Pancreatic somatostatinoma with obscure inhibitory syndrome and mixed pathological pattern
Pancreatic somatostatinoma with obscure inhibitory syndrome and mixed pathological pattern
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具有不明抑制综合征和混合病理模式的胰腺生长抑素瘤
DOI：
10.1631/jzus.b0900166
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发表时间：
2010-01
影响因子：
5.1
通讯作者：
Wu, Yu-lian
中科院分区：
文献类型：
--
作者：
Fu, Yan-biao;Zhang, Bo;Xie, Qiu-ping;Gao, Shun-liang;Wu, Yu-lian
生长抑素瘤是一种非常罕见的神经内分泌肿瘤，起源于D细胞，占所有胃肠道内分泌肿瘤的不到1%。十二指肠是这种肿瘤最常见的部位，其次是胰腺。我们在此报告一位46岁的中国女性，罹患胰脏生长抑素瘤，表现为典型的“抑制性”症候群，但症状不明显且似乎不相关。此病例也因其巨大的肿瘤大小和混合的病理模式而独特。进行了远端胰腺切除术，患者自手术以来一直保持良好。由于生长抑素瘤的症状可能是模糊和不典型的，临床医生应该审查所有的临床表现，以获得准确的诊断。积极手术是提高生存率的首选方法。
Somatostatinoma is a very rare neuroendocrine tumor that originates from D cells and accounts for less than 1% of all gastrointestinal endocrine tumors. The duodenum is the most frequent site for this tumor, followed by the pancreas. We here describe a 46-year-old Chinese woman who developed pancreatic somatostatinoma presenting with the characteristic “inhibitory” syndrome, but the symptoms were obscure and seemingly uncorrelated. This case is also unique for its large tumor size and mixed pathological pattern. Distal pancreatectomy was performed, and the patient has remained well since operation. As the syndromes of somatostatinoma may be obscure and atypical, clinicians should review all clinical findings to obtain an accurate diagnosis. Aggressive surgery is preferred to improve the survival.
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影响因子：
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作者：
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通讯作者：
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影响因子：
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