Cardiac, Thoracic, and Vascular: Lung Flashcards
Lung: Anatomy
- The lungs are divided into three lobes with 10 segments
on the right and two lobes with nine segments on the
left (Fig. 18-1). The decreased number of divisions on
the left can be thought of as space taken up by the
heart. The right mainstem bronchus forms a gentler
curve with the trachea than does the left mainstem
bronchus (Fig. 18-2). Therefore, aspirated foreign
bodies are more likely to lodge in the right mainstem
bronchus. In aspiration pneumonia, the aspirated
material is most likely to deposit in the most depen-
dent portions of the lungs. For a supine individual,
these are the posterior segments of the upper lobes
and the superior segments of the lower lobes. The
arterial supply to the lungs is through the pulmonary
arteries as well as the bronchial arteries, which arise
from the aorta and intercostal vessels.
Benign Tumors of the Trachea and Bronchii: Pathology
- Types of benign tumors include squamous papilloma,
angioma, fibroma, leiomyoma, and chondroma.
Squamous papillomatosis is associated with human
papilloma viruses 6 and 11.
Benign Tumors of the Trachea and Bronchii: Epidemology
- Truly benign neoplasms of the trachea and bronchi
are rare.
Benign Tumors of the Trachea and Bronchii: History
- Patients commonly present with recurrent pneumo-
nias, cough, or hemoptysis.
Benign Tumors of the Trachea and Bronchii: Physical Examination
- Patients may have decreased breath sounds on the
affected side, with the additional signs and symptoms
owing to postobstructive pneumonia.
Benign Tumors of the Trachea and Bronchii: Diagnostic Evaluation
- Chest radiography may demonstrate a mass, and
there is often a postobstructive pneumonia if the
lesion significantly narrows the bronchial lumen.
Benign Tumors of the Trachea and Bronchii: Treatment
- Angiomas frequently regress, and observation is rec-
ommended. Other lesions require surgical removal
to relieve symptoms and establish a diagnosis. This
may require partial lung resection or sleeve resection,
where a segment of bronchus is removed and pri-
marily reanastomosed. Squamous papillomatosis has
a high recurrence rate.
Tracheobronchial Tumors with Malignant Potential
Tumors with malignant potential include bronchial
carcinoids, adenoid cystic carcinoma, and mucoepi-
dermoid tumors. Carcinoid tumors, which are malignant
in approximately 10% of patients, may cause parane-
oplastic syndromes through release of various substances,
including histamine, serotonin, vasoactive intestinal
peptide, gastrin, growth hormone, insulin, glucagon, and
catecholamines.
Tracheobronchial Tumors with Malignant Potential: Epidemiology
- These tumors make up fewer than 5% of all pulmonary
neoplasms and have no obvious age or sex predilec-
tion. Carcinoids make up approximately 1% of all lung
tumors; adenoid cystic carcinoma, approximately 0.5%;
and mucoepidermoid, approximately 0.2%.
Tracheobronchial Tumors with Malignant Potential: History
- Patients most commonly complain of cough, dyspnea,
hemoptysis, or recurrent pneumonia. Less frequently,
carcinoid tumors may produce carcinoid syndrome,
with complaints of flushing and diarrhea, as well as
manifestations of specific hormone excess. This syn-
drome only occurs in approximately 3% of patients
with carcinoid tumors.
Tracheobronchial Tumors with Malignant Potential: Physical Examination
- The patient may have respiratory compromise or
decreased breath sounds. Carcinoid tumors may cause
valvular heart disease with signs of pulmonic stenosis or
tricuspid regurgitation.
Tracheobronchial Tumors with Malignant Potential: Diagnostic Evaluation
- Chest radiography may reveal a lesion or postobstruc-
tive pneumonia. Bronchoscopy is useful to obtain tissue
diagnosis and define bronchial anatomy. Computed
omography (CT) of the chest is routine for preoper-
ative planning.
Tracheobronchial Tumors with Malignant Potential: Treatment
- These tumors should all be resected. Long-term sur-
vival for carcinoid tumors is 80%; for adenoid cystic
carcinoma and mucoepidermoid tumors, the progno-
sis is also favorable.
Lung Cancer: Epidemiology
- Lung cancer is the leading cause of cancer-related death
for both men and women in North America, responsi-
ble for greater than 150,000 deaths each year in the United States and accounting for almost 30% of all cancer-related
deaths. More than 80% of lung cancers are smoking-
related (Fig. 18-3). In the United States, more people
die each year from lung cancer than from breast, pros-
trate, and colorectal cancers combined. Lung cancer
kills more men than prostate cancer and more women
than breast cancer. Lung cancer incidence rates among
women continue to increase. Deaths from lung can-
cer in women have increased 400% between 1960
and 1990. Smoking cessation significantly reduces
an individual’s risk of developing lung cancer, although
the level of risk remains greater than for nonsmokers.
Asbestos, formaldehyde, radon gas, arsenic, uranium,
chromates, and nickel have been identified as carcino-
gens, especially when combined with smoking.
Lung Cancer: Pathology
- Lung cancer is divided into small-cell lung cancer
(SCLC; 20% to 25%) and non–small-cell lung cancer
(NSCLC; 75% to 80%). NSCLC is further divided
into squamous cell carcinoma (30%), adenocarcinoma
(35%), and large-cell carcinoma (10%). SCLC is usually
centrally located and may be associated with parane-
oplastic syndromes. Approximately 5% of patients have
symptoms of inappropriate secretion of antidiuretic
hormone, whereas 3% to 5% have Cushing’s syndrome
from adrenocorticotropin production. Squamous cell
cancer usually occurs centrally and can be associated
with symptoms of hypercalcemia secondary to produc-
tion of a substance similar to parathyroid hormone.
Adenocarcinoma typically occurs at the periphery.
Lung Cancer: History
- Most patients come to seek medical attention as a
result of signs and symptoms indicating advanced dis-
ease. Ninety percent of patients with lung cancer are
symptomatic at the time of diagnosis. Worsening
cough with increased sputum production and hemop-
tysis often indicates airway obstruction by tumor. A
history of recurrent pneumonia requiring antibiotic
therapy is common. Persistent chest, back, or shoulder
pain is related to nerve involvement or direct tumor
invasion. Bone pain indicates distant skeletal metas-
tases, whereas neurologic symptoms indicate brain
metastases. Systemic symptoms include fatigue, loss of
appetite, and unintentional weight loss.
Lung Cancer: Physical Examination
- Chest auscultation may reveal diminished breath
sounds owing to pneumonia or malignant pleural effu-
sion. Supraclavicular lymphadenopathy may be pres-
ent. Recent onset of hoarseness indicates involvement
of the recurrent laryngeal nerve. Horner syndrome
(ptosis, myosis, and anhydrosis) results from a superior
sulcus tumor causing neural invasion. Superior vena
cava syndrome and Pancoast syndrome (shoulder and
arm pain on the affected side) may occur. Paralysis of
the diaphragm indicates phrenic nerve involvement.
Patients with advanced disease are usually ill-appearing
and exhibit significant weight loss.