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首页> 外文期刊>Brain tumor pathology >Diencephalic pediatric low-grade glioma harboring the BRAF V600E mutation presenting with various morphologies in sequential biopsy specimens
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Diencephalic pediatric low-grade glioma harboring the BRAF V600E mutation presenting with various morphologies in sequential biopsy specimens

机译:Diencephalic儿科低级胶质瘤患BRAF V600E突变,呈现序贯活检标本中的各种形态

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摘要

A 5-year-old boy underwent biopsy of an intra-axial calcified tumor in the hypothalamus, which was incidentally found. Based on the presence of ganglion-like cells combined with glial cell element, the pathological diagnosis was ganglioglioma. Because the tumor grew gradually in size over the next 2 years, he underwent chemotherapy with temozolomide. However, at 8 years of age, the boy developed hydrocephalus and the cystic lesion had re-grown. Endoscopic cyst fenestration and tumor biopsy was performed, and pathological diagnosis was tentatively oligodendroglioma based on the presence of tumor cells with a perinuclear halo. At 10 years of age, hydrocephalus recurred and the cystic lesion had re-grown. A second round of endoscopic cyst fenestration and tumor biopsy led to a pathological diagnosis of pilocytic astrocytoma due to a biphasic appearance with areas of dense tumor cells and microcystic areas, tumor cells with eosinophilic processes, and the presence of an eosinophilic granular body. Genetic analysis of the first biopsy successfully identified the BRAF V600E mutation. Because pathological diagnosis of diencephalic low-grade glioma harboring BRAF V600E would be sometimes difficult due to pathological variations, pathological diagnosis should be performed under the consideration of molecular diagnosis of BRAF V600E for optimal diagnosis and treatment.
机译:一个5岁的男孩在下丘脑中接受了轴上慢性钙化肿瘤的活检,偶然发现。基于神经节细胞的存在与胶质细胞元素联合,病理诊断是神经糖瘤。由于肿瘤在未来2年内逐渐增长,因此他接受了用替替莫替莫啶疗法进行化疗。然而,在8岁时,该男孩开发了脑积水,囊性病变已经重新种植。进行内镜囊肿衰减和肿瘤活检,并且基于肿瘤细胞的存在,病理诊断是延长寡核瘤,其肿瘤细胞与PerinuclecloO晕。在10岁时,脑积水重复,囊性病变重新种植。第二轮内窥镜囊肿衰生和肿瘤活组织检查导致硫胺星形细胞瘤的病理诊断由于具有致密肿瘤细胞和微肾域区域的面积,具有嗜酸性粒细胞的肿瘤细胞和嗜酸性粒细胞的存在。第一活检的遗传分析成功鉴定了BRAF V600E突变。由于Diencephalic低级胶质瘤的病理诊断患BRAF v600E有时会因病理变异而困难,因此应在考虑BRAF V600E的分子诊断下进行病理诊断进行最佳诊断和治疗。

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