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Histological classification of intraepithelial neoplasias and
microinvasive squamous carcinoma of the esophagus. Am J Surg Pathol.1989
Aug;13(8):685-90
We reviewed a
total of 119 resected esophagi with intraepithelial neoplasias of low
grade (including slight or moderate dysplasias), high grade (including
severe dysplasia and carcinoma in situ), or microinvasive squamous
carcinoma (i.e., not invasive beyond the submucosa and without
metastases in regional lymph nodes). Epithelial buds bulging into the
stroma were noted in noninvasive intraepithelial lesions. The most
severe degree of histological alteration was used to characterize each
case. Of the 119 cases, five were low-grade, 38 were high-grade, and the
remaining 76 specimens contained microinvasive squamous carcinoma. Of
these, 23 invaded only the lamina propria. Nine invaded the muscularis
mucosae, 16 invaded the inner half of the submucosa, and the remaining
28 invaded the outer half of the submucosa. Epithelial buds were divided
according to their configuration into types I, II, and III. Grade I was
characterized by regular epithelial buds of the same size, grade II had
regular buds that varied in size, and grade III had irregular buds
(i.e., buds of varying length and width with irregular contours). Our
study of 66 specimens with microinvasive squamous carcinoma showed that
one of the two specimens that had low grade dysplasia also had type III
buds, while 56 of the remaining 64 (87.7%) with high grade dysplasia
also had type III buds. Microinvasion originated at the tip of the type
III epithelial buds in 12 specimens. Similar results have been
demonstrated in experimental animals. We conclude that in the esophageal
mucosa, there is a close relationship among the degree of squamous
cellular atypia, the formation of epithelial buds, and the progression
toward invasive carcinoma.
Superficial
esophageal carcinoma: a report of 27 cases in Japan.Am
J Gastroenterol.1991 Dec;86(12):1723-8.
Twenty-seven
patients with superficial esophageal carcinoma were investigated to
determine their clinical and pathological features. All 21 male patients
were habitual drinkers, and 17 were heavy smokers. Histological
examination showed that three tumors were intraepithelial, five were
mucosal, and 19 were submucosal. Fifteen of the 27 patients were
asymptomatic, including seven of the eight with intraepithelial or
mucosal carcinoma. Twelve of the 13 patients with polypoid tumors had
submucosal invasion, whereas two patients with flat tumors and four of
the seven with erosive tumors had either intraepithelial or mucosal
carcinoma. Six of the eight patients with intraepithelial or mucosal
carcinoma had normal routine radiological studies. All these eight
patients had no lymph node involvement, whereas four of the 19 with
submucosal carcinoma had lymph node metastases. An aggressive approach
to endoscopy in asymptomatic high-risk individuals (middle-aged male
drinkers and smokers) may increase the detection of early esophageal
carcinoma, although the cost-effectiveness should be evaluated further.
In addition, in the interest of prevention, our results show that
encouraging people to stop smoking and limit their alcohol intake to an
occasional drink might be an important factor in lessening the risk for
esophageal carcinoma.
Superficial squamous
cell carcinoma of the esophagus. A report of 76 cases and review of the
literature.Am J Surg Pathol.1989 Jul;13(7):535-46.
Superficial
squamous carcinoma of the esophagus, defined as carcinoma limited to
mucosa or submucosa regardless of lymph node status, is being
increasingly recognized in the Western hemisphere. Seventy-six cases of
this entity are herein presented. Five macroscopic types were
recognized: normal flat (eight cases), coarse (21 cases), verrucous (25
cases), polypoid (17 cases), and ulcerating infiltrating (five cases).
Histological typing included 65 conventional squamous cell carcinomas,
six squamous carcinomas with spindle cell features, and five adenoid
cystic carcinomas. Four cases were strictly intraepithelial, 10 cases
were confined to the mucosa, nine cases encroached onto the muscularis
mucosae, and 53 extended into the submucosa. Cases with intraepithelial
and infiltrating carcinomas confined to the mucosa showed no lymph node
involvement. Thirty percent of cases extending into the submucosa
developed lymph node metastases. Thirty-eight patients survived surgical
resection from 1 to 96 months; 34 of these 38 were free of neoplastic
disease. Fourteen patients had an associated bronchial or
oropharyngolaryngeal carcinoma either simultaneously or asynchronously.
We conclude that patients with superficial squamous carcinoma of the
esophagus can benefit from early diagnosis and prompt surgery.
Basaloid-squamous carcinoma of the esophagus. A clinicopathologic, DNA
ploidy, and immunohistochemical study of seven cases. Am J Surg
Pathol.1996 Apr;20(4):453-61.
Basaloid-squamous carcinoma (BSC) of the esophagus is a rare but
interesting neoplasm that occurs primarily in the upper aerodigestive
tract. In this study, we reviewed 371 cases of esophageal malignancies
and detected seven cases (1.9%) of BSC. The clinicopathologic features,
light and electron microscopic findings, and immunohistochemical
localization of various differentiation-related antigens, including
cytokeratin (CK) subtypes, p53, and epidermal growth factor receptor (EGFR),
were examined. DNA ploidy was also determined in an effort to
characterize the biologic features of these tumors. The tumors were
classified as stage I (n = 1), IIB (n = 3), III (n = 2) or IV (n = 1).
Six patients had lymph node metastasis, in four the metastatic carcinoma
exhibited basaloid components. Histologically, all the tumors displayed
a biphasic pattern of basaloid and squamous components. The former
predominated in three cases, the latter in four cases. All the tumors
contained solid growth of basaloid cells with microcystic patterns and
stromal hyalinosis as well as palisading of cells. Ultrastructurally,
markedly replicated basement membrane was observed. Immunohistochemistry
revealed staining with only CK 14 and CK 19 antibodies in the periphery
of the basaloid tumor nests. These antibodies were also positive in the
basal layer of normal esophagus. Diffuse immunoreactivity for EGFR was
demonstrated in all the tumors. Five tumors displayed p53 nuclear
immunoreactivity. All of the basaloid components demonstrated aneuploidy
by DNA image cytometry. We conclude that BSC is a distinct type of
esophageal carcinoma that should be differentiated from the usual types
of esophageal carcinoma and may be associated with aggressive biologic
behavior.
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