Chest Wall, Pleura and Mediastinum (TCVS) Flashcards
All of the following increase the risk or tracheal stenosis EXCEPT
A. Age over 70years
B. Radiation
C. Male gender
D. Excessive corticosteroid therapy
Answer: C
Intubation-related risk factors include:
1) prolonged intubation;
2) high tracheostomy through the first tracheal ring or cricothyroid membrane;
3) transverse rather than vertical incision on the trachea;
4) oversized tracheostomy tube;
5) prior tracheostomy or intubation; and
6) traumatic intubation.
Stenosis is also more common in older patients, in females, after radiation, or after excessive corticosteroid therapy, and in the setting of concomitant diseases such as autoimmune disorders, severe reflux disease, or obstructive sleep apnea and the setting of severe respiratory failure.
However, even a properly placed tracheostomy can lead to tracheal stenosis because of scarring and local injury.
Mild ulceration and stenosis are frequently seen after tracheostomy removal.
Use of the smallest tracheostomy tube possible, rapid downsizing, and a vertical tracheal incision minimize the risk for post-tracheostomy stenosis.
(See Schwartz 10th ed., p. 607.)
Adenoid cystic carcinomas
A. Spread submucosally
B. Exhibit aggressive growth
C. Are not radiosensitive
D. Have a 5-year survival rate of >50%
Answer: A
Squamous cell carcinomas often present with regional lymph node metastases and are frequently unresectable at presentation.
Their biologic behavior is similar to that of squamous cell carcinoma of the lung. Adenoid cystic carcinomas, a type of salivary gland tumor, are generally slow-growing, spread submucosally, and tend to infiltrate along nerve sheaths and within the tracheal wall.
Although indolent in nature, adenoid cystic carcinomas are malignant and can spread to regional lymph nodes, lung, and bone.
Squamous cell carcinoma and adenoid cystic carcinomas represent approximately 65% of all tracheal neoplasms.
The remaining 35% comprises small cell carcinomas, mucoepidermoid carcinomas, adenocarcinomas, lymphomas, and others.
Postoperative mortality, which occurs in up to 10% of patients, is associated with the length of tracheal resection, use of laryngeal release, the type of resection, and the histologic type of the cancer.
Factors associated with improved long- term survival include complete resection and use of radiation as adjuvant therapy in the setting of incomplete resection.
Due to their radiosensitivity, radiotherapy is frequently given post-operatively after resection of both adenoid cystic carcinomas and squamous cell carcinomas.
A dose of 50 Gray or greater is usual. Nodal positivity does not seem to be associated with worse survival.
Survival at 5 and 10 years is much better for adenoid cystic (73 and 57%, respectively) than for tracheal cancers (47 and 36%, respectively; P <0.05).
For patients with unresectable tumors, radiation may be given as the primary therapy to improve local control, but is rarely curative.
For recurrent airway compromise, stenting or laser therapies should be considered part of the treatment algorithm.
(See Schwartz 10th ed., pp. 610–611.)
Which of the following is NOT a non-small-cell tumor of the lung?
A. Squamous cell carcinoma
B. Adenocarcinoma
C. Carcinoid tumor
D. Large-cell carcinoma
Answer: C
The term non–small-cell lung carcinoma (NSCLC) includes many tumor cell types, including large cell, squamous cell, and adenocarcinoma.
Historically, these subtypes were considered to be a uniform group based on limited understanding of the distinct clinical behaviors of the subtypes as well as the act that there were few treatment options available.
With increasing understanding of the molecular biology underlying these tumor subtypes, however, the approach to diagnosis and management and the terminology used in describing these tumors is evolving rapidly.
(See Schwartz 10th ed., p. 614.)
The most common pattern of benign calcifcation in hamartomas is
A. Solid
B. Diffuse
C. Central
D. Popcorn
Answer: D
Computed tomography (CT) indings characteristic of benign lesions include small size, calcification within the nodule, and stability over time.
Four patterns of benign calcification are common: diffuse, solid, central, and laminated or “popcorn.”
Granulomatous infections, such as tuberculosis, can demonstrate the first three patterns, whereas the popcorn pattern is most common in hamartomas.
In areas of endemic granulomatous disease, differentiating benign versus malignant can be challenging.
Infectious granulomas arising from a variety of organisms account for 70 to 80% of this type of benign solitary nodules; hamartomas are the next most common single cause, accounting or about 10%.
(See Schwartz 10th ed., p. 622.)
For an adenocarcinoma that has pleural invasion, tumor necrosis, and has lymphovascular invasion the correct subtype is
A. Minimally invasive adenocarcinoma (MIA)
B. Lepidic predominant adenocarcinoma (LPA)
C. Invasive adenocarcinoma
D. Adenocarcinoma in situ
Answer: B
If lymphovascular invasion, pleural invasion, tumor necro- sis, or more than 5 mm of invasion are noted in a lesion that has lepidic growth as its predominant component, minimally invasive adenocarcinoma (MIA) is excluded, and the lesion is called lepidic predominant adenocarcinoma (LPA), and the size of the invasive component is recorded for the T stage.
(See Schwartz 10th ed., p. 615.)
The grade of neuroendocrine carcinoma (NEC) that is associated with hemoptysis, pneumonia, and tumor cells arranged in cords and clusters is
A. Grade VI NEC
B. Grade IV NEC
C. Grade II NEC
D. Grade I NEC
Answer: D
Grade I neuroendocrine carcinoma (NEC) (classic or typical carcinoid) is a low-grade NEC; 80% arise in the epithelium of the central airways.
It occurs primarily in younger patients. Because of the central location, it classically presents with hemoptysis, with or without airway obstruction and pneumonia.
Histologically, tumor cells are arranged in cords and clusters with a rich vascular stroma. This vascularity can lead to life-threatening hemorrhage with even simple bronchoscopic biopsy maneuvers.
Regional lymph node metastases are seen in 15% of patients, but rarely spread systemically or cause death.
(See Schwartz 10th ed., p. 617.)
Which of the following is NOT a known predictive or prognostic tumor marker for adenocarcinoma?
A. EGFR
B. KRAS
C. AFP
D. EML4-ALK
Answer: C
Establishing a clear histologic diagnosis early in the evaluation and management of lung cancer is critical to effective treatment.
Molecular signatures are also key determinants of treatment algorithms or adenocarcinoma and will likely become important for squamous cell carcinoma as well.
Currently, differentiation between adenocarcinoma and squamous cell carcinoma in cytologic specimens or small biopsy specimens is imperative in patients with advanced stage disease, as treatment with pemetrexed or bevacizumab-based chemotherapy is associated with improved progression-free survival in patients with adenocarcinoma but not squamous cell cancer.
Furthermore, life-threatening hemorrhage has occurred in patients with squamous cell carcinoma who were treated with bevacizumab.
Finally, EGFR mutation predicts response to EGFR tumor kinase inhibitors and is now recommended as first-line therapy in advanced adenocarcinoma.
Because adequate tissue is required for histologic assessment and molecular testing, each institution should have a clear, multidisciplinary approach to patient evaluation, tissue acquisition, tissue handling/processing, and tissue analysis.
In many cases, tumor morphology differentiates adenocarcinoma rom the other histologic subtypes. If no clear morphology can be identified, then additional testing or one immunohistochemistry marker for adenocarcinoma and one for squamous cell carcinoma will usually enable differentiation.
Immunohistochemistry for neuroendocrine markers is reserved for lesions exhibiting neuroendocrine morphology.
Additional molecular testing should be performed on all adenocarcinoma specimens for known predictive and prognostic tumor markers (eg, EGFR, KRAS, and EML4-ALK fusion gene).
Ideally, use of tissue sections and cell block material is limited to the minimum necessary at each decision point.
This emphasizes the importance of a multidisciplinary approach; surgeons and radiologists must work in direct cooperation with the cytopathologist to ensure that tissue samples are adequate or morphologic diagnosis as well as providing sufficient cellular material to enable molecular testing.
(See Schwartz 10th ed., p. 627.)
Desmoid tumors
A. Arise from the periosteum of the rib
B. Are treated with wide local excision with a 2- to 4-cm margin
C. Require radical excision (sacrificing neurovascular structures) to obtain 4-cm margins
D. Require chemotherapy to treat or prevent metastatic disease
Answer: B
Because the lesions have low cellularity and poor yield with fine needle aspiration (FNA), an open incisional biopsy or lesions over 3 to 4 cm is often necessary.
Surgery consists of wide local excision with a 2- to 4-cm margin and intraoperative frozen section assessment of resection margins.
Typically, chest wall resection, including the involved rib(s) and one rib above and below the tumor with a 4- to 5-cm margin of rib, is required.
A margin of less than 1 cm results in much higher local recurrence rates.
If a major neurovascular structure would have to be sacrificed, leading to high morbidity, then a margin of less than 1 cm would have to suffice.
Survival after wide local excision with negative margins is 90% at 10 years.
(See Schwartz 10th ed., p. 666.)
A 57-year-old non-small-cell lung cancer patient with a potentially resectable tumor found on computed tomography (CT) scan who can walk on a flat surface indefinitely without oxygen or stopping to rest, secondary to dyspnea will most likely tolerate
A. Lobectomy
B. Pneumonectomy
C. Single-lung ventilation
D. Wedge resection
Answer: A
Patients with potentially resectable tumors require careful assessment of their functional status and ability to tolerate either lobectomy or pneumonectomy.
The surgeon should first estimate the likelihood of pneumonectomy, lobectomy, or possibly sleeve resection, based on the CT images.
A sequential process of evaluation then unfolds.
A patient’s history is the most important tool for gauging risk. Specific questions regarding performance status should be routinely asked. If the patient can walk on a flat surface indefinitely, without oxygen and without having to stop and rest secondary to dyspnea, he will be very likely to tolerate lobectomy.
If the patient can walk up two lights of stairs (up two standard levels), without having to stop and rest secondary to dyspnea, he will likely tolerate pneumonectomy.
Finally, nearly all patients, except those with carbon dioxide (CO2) retention on arterial blood gas analysis, will be able to tolerate periods of single-lung ventilation and wedge resection.
(See Schwartz 10th ed., pp. 635–636.)
An “onion-peel” appearance of a rib on CT is suggestive of
A. Chondroma
B. Ewing sarcoma
C. Plasmacytoma
D. Osteosarcoma
Answer: B
Primitive neuroectodermal tumors (PNEs) (neuroblastomas, ganglioneuroblastomas, and ganglioneuromas) derive from primordial neural crest cells that migrate from the mantle layer of the developing spinal cord.
Histologically, PNEs
and Ewing sarcomas are small, round cell tumors; both possess a translocation between the long arms of chromosomes 11 and 22 within their genetic makeup.
They also share a consistent pattern of proto-oncogene expression and have been found to express the product of the MIC2 gene.
Ewing sarcoma occurs in adolescents and young adults who present with progressive chest wall pain, but without the presence of a mass.
Systemic symptoms of malaise and fever are often present.
Laboratory studies reveal an elevated erythrocyte sedimentation rate and mild white blood cell elevation.
Radiographically, the characteristic onion peel appearance is produced by multiple layers of periosteum in the bone formation. Evidence of bony destruction is also common.
The diagnosis can be made by a percutaneous needle biopsy or an incisional biopsy.
(See Schwartz 10th ed., p. 669.)
Pancoast tumors are identified as involving all of the following except:
A. The chest wall at or below the second rib.
B. Tumors of the parietal pleura or deeper structures overlying the first rib.
C. The superior sulcus.
D. The extreme apex of the chest.
Answer: A
Carcinoma arising in the extreme apex of the chest with associated arm and shoulder pain, atrophy of the muscles of the hand, and Horner syndrome presents a unique challenge to the surgeon.
Any tumor of the superior sulcus, including tumors without evidence for involvement of the neurovascular bundle, is now commonly known as Pancoast tumors, after Henry Pancoast who described the syndrome in 1932.
The designation is reserved for tumors involving the parietal pleura or deeper structures overlying the first rib.
Chest wall involvement at or below the second rib is not a Pancoast tumor.
Treatment is multidisciplinary; due to the location of the tumor and involvement of the neurovascular bundle that supplies the ipsilateral extremity, preserving postoperative function of the extremity is critical.
(See Schwartz 10th ed., p. 642.)
The most likely cause of aspiration pneumonia is
A. A mixture of aerobes and anaerobes
B. Aerobes only
C. Anaerobes only
D. Gram-negative bacteria
Answer: C
Normal oropharyngeal secretions contain many more Streptococcus species and more anaerobes (approximately 1 × 108 organisms/mL) than aerobes (approximately 1 × 107 organisms/mL).
Pneumonia that follows from aspiration, with or without abscess development, is typically poly- microbial.
An average of two to four isolates present in large numbers have been cultured from lung abscesses sampled percutaneously.
Overall, at least 50% of these infections are caused by purely anaerobic bacteria, 25% are caused by mixed aerobes and anaerobes, and 25% or fewer are caused by aerobes only.
In nosocomial pneumonia, 60 to 70% of the organisms are gram-negative bacteria, including Klebsiella pneumoniae, Haemophilus influenzae, Proteus species, Pseudomonas aeruginosa, Escherichia coli, Enterobacter cloacae, and Eikenella corrodens.
Immunosuppressed patients may develop abscesses because of the usual pathogens as well as less virulent and opportunistic organisms such as Salmonella species, Legionella species, Pneumocystis carinii, atypical mycobacteria, and fungi.
(See Schwartz 10th ed.,p.650.)
Laboratory evaluation of a chest wall mass showing elevated erythrocyte sedimentation rates indicates
A. Osteosarcoma
B. Plasmacytoma
C. Ewing sarcoma
D. Multiple myeloma
Answer: C
Laboratory evaluations are useful in assessing chest wall masses or the following:
- Plasmacytoma: Serum protein electrophoresis demonstrates a single monoclonal spike, which is measuring the overproduction of one immunoglobulin rom the malignant plasma cell clone.
- Osteosarcoma: Alkaline phosphatase levels may be elevated.
- Ewing sarcoma: Erythrocyte sedimentation rates may be elevated.
(See Schwartz 10th ed., able 19-18, p. 665.)
The most common benign chest wall tumor is
A. Chondromas
B. Osteochondromas
C. Desmoid tumors
D. Fibrous dysplasia
Answer: A
Chondromas, seen primarily in children and young adults, are one of the more common benign tumors of the chest wall.
They usually occur at the costochondral junction anteriorly and may be confused with costochondritis, except that a painless mass is present.
Radiographically, lesion is lobulated and radiodense; it may have diffuse or focal calcifications; and it may displace the bony cortex without penetration.
Chondromas may grow to huge sizes if left untreated.
Treatment is surgical resection with a 2-cm margin.
Large chondromas may harbor well-differentiated chondrosarcoma and should be managed with a 4-cm margin to prevent local recurrence.
(See Schwartz 10th ed., p. 666.)
Which of the following is an indication for surgical drainage of a lung abscess?
A. Abscess >3 cm in diameter.
B. Hemoptysis.
C. Failure to decrease in size after 1 week of antibiotic therapy.
D. Persistent ever.
Answer: B
Surgical drainage of lung abscesses is uncommon since drainage usually occurs spontaneously via the tracheobronchial tree.
Indications for intervention are:
- Failure of medical therapy
- Abscess under tension
- Abscess increasing in size during appropriate treatment
- Contralateral lung contamination
- Abscess >4–6 cm in diameter
- Necrotizing infection with multiple abscesses, hemoptysis, abscess
rupture, or pyopneumothorax - Inability to exclude a cavitating carcinoma
What percentages of chest wall masses are malignant?
A. 10–20%
B. 20–30%
C. 50–80%
D. 40–50%
Answer: C
Patients with chest wall tumors, regardless of etiology, typically complain of a slowly enlarging palpable mass (50–70%), chest wall pain (25–50%), or both.
Interestingly, growing masses are often not noticed by the patient until they suffer a trauma to the area.
Pain from a chest wall mass is typically localized to the area of the tumor; it occurs more often and more intensely with malignant tumors, but it can also be present in up to one-third of patients with benign tumors.
With Ewing sarcoma, fever and malaise may also be present.
Benign chest wall tumors tend to occur in younger patients (average age 26 years), whereas malignant tumors tend to be found in older patients (average age 40 years).
Overall, between 50 and 80% of chest wall tumors are malignant.
(See Schwartz 10th ed., p. 665.)
The population most at risk for developing active tuberculosis is
A. Elderly
B. Minorities
C. Urban residents
D. Human immunodeficiency virus (HIV) infected
Answer: D
Tuberculosis is a widespread problem that affects nearly one-third of the world’s population. Between 8.3 and 9 million new cases of tuberculosis and 12 million prevalent cases (range 10–13 million) were estimated worldwide in 2011 according to the World Health Organization. Only 10,521 new cases were reported to the World Health Organization in the United States in 2011.
Human immunodeficiency virus (HIV) infection is the strongest risk factor for developing active tuberculosis. The elderly, minorities, and recent immigrants are the most common populations to have clinical manifestations of inection, yet no age group, sex, or race is exempt from infection.
In most large urban centers, reported cases of tuberculosis are more numerous among the homeless, prisoners, and drug-addicted populations.
Immunocompromised patients additionally contribute to an increased incidence of tuberculosis infection, often developing unusual systemic as well as pulmonary manifestations.
(See Schwartz 10th ed., p. 654.)
The fungi associated with the highest mortality rate due to invasive mycoses in the United States is
A. Aspergillus
B. Cryptococcus
C. Candidia
D. Mucor
Answer: A
The genus Aspergillus comprises over 150 species and is the most common cause of mortality due to invasive mycoses in the United States.
It is typically acute in onset and life-threatening and occurs in the setting of neutropenia, chronic steroid therapy, or cytotoxic chemotherapy.
It can also occur in the general intensive care unit population of critically ill patients, including patients with underlying chronic obstructive pulmonary disease (COPD), postoperative patients, patients with cirrhosis or alcoholism, and post-inluenza patients, without any of these factors present.
The species most commonly responsible for clinical disease include A. fumigatus, A. flavus, A. niger, and A. terreus.
Aspergillus is a saprophytic, filamentous fungus with septate hyphae.
Spores (2.5–3 μm in diameter) are released and easily inhaled by susceptible patients; because the spores are microns in size, they are able to reach the distal bronchi and alveoli.
(See Schwartz 10th ed., p. 655.)
A patient presenting with a history and findings of dyspnea, wheezing, hemoptysis, and a mediastinal mass in the visceral compartment yields a diagnosis of
A. Lymphoma
B. Thymoma with myasthenia gravis
C. Mediastinal granuloma
D. Germ cell tumor
LYMPHOMA
- Hx/PE: Night sweats, weight loss, fatigue, extrathoracic adenopathy, elevated erythrocyte sedimentation rate or C-reactive protein level, leukocytosis
- Location: Any compartment
THYMOMA WITH MYASTHENIA GRAVIS
- Hx/PE: Fluctuating weakness, early fatigue, ptosis, diplopia
- Location: Anterior
MEDIASTINAL GRANULOMA
- Hx/PE: Dyspnea, wheezing, hemoptysis
- Location: Visceral (middle)
GERM CELL TUMOR
- Hx/PE: Male gender, young age, testicular mass, elevated levels of human chorionic gonadotropin and/or α- fetoprotein
- Location: Anterior
A patient with an anterior mediastinal mass and elevated serum α- etoprotein (AFP) most likely has
A. A teratoma
B. A nonseminomatous germ-cell tumor
C. A seminomatous germ-cell tumor
D. Metastatic hepatocellular carcinoma
Answer: B
The use of serum markers to evaluate a mediastinal mass can be invaluable in some patients. For example, nonseminomatous and seminomatous germ-cell tumors can frequently be diagnosed and often distinguished from one another by the levels of α- etoprotein (AFP) and human chorionic gonadotropin (hCG).
In over 90% of nonseminomatous germ-cell tumors, either the AFP or the hCG level will be elevated. Results are close to 100% specificic if the level of either AFP or hCG is greater than 500 ng/mL.
Some centers institute chemotherapy based on this result alone, without biopsy confirmation of the diagnosis. In contrast, the AFP level in patients with mediastinal seminoma is always normal; only 10% will have elevated hCG, which is usually less than 100 ng/mL.
Other serum markers, such as intact parathyroid hormone level or ectopic parathyroid adenomas, may be useful for diagnosing and also for intraoperatively confirming complete resection.
After successful resection of a parathyroid adenoma, this hormone level should rapidly normalize.
(See Schwartz 10th ed., p. 672
The primary site for male patients with malignant pleural effusions is
A. Gastrointestinal tract
B. Lung
C. Genitourinary tract
D. Melanoma
Answer: B
Malignant pleural effusions may occur in association with a number of different malignancies, most commonly lung cancer, breast cancer, and lymphomas, depending on the patient’s age and gender.
(p. 132 Schwartz ABSITE)
Eosinophilic granulomas are associated with
A. Langerhans cell histiocytosis (LCH)
B. Parasitic infections
C. Crohn disease
D. Gardner syndrome
Answer: A
Eosinophilic granulomas are benign osteolytic lesions. Eosinophilic granulomas of the ribs can occur as solitary lesions or as part of a more generalized disease process of the lymphoreticular system termed Langerhans cell histiocytosis (LCH).
In LCH, the involved tissue is infiltrated with large numbers of histiocytes (similar to Langerhans cells seen in skin and other epithelia), which are often organized as granulomas.
The cause is unknown. Of all LCH bone lesions, 79% are solitary eosinophilic granulomas, 7% involve multiple eosinophilic granulomas, and 14% belong to other forms of more systemic LCH.
Isolated single eosinophilic granulomas can occur in the ribs or skull, pelvis, mandible, humerus, and other sites. They are diagnosed primarily in children between the ages of 5 and 15 years.
Because of the associated pain and tenderness, they may be confused with Ewing sarcoma or with an inflammatory process such as osteomyelitis.
Healing may occur spontaneously, but the typical treatment is limited surgical resection with a 2-cm margin.
(See Schwartz 10th ed., p. 666.)
A chylothorax is likely to be present in a patient whose pleural fluid analysis results show a triglyceride level of
A. 80mg/100mL
B. 100mg/100mL
C. 45mg/100mL
D. 130mg/100mL
Answer: D
Laboratory analysis of the pleural fluid shows a high lymphocyte count and high triglyceride levels.
If the triglyceride level is greater than 110 mg/100 mL, a chylothorax is almost certainly present (a 99% accuracy rate).
If the triglyceride level is less than 50 mg/mL, there is only a 5% chance of chylothorax.
(See Schwartz 10th ed., p. 686.)
Osteosarcoma of the rib
A. Is considered nonoperable if pulmonary metastases are present
B. Is treated with radiation therapy before resection
C. Is treated with adjuvant chemotherapy before resection
D. Requires excision with a 6-cm margin
Answer: C
While osteosarcomas are the most common bone malignancy, they represent only 10 to 15% of all malignant chest wall tumors.
They primarily occur in young adults as rapidly enlarging, painful masses; however, osteosarcomas can occur in older patients as well, sometimes in association with previous radiation, Paget disease, or chemotherapy.
Radiographically, the typical appearance consists of spicules of new periosteal bone formation producing a sunburst appearance.
Osteosarcomas have a propensity to spread to the lungs, and up to one-third of patients present with metastatic disease.
Osteosarcomas are potentially sensitive to chemotherapy. Currently, preoperative chemotherapy is common. After chemotherapy, complete resection is performed with wide (4-cm) margins, followed by reconstruction.
In patients presenting with lung metastases that are potentially amenable to surgical resection, induction chemotherapy may be given, followed by surgical resection of the primary tumor and of the pulmonary metastases.
Following surgical treatment of known disease, additional maintenance chemotherapy is usually recommended.
(See Schwartz 10th ed., p. 667.)