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Neurofibromatosis 1 Presenting with Multiple Duodenal Gists Associated with a Somatostatin-Producing D Cell Neoplasm

机译:神经纤维瘤病1呈现与生长抑素产生的D细胞肿瘤相关的多个十二指肠。

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摘要

The co-existence of a duodenal somatostatin-producing D cell neoplasm and multiple duodenal gastrointestinal stromal tumours (GISTs) in a 61-year-old woman with neurofibromatosis type 1 is reported. Histologically, the D cell neoplasm showed a glandular pattern with psammoma bodies and was metastatic to regional lymph nodes and liver at the time of surgery. Tumour cells were monomorph and showed intense and diffuse immunoreactivity for somatostatin, focal positivity for calcitonin, while were negative for other gastroenteropancreatic hormones including insulin, glucagon, pancreatic polypeptide, serotonin and gastrin. Four submucosal and subserosal GISTs, ranging from 5 to 15 mm in diameter, were composed of uniform spindle-shaped cells lacking mitoses and contained numerous skeinoid fibres. The tumours were positive for CD117, DOG1, vimentin and CD34 and did not have KIT or PDGFRA mutations. The clinical and pathological importance of this unusual association is discussed.
机译:据报道,一名61岁的患有1型神经纤维瘤病的妇女存在十二指肠生长抑素的D细胞肿瘤与多发十二指肠胃肠道间质瘤(GIST)并存。从组织学上讲,D细胞肿瘤显示为具有腺瘤体的腺样,并在手术时转移至局部淋巴结和肝脏。肿瘤细胞是单形的,对生长抑素表现出强烈而弥漫的免疫反应,对降钙素有局灶性阳性,而对其他胃肠道胰激素,包括胰岛素,胰高血糖素,胰多肽,血清素和胃泌素则呈阴性。四个粘膜下和浆膜下GIST的直径范围为5至15 mm,由缺乏有丝分裂的均匀纺锤状细胞组成,并包含许多类蛇形纤维。肿瘤的CD117,DOG1,波形蛋白和CD34呈阳性,没有KIT或PDGFRA突变。讨论了这种异常关联的临床和病理重要性。

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