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Precocious puberty caused by hCG-producing germinoma involving the bilateral basal ganglia and cerebral white matter without 1ypical radiologic findings: case report

机译:由产生hCG的生殖细胞瘤引起的性早熟,涉及双侧基底神经节和脑白质,无1例典型影像学表现:病例报告

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摘要

An 8-year-old boy presented with a rare case of germinoma involving the bilateral basal ganglia and cerebral white matter manifesting as precocious puberty. Magnetic resonance (MR) imaging at the initial presentation demonstrated mild hyperintense areas in the bilateral basal ganglia and corpus callosum on T1-weighted images, and a small hyperintense spot in the right internal capsule on T2-weighted images. Human chorionic gonadotropin (hCG) level was elevated in the cerebrospinal fluid (CSF), so we strongly suspected that threre was a hCG-producing germinoma originating in the bilateral basal ganglia. Stereotactic biopsy was performed. Histological examination revealed two-cell pattern germinoma. After three cycles of combination chemotherapy consisting of ifosfamide, cisplatin, and etoposide, followed by whole brain irradiation with a total dose of 24 Gy, the CSF hCG level fell below the detection limit, but MR imaging demonstrated no significant change. Intracranial hCG-producing germinoma should besuspected in patients presenting with precocious puberty and elevated CSF hCG level. Moreover, slight intensity change on MR imaging is important to identify germinoma arising from the basal ganglia in the early stage.
机译:一个8岁男孩表现出罕见的生殖器瘤病例,涉及双侧基底神经节和表现为性早熟的脑白质。最初呈现的磁共振成像(MR)在T1加权图像上显示了双侧基底神经节和call体中的轻度高信号区,在T2加权图像上右内囊中有一个小的高信号点。人绒毛膜促性腺激素(hCG)的水平在脑脊髓液(CSF)中升高,因此我们强烈怀疑苏雷是源自双侧基底神经节的产生hCG的生殖细胞瘤。进行立体定向活检。组织学检查发现两细胞型生殖器瘤。在由异环磷酰胺,顺铂和依托泊苷组成的三个联合化疗周期之后,然后以总剂量24 Gy进行全脑照射,脑脊液hCG水平降至检测限以下,但MR影像显示无明显变化。表现为性早熟和脑脊液hCG水平升高的患者应怀疑颅内产生hCG的生殖细胞瘤。此外,MR成像上的轻微强度变化对于识别早期由基底节产生的生殖瘤很重要。

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