Alexandre Jourdan , Syeda Maria Ahmad Zaidi , Haissan Iftikhar , Shahzada Ahmed
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Abstract
Background
Pituitary metastasis is a rare entity, with majority of the primary tumors reported from breast or lung origins. We present a case with pituitary metastasis as the first clinical presentation of underlying ovarian carcinoma.
Case
A 48-year-old female presented with visual disturbances and hyponatremic episodes. After management of her hyponatremia and resulting diabetes insipidus, detailed imaging was carried out which revealed a 35 mm x 35 mm x 20 mm (TS x CC x AP) pituitary mass, extending into the cavernous sinuses and suprasellar compartment, causing compression of the optic chiasma. Debulking was performed via the endoscopic trans-sphenoidal approach, and biopsy was consistent with metastatic high-grade ovarian serous carcinoma (WT1 + and estrogen receptor+). A CT chest-abdomen-pelvis revealed a 10 cm right ovarian mass with bilateral adrenal nodules. Postoperatively, patient developed CSF rhinorrhea and meningitis. Despite, reconstructive efforts, the patient continued to decline and was referred to palliation. She succumbed to her illness during her hospital admission.
Conclusion
Our case underscores the importance of considering pituitary metastasis when encountering DI or pituitary insufficiency in a middle-aged patient with a sellar mass.
背景垂体转移瘤是一种罕见肿瘤,原发肿瘤大多来自乳腺或肺部。我们报告了一例以垂体转移为首发临床表现的卵巢癌病例。病例一名 48 岁女性,因视力障碍和低钠血症发作而就诊。在对她的低钠血症和由此引起的糖尿病进行治疗后,进行了详细的影像学检查,发现了一个 35 毫米 x 35 毫米 x 20 毫米(TS x CC x AP)的垂体肿块,肿块延伸至海绵窦和黄上部,导致视神经椎体受压。通过内窥镜经蝶窦方法进行了切除,活检结果与转移性高级别卵巢浆液性癌(WT1 + 和雌激素受体 +)一致。胸部-腹部-盆腔 CT 显示右侧卵巢肿块 10 厘米,双侧肾上腺结节。术后,患者出现鼻出血和脑膜炎。尽管进行了重建工作,但患者病情仍在继续恶化,被转至姑息治疗。结论:我们的病例强调了当中年蝶窦肿块患者出现DI或垂体功能不全时考虑垂体转移的重要性。