnea, stridor, SVC syndrome due to
mass effects are uncommonmass effects are uncommon
Primary Mediastinal Hodgkin’s LymphomaPrimary Mediastinal Hodgkin’s Lymphoma
PresentationPresentation
Incidental mediastinal mass on chest xray is 2nd mostIncidental mediastinal mass on chest xray is 2nd most
common presentation after asymptomaticcommon presentation after asymptomatic
lymphadenopathylymphadenopathy
Mass is usually large, rarely causes retrosternal chestMass is usually large, rarely causes retrosternal chest
pain, cough, dyspnea, effusions or SVC syndromepain, cough, dyspnea, effusions or SVC syndrome
Bimodal age distributionBimodal age distribution
““B” symptoms: fever, weight loss (>10% body wt in 6B” symptoms: fever, weight loss (>10% body wt in 6
months), night sweatsmonths), night sweats
Generalized pruritus presentGeneralized pruritus present
A chest CT exam shows the mass to extend from the neck to the
diaphragm, compressing the tracheal and left mainstem bronchus leading to
left lower lobe atelectasis. The chest wall mass is partially eroding the
sternum.
Dx:Lymphoma, Hodgkin, Anterior Mediastinal, Sternal
Involvement
Two contiguous slices
from an enhanced chest
CT exam show a
homogenous, solid,
anterior mediastinal mass
and a large right pleural
effusion.
Dx-Lymphoma
Non-Hodgkin,
Anterior Mediastinal
Mediastinal Germ CellTumorsMediastinal Germ CellTumors
Primary extragonadal germ cell tumors comprisePrimary extragonadal germ cell tumors comprise
2% to 5% of all germ cell tumors2% to 5% of all germ cell tumors
Approximately two thirds of these tumors occur inApproximately two thirds of these tumors occur in
the mediastinumthe mediastinum
The mediastinum is the most common site ofThe mediastinum is the most common site of
primary extragonadal germ cell tumors in youngprimary extragonadal germ cell tumors in young
adultsadults
Represent 10-15% of adult anterosuperiorRepresent 10-15% of adult anterosuperior
mediastinal tumorsmediastinal tumors
they presumably arise from germ cells that migrate alongthey presumably arise from germ cells that migrate along
the urogenital ridge during embryonic development .the urogenital ridge during embryonic development .
The embryologic urogenital ridge extends from C6 to L4The embryologic urogenital ridge extends from C6 to L4
and after malignant transformation of displaced germand after malignant transformation of displaced germ
cells, explains the development of primary germ cellcells, explains the development of primary germ cell
tumors outside the gonadstumors outside the gonads
Mediastinal Germ CellTumorsMediastinal Germ CellTumors
MediastinalTeratomasMediastinalTeratomas
Most common mediastinal germ cell tumorMost common mediastinal germ cell tumor
Three types:Three types:
• Mature: benign, well-differentiatedMature: benign, well-differentiated
• Immature: contains >50% immature components, may recurImmature: contains >50% immature components, may recur
or metastasizeor metastasize
• Malignant: a mature teratoma that contains a focus ofMalignant: a mature teratoma that contains a focus of
carcinoma, sarcoma or malignant GCTcarcinoma, sarcoma or malignant GCT
MatureTeratomaMatureTeratoma
Occurs in children and young adultsOccurs in children and young adults
Usually asymptomatic, but if large enough, may causeUsually asymptomatic, but if large enough, may cause
chest pain, dyspnea, cough or other symptoms ofchest pain, dyspnea, cough or other symptoms of
mediastinal compressionmediastinal compression
Contains derivatives of all three primitive germ layersContains derivatives of all three primitive germ layers
includingincluding
• Ectoderm: teeth, skin, hairEctoderm: teeth, skin, hair
• Mesoderm: cartilage and boneMesoderm: cartilage and bone
• Endoderm: bronchial, intestinal and pancreatic tissueEndoderm: bronchial, intestinal and pancreatic tissue
Expectoration of hair (trichoptysis) is rare butExpectoration of hair (trichoptysis) is rare but
pathognomonicpathognomonic
Mediastinal SeminomaMediastinal Seminoma
Represents 40% of malignant mediastinal GCTsRepresents 40% of malignant mediastinal GCTs
Afflicts Caucasian men in 20s-30sAfflicts Caucasian men in 20s-30s
Only rarely represents a metastatic lesion from aOnly rarely represents a metastatic lesion from a
testicular primary tumor, but testicular USG istesticular primary tumor, but testicular USG is
usually performed to rule this outusually performed to rule this out
If any other germ cell tumor histology is identifiedIf any other germ cell tumor histology is identified
in the tumor, it is treated as a mixed NSGCTin the tumor, it is treated as a mixed NSGCT
AFP normal,AFP normal, ββ-HCG may be elevated in 10%-HCG may be elevated in 10%
Mediastinal SeminomaMediastinal Seminoma
PresentationPresentation
Slow growing tumor, usually symptomatic at diagnosisSlow growing tumor, usually symptomatic at diagnosis
Commonly presents with chest pain, dyspnea, cough,Commonly presents with chest pain, dyspnea, cough,
weight lossweight loss
Presents infrequently with SVC syndromePresents infrequently with SVC syndrome
Bulky, lobulated, homogeneous mass, no calcificationsBulky, lobulated, homogeneous mass, no calcifications
Usually not invasive, but many have metastasized toUsually not invasive, but many have metastasized to
regional lymph nodes, lung and/or bone by the time ofregional lymph nodes, lung and/or bone by the time of
diagnosisdiagnosis
Mediastinal NonseminomatousMediastinal Nonseminomatous
Germ CellTumorsGerm CellTumors
NSGCTs of the mediastinum have a worse prognosis thanNSGCTs of the mediastinum have a worse prognosis than
mediastinal seminomas or teratomasmediastinal seminomas or teratomas
Occur in men in the 20-40 age groupOccur in men in the 20-40 age group
20% of patients also have Klinefelter’s syndrome20% of patients also have Klinefelter’s syndrome
Tracheal tumorsTracheal tumors
Extremely rare tumors.Extremely rare tumors.
Comprise of 0.1 to 0.4 %of all diagnosed malignanciesComprise of 0.1 to 0.4 %of all diagnosed malignancies
Two types: squamous cell carcinoma M:F=3:1 Age:6Two types: squamous cell carcinoma M:F=3:1 Age:6thth
decadedecade
adenoid cystic carcinomas M:F=1:1 younger ageadenoid cystic carcinomas M:F=1:1 younger age
Clinical feature: cough, dysnoea, dysphagia,stridorClinical feature: cough, dysnoea, dysphagia,stridor
hemoptysis, dysphoniahemoptysis, dysphonia
Clinical PresentationClinical Presentation
Asymptomatic massAsymptomatic mass
Incidental discovery – most commonIncidental discovery – most common
50% of all mediastinal mass are asymptomatic50% of all mediastinal mass are asymptomatic
80% of such mass are benign80% of such mass are benign
More than half are malignant if with symptomsMore than half are malignant if with symptoms
Clinical PresentationClinical Presentation
11 Effects on Compression or invasion ofEffects on Compression or invasion of
adjacent tissuesadjacent tissues
Chest painChest pain, from traction on mediastinal mass, tissue invasion,, from traction on mediastinal mass, tissue invasion,
or bone erosion is commonor bone erosion is common
CoughCough, because of extrinsic compression of the trachea or, because of extrinsic compression of the trachea or
bronchi, or erosion into the airway itselfbronchi, or erosion into the airway itself
Hemoptysis, hoarseness or stridorHemoptysis, hoarseness or stridor
Pleural effusion, invasion or irritation of pleural spacePleural effusion, invasion or irritation of pleural space
Dysphagia, invasion or direct invasioin of the esophagusDysphagia, invasion or direct invasioin of the esophagus
Pericarditis or pericardial tamponadePericarditis or pericardial tamponade
Right ventricular outflow obstruction and cor pulmonaRight ventricular outflow obstruction and cor pulmonalele
Clinical PresentationClinical Presentation
22 Effects on Compression of nervesEffects on Compression of nerves
Hoarseness, invading or compressing the nerves recurrentHoarseness, invading or compressing the nerves recurrent
laryngeal nervelaryngeal nerve
Horners syndrome, involvement of the sympatheticHorners syndrome, involvement of the sympathetic
gangliaganglia
Dyspnea, from phrenic nerve involvement causingDyspnea, from phrenic nerve involvement causing
diaphragmatic paralysisdiaphragmatic paralysis
Tachycardia, secondary to vagus nerve involvemenTTachycardia, secondary to vagus nerve involvemenT
Clinical PresentationClinical Presentation
Superior vena cavaSuperior vena cava
Vulnerable to extrinsic compression and obstruction because it is thinVulnerable to extrinsic compression and obstruction because it is thin
walled and its intravascular pressure is low.walled and its intravascular pressure is low.
Superior vena cava syndromeSuperior vena cava syndrome
Results from the increase venous pressure in the upper thorax , headResults from the increase venous pressure in the upper thorax , head
and neckand neck
characterized by dilation of the collateral veins in the upper portion ofcharacterized by dilation of the collateral veins in the upper portion of
the head and thorax and edema oand phlethora of the face, neck andthe head and thorax and edema oand phlethora of the face, neck and
upper torso, suffusion and edema of the conjunctiva and cerebralupper torso, suffusion and edema of the conjunctiva and cerebral
symptoms such as headache, disturbance of consciousness and visualsymptoms such as headache, disturbance of consciousness and visual
distortiondistortion
Bronchogenic carcinoma and lymphoma are the most commonBronchogenic carcinoma and lymphoma are the most common
etiologiesetiologies
Clinical PresentationClinical Presentation
Systemic symptoms and syndromesSystemic symptoms and syndromes
Fever, anorexia, weight loss and other non specificFever, anorexia, weight loss and other non specific
symptoms of malignancy .symptoms of malignancy .
1/3 have chest pain, cough or dyspnea on presentation
Myasthenia gravis occurs in 30-50% of pts with thymoma. All pts should have antiacetylcholine receptor antibodies measured prior to surgery and subsequently
Hypogammaglobulinemia occurs in 10% of pts with thymoma
Pure red cell aplasia occurs in 5%, but thymoma occurs in 50% of pts with red cell aplasia