| 12. Esophageal
Neoplasms |
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123 |
A large number of different tumors can involve the
esophagus ( Table
5). The
vast majority are extremely rare and often do not produce clinical
disease. Unfortunately, the most common esophageal neoplasm is squamous
cell carcinoma, which has a five-year survival rate (< 10%) that is
among the lowest for any neoplastic disease.
TABLE 5. Classification of esophageal
tumors
Benign tumors
Epithelial origin
Squamous cell papilloma
Non-epithelial origin
Leiomyoma
Granular cell tumor
Hemangioma
Lymphangioma
Malignant tumors
Epithelial origin
Squamous cell carcinoma
Adenocarcinoma
Adenoid cystic carcinoma
Mucoepidermoid carcinoma
Adenosquamous carcinoma
Undifferentiated carcinoma; small-cell carcinoma
Non-epithelial origin
Leiomyosarcoma
Carcinosarcoma
Malignant melanoma
Secondary tumors
Malignant melanoma
Breast carcinoma
Tumor-like lesions
Fibrovascular polyp
Heterotopia
Congenital cyst
Glycogen acanthosis
| 12.1 Benign
Tumors |
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123 |
Leiomyoma
is the most common benign esophageal tumor. Esophageal leiomyomas may
produce dysphagia and retrosternal chest pain, but in most cases are
asymptomatic. Unlike gastric leiomyomas, they rarely hemorrhage. On
barium x-ray a characteristic smooth, round luminal defect is seen
projecting from one wall. Its endoscopic appearance is a clearly
demarcated projection into the lumen; the overlying mucosa is normal.
Endoscopic biopsy is not helpful, as the lesion is submucosal and
cannot be reached with biopsy forceps. If leiomyomas are symptomatic,
surgical enucleation is indicated.
Squamous cell papillomas consist of
frond-like projections of the lamina propria that are covered by
squamous epithelium and develop at several sites simultaneously. They
rarely grow large enough to produce dysphagia. They occur in
association with acanthosis nigricans and tylosis. Except when
associated with tylosis, these lesions are not considered to be
precursors of squamous cell carcinoma.
Fibrovascular
polyps consist of a core of loose fibrous connective tissue, fat
and blood vessels covered by a thick layer of squamous epithelium.
Such a polyp may become quite large, with a very long stalk that
permits the lesions to flop back and forth in the esophageal lumen.
Patients with this lesion have presented with regurgitation of the
free end of the polyp into the mouth; in other instances, the
regurgitated polyp has caused sudden death by obstructing the larynx.
Granular
cell tumors are submucosal lesions with intact mucosal covering
that are usually picked up incidentally at endoscopy. They may
originate from neural elements. They rarely cause symptoms, although
there have been occasional reports of dysphagia due to large granular
cell tumors. There have also been rare reports of malignant granular
cell tumors in the esophagus. Symptomatic tumors need to be removed
surgically.
Carcinoma
of the esophagus is a relatively uncommon malignancy in Canada, with
only 3 to 4 new cases per 100,000 population per year in males and
just over 1 new case per 100,000 population per year in females.
Nevertheless, because of its poor prognosis, esophageal cancer ranks
among the 10 leading causes of cancer death in Canadian men 45 years
of age and older.
Although
several different types of primary and secondary malignancies can
involve the esophagus (Table
5),
squamous cell carcinoma and adenocarcinoma are by far the most
common esophageal malignancies.
Adenocarcinoma
used to make up approximately 10% of all esophageal cancers.
However, its incidence has been increasing in recent decades such
that now it comprises up to 30-40% of esophageal cancers in North
America. Rarely, primary esophageal adenocarcinomas arise from
embryonic remnants of columnar epithelium or from superficial or
deep glandular epithelium. In most instances, adenocarcinoma arises
from metaplastic Barrett's epithelium in the distal esophagus.
Adenocarcinoma of the cardia of the stomach may also involve the
distal esophagus and give the appearance that the cancer arises from
the esophagus.
The
true incidence of Barrett's-related cancer is uncertain, but most
studies suggest that patients with Barrett's esophagus will develop
adenocarcinoma at a rate of about 0.5% per year. This is a
significant problem given the large number of reflux patients with
Barrett's metaplasia. Because dysplasia develops prior to frank
carcinoma in Barrett's epithelium, most experts suggest that these
patients should undergo surveillance endoscopy with multiple
biopsies every one to two years to identify those who are likely to
progress to cancer (Section 7).
The
clinical presentation and diagnostic evaluation of patients with
adenocarcinoma of the esophagus are similar to squamous cell
carcinoma (Section 12.2.2). These lesions are not radiosensitive and
their response to various chemotherapeutic agents is not very
satisfactory. Surgical resection or palliation with laser,
photodynamic therapy, peroral dilation and/or stent placement are
the preferred treatments. The prognosis is similar to that for
gastric adenocarcinoma - i.e., an overall five-year survival rate of
< 10%.
| 12.2.2 SQUAMOUS
CELL CARCINOMA |
|
The
occurrence of squamous cell carcinoma of the esophagus shows
striking geographic variability, with high frequencies in certain
regions of Iran, Africa, China and the former USSR. This has led to
several theories concerning certain environmental agents that may be
important etiologically (Table
6). In North America, squamous cell carcinoma is
associated with alcohol ingestion, tobacco use and lower
socioeconomic status. It is also significantly more common in blacks
and in males.
Characteristically
these cancers extend microscopically in the submucosa for
substantial distances above and below the area of the gross
involvement. They also have a propensity to extend through the
esophageal wall and to regional lymphatics quite early. Furthermore,
they usually produce symptoms only when they have become locally
quite advanced. For these reasons approximately 95% of these cancers
are diagnosed at a time when surgical cure is impossible.
In
most studies, the mid-esophagus is the most common site of origin;
however, others have reported distal cancers to be most common. The
lungs and liver are the most common sites of distant metastases.
Most
patients present with progressive, predictable dysphagia and weight
loss. Other symptoms include odynophagia, chest pain (which may
radiate to the mid-scapular region), hoarseness (due to recurrent
laryngeal nerve involvement) and blood loss.
Pulmonary complications due to either direct
aspiration or esophagorespiratory fistulas are also quite common
during the course of the disease. Physical examination is usually
negative aside from signs of weight loss. Hepatomegaly or enlarged
cervical or supraclavicular lymph nodes may be detected in cases of
disseminated metastases.
Barium swallow is usually diagnostic, although
small cancers can be missed in up to 30% of cases. Endoscopy with
multiple directed biopsies combined with brush cytology is required
to confirm the diagnosis. This should be followed by careful
attempts to stage the disease prior to deciding on therapeutic
intervention. In addition to a careful physical examination, chest
x-ray and blood tests for transaminases, alkaline phosphatase and
bilirubin, an ultrasound of the abdomen should be performed to look
for liver metastasis. If this is negative, one should proceed to a
CT scan of the thorax in order to define the extent of local spread.
Unfortunately the CT scan lacks sensitivity in this regard.
Endoscopic ultrasound appears promising in accurately assessing
depth of tumor involvement and presence or absence of enlarged
mediastinal lymph nodes. If the above investigations are negative,
some experts recommend bronchoscopy, mediastinoscopy and scalene
node biopsy prior to attempting surgical resection.
Treatment results of squamous cell carcinoma of
the esophagus are discouraging. Although it is traditionally taught
that surgical resection is the only chance for a cure, there is no
convincing evidence that "curative" surgery is better than
"curative" radiotherapy. These tumors are quite
radiosensitive; however, most centers give radiotherapy to patients
who have advanced unresectable tumors or other health problems that
make them poor surgical candidates. This understandably leads to
very poor overall survival following radiotherapy. In the few
reports where radiotherapy is used as the primary mode of therapy in
patients who might otherwise be considered surgical candidates, the
five-year survival rate is as high as 17%, which compares quite
favorably to surgical results. Both forms of treatment have
significant morbidity, and the mortality following esophageal
resection is at least 10%. Controlled trials are needed, but in only
a small proportion of the total population of esophageal cancer
patients is cure a realistic goal. In the majority the disease is
too far advanced. New regimens that combine radiotherapy and
chemotherapy, with or without surgery, are currently being
evaluated.
The goal of treatment has to be palliation in
most patients. Both radiotherapy and modified surgery can be used in
this setting; however, other modalities are often necessary. The
dysphagia can be relieved with peroral dilation, but in many
patients this becomes exceedingly difficult as the disease
progresses. If this is the case, a prosthetic device can sometimes
be placed across the tumor to maintain luminal patency. These stents
can work quite well, although tube blockage, tube migration and
erosion through the esophageal wall are important complications.
These prosthetic devices are the best treatment for an
esophagorespiratory fistula. Endoscopic Nd-YAG laser therapy has
been used to destroy tumors that obstruct the esophageal lumen. This
appears to be a very useful form of palliation, but it is expensive
and has not as yet been documented to be superior to dilation and
stent placement. Photodynamic therapy has recently been approved for
palliation of neoplastic dysphagia. This involves using a
photosensitizing compound that accumulates in cancer cells, which
leads to their destruction when they are exposed to light of a
certain wavelength. The caring physician must also provide emotional
support, nutritional support and adequate pain therapy for these
unfortunate patients.
TABLE 6. Esophageal squamous
cell carcinoma: possible etiological factors
Alcohol
Tobacco
Nutritional exposures
Nitrosamines; 'bush teas' containing tannin and/or diterpene phorbol
esters
Nutritional deficiencies (riboflavin, niacin, iron)
Chronic esophagitis
Achalasia
Previous lye-induced injury
Tylosis
Plummer-Vinson (Paterson-Kelly) syndrome
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