Ohtsuki Y, Sonobe H, Mizobuchi T, Takahashi K, Hayashi K, Iwata J, Tahara E
Department of Pathology, Kochi Medical School, Japan.
Acta Pathol Jpn. 1989 Feb;39(2):141-6. doi: 10.1111/j.1440-1827.1989.tb01492.x.
We report the immunohistochemical and ultrastructural features of a case of duodenal carcinoid (somatostatinoma) combined with cutaneous-type von Recklinghausen's disease in a 65-year-old woman. The duodenal tumor located at the 2nd portion was composed of tumor cells arranged in a trabecular, glandular or nest-like pattern, occasionally associated with eosinophilic globules in the glandular structures. The tumor cells mostly showed strong immunoreactivity with anti-somatostatin antibody. Electron microscopy revealed that every tumor cell contained intracytoplasmic granules with electron-dense cores, 100-300 nm in size, in varying numbers, and intracytoplasmic lumina were rarely detected. The present case including identical cases reported so far suggest that the disease entity is likely to be a combination of duodenal somatostatinoma and von Recklinghausen's disease and/or phaeochromocytoma. This is the tenth case of duodenal carcinoid associated with von Recklinghausen's disease and/or phaeochromocytoma in the world literature and the third case reported as duodenal somatostatinoma.
我们报告了一例65岁女性十二指肠类癌(生长抑素瘤)合并皮肤型冯雷克林霍增氏病的免疫组化和超微结构特征。位于十二指肠第二部的肿瘤由呈小梁状、腺管状或巢状排列的肿瘤细胞组成,腺管结构中偶尔可见嗜酸性小球。肿瘤细胞大多对抗生长抑素抗体呈强免疫反应性。电子显微镜检查显示,每个肿瘤细胞都含有数量不等的、大小为100 - 300纳米、核心电子密度高的胞质颗粒,很少检测到胞质内管腔。本病例以及迄今为止报告的相同病例表明,该疾病实体可能是十二指肠生长抑素瘤与冯雷克林霍增氏病和/或嗜铬细胞瘤的组合。这是世界文献中第十例与冯雷克林霍增氏病和/或嗜铬细胞瘤相关的十二指肠类癌,也是第三例报告为十二指肠生长抑素瘤的病例。