Liang Jing, Liu Shangmei
Department of Pathology, Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100021, China.
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Zhonghua Zhong Liu Za Zhi. 2014 Jul;36(7):522-8.
The aim of this study was to investigate the clinicopathological features of different histological types of primary gastric neuroendocrine neoplasms (including the esophagogastric junction), and to analyze the characteristics and difficulties in diagnosis of all the subtypes of this disease.
75 cases of primary gastric neuroendocrine neoplasms (including the esophagogastric junction) were included in this study. The expressions of several markers including somatostatin, synaptophysin, chromogranin A, CD56, S-100, neuron-specific enolase and CD57 were assayed in all the specimens by immunohistochemical staining, and their significance in the diagnosis and prognosis of gastric neuroendocrine neoplasms were assessed. In addition, the relationship between various clinical parameters such as tumor location, histological types, depth of invasion and metastasis was also analyzed.
The incidence of gastric neuroendocrine neoplasms accounted for 1.5% of gastric cancer in the same period, and the proportion of each subtype was 53.3% (40/75) in G3, 29.3% (22/75) in MANEC, 16.0% in G1(12/75), and 1.3% (1/75) in G2, respectively. 41.7% (5/12) of the G1 showed multifocal lesions, accompanyied with neuroendocrine cell hyperplasia in the gastric mucosa. 54.67% (41/75) of the NEN located in the esophagogastric junction. The lymph node metastasis of MANEC is unique. The coincidence rate in diagnosis of preoperative biopsies and postoperative specimen was 75.0% (9/12) in G1, 72.7% (16/22) in MANEC, and 25.0% (10/40) in G3, respectively.
Gastric neuroendocrine neoplasms occur mainly in the esophagogastric junction, and most of them were highly malignant. The coincidence rate of preoperative and postoperative pathological diagnosis for primary gastric neuroendocrine neoplasms is low. Therefore, it should be very cautious when diagnosis of this disease is made in a preoperative biopsy.
本研究旨在探讨不同组织学类型的原发性胃神经内分泌肿瘤(包括食管胃交界部)的临床病理特征,并分析该疾病各亚型的诊断特点及难点。
本研究纳入75例原发性胃神经内分泌肿瘤(包括食管胃交界部)。通过免疫组织化学染色检测所有标本中生长抑素、突触素、嗜铬粒蛋白A、CD56、S-100、神经元特异性烯醇化酶和CD57等几种标志物的表达,并评估其在胃神经内分泌肿瘤诊断和预后中的意义。此外,还分析了肿瘤位置、组织学类型、浸润深度和转移等各种临床参数之间的关系。
胃神经内分泌肿瘤的发病率占同期胃癌的1.5%,各亚型比例分别为G3型53.3%(40/75)、混合性腺神经内分泌癌(MANEC)29.3%(22/75)、G1型16.0%(12/75)、G2型1.3%(1/75)。G1型中41.7%(5/12)表现为多灶性病变,伴有胃黏膜神经内分泌细胞增生。54.67%(41/75)的神经内分泌肿瘤位于食管胃交界部。MANEC的淋巴结转移具有独特性。G1型术前活检与术后标本诊断符合率分别为75.0%(9/12),MANEC为72.7%(16/22),G3型为25.0%(10/40)。
胃神经内分泌肿瘤主要发生于食管胃交界部,且大多恶性程度高。原发性胃神经内分泌肿瘤术前与术后病理诊断符合率低。因此,术前活检诊断该病时应非常谨慎。