Rode J, Dhillon A P, Cotton P B, Woolf A, O'Riordan J L
J Clin Pathol. 1987 May;40(5):546-51. doi: 10.1136/jcp.40.5.546.
Three cases of carcinoid tumour of the stomach associated with primary hyperparathyroidism had the clinical and pathological features of a pluriglandular syndrome. Two of the patients showed multiple small polypoid carcinoids in the non-antral stomach, in conjunction with a parathyroid adenoma in one and parathyroid hyperplasia in the other case. One of these patients was also suffering from pernicious anaemia. A third patient had a large metastasising carcinoid arising in the gastric body and a parathyroid adenoma. Immunohistochemical stains for PGP 9.5 were positive in the carcinoids of all three cases. In all cases the carcinoids showed immunoreactivity for gastrin. A positive family history of endocrine hyperplasia and neoplasia was established in one case. It is suggested that patients with gastrointestinal carcinoids and their families should be evaluated for hyperparathyroidism, and patients with hyperparathyroidism presenting with upper gastrointestinal symptoms should undergo endoscopy to rule out gastric carcinoid tumours.
三例胃类癌瘤合并原发性甲状旁腺功能亢进症患者具有多腺体综合征的临床和病理特征。其中两名患者在非胃窦部胃内出现多个小息肉样类癌,一例伴有甲状旁腺腺瘤,另一例为甲状旁腺增生。这两名患者中的一名还患有恶性贫血。第三名患者在胃体部出现一个大的转移性类癌和一个甲状旁腺腺瘤。所有三例类癌的PGP 9.5免疫组化染色均为阳性。所有病例中的类癌均显示胃泌素免疫反应阳性。其中一例有内分泌增生和肿瘤的阳性家族史。建议对胃肠道类癌患者及其家族进行甲状旁腺功能亢进症评估,而出现上消化道症状的甲状旁腺功能亢进症患者应接受内镜检查以排除胃类癌瘤。