Tri-modal management of primary small cell carcinoma of the pancreas (SCCP): a rare neuroendocrine carcinoma (NEC)

被引:0
|
作者
Elzein, Safa [1 ]
Bao, Fei [2 ]
Lin, Ray [3 ]
Schnickel, Gabriel [4 ]
Lowy, Andrew M. [4 ]
Botta, Gregory P. [5 ]
机构
[1] Scripps Clin Green Hosp, Dept Internal Med, 10666 N Torrey Pines Rd, La Jolla, CA 92037 USA
[2] Scripps Clin Green Hosp, Dept Pathol, 10666 N Torrey Pines Rd, La Jolla, CA 92037 USA
[3] Scripps Hlth Radiat Oncol, 10666 N Torrey Pines Rd, La Jolla, CA 92037 USA
[4] Univ Calif San Diego, Moores Canc Ctr, Dept Surg, Div Surg Oncol, 3855 Hlth Sci Rd, La Jolla, CA 92037 USA
[5] Univ Calif San Diego, Moores Canc Ctr, Dept Med, Div Hematol Oncol, 3855 Hlth Sci Rd, La Jolla, CA 92037 USA
关键词
Small cell; Carcinoma; Pancreas; Neuroendocrine carcinoma; CHROMOGRANIN-A; HIGH-GRADE; TUMORS; DIAGNOSIS; MARKERS; CANCER;
D O I
10.1186/s12876-021-01901-7
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Primary small cell carcinoma of the pancreas (SCCP) is a rare malignant neuroendocrine carcinoma (NEC). Typically, it presents with lymphovascular invasion as well as metastasis at the time of diagnosis which portends a dismal prognosis. Treatment is typically based on therapy used for other aggressive NECs such as small cell lung cancer. Although multimodal surgery, radiation and chemotherapy may improve prognosis, the outcome generally remains poor. Case presentation Here we present a primary SCCP managed with neoadjuvant multi-agent chemotherapy combined with radiotherapy and surgery Conclusions Multi-disciplinary therapy resulted in an ongoing 28 + month radiographic complete response and overall survival.
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页数:7
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