diseases of the mediastinum & mediastinal masses dr. waseem hajjar md, frcs, assistant professor...
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Diseases of the Mediastinum &
Mediastinal Masses
Dr. Waseem HAJJAR MD, FRCS,Assistant Professor &
Consultant thoracic surgeonKKUH, King Saud University
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The Mediastinum is the region in the chest between the pleural cavities that contain the heart and other thoracic viscera except the lungs
Boundaries Lateral - parietal pleuraAnterior - sternumPosterior - vertebral column and paravertebral
guttersSuperior -thoracic inletInferior - diaphragm
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Mediastinal Anatomy
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Normal Mediastinum
Anterior mediastinumEverything lying forward of and superior to the heart
shadowBoundaries
Sternum, first rib, imaginary curved line following the anterior heart border and brachiocephalic vessels from the diaphragm to the thoracic inlet
ContentsThymus gland, substernal extension of the thyroid
and parathyroid gland and lymphatic tissues
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Normal Mediastinum
Middle mediastinumDorsal to the anterior mediastinum, extends from the
lower edge of the sternum along the diaphragm and then cephalad along the posterior heart border and posterior wall of the trachea
ContentsHeart, pericardium, aortic arch and its major branches,
innominate veins and superior vena cava, pulmonary arteries and hila, trachea, group of lymph nodes, phrenic and upper vagus nerve
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Normal Mediastinum
Posterior MediastinumOccupies the space between the back of the heart and
trachea and the front of the posterior ribs, and paravertebral gutter
It extends from the diaphragm cephalad to the first rib Contents
Esophagus, descendng aorta, azygos and hemiazygos vein, paravertebral lymph nodes, thoracic duct, lower portion of the vagus nerve and the symphathetic chain
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Clinical Presentation
Asymptomatic massSpecific disease entities according to anatomical, and
embryologic origin50% of all mediastinal mass are asymptomatic80% of such mass are benignIncidental discovery – most common (routine CXR)Silent in early phaseMainly cause pressure symptomsMore than half are malignant if with symptoms
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Clinical Presentation
Effects on Compression or invasion of adjacent tissues
Chest pain, from traction on mediastinal mass, tissue invasion,
or bone erosion is common
Cough, because of extrinsic compression of the trachea or
bronchi, or erosion into the airway itself
Hemoptysis, hoarseness or stridor
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Clinical Presentation
Pleural effusion, invasion or irritation of pleural space
Dysphagia, invasion or direct invasioin of the esophagus
Pericarditis or pericardial tamponade
Right ventricular outflow obstruction and cor pulmonale
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Clinical Presentation
• Superior vena cava
– Vulnerable to extrinsic compression and obstruction because it is thin walled and its
intravascular pressure is low, and relatively confined by lymph nodes and other rigid
structures
• Superior vena cava syndrome
– Results from the increase venous pressure in the upper thorax , head and neck
– characterized by dilation of the collateral veins in the upper portion of the head and
thorax and edema oand phlethora of the face, neck and upper torso, suffusion and
edema of the conjunctiva and cerebral symptoms such as headache, disturbance of
consciousness and visual distortion
• Bronchogenic carcinoma and lymphoma are the most common etiologies
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Clinical Presentation
• Hoarseness, invading or compressing the nerves
• Horners syndrome, involvement of the sympathetic ganglia
• Dyspnea, from phrenic nerve involvement causing
diaphragmatic paralysis
• Tachycardia, secondary to vagus nerve involvement
• Clinical manifestations of spinal cord compression
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Clinical Presentation
• Systemic symptoms and syndromes
• Fever, anorexia, weight loss and other non specific symptoms
of malignancy and granulomatous inflammation
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Techniques for visualizing the mediastinum and its content & obtaining tissue Bx
• Chest PA & Lateral• Chest Ct with oral & i/v contrast• Fluoroscopy• Bronchoscopy• Esophagogram (Barrium swallow)• Isotope Scanning
• FNA• True cut Needle Bx• Medistinoscopy• VATS• Thoracotomy
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43 y/o female w/ Hx of asthma presents with progressive SOB, dysphagia , fatigability for 5 months. No wheeze or cough, EKG normal. CXR showed
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• FILM FINDINGS:-Mass just lateral to main
pulmonary artery - thick-walled smoothly-
marginated- No calcification
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Thymoma• Anterior mediastinum• Most common (20%)of mediastinal tumor in adults but
rarely seen in children• Equal frequency in males and females • 30 – 50 yrs• 50% are asymptomatic• Various Classification : Lymphocytic, Epithelial, Spindle Cell• Most encapsulated; 35% invasive (but histologically
benign!)• Parathymic syndromes – 30-50% myasthenia gravis, – less common– hypogammaglobulinema (10%), pure
red cell aplasia (5%)
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Thymoma (Staging)
• Stage I : contained within an intact capsule
• Stage II: extension through the capsule to surrounding fat, pleura, pericardium
• Stage III : Intrathoracic metastasis• Stage IV: Extrathoracic Metastasis
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Thymoma(Treatment)
• Stage I : Surgical resection Recurrence 2-12%• Stage II & III : Surgery + Radiotherapy• Stage IV : Multimodality Induction chemotherapy,
surgery + post op Radiotherapy• complete surgical resection – usually good prognosis• 2-12% of resected encapsulated thymomas recur• invasive thymoma has much worse prognosis– 50% 5-
yr survival, compared to 75% in noninvasive.• Survival not affected by the presence of Myasthenia
Gravis
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23-year-old female had a 8-week history of fever and night sweats accompanied by a 8kg weight loss
Left anteriorMediastinal mass
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A CT was ordered to further characterize the mass:
• Film findings:-large, Inhomogeneou
solid, antero left mediastinal
Mass.No calcium. No fat.
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PATHOLOGY
• A percutaneous CT guided truecut biopsy was performed
• Pathology reported the presence of Reed- Sternberg cells.• What is the diagnosis?
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Lymphoma
• 5-10% is mediastinal primary• Second most common Anterior Mediastinal Mass in
Adults• Malignant > Hodgkin’s & non-Hodgkin’s• Surgeon’s primary role is to provide sufficient tissue
for diagnosis and to assist in pathologic staging.• Dx: Mediastinoscopy, thoracotomy ,True cut Bx• Rx: Chemotherapy or XRT• Prognosis: Varies with tumor histology
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18 y/o female with R upper chest and shoulder pain x 1 month. Exacerbated by movement and inspiration. No findings on PE. Working Dx is musculoskeletal injury. A CXR done
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CHEST CT
- CT shows mass with areas of:•fat•fluid•soft tissue Likely
diagnosis ?
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Germ Cell Tumors• The mediastinum is the most common location for extragonadal
germ cell tumors (GCTs) in adults• GCTs can be either benign (teratomas, dermoid cysts) or
malignant (seminomas, non-seminomatous GCTs).• Mature teratoma – most common mediastinal germ cell tumour.• All ages – particularly young adults (F>M)• Presentation – mostly asymptomatic , incidentally diagnosed on X-
ray, CT., may cause cough, dyspnea, pain• CXR: well-circumscribed, round or lobulated, calcifications in up
to 26%• CT: well-marginated, lobulated, cystic component 88%, fat 50-
75%,calcification 25-50%, fat-fluid levels diagnostic, but rare (<10%)
• Surgical excision is curative
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Malignant Nonteratomatous Germ Cell Tumors
• Usually in the third and fourth decades of life• Symptoms: chest pain, cough, dyspnea, and hemoptysis• The superior vena cava syndrome occurs commonly• Diagnostic imaging: A large anterior mediastinal mass• Serologic measurements (α-fetoprotein and β-hCG) useful for:
– differentiating seminomas from nonseminomas tumors, – assessing response to therapy,– diagnosing relapse or failure of therapy
• Seminomas rarely produce β-hCG and never produce α-fetoprotein• More than 90% of nonseminomas secrete one or both of these
hormones• seminomas are radiosensitive and nonseminomas are relatively
radiosensitive
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A 46-year-old woman came to you with complain of a persistent cough for the past 3 weeks and mild dysphagia. O/E she has no respiratory distress. There is an enlarged left lobe of the thyroid gland, without any cervical adenopathy.
-Film Findings :-Trachea deviated to
right. LeftanterosuperiorMediastinal massextending intoCervical region
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Substernal Thyroid Tissues
• Goiters usually are considered substernal (also referred to as mediastinal, intrathoracic, or retrosternal) when more than 50% of the thyroid parenchyma is located below the sternal notch
• Mediastinal goiters are classified as primary or secondary• Primary mediastinal goiters, also referred to as ectopic or
aberrant goiters, uncommon, 1% of all surgically excised goiters
• Secondary mediastinal goiters are a much more common, 5–15% of all goiters demonstrate some extension into the mediastinum
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• Radiographic:– Chest x-ray mediastinal mass, superior mediastinal
widening, tracheal deviation or compression– Chest CT scans define the full extent and anatomic
relationships of the substernal thyroid to surrounding structures and to facilitate preoperative planning
• serum thyroid-stimulating hormone measurement If hyperthyroidism is present antithyroid medications and beta blockade should be undertaken before elective resection
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A 25-year-old man incidentally discovered, asymptomatic, isolated, rounded paravertebral mass on CXR and further CT scan showed following findings. The most likely diagnosis is
“Dumb-bell”Tumor
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Neurilemmoma(Schwannoma)
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Neurogenic tumours
• most common tumours to arise in the posterior mediastinum.
• peripheral nerves – neurofibroma, schwannoma, malignant tumours of nerve sheath origin.• Tumours arising from sympathetic ganglia.• Peripheral nerve tumours typically originate in an
intercostal nerve in the paravertebral region. • Neurofibromas and Schwannomas present as well-defined
round or oval posterior mediastinal masses.
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Mesenchymal Tumors
• Lipoma, Fibroma, Mesothelioma• Superior or Anterior mediastinal location• Diagnosis with CT scan
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Benign Cysts
• Most Common in Middle mediastinum• 20% of mediastinal masses• Usually asymptomatic• Bronchogenic cyst(32%), pericardial
cyst(35%), enteric cyst(12%), thymic cyst, and thoracic duct cyst
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Pericardial Cyst
• Thin-walled, mesothelial cell lining• most common in Right C-P angle • Simple cysts are almost always
asymptomatic• Rare cardiac impingement
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Pericardial Cyst
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Bronchogenic Cysts
• 30 - 60% of all mediastinal cysts• Lined by ciliated respiratory epithelium• May contain cartilages or mucous• Communicate with tracheobronchial trees• May become infected• Wheezing, dyspnea, recurrent pulmonary
infections
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Bronchogenic Cyst
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Aortic Aneurysm
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Paratracheal Lymphadenopathy
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Pleuro-pulmonary infection
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Infectious A.Lung Abscess
Causes Clinical Features
‒ Copious production of foul smelling sputum
Investigation‒ C X R
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Treatment Abx Drainage
‒ Internal‒ External
Pulmonary resection Indications
1. Failure of medical RX2. Giant abscess ( >6cm)3. Haemorrhage4. Inability to R/O carcinoma5. Rupture with resulting empyema
Type of Resection‒ Lobectomy
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B. BronchiectasisDef.Bronchial dilatationCause
Congenital Infection Obstruction
Clinical Features Cough Dyspnea Haemoptysis (50%) Clubbing
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Investigation Bronchogram CT Bronchoscopy
Treatment Medical
‒ Resolve most cases
Surgical‒ Failure of medical Rx‒ Patient with localized disease
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C. Tuberculosis* 30,000 new cases occur
annually in U.S.A Cause
‒ Pulmonary‒ Extra-pulmonary
Investigation‒ C X R
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Treatment‒ Medical‒ Surgical
Failure of medical Rx Destroyed lobe or lung Pulmonary haemorrhage Persistent open cavity with + ve
sputum Persistent broncho pulmonary
fistula
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Hydatid cystCause
Echinococcus granulosus
DiagnosisTreatment
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Thoracic empyema
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Striffeler H, Gugger M, Im Hof V, Cerny A, Furrer M, Ris HB. Ann Thorac Surg 1998;65:319-323.
Striffeler H, Ris HB, Würsten HU, Im Hof V, Stirnemann P, Althaus U. Eur J Cardiothorac Surg 1994;8:585-588.
• Thoracic empyema is the collection of pus or the presence of infected fluid within the pleural cavity.
• Pleural empyema affects a large number of patients and may lead to severe and disabling sequelae in cases of inappropriate diagnosis or treatment.
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