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Autoimmune hypophysitis presenting with intracranial multi-organ involvement: three case reports and review of the literature

机译:表现为颅内多器官受累的自身免疫性垂体炎:三例病例报告并文献复习

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Background Autoimmune hypophysitis very rarely spreads to nearby organs outside the pituitary tissue, for unknown reasons, with only 5 reported cases of hypophysitis spreading over the cavernous sinus. Case presentation Three patients presented with cases of non-infectious hypophysitis spreading outside the pituitary tissue over the cavernous sinus. All three cases were diagnosed with histological confirmation by transsphenoidal surgery, and the patients showed remarkable improvement with postoperative pulse dose steroid therapy, including disappearance of abnormal signal intensities in the bilateral hypothalami on magnetic resonance imaging, resolution of severe stenosis of the internal carotid artery, and normalization of swollen pituitary tissues. Two of 3 cases fulfilled the histological criteria of immunoglobulin G4-related disease, although none of the patients had high serum immunoglobulin G4 level. Conclusion The true implications of such unusual spreading of hypophysitis to nearby organs are not fully understood, but the mechanism of occurrence might vary according to the timing of inflammation in this unusual mode of spreading. Pulse dose steroid therapy achieved remarkably good outcomes even in the patient with progressive severe stenosis of the internal carotid artery and rapid visual deterioration.
机译:背景自身免疫性垂体炎极少扩散至垂体组织外的附近器官,原因不明,仅5例报告的垂体炎病例遍布海绵窦。病例报告3例患者出现非传染性垂体瘤扩散到垂体组织,垂体组织超出海绵窦。这三例均经经蝶窦手术诊断为组织学证实,术后接受脉冲剂量类固醇治疗后患者表现出明显改善,包括磁共振成像中双侧下丘脑异常信号强度的消失,颈内动脉严重狭窄的缓解,和垂体肿大正常化。 3例中有2例符合免疫球蛋白G4相关疾病的组织学标准,尽管无一例患者的血清免疫球蛋白G4高。结论这种垂体异常扩散到附近器官的真正含义尚不完全清楚,但在这种异常扩散方式下,其发生机制可能会根据炎症的时机而有所不同。即使在颈内动脉进行性严重狭窄且视觉快速恶化的患者中,脉冲剂量类固醇疗法也取得了非常好的效果。

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