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Thoracic Review
Anatomy
Azygous Vein- Runs on the right side and drains into the SVC
Thoracic duct- Originates around L1/L2 goes through AORTIC hiatus crosses
towards left side at T4/T5  drains into the Left Subclavian (IJ junction)
Phrenic Nerve- Anterior to hilum
Vagus Nerve- Posterior to hilum
Main resp muscles- diaphragm (80%) and intercostals (20%). When with increased
work of breathing employ SCM, levators, serratus, scalenes.
Sup-Inferior change in volume
Anatomy Continued
Right Lung has 3 lobes and accounts for 55% of the volume
Left Lung has 2 lobes and accounts for 45% of the volume
(lingual)
Left Lung has 2 lobes and accounts for 45% of the volume
(lingual)
Type 1- gas exchange
Type 2- surfactant production
There are an equal amount of type 1 and type 2
pneumocytes, although there are more type 1 pneumocytes
on the air exchange surface
Post-Op
FEV1>0.8 OR >40% of predicted post op
Use VQ scan if close. Best predictor of pulmonary complications
DLCO>10 (oxygen exchange. Hgb also plays a role in this)
No resection if:
PCO2>50; PO2<60; VO2 max <10-12ml/min/kg
Segmentectomy- Persistent Air Leak
Lobectomy- Atelectasis
Pneumonectomy- Arrythmias
Lung Cancer
Lung Cancer:
Asymptomatic, cough, hemoptysis, pain, weight loss
MCC of cancer death
*prognostic factor indicator: nodal involvement
Mets: Brain (1), other lung, bone, liver, adrenals
5 yr survival: ~30 w/ resection. ~10 otherwise
Lung Cancer Types
Types:
Non-small cell:
MOST COMMON lung cancer (80% of lung cancer)
Squamous, central, smoking
PTHrP (hypercalcemia)
Adenocarcinoma, peripheral (MOST COMMON NON SMALL CELL)
TX: Resection, Carboplatin, Taxol, XRT
Small cell:
Neuroendocrine. Poor prognosis. Even stage 1 disease: 50% 5 yr survival.
ACTH (MC paraneoplastic syndrome), ADH
TX: Chemo-rads most typical given late presentation; Cisplatin; Etoposide
Mesothelioma:
Asbestos exposure. Ship builder, old houses/buildings. Aggressive local invasion, nodal
invasion, and distant mets
Aggressive
Lung Cancer Types Continued
Bronchoealveolar CA:
alveolar walls; multifocal; pneumonia
Carcinoid:
Neuroendocrine. Central. Coughing, flushing, diarrhea, hemoptysis
Typical 90% 5 yr; Atypical 60% 5yr
RF for recurrence: >3cm; + nodes
TX: resection
Mets:
Can be resectable IF no other mets. Colon, Renal, Sarcoma, Melanoma, Ovarian, Endometrial
mets to lung
Work Up
Imaging: CT- T & N; PET- M
Mediastinoscopy: For central tumors. CANNOT reach aorto-pulm nodes
If positive, unresectable
Structures
Left- RLN, esophagus, aorta, PA
Right- Azygous, SVC
Anterior- innominate
Chamberlain: though 2nd rib space. Anterior/ Parasternal thoracotomy.
Reaches AP space
Bronchoscopy: central tumors
Non-resectable: N2 (ipsilat nodes onwards)
Lesions
Coin lesions:
10% malignant. Need repeat imaging +/- biopsy if
suspicious
MC- granuloma or hamartoma
If Cancer: adenocarcinoma
50yo cutoff: less-> <5%; greater-> >50% malignant
Bronchial Adenoma:
Carcinoid, mucoepidermoid, mucous, adenoid
Slow growing
Resect +/- XRT (especially adenoid cystic)
Hamartoma:
Benign, see calcifications. Popcorn lesions
TX: repeat imaging (6mo) +/- resection
Lesions Continued
Pancoast tumors:
Can invade chest wall
Horners syndrome: 2/2 compression of sympathetic chain ptosis, miosis, anhydrosis
Ulnar nerve compression
SVC syndrome: head, neck, upper extremity swelling.
TX: XRT
Mediastinal Masses
Asymptomatic, cough, hemoptysis, dyspnea
If Neuroendocrine Typically posterior mediastinum
If asymptomatic 90% benign; symptomatic 50:50
MCC of adenopathy- lymphoma
Anterior: T’s- thymoma (#1 adults), thyroid, T cell, Teratoma, parathyroid
Middle: heart, trachea, ascending aorta bronchogenic cysts, pericardial cysts, enteric
cysts, lymphoma
Posterior: esophagus, neurogenic, lymphoma
Mediastinal Masses Continued
All thymomas require resection. 50% malig, 50% symp, 50% myasthenia gravis
Myasthenia Gravis- Antibody to anticholinesterase receptor. TX: Anticholinesterase
inhibitor, steroid, plasmapheresis. Thymus removal (even without mass can improve
symptoms)
Lambert-Eaton- autoimmune presynaptic regulation malfunction. Associated with small
cell. Gets better with time. TX: Guanidine Hydrochloride
Mediastinal Masses Continued
Germ cell tumor:
Teratoma- MC germline tumor. Resect because can be malignant. +/- chemo if malignant
Seminoma- MC MALIGNANT- NEGATIVE FOR AFP. Can have positive bHCG
XRT
Non Seminoma- elevated bHCG and AFP
Chemo: cisplatin, bleomycin, etoposide. Surgery for residual disease
Cyst:
Bronchiogenic resect; Pericardial can ;eave alone
Neurogenic Tumors:
painful, neuro symptoms/deficts
MC- neurolemmoma/schwannoma
Paraganglionoma VHL; catecholamine
Trachea
MC benign: Papilloma (adult); Hemangioma (children)
MC malignant: squamous cell (adult); carcinoid (children
After surgery:
Early edema reintubation, racemic epinephrine, steroids
Post-intubation stenosis:
Typically at cuff site for ET tube/stoma site
TX: serial dissection  endoscopic resection/laser  tracheal resection
Traheo-innominate fistula:
Bad problem to have. Herald bleed. Hemoptysis. To avoid, keep trach high (between
2nd and 3rd rings)
TX: Utley maneuver. Median sternotomy. Ligate and resect innominate artery
Trachea Continued
TEF:
Congenital vs prolonged intubation
TX: resection, reanastamosis, hyoid flap between esophagus and trachea
Other things in the lung
Lung abscess:
Necrotic area. Typically from aspiration. Typically in RLL. Think of Staph
TX: ABX drainage  surgery if with complication (hemorrhage) or to rule out cancer
Empyema:
Pneumona/parapneumonic effusion
Pleuritic chest pain, fever, cough, SOB. High cells/proteins in fluid. + stain/culture
Exudative (1st week)- chest tube/abx
Fibroproliferative (2nd week)- above + VATs/decortication
Organized (3rd week onwards)- likely will need decortication. Adjuncts: intrapleural
tPA/Elpesser flap
Other things in the lung continued
Chylothorax:
high lymphocytes and Triglycerides (>110). Sudean red stain
Trauma, iatrogenic, lymphoma, infection.
T5 and above= left// T6 and below= right
TX: chest tube, octreotide, low fat diet  ligate
If malignant: chemo/XRT
Hemoptysis:
Massive if >600 over 24hrs (likely from bronchial arteries)
MCC- infection
TX: bleeding side DOWN (keep visual field dry). Rigid bronch. May require resection/artery
embolization
Spontaneous Pneumo:
Recurrence increases the more episodes you have
Chest tube. PLeurodesis
Quick Hits
Endometriosis symptoms + difficulty breathing: pneumothorax (catamenial)
Residual hemothorax/ clotted hemothorax surgery
White out:
Shift away from white out  effusion
Shift toward white out  collapse
Tuberculosis:
lung apices. Caseating granuloma
Homeless, travel, hospital
TX: INH, rifampin, pyrazinamide
Sarcoidosis- non caseating granuloma
AVMs- embolize
Chest wall tumors- benign: osteochondroma; malignant: chondrosarcoma

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Thoracic review

  • 2. Anatomy Azygous Vein- Runs on the right side and drains into the SVC Thoracic duct- Originates around L1/L2 goes through AORTIC hiatus crosses towards left side at T4/T5  drains into the Left Subclavian (IJ junction) Phrenic Nerve- Anterior to hilum Vagus Nerve- Posterior to hilum Main resp muscles- diaphragm (80%) and intercostals (20%). When with increased work of breathing employ SCM, levators, serratus, scalenes. Sup-Inferior change in volume
  • 3. Anatomy Continued Right Lung has 3 lobes and accounts for 55% of the volume Left Lung has 2 lobes and accounts for 45% of the volume (lingual) Left Lung has 2 lobes and accounts for 45% of the volume (lingual) Type 1- gas exchange Type 2- surfactant production There are an equal amount of type 1 and type 2 pneumocytes, although there are more type 1 pneumocytes on the air exchange surface
  • 4. Post-Op FEV1>0.8 OR >40% of predicted post op Use VQ scan if close. Best predictor of pulmonary complications DLCO>10 (oxygen exchange. Hgb also plays a role in this) No resection if: PCO2>50; PO2<60; VO2 max <10-12ml/min/kg Segmentectomy- Persistent Air Leak Lobectomy- Atelectasis Pneumonectomy- Arrythmias
  • 5. Lung Cancer Lung Cancer: Asymptomatic, cough, hemoptysis, pain, weight loss MCC of cancer death *prognostic factor indicator: nodal involvement Mets: Brain (1), other lung, bone, liver, adrenals 5 yr survival: ~30 w/ resection. ~10 otherwise
  • 6. Lung Cancer Types Types: Non-small cell: MOST COMMON lung cancer (80% of lung cancer) Squamous, central, smoking PTHrP (hypercalcemia) Adenocarcinoma, peripheral (MOST COMMON NON SMALL CELL) TX: Resection, Carboplatin, Taxol, XRT Small cell: Neuroendocrine. Poor prognosis. Even stage 1 disease: 50% 5 yr survival. ACTH (MC paraneoplastic syndrome), ADH TX: Chemo-rads most typical given late presentation; Cisplatin; Etoposide Mesothelioma: Asbestos exposure. Ship builder, old houses/buildings. Aggressive local invasion, nodal invasion, and distant mets Aggressive
  • 7. Lung Cancer Types Continued Bronchoealveolar CA: alveolar walls; multifocal; pneumonia Carcinoid: Neuroendocrine. Central. Coughing, flushing, diarrhea, hemoptysis Typical 90% 5 yr; Atypical 60% 5yr RF for recurrence: >3cm; + nodes TX: resection Mets: Can be resectable IF no other mets. Colon, Renal, Sarcoma, Melanoma, Ovarian, Endometrial mets to lung
  • 8. Work Up Imaging: CT- T & N; PET- M Mediastinoscopy: For central tumors. CANNOT reach aorto-pulm nodes If positive, unresectable Structures Left- RLN, esophagus, aorta, PA Right- Azygous, SVC Anterior- innominate Chamberlain: though 2nd rib space. Anterior/ Parasternal thoracotomy. Reaches AP space Bronchoscopy: central tumors Non-resectable: N2 (ipsilat nodes onwards)
  • 9. Lesions Coin lesions: 10% malignant. Need repeat imaging +/- biopsy if suspicious MC- granuloma or hamartoma If Cancer: adenocarcinoma 50yo cutoff: less-> <5%; greater-> >50% malignant Bronchial Adenoma: Carcinoid, mucoepidermoid, mucous, adenoid Slow growing Resect +/- XRT (especially adenoid cystic) Hamartoma: Benign, see calcifications. Popcorn lesions TX: repeat imaging (6mo) +/- resection
  • 10. Lesions Continued Pancoast tumors: Can invade chest wall Horners syndrome: 2/2 compression of sympathetic chain ptosis, miosis, anhydrosis Ulnar nerve compression SVC syndrome: head, neck, upper extremity swelling. TX: XRT
  • 11. Mediastinal Masses Asymptomatic, cough, hemoptysis, dyspnea If Neuroendocrine Typically posterior mediastinum If asymptomatic 90% benign; symptomatic 50:50 MCC of adenopathy- lymphoma Anterior: T’s- thymoma (#1 adults), thyroid, T cell, Teratoma, parathyroid Middle: heart, trachea, ascending aorta bronchogenic cysts, pericardial cysts, enteric cysts, lymphoma Posterior: esophagus, neurogenic, lymphoma
  • 12. Mediastinal Masses Continued All thymomas require resection. 50% malig, 50% symp, 50% myasthenia gravis Myasthenia Gravis- Antibody to anticholinesterase receptor. TX: Anticholinesterase inhibitor, steroid, plasmapheresis. Thymus removal (even without mass can improve symptoms) Lambert-Eaton- autoimmune presynaptic regulation malfunction. Associated with small cell. Gets better with time. TX: Guanidine Hydrochloride
  • 13. Mediastinal Masses Continued Germ cell tumor: Teratoma- MC germline tumor. Resect because can be malignant. +/- chemo if malignant Seminoma- MC MALIGNANT- NEGATIVE FOR AFP. Can have positive bHCG XRT Non Seminoma- elevated bHCG and AFP Chemo: cisplatin, bleomycin, etoposide. Surgery for residual disease Cyst: Bronchiogenic resect; Pericardial can ;eave alone Neurogenic Tumors: painful, neuro symptoms/deficts MC- neurolemmoma/schwannoma Paraganglionoma VHL; catecholamine
  • 14. Trachea MC benign: Papilloma (adult); Hemangioma (children) MC malignant: squamous cell (adult); carcinoid (children After surgery: Early edema reintubation, racemic epinephrine, steroids Post-intubation stenosis: Typically at cuff site for ET tube/stoma site TX: serial dissection  endoscopic resection/laser  tracheal resection Traheo-innominate fistula: Bad problem to have. Herald bleed. Hemoptysis. To avoid, keep trach high (between 2nd and 3rd rings) TX: Utley maneuver. Median sternotomy. Ligate and resect innominate artery
  • 15. Trachea Continued TEF: Congenital vs prolonged intubation TX: resection, reanastamosis, hyoid flap between esophagus and trachea
  • 16. Other things in the lung Lung abscess: Necrotic area. Typically from aspiration. Typically in RLL. Think of Staph TX: ABX drainage  surgery if with complication (hemorrhage) or to rule out cancer Empyema: Pneumona/parapneumonic effusion Pleuritic chest pain, fever, cough, SOB. High cells/proteins in fluid. + stain/culture Exudative (1st week)- chest tube/abx Fibroproliferative (2nd week)- above + VATs/decortication Organized (3rd week onwards)- likely will need decortication. Adjuncts: intrapleural tPA/Elpesser flap
  • 17. Other things in the lung continued Chylothorax: high lymphocytes and Triglycerides (>110). Sudean red stain Trauma, iatrogenic, lymphoma, infection. T5 and above= left// T6 and below= right TX: chest tube, octreotide, low fat diet  ligate If malignant: chemo/XRT Hemoptysis: Massive if >600 over 24hrs (likely from bronchial arteries) MCC- infection TX: bleeding side DOWN (keep visual field dry). Rigid bronch. May require resection/artery embolization Spontaneous Pneumo: Recurrence increases the more episodes you have Chest tube. PLeurodesis
  • 18. Quick Hits Endometriosis symptoms + difficulty breathing: pneumothorax (catamenial) Residual hemothorax/ clotted hemothorax surgery White out: Shift away from white out  effusion Shift toward white out  collapse Tuberculosis: lung apices. Caseating granuloma Homeless, travel, hospital TX: INH, rifampin, pyrazinamide Sarcoidosis- non caseating granuloma AVMs- embolize Chest wall tumors- benign: osteochondroma; malignant: chondrosarcoma