Bertulli Lorenzo, Bertani Giulio Andrea, Gianelli Umberto, Mantovani Giovanna, Rampini Paolo Maria, Locatelli Marco
Unit of Neurosurgery, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Unit of Neurosurgery, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
World Neurosurg. 2017 Sep;105:1036.e5-1036.e9. doi: 10.1016/j.wneu.2017.06.055. Epub 2017 Jun 16.
Autoimmune hypothalamitis, which is among the causes of acquired central diabetes insipidus, has seldom been described in the literature. This condition is probably provoked by the production of anti-vasopressin-secreting cell antibodies and antihypothalamus antibodies and is often associated with pituitary or polyendocrine autoimmunity. Correct diagnosis and immediate treatment are essential to avoid the progression of the pathologic process.
A woman diagnosed with central diabetes insipidus 12 years ago, who had panhypopituitarism and mild memory deficit, came to our attention. She refused radiologic studies. Magnetic resonance imaging performed in our unit showed a contrast-enhancing hypothalamic lesion. Lumbar puncture was negative for neoplastic markers. We decided to perform a biopsy of the lesion to obtain a histopathologic examination of the tissue and chose an endoscopic transventricular approach to reach the floor of the third ventricle. Autoimmune hypothalamitis was diagnosed and treatment with steroids and azathioprine was started. The lesion size decreased and was stable after 17 months of follow-up.
The endoscopic transventricular approach has proved to be an effective and safe way to obtain tissue samples for histopathologic examination from a region that is usually difficult to reach; it also gives direct visualization of the lesion, which makes sampling easier. The lesion size decreased after treatment but no clinical improvement was detected, either on the cognitive or on the endocrinologic side.
自身免疫性下丘脑炎是后天性中枢性尿崩症的病因之一,在文献中鲜有描述。这种情况可能是由抗血管加压素分泌细胞抗体和抗下丘脑抗体的产生所引发,且常与垂体或多内分泌自身免疫相关。正确诊断和及时治疗对于避免病理过程的进展至关重要。
一名12年前被诊断为中枢性尿崩症的女性引起了我们的注意,她患有全垂体功能减退和轻度记忆缺陷。她拒绝进行放射学检查。我们单位进行的磁共振成像显示下丘脑有一个强化病变。腰椎穿刺肿瘤标志物检查为阴性。我们决定对病变进行活检以获取组织的组织病理学检查,并选择经脑室内镜入路到达第三脑室底部。诊断为自身免疫性下丘脑炎,并开始使用类固醇和硫唑嘌呤治疗。随访17个月后,病变大小减小且稳定。
经脑室内镜入路已被证明是一种有效且安全的方法,可从通常难以到达的区域获取用于组织病理学检查的组织样本;它还能直接观察病变,使取样更容易。治疗后病变大小减小,但在认知或内分泌方面均未检测到临床改善。