Jaiswal Sushila, Vij Mukul, Jaiswal Awadhesh Kumar, Chand Gyan, Behari Sanjay, Kumarjain Vijendra
Sanjay Gandhi Postgraduate Institute of Medical Sciences, Department of Pathology, Lucknow, India.
Turk Neurosurg. 2012;22(1):127-33. doi: 10.5137/1019-5149.JTN.3398-10.0.
Bone formation in pituitary adenoma is an extremely rare finding. Only five previous cases have been published. This is the sixth case report of an ossifying pituitary adenoma and the first case report of a pituitary adenoma with bone formation coexisting with WHO grade II astrocytoma. MRI imaging revealed an unusual eggshell cap-like calcified structure surrounding the tumor. Histologically, the adenoma contained irregularly anastomosing trabeculae with well-formed lacunae and osteoblasts along the margins. Our second case concerns a 25-year-old male patient who presented with complains of off and on headache for 12 months. MRI (head) revealed a 4x3cm well defined rounded lesion in the sella and suprasellar extension that was isointense in T1, hyperintense on T2 with cystic areas and homogenous contrast enhancement. On morphological examination, a cellular tumor admixed with foci of large ganglion cells embedded in a neuropil stroma was noted. On immunohistochemistry, tumor cells were focally positive for pancytokeratin, growth hormone and synaptophysin; and ganglion cells were positive for neurofilament and synaptophysin. No GFAP positive cells were seen. The Ki67 index was < 1%. Based on these findings, a diagnosis of gangliocytoma associated with pituitary adenoma was considered.
垂体腺瘤中的骨形成是一种极其罕见的现象。此前仅发表过5例相关病例。本文是骨化性垂体腺瘤的第6例病例报告,也是垂体腺瘤骨形成与世界卫生组织II级星形细胞瘤并存的首例病例报告。磁共振成像(MRI)显示肿瘤周围有异常的蛋壳样钙化结构。组织学上,腺瘤包含不规则吻合的小梁,边缘有形成良好的陷窝和成骨细胞。我们的第二例病例是一名25岁男性患者,主诉间断性头痛12个月。头颅MRI显示蝶鞍区有一个4×3cm边界清晰的圆形病变,向鞍上延伸,T1加权像呈等信号,T2加权像呈高信号,有囊性区域,增强扫描呈均匀强化。形态学检查发现一个细胞性肿瘤,混有散在的大神经节细胞,包埋于神经毡基质中。免疫组化显示,肿瘤细胞局灶性表达全细胞角蛋白、生长激素和突触素;神经节细胞表达神经丝和突触素。未见胶质纤维酸性蛋白(GFAP)阳性细胞。Ki67指数<1%。基于这些发现,考虑诊断为与垂体腺瘤相关的神经节细胞瘤。