Rahimi Kurosh, Gologan Adrian, Haliotis Tina, Lamoureux Esther, Chetty Runjan
Departments of Pathology, The Jewish General Hospital, Montreal and University Health Network, University of Toronto Toronto, Canada.
Int J Clin Exp Pathol. 2008 May 20;2(6):608-13.
Gastrointestinal stromal tumor (GIST) and mantle cell lymphoma involving the appendix are rare as individual disease entities. Their coexistence has not been previously reported in the literature. We describe a 65-year old female who presented with extensive ileocecal mantle cell lymphoma, which extended to the appendix. The appendix was involved by mantle cell lymphoma and an incidental coexistent GIST was noted in the appendiceal wall. The GIST was CD117 positive but did not harbor mutations in the c-kit and PDGFR genes. In addition, it was unusual in showing S-100 immunoreactivity and ultrastructural evidence of autonomic nerve differentiation. This is the first description of the association of a GIST with autonomic nerve differentiation coexisting with mantle cell lymphoma in the appendix.
胃肠道间质瘤(GIST)和累及阑尾的套细胞淋巴瘤作为单独的疾病实体较为罕见。此前文献中尚未报道过它们的共存情况。我们描述了一名65岁女性,她患有广泛的回盲部套细胞淋巴瘤,该淋巴瘤已蔓延至阑尾。阑尾受累于套细胞淋巴瘤,并且在阑尾壁上发现了一个偶然并存的GIST。该GIST的CD117呈阳性,但c-kit和PDGFR基因未发生突变。此外,其表现出S-100免疫反应性以及自主神经分化的超微结构证据,这一点很不寻常。这是首次描述阑尾中存在自主神经分化的GIST与套细胞淋巴瘤共存的情况。