Liang Peter S, Shaffer Kitt
Radiol Case Rep. 2015 Dec 7;2(3):90. doi: 10.2484/rcr.v2i3.90. eCollection 2007.
Carcinoid tumors are rare and slow growing malignancies derived from enterochromaffin cells. Two-thirds of carcinoid tumors arise in the gastrointestinal tract, and in 3% of these cases the primary site cannot be determined. Presenting symptoms depend on the location of the primary tumor but may be nonspecific, and in 13% of patients distant metastases are discovered on diagnosis. The classic carcinoid syndrome occurs in less than 10% of cases and only after metastasis to the liver. We present a case of a young woman with a gastrointestinal carcinoid tumor of unknown site that had metastasized to the liver. We also provide a review of the current diagnostic modalities. Familiarity with the signs and symptoms of carcinoid tumors and the diagnostic techniques thereof may facilitate early detection and improved outcome.
类癌肿瘤是起源于肠嗜铬细胞的罕见且生长缓慢的恶性肿瘤。三分之二的类癌肿瘤发生于胃肠道,其中3%的病例无法确定原发部位。出现的症状取决于原发肿瘤的位置,但可能不具有特异性,13%的患者在诊断时发现有远处转移。典型的类癌综合征不到10%的病例会出现,且仅在转移至肝脏后出现。我们报告一例年轻女性患者,患有部位不明的胃肠道类癌肿瘤并已转移至肝脏。我们还对当前的诊断方法进行了综述。熟悉类癌肿瘤的体征和症状及其诊断技术可能有助于早期发现并改善预后。