Discussion
Diagnosis With Brief Discussion
- Diagnosis
- Spindle cell carcinoma of the esophagus
- Radiologic Findings
- Axial unenhanced CT image, obtained at the time of presentation, shows the distal esophagus, which is expanded by a mass of soft-tissue attenuation. Axial contrast-enhanced CT shows intense enhancement of the mass. Coronal contrast-enhanced CT shows a huge sausage-shaped mass filling the midesophagus. Endoscopic image shows a large lobulated mass that occupies almost the entire middle esophagus. Photograph of the sectioned mass shows a yellow-tan internal structure. CT postop. 6 months shows a large recurrent pleural mass, which was confirmed with transthoracic needle biopsy.
- Brief Review
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Spindle cell carcinoma of the esophagus is rare (0.5~2.8 % of all esophageal neoplasm). The current understanding of this tumor is that it originates from an epithelial cell with divergent bidirectional differentiation.
Spindle cell carcinoma usually affects middle-aged men (male-to-female ratio, 4:1 to 9:1). Presenting symptoms are nonspecific; the most common are dysphagia and weight loss, followed by pain. Most spindle cell tumors (more than 90%) arise from the middle and distal esophagus. Most patients present early in the disease process, infrequently invading the esophageal wall, due to its intraluminal location and rapid growth (doubling time, 2.2~5 months). The tumor frequently spreads loco-regionally or metastasizes to the lung and liver (38~50%).
The surface of spindle cell carcinoma may be smooth, lobulated, or scalloped, and a cupola, or domelike shape, is usually seen at the proximal interface with the esophageal lumen. Focal ulcerations and luminal obstruction are infrequent.
At CT, spindle cell tumor is seen as an expansile, low-attenuation, intraluminal mass, with differentials including fibrovascular polyp, myofibroma, pedunculated lipoma, and leiomyoma (benign) and adenocarcinoma of the esophagus, leiomyosarcoma, fibrosarcoma, rhabdomyosarcoma, melanoma, oat cell carcinoma, and lymphoma (malignancies). The treatment and prognosis spindle cell tumor are not well defined due to its rarity. Esophageal resection with gastric pull-through is the most accepted treatment option. The 5-year survival rates of patients with spindle cell carcinoma (slightly more than 20%) are similar to those of patients with squamous cell carcinoma.
- References
- 1. Sadej P, Feld RI, Toll AD, Palazzo JP. AIRP best cases in radiologic-pathologic correlation: spindle cell carcinoma of the esophagus. Radiographics. 2011 Nov-Dec;31(7):2035-9.
2. Takahashi T, Hokamura N. A case of esophageal spindle cell carcinoma. Jpn J Clin Oncol. 2011 Oct;41(10):1238-9.
- Keywords
- esophagus, malignant tumor,