Sharma M C, Gaikwad S, Mahapatra A K, Menon P S, Sarkar C
Department of Pathology, All India Institute of Medical Sciences, New Delhi.
Am J Surg Pathol. 1998 Dec;22(12):1538-41. doi: 10.1097/00000478-199812000-00011.
A rare case of hypothalamic hamartoma with unusual radiologic and histopathological features is described, possibly the first of its type in English literature. A 1.5-year-old female child presented with precocious puberty. MR scan of the brain revealed a pedunculated hypothalamic mass, most of which was isointense with normal brain on T1- and T2-weighted images. However, a sizeable component of the lesion was hyperintense on T1-weighted images, suggestive of adipose tissue. Microscopically, the lesion was a hamartoma composed of an admixture of neuroectodermal elements, namely glial cells, neurons, and nerve bundles along with mesenchymal elements in the form of fibroadipose tissue.
本文描述了一例罕见的下丘脑错构瘤,具有不寻常的放射学和组织病理学特征,可能是英文文献中首例此类病例。一名1.5岁女童出现性早熟。脑部磁共振成像(MR)扫描显示一个带蒂的下丘脑肿块,其大部分在T1加权和T2加权图像上与正常脑组织等信号。然而,病变的相当一部分在T1加权图像上呈高信号,提示脂肪组织。显微镜下,病变为错构瘤,由神经外胚层成分(即胶质细胞、神经元和神经束)与纤维脂肪组织形式的间充质成分混合组成。