Xanthogranulomatous hypophysitis masquerading as pituitary macroadenoma

Debadutta Senapati, Sudhansu Mishra, Sanjib Mishra, Tapaprakash Behera
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Abstract

Xanthogranulomatous hypophysitis (XGH) is an inflammatory disease of the pituitary gland that has clinical presentation and radiologic features similar to a neoplastic lesion. We report a rare case of XGH in an elderly male of 61-year-old age presenting with features of a pituitary macroadenoma with apoplexy. Clinical features and radiologic findings can be confusing and misleading. Surgical resection is the preferred method for treatment and establishing the final diagnosis from biopsy. Attention should be paid to the management of hypopituitarism and diabetes insipidus. Preoperative diagnosis is difficult and a high level of clinical suspicion of inflammatory disorders is necessary for correct diagnosis and optimal management.
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伪装成垂体大腺瘤的黄色肉芽肿性垂体炎
黄色肉芽肿性垂体炎(XGH)是一种垂体炎性疾病,其临床表现和放射学特征与肿瘤病变相似。我们报告一个罕见的病例XGH在61岁的老年男性表现为垂体大腺瘤与中风的特征。临床特征和放射学表现可能令人困惑和误导。手术切除是首选的治疗方法,并从活检中确定最终诊断。垂体功能低下和尿崩症的处理应引起重视。术前诊断困难,临床高度怀疑炎症性疾病是正确诊断和最佳治疗的必要条件。
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