Abstract
BackgroundPrimary small cell carcinoma (SCC) of the esophagus is a rare and aggressive tumor with poor prognosis. In this study, we report the clinicopathological characteristics of 21 cases of small cell carcinoma of the esophagus treated at the Cancer Center of Sun Yat-Sen University, with particular focus on the histologic and immunohistochemical findings.MethodsTwenty-one patient records were reviewed including presenting symptoms, demographics, disease stage, treatment, and follow-up. Histologic features were observed and immunohistochemical detection of cytokeratin (CK), epithelial membrane antigen (EMA), neuron specific enolase (NSE), synaptophysin (Syn), chromogranin A (CgA), neuronal cell adhesion molecules (CD56), thyroid transcriptional factor-1 (TTF-1) and S100 protein (S100) was performed.ResultsThe median age of patients in the study was 56 years, with a male-to-female ratio of 3.2:1. Histologically, there were 19 "homogenous" SCC esophageal samples and 2 samples comprised of SCC and well-differentiated squamous cell carcinoma. The percentages of SCC samples with positive immunoreactivity were Syn 95.2%, CD56 76.2%, TTF-1 71.4%, NSE 61.9%, CgA 61.9%, CK 57.1%, EMA 61.9%, and S100 19.0%, respectively. The median patient survival time was 18.3 months after diagnosis. The 2-year survival rate was 28.6%.ConclusionOur study suggests that esophageal SCC has similar histology to SCC that arises in the lung compartment, and Chinese patients have a poor prognosis. Higher proportion of positive labeling of Syn, CD56, CgA, NSE, and TTF-1 in esophageal SCC implicate that they are valuably applied in differential diagnosis of the malignancy.
Highlights
Primary small cell carcinoma (SCC) of the esophagus is a rare and aggressive tumor with poor prognosis
A total of 21 cases were diagnosed as small cell carcinoma of the esophagus, using histological criteria for esophageal small cell carcinoma [13] and pulmonary small cell carcinoma [14] prepared by the World Health Organization
Clinical features Between 1989 and 2005, twenty-one Chinese patients were diagnosed with primary SCC, representing 0.05% (21/4050) of all patients with esophageal malignancies seen in our hospital
Summary
Twenty-one patient records were reviewed including presenting symptoms, demographics, disease stage, treatment, and follow-up. Histologic features were observed and immunohistochemical detection of cytokeratin (CK), epithelial membrane antigen (EMA), neuron specific enolase (NSE), synaptophysin (Syn), chromogranin A (CgA), neuronal cell adhesion molecules (CD56), thyroid transcriptional factor-1 (TTF-1) and S100 protein (S100) was performed. Immunological markers included pancytokeratin (CK; mouse monoclonal antibody; Clone:AE1/AE3; Cat No 18-0132; Zymed, CA), epithelial membrane antigen (EMA; mouse monoclonal antibody; Clone:MC-5; Cat No MU182-UC; BioGenex, CA), neuron specific enolase (NSE; mouse monoclonal antibody; Clone:NSE-1G4; Cat No 18-01963; Zymed, CA), synaptophysin (Syn; mouse monoclonal antibody; Clone:snp; Cat No MU363-UC; BioGenex, CA), chromogranin A (CgA; mouse monoclonal antibody; Clone:LK2H10; Cat No MU126-UC; BioGenex, CA), neuronal cell adhesion molecule (CD56; mouse monoclonal antibody; Clone:123C3; Cat No.18-0152; Zymed, CA), Thyroid Transcriptional Factor-1 (TTF-1; mouse monoclonal antibody; Clone:8G7G3/1; Cat No.18-0221; Zymed, CA) and S100 protein (S100; mouse monoclonal antibody; Clone:4C4.9; Cat No Z2055; Zeta, CA). Immunostaining labeling intensities were defined as: +, less than 10% of the positive tumor cells; ++, 10%–50% of the positive tumor cells; +++ more than 50% of the positive tumor cells; - negative labeling
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