Approach to the Solitary Pulmonary Nodule
The Solitary Pulmonary Nodule •
• • •
The term “solitary pulmonary nodule” (SPN) describes a well-circumscribed, rounded, smooth edged, dense pulmonary lesion, 3 cm or less in diameter, that is completely surrounded by lung parenchyma Is NOT associated with atelectasis , pleural effusion or adenopathy , does not touch the hilum or mediastinum “Coin lesion” .The older term “coin lesion” has been replaced by SPN since these lesions are spherical, not flat. Lesions > 3 cm called “MASSES” and often malignant
The Solitary Pulmonary Nodule • • •
Since the SPN by definition is a radiographic finding, radiologic workup is intrinsic to the diagnostic workup The initial step in evaluation is to determine whether the abnormality is in fact a solitary pulmonary nodule. This assessment is important because up to 20% of suspected nodules prove to be entities mimicking a solitary pulmonary nodule such as rib fractures, skin lesions, or composite areas of increased opacity
The Solitary Pulmonary Nodule • • • • •
Incidence of cancer from 10 – 70% Found on 0.09 to 0.20 % of all CXRs (approximately 1 in 500) 150,000 SPNs found annually 90% Solitary pulmonary nodules are most
often detected incidentally when a chest xray is taken for other reasons. •
Increased further with incidental findings on CT
Why is it concerning? • • •
SPN are concerning for what they could represent The absolute #1 concern is if the SPN is the harbinger of a malignancy What is more critical is the fact that the earlier you diagnose the malignancy the better the survival rate will be
Why is it concerning •
Chest. 1997 Jun;111(6):1486-7 • •
•
Patients with stage IA (T1N0M0) disease have the best prognosis. These patients have a 61 to 75% 5-year survival following surgical resection
Radiol Clin North Am 2000; 38:1–9 • •
Unfortunately almost 50% of patients have extrathoracic spread by the time of diagnosis these patients only had a 15% 5 year survival
Why is it concerning? •
•
•
With these numbers in mind, it is absolutely critical to give the SPN the attention it deserves If not worked up properly it will effectively push patients who do carry a malignancy with in the SPN from the 75% survival into the 15% survival That is just unacceptable
Solitary Pulmonary Nodule • • • •
Basic strategy is to identify malignant versus benign Nodules prove to be malignant in 40% of cases Most often Bronchogenic carcinoma (25% ) Most common benign is hamartoma
Solitary pulmonary nodule A solitary nodule is assumed to be primary lung cancer until proved otherwise . One must consider the relationship of age to the incidence of malignancy . Age (Yr)
Malignancy (%)
35-44
15
45-49
26
50-59
41
60-69
50
70-79
70
Most solitary pulmonary nodules should be resected after through investigations, shows that systemic dissemination has not yet occured . Review of previous chest films may help determine the growth pattern of the nodule . A malignant nodule will usually have a doubling time of 20-500
Early Resection • • •
Studies have proven that early resection results in 5-year survival rate of 50% If nodule is 1cm or less rate is about 80% Survival rate after discovery of bronchogenic carcinoma is 15% and hence the importance of early discovery in terms of cure
Differential Diagnosis • Neoplasms • Malignant – • Metastasis, • Primary Lung Carcinoma • Benign Tumors
• Inflammatory • Granulomas • TB, • Histo, • Sarcoid, etc.),
• • • • •
Abscess, Hydatid Cyst, Fungus Ball, Org. Pneumonia, Bronchiectatic cyst
Differential Diagnosis • Vascular • Infarct, • Pulm Vein anomaly, • Rheum Nodule, • Wegener’s, • AVM, • Pulm Art Aneurys (behcets disease) • Developmental • Bronchogenic cyst, • Pulmonary sequestration
• Nipple shadow
It is important to note that the majority of SPN are of a benign etiology
Benign nodules • • • • • • • • • • • •
Hamartoma 8% (popcorn lesion) Granuloma Rheumatoid granuloma, Healed infarct, Pulmonary anurysm, Wagener’s granulomatosis Hemangioma Schwannoma Fibroma Lipoma Leiomyoma Teratoma
SO now if we have a patient with an SPN on CXR or CT what to be done?
Postgrad Med 2003;114(2):29-35
• • • • • • •
Ask (history, profession, habits, sign, symptoms) Assess (X-ray, age, size, shape, margins, calcification, position,) Assign (benign or malignant) Advice (Follow up) Arrange (CT, PET) Attain (Biopsy) Attempt (Surgical Resection)
Assessing Growth • • • •
There are three categories to place the patient in assessing growth No change in two years / or Growth Rate of benign nature Indeterminate because of no old studies Growth Rate of possible malignancy
No change in two years • •
Radiologic stability is the best predictor of a benign etiology. Since the 1950’s it has been well established that if the SPN has not grown in 2 years it is benign. (JAMA 1958; 166:210–215 )
•
If old radiographs show no change in two years, no further work up is needed
Benign vs. Malignant Doubling Time • •
•
•
The time it takes for the apparent volume to double is referred to as the doubling time one doubling in volume is equivalent to the nodule diameter increasing by only 26% to 28% Benign nodules representing acute inflammatory changes have a doubling time of less than 20 days In contrast, stable granulomas and hamartomas may enlarge slowly and have a doubling time of more than 500 days
Semin Ultrasound CT MR 2000;21(2):97-115
Benign vs. Malignant Doubling Time •
•
If the SPN has a doubling time of <20 days or >500 days the patient is in the clear and can be followed If however the SPN doubling time falls in between 20 and 500 days the SPN must be assumed malignant until proven otherwise and surgical intervention is now recommended. Postgrad Med 1997;101(3):145-50
Growth of a Nodule • • •
Malignant nodules grow at a constant rate expressed as doubling time This usually falls between 20 and 500 days with a median of 120 days An increase of 28% in nodule diameter indicates doubling
Growth of a Nodule • •
•
Benign lesions grow slowly with doubling time exceeding 500 days It is almost conclusively a benign lesion if size is stable for 2 years ( doubling time exceeding 720 days ) A doubling time of less than 20 days signifies inflammatory process
Growth Rate: Doubling Time • • • •
Volume = 4/3 Π r 3 28% increase in diameter results in doubling of volume Non-malignant disease: less than 20 days or greater than 500 days Malignant lesions: 20 to 500 days Av.120
Malignant Doubling Time •
• •
With the numbers crunch, biopsy in this case is not worth the risks because a malignant diagnosis would not change resection therapy So in this case, surgical resection is highly recommended If the patient is reluctant or the risk of surgery is really high and if diagnosis is likely to be sure of before going to the OR, then biopsy can be undertaken.
Benign vs Malignant • • • • • • •
Age <40 nodule diameter<1.5 never smoked nodule edge type1 doubling time >500 d calcification in benign Needle Bx: benign dis
• • • • • • • •
•
Needle Bx: Nonspecific
>40 >1.5 ever smoked type3 20 to 500 days indeterminate pattern malignant disease suspicious cells
High Resolution CT •
•
HRCT is the most sensitive and specific for assessing the size, shape, calcification and edge of a nodule Type 1 Type 2 Type 3 Type 4
Likelihood of cancer with the appearance of a nodule's edge • • • •
Type 1 nodules :smooth, regular edge….20%. Type 2 nodules: smooth, irregular edge…. 33%. Type 3 nodules: spiculated edge…. 83%. Type 4 nodules: fuzzy, multispiculated edge or corona radiata…. 93%
Factors Influencing Probability of Malignancy • • • •
Size Growth rate Number Density
• • • •
Patient age Gender Smoking history Occupational history
LUNG NODULE MALIGNANT FEATURES • • •
New or growing lesion Spiculated margin Large size (>3cm)
Spiculated nodule
MALIGNANT
MALIGNANT
Irregular contour
Spiculated margin
Bronchus leads to it
MALIGNANT
LUNG NODULE DEFINITE BENIGN CHARACTERISTICS
• • • • •
Absence of growth for 2 years Definite benign calcifications Extensive calcification Smooth margins Small size (< 3 cm)
Very white (like bone) BENIGN
BENIGN
Smooth margin
BENIGN
BENIGN
BENIGN
Note the smooth contour
BENIGN GRANULOMA
Homogeneous white= benign calcification
Very subtle nodule
There it is
SMOOTH BENIGN
Postgrad Med 2003;114(2):29-35
Indeterminate Growth Rate •
•
This is where the real dilemma is created and every radiological and clinical clue must be taken into consideration to make a decision. First step is to look at all patterns of the SPN and determine if a “typically benign or malignant pattern can be found”
Calcification • • •
Radiographic pattern of calcium deposition is helpful Benign lesions tend to have central, laminated (bull’s eye), diffuse or popcorn pattern Malignant lesions have speckled or eccentric pattern
TYPES OF CALCIFICATION •
BENIGN • • • •
•
Central = granuloma Nodule completely calcified = granuloma Popcorn = hamartoma Target = granuloma
MALIGNANT • •
Spicculated or punctate = malignant Eccentric = malignant
Benign Calcifications
Popcorn calcification= hamartoma
BENIGN
Hamartoma • • • • • • •
Regarded as benign developemental deformity 1-3cms lesion containing cartilage, epithelium, fibro-fatty tissue Single, may be multiple Slow growing Ussually periphral Central calcification males
Popcorn Calcification • •
Classic “popcorn” pattern often seen in hamartomas HRCT can show fat and cartilage in half of cases
HAMARTOM A
Hamartoma
Fat • •
Fat on CT benign hamartoma can be diagnosed with confidence
Benign Calcification: Popcorn Calcification
Popcorn Calcification •
•
Popcorn calcification or Chondroid Calcification Pattern typical of hamartomas
Granulomas • • •
About 40% of all SPNs are granulomas—small, granular inflammatory lesions. The word "granuloma" comes from the Latin word "granum," meaning "grain" or "seed." Granulomas are characterized by a nodular appearance and a unique cellular pattern that can be seen through a microscope.
Benign Calcification: Central Calcification
Calcification • •
Laminated or central pattern Typical of granuloma
Histoplasmoma • • • • • • •
Tend to B\L multiple with LN Rarely slowly progressive apical or post. pulm.nodule Usually in presence of pre exist. lung ds. B’ectatic or emphysema Calcified centre smtime with calcified laminae Prevalent in USA,also in many other tropical parts Self limiting in 2-3 wks Remnant calcified granuloma in lung .
a
Histoplasmoma
Solid or Central Calcification •
A solid calcified SPN is found in association with prior granulomatous infection, most commonly histoplasmosis or tuberculosis
Histoplasmoma
Hydatid cyst • • • • • • • •
Echinococcus infection Human accidental intermediate host Slow steadily growing Spherical lession with well defined edges or uniform density Ussually multiple and bilateral May rupture to give salty expectoration Thus cyst with level,… later calcified walls Casoni test ,latex agglutination ,complement fixation test diagnostic
Hydatid cyst in lung. This patient had a single large cyst in the left lung.
Rheumatoid nodules • • • • • • • •
A \ w arthritis , fibrosis > Men, middle age, RA factor may be positive May have chylous pleural effussion, Single or multiple nodules With or without cavitation Ussually 1-3 cms may be upto 10 cms , Subpleural commonly Nodule in coalminers “Caplan Syndrome”
Arteriovenous malformation
Other benign tumors • • • • •
fibromas (fibrous connective tissue), lipomas (fat), leiomyomas (smooth muscle), hemangiomas (dilated blood vessels), papillomas (epithelial cells).
Speckled or Punctate Calcification •
•
•
Speckled or Punctate calcifications Represent malignant calcification and Should not be taken as benign
Eccentric Calcification • •
Eccentric Calcification a sign of malignant potential
Calcification • •
Suggests benign diagnosis With CT the reference standard, • • •
CXR has sensitivity 50%, specificity 87%, and PPV 93% for identifying calcification
Postgrad Med 2003;114(2):29-35
Radiological Findings • •
If you have definitive findings suggestive of benign pattern than no further work up is needed. If still no answer after SCTIE or other radiologic finding further work up is needed
Size • • • •
Size of the SPN can also help out at this point to help make a decision In general, smaller nodules are more likely to be benign and larger lesions malignant 80% of benign SPNs are less than 2 cm in diameter However, small size is not necessarily reliable evidence of benignity because 15% of malignant nodules are less than 1 cm in diameter approximately 42% are less than 2 cm in diameter Radiographics 20:43, 2000
Size of SPN • •
Most SPN are less than 2 cm in diameter Malignant nodules • • • •
40% less than 2 cm 15% less than 1 cm 1% less than 7 mm 0% less than 5 mm
Margins • • • •
Smooth, well-defined margins most often indicate a benign nodule However 21% of malignant nodules have a smooth welldefined margin a lobulated margin may reflect uneven growth of a SPN and can indicate malignancy although 25% of benign nodules, particularly hamartomas, are lobulated Radiology 179:469, 1991
Patterns of Margins • •
• •
Corona radiata sign Fine linear strands extending 4-5 mm outward Spiculated on CXRs 84 – 90% are malignant
Patterns of Margins
Patterns of Margins
Spiculated lipoid pneumonia
Patterns of Margins • • •
Scalloped border Intermediate probability of cancer Smooth border suggestive of benign diagnosis
Other Characteristics •
•
Air bronchograms and pseudocavitation more commonly malignant Cavitation with thick (>15 mm vs < 5 mm) more often maligant
Air Bronchograms
Cavitation •
• • •
Although cavitation can occur in necrotic malignant SPNs, inflammatory lesions can also cavitate. The thickness of the cavity wall can be helpful in distinguishing benign from malignant lesions. Cavities with a greatest wall thickness less than 5 mm are almost always benign whereas most of those with a maximal wall thickness greater than 15 mm are malignant
Cavitation Thick walled cavity which came back as squamous cell carcinoma.
RADIOGRAPHIC PRESENTATIONS OF LUNG CANCER • • • •
Mass or nodule Atelectasis (lung collapse) Non-resolving pneumonia Mediastinal lymph node enlargement
ADENOCARCINOMA • • • •
•
Peripheral Spiculated < 4 cm Uncommon Hilar and mediastinal lymph node enlargement Early metastases to brain, adrenals, liver, bone Can arise from an existing scar - scar carcinoma
Peripheral
ADENOCARCINOMA
Small
ADENOCARCINOMA
ADENOCARCINOMA
SQUAMOUS CELL CARCINOMA •
Central endobronchial • •
post obstructive pneumonia atelectasis
Calcified granuloma
Central hilar
SQUAMOUS CELL CARCINOMA
Ascending aorta
SVC
Main pulmonary artery
Central hilar mass
Descending aorta
SQUAMOUS CELL CARCINOMA
SQUAMOUS CELL CARCINOMA •
Apical - Pancoast or superior sulcus tumour
PANCOAST TUMOUR
Destroyed 3rd rib
Destroyed 3rd rib
Mass
PANCOAST TUMOUR
SQUAMOUS CELL CARCINOMA • •
Slow growing (1 - 10 cm) Cavitation (10 - 20%) •
•
DDx - lung abscess
Late metastases
Central cavity
DDX - Lung abscess
SQUAMOUS CELL CARCINOMA
SMALL CELL LUNG CANCER • • •
Central > peripheral Massive hilar and mediastinal adenopathy Early distant spread
Large mass
Large mediastinal nodes
SMALL CELL CARCINOMA
SMALL CELL CARCINOMA
LARGE CELL CARCINOMA • • •
Large peripheral mass ~ 7 cm Rapid growth Early distant spread
LARGE CELL CARCINOMA
Large peripheral mass
LARGE CELL CARCINOMA
Large peripheral mass
LARGE CELL CARCINOMA
LARGE CELL CARCINOMA
Large peripheral mass
LARGE CELL CARCINOMA
BRONCHIOLOALVEOLAR CARCINOMA • • •
Peripheral nodule Non-resolving focal “pneumonia” Diffuse bilateral “pneumonia” • •
hilar and mediastinal nodal enlargement uncommon distant spread uncommon
Looks like pneumonia but …….
Air bronchogram
BRONCHIOLOALVEOLAR CARCINOMA
Air bronchogram
Multifocal
BRONCHIOLOALCEOLAR CELL CARCINOMA
Air space disease
No Specific Pattern Found • • •
With no specific finding, all risk factors must be taken into account. Trying to milk the SPN for as much information it can be It may help stratify the risk in the patient
Indeterminate SPN •
•
After milking the SPN for all its characteristics it is now important to milk the patient for all relevant information Key points include: • • • • •
smoking history; symptoms; comorbid conditions (particularly severe emphysema); history and type of prior malignancy; prior infections and environmental exposures.
Work-up of SPN: CXR • • • •
No change in two years - no further evaluation Characteristic calcifications of benign disease Lateral films for “hidden” lesions Initial CXR then serial CT Scans
Decision Making
Postgrad Med 2003;114(2):29-35
N Engl J Med 348:2535-2542
Clinical Decision •
• • • • •
Now after evaluating the entire clinical picture and clinically identifiable risks its time to determine where they fall into Low, Moderate or High risk Pretest probability of cancer determines most costeffective strategy Low : radiographic follow-up Intermediate : CT and PET High : CT followed by biopsy or surgery Very high : surgery*
Low risk indeterminate SPN • • • • • • •
30 year old male, never smoked, nodule is <1cm with no previous studies, no environmental exposure, Review all prior CXR No specific pattern found Get CT scans found on CT not seen on CXR
• •
If probability of cancer is <10% wait and watch Can follow for two years
Moderate Risk • • • • • •
Now we have a patient who isnt clearly low risk. Maybe older age, questionable smoke or environmental history but not quite screaming high risk, what to do? If it is high thoracotomy should intervene Bronch & NAB reserved for pt who are reluctant to go for surgery before Dx PET SCAN is now recommended
• •
PET is slightly more effective,noninvasive If PET is +ve but other criteria are low for malignancy, then ANB is needed to R/O infectious granulomas
CT Scan •
CT can help distinguish a solitary pulmonary lesion from multiple pulmonary nodules
•
CT Scan with contrast to evaluate mediastinum Serial scans at 3, 6, 12, and 24 months Can consider trial of antibiotics prior to repeat scan in 6 weeks Newer CT techniques
• • •
• •
Volumetric analysis Multi-slice scanner
Contrast-Enhanced CT • •
• • •
Degree on enhancement on spiral CT after injection of contrast One study used an increase in attenuation of 20 Hounsfield units as threshold for malignant lesions Sensitivity 95-100%, specificity 70-93%* Local expertise varies *Zhang, Radiology
Spiral CT with IV contrast Enhancement (SCTIE) •
•
•
Computed tomography (CT) (particularly thinsection CT) is 10–20 times more sensitive than standard radiography and allows objective, quantitative assessment of calcification SCTIE the imaging modality of choice for the SPN and should be obtained on all newly diagnosed SPNs A number of benign etiologies for SPNs have a characteristic appearance on CT
CT Densitometry • • • •
Involves measurement of attenuation values Expressed in Hounsfield units, as compared to reference “phantom” Usually higher for benign nodules Allows for identification of 35 – 55% of subsequently identified benign lesions
CT Densitometry • • •
One large, multicenter trial, only 1 of 66 nodules identified as benign later found to be malignant* Cutoff used was 264 Hounsfield units More conventional cutoff is 185, which yielded a higher false negative rate
*Zerhouni, Radiology
Lung cancer screening New CT techniques detect suspicious nodules 3x more than CXR, malignant tumors 4x and stage 1 tumors 6x
Henschke et al: Early Lung Cancer Action Project: overall design and findings from baseline screening. Lancet, 1999;354:99-105
PET Scan •
Highly valuable noninvasive tool
PET SCAN •
•
Positron emission tomography (PET) with 18-fluorodeoxyglucose (FDG) has proven to be an excellent mode of tumor imaging 18-FDG (fluorodeoxyglucose) • •
increased uptake by metabolically active cells does not enter glycolysis
PET SCAN •
•
•
Increased activity is demonstrated in cells with high metabolic rates, as is seen in tumors and areas of inflammation Taken up by cells in glycolysis but is bound within cells and cannot enter normal glycolytic pathway It can also tell us about if any metastatic disease is present thus altering treatment
Limitations Positron Emission Tomography •
•
However the spatial resolution of PET is currently 7 to 8 mm, and so the imaging of SPNs < 1 cm is unreliable False negatives in tumors with low uptake such as bronchoalveolar cell carcinoma It is 95% sensitive for identifying malignancy and 85% specific
Limitations Positron Emission Tomography •
•
False positive results may occur in lesions that contain active infection or inflammatory tissue (histoplasmomas) High post test likelihood of malignancy (14%) in high risk patients with negative PET
Thoracic PET Scan: Potential Sources of Error •
False Positive Results:
Metabolically active infectious or inflammatory lesions:
•
False Negative Results:
Tumors with low metabolic activities:
Sarcoidosis. Rheumatoid nodules. TB. Fungal granuloma. Others.
Bronchoalveolar CA. Carcinoid tumors. Mets: renal cell and testis.
Small tumors-<1cm.
Hyperglycemia-keep sugars below 150mg%.
PET Scan •
Allows more accurate identification of tumors, lymph nodes, and metastatic disease
•
May provide staging information Up to 14% of patients otherwise eligible for surgery have occult extra thoracic disease on whole-body PET
•
•
Benign disease • •
96% sensitivity 88% specificity
Malignant disease 96% sensitivity 77% specificity
Pet Scan •
•
Gould et al performed a meta-analysis of the literature on pulmonary nodules and masses and PET scanning and found an overall sensitivity of 96.8% and specificity of 77.8% for detecting malignancy. PET scans also have a 96% sensitivity and 88% specificity with 94% accuracy in the diagnosis of benign nodules JAMA 2001; 285:914–924
Utilization of PET Scans • •
• • •
Negative PET in high risk patients still need tissue diagnosis…so why get it? PET not usually indicated unless it will change management
So depending on the PET Scan result we can base our treatment If PET is positive than we can refer the patient to CT Surgery for resection options If PET is negative than can follow
Positron Emission Tomography • • •
CT combined with PET for staging was often superior to conventional approaches Reduced number of surgeries by 15% Cost savings per patient
*Gambhir, J Clin Oncol
Positron Emission Tomography •
More expensive than other imaging modalities
*http://cms.hhs.gov, Dec
PET Images
Pieterman, NEJM 2000;343:254-
PET Images
Pieterman, NEJM 2000;343:254-
Integrated PET and CT
Lardinos, NEJM 2003;348:2500 -7
Integrated PET and CT
Lardinos, NEJM 2003;348:2500 -7
Sample Pre-biopsy Algorithm CHEST 2004; 125:1522-1529
Biopsy •
Bronchoscopic biopsy
•
CT guided • Transthoracic needle aspiration (TTNA) Transthorathic needle aspiration (TTNAB) has a sensitivity of 80% to 90% • Fine needle aspiration (FNA) Surgical • Video Assisted Thoracic Surgery (VATS) • Open
•
BRONCHOSCOPY
Bronchoscopy • • • • •
Limited role Transbronchial needle aspiration of mediastinal lymph nodes Useful for large central lesions and endobronchial lesions Can detect infection No use in peripheral nodules
Bronchoscopy •
Useful for lesions at least 2 cm
INDICATION FOR BRONCHOSCOPIC BIOPSY •
Central lesion ie. Near hilum
Bronchoscopy •
• • •
Diagnostic yield varies in literature from 20 – 80%, depending on size of nodule and patient population Yield depends on nodule size and proximity to bronchial tree Yield 10% for < 1.5 cm, and 40 – 60% for > 2 – 3 cm 70% yield when CT reveals a bronchus leading to lesion
Bronchoscopy • • • • •
Relatively low risk Overall complication rate 5% 3% risk of pneumothorax 1% risk of hemorrhage 0.24% risk of death
INDICATIONS FOR FNAB • •
Peripheral lesion Central lesion without significant distal collapse
DIAGNOSTIC YIELD OF FNAB •
90 - 97%
FNAB TECHNIQUE • • •
Out-patient procedure 22G needle Image guidance • • •
fluoroscopy computed tomography ultrasound
Transthoracic FNA (TTFNA) • • • • •
Diagnostic yield up to 95% in peripheral lesions Higher complication rate Pneumothorax (10 - 30%) Hemoptysis (30%) About 5% of these require chest tube
What are the limitations of Needle Biopsy of Lung Nodules? •
• •
In a small number of cases, the tissue obtained during a biopsy may not be adequate for diagnosis. Needle biopsy is not cost-effective for small lesions one to two millimeters in diameter. The needle is too difficult to position into the nodule and the nodule is too small to provide enough tissue for an accurate diagnosis.
What are the limitations of Needle Biopsy of Lung Nodules? •
For patients with certain conditions a needle biopsy may not be recommended. • • • • • •
•
emphysema, lung cysts, blood coagulation disorder of any type, insufficient blood oxygenation, pulmonary hypertension, and certain heart failure conditions,
Alternatives to lung biopsy usually include continued follow-up with imaging and surgical removal of the abnormality.
CT-guided fine-needle aspiration biopsy •
The use of CT-guided fine-needle aspiration biopsy in solitary pulmonary nodules has been condemned historically as often being an unnecessary step in the workup of these patients.
Sample Post-biopsy Algorithm CHEST 2004; 125:1522-1529
Thracoscpic Resctn of Lung Nodules
Lung cancer: Surgical options • • • • •
VATS Segmentectomy Lobectomy Sleeve resection Pneumonectomy
Surgery •
• •
Thoracotomy to resect a malignant nodule carries significant death of 3% to 4% but for a benign lesion it is 0.3% Thoracoscopy carries less significant morbidity and lessens hospital stay It is not known if the 5-years survival is different between the two approaches
High Risk Patient • • • • •
68 year old male, 100 pack years of smoking, Used to work with asbestos, and Coughing up blood RIGHT TO THE OR for resection.
Conclusion • •
•
The main point is to make sure you give the SPN the respect it deserves. With timely diagnosis we can effectively prevent morbidity and mortality for our patients There is just no excuse for a patient to die because we did not work up the patient in a timely fashion.
Medicolegal Aspects •
•
Physicians should discuss the possibility of lung cancer presenting as a SPN in those patients who have lesions that cannot be confirmed to be benign based on their presence on old films with over 2 years of stability, or classic calcification typical of a benign lesion. Patients should play an active role in the decision to remove, evaluate with invasive procedures, or observe their SPN.
Medicolegal Aspects • •
•
The pros and cons of pulmonary resection should be discussed and a recommendation made. This should be carefully documented in the patient record, and if observation is chosen, advice for follow up given. Then, it is important for the physician to insure that follow up actually occurs.
Postgrad Med 2003;114(2):29-35
Postgrad Med 2003;114(2):29-35
Postgrad Med 2003;114(2):29-35
Postgrad Med 2003;114(2):29-35
Primary Tumor (T)
Description
T1
A small tumor that is not locally advanced or invasive Criteria: <3 cm in size; surrounded by lung or visceral pleura; not extending into the main bronchus
T2
A larger tumor that is minimally advanced or invasive Criteria: >3 cm in size; may invade the visceral pleura; may extend into the main bronchus but remains >2 cm from the main carina; may cause segmental or lobar atelectasis
T3
Any size tumor that is locally advanced or invasive up to but not including the major intrathoracic structures Criteria: any size; may involve the chest wall, diaphragm, mediastinal pleura, parietal pericardium; main bronchus within 2 cm of the main carina (not involving the main carina); may cause atelectasis of the entire lung
T4
Any size tumor that is advanced or invasive into the major intrathoracic structures Criteria: any size; invades the mediastinum, heart, great vessels, trachea, esophagus, vertebral body, main carina; malignant pericardial or pleural effusion; presence of satellite tumor nodule(s) within the primary tumor lobe
Regional Lymph Node Involvement (N)
Description
N1
Metastatic disease to nodes within the ipsilateral lung Criteria: direct extension to intrapulmonary nodes; metastasis to ipsilateral peribronchial and/or hilar nodes (nodal stations 10 through 14)
N2
Metastatic disease to nodes beyond the ipsilateral lung but not contralateral to the primary tumor Criteria: metastasis to the ipsilateral mediastinal and/or subcarinal nodes (nodal stations 1 through 9)
N3
Metastatic disease to nodes distant to those included in N2 Criteria: metastasis to contralateral mediastinal and/or hilar nodes, ipsilateral or contralateral scalene and/or supraclavicular nodes
Metastases (M)
Description
MO
Local or regional disease, no distant metastases
M1
Disseminated disease, distant metastases present