Collision tumor of the sellar region

J. Gong, Yan-yan Su, S. Lei, Xiao-Yu Liu, Shang-fu Zhang
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引用次数: 1

Abstract

Objective To summarize clinical and pathological features, diagnosis and differential diagnosis, as well as treatment and prognosis through analyzing one case of collision tumor in the sellar region (pituitary adenoma combined with malignant triton tumor).  Methods and Results A 59-year-old male was admitted to hospital with decreased vision, vision field defect and dizziness. Head MRI demonstrated space-occupying lesion in the sellar region. Therefore, the patient underwent a transsphenoidal surgery with subtotal tumor resection. Three months later, the patient was admitted to hospital again with vision loss and headache. Head CT demonstrated space-occupying lesions in sellar/suprasellar region, therefore, the patient underwent saddle tumor resection. Histological findings revealed that the tumor was composed of two different types of tumors, one was pituitary adenoma with epithelial cells arranged in nest-like and trabecular pattern, and the other was diffused spindle cell tumor. The two tumors were distributed separately or mixed togenther. The morphology of spindle cell tumor was bland with scarce mitosis in the first surgery, whereas additional features including increased cell density, dark nuclei, frequent mitosis and scattering distributed rhabdomyoblasts were found in the second surgery. Immunohistochemically, the pituitary adenoma (epithelial cell region) cells were positive for cytokeratin 8 (CK8), chromogranin A (CgA), synaptophysin (Syn) and thyroid stimulating hormone (TSH), while the malignant triton tumor cells (spindle cell region) were positive for CD56, CD57, calretinin (CR) and focally positive for S-100 protein (S-100), desmin (Des) and myogenin. Ultrastructural findings revealed abundant rough endoplasmic reticules and secretary granules in the cytoplasm of pituitary adenoma cells, and discontinuous basal lamina located outside the spindle cell membrane. The final pathological diagnosis was sellar collision tumor (non-functional TSH adenoma combined with malignant triton tumor). The patient died 6 months after the second surgery.  Conclusions Collision tumor of the sellar region with pituitary adenoma and malignant triton tumor is a rare tumor which can hardly be diagnosed by clinical and neuroimaging examination. The diagnosis relies on morphological characteristics, immunophenotype and ultrastructural features. The prognosis of collision tumor with malignant triton tumor component is poor. DOI: 10.3969/j.issn.1672-6731.2017.11.009
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鞍区碰撞瘤
目的通过分析1例鞍区碰撞瘤(垂体腺瘤合并恶性甲状腺瘤)的临床病理特点、诊断与鉴别诊断、治疗及预后。方法与结果男性1例,59岁,因视力下降、视野缺损、头晕入院。头部MRI显示鞍区占位性病变。因此,患者接受了经蝶窦手术和肿瘤次全切除。3个月后,患者因视力下降和头痛再次入院。头部CT显示鞍区/鞍上区占位性病变,因此患者行鞍区肿瘤切除术。组织学结果显示,肿瘤由两种不同类型的肿瘤组成,一种是垂体腺瘤,上皮细胞呈巢状和小梁状排列,另一种是弥漫性梭形细胞瘤。两个肿瘤分别分布或混在一起。梭形细胞肿瘤在第一次手术中形态平淡,很少有丝分裂,而在第二次手术中发现细胞密度增加,细胞核暗,有丝分裂频繁,横纹肌母细胞分散分布。免疫组化结果显示,垂体腺瘤(上皮细胞区)细胞角蛋白8 (CK8)、嗜铬粒蛋白A (CgA)、突触素(Syn)、促甲状腺激素(TSH)阳性,而恶性triton肿瘤(梭形细胞区)细胞CD56、CD57、calretinin (CR)阳性,S-100蛋白(S-100)、desmin (Des)、肌原素(myogenin)局部阳性。超微结构显示垂体腺瘤细胞胞质内有丰富的粗面内质网和秘书颗粒,纺锤体细胞膜外有不连续的基底膜。最终病理诊断为鞍部碰撞瘤(无功能TSH腺瘤合并恶性triton瘤)。患者在第二次手术后6个月死亡。结论鞍区碰撞瘤合并垂体腺瘤及恶性三角瘤是一种罕见的肿瘤,临床及神经影像学检查难以诊断。诊断依赖于形态学特征、免疫表型和超微结构特征。碰撞瘤合并恶性triton肿瘤成分预后较差。DOI: 10.3969 / j.issn.1672-6731.2017.11.009
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中国现代神经疾病杂志
中国现代神经疾病杂志 Medicine-Neurology (clinical)
CiteScore
0.40
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0.00%
发文量
4914
审稿时长
10 weeks
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