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Symptomatic hypopituitarism revealing primary suprasellar lymphoma

机译:有症状的垂体功能低下提示原发性上鞍上淋巴瘤

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Background The most common cause of hypopituitarism is pituitary adenoma. However, in the case of suprasellar masses different etiologies are possible. We report an unusual case of primary suprasellar lymphoma presented with hypopituitarism. Case presentation A 26 year old woman presented with amenorrhea, galactorrhea and neurological disorders. Also, the laboratory work-up revealed partial hypopituitarism. The magnetic resonance imaging of the head showed a suprasellar mass. A presumptive diagnosis of granulomatous processes was made and the patient was given steroid therapy. Repeated brain MRI detected new lesions in the brain with regression of the suprasellar mass. Stereotactic biopsy of the paraventricular lesion revealed the diagnosis of B-cell lymphoma. Conclusion This case presentation reports a rare cause of hypopituitarism. Primary suprasellar lymphoma is extremely rare and represented a real diagnostic challenge. Besides, suprasellar masses are varied in aetiology and can present diagnostic problems for a radiologist. Also, because of the increased incidence of PCNSL, lymphoma must be kept in mind in the differential diagnosis of lesions in the suprasellar region.
机译:背景技术垂体功能低下的最常见原因是垂体腺瘤。但是,对于超肿块,可能有不同的病因。我们报告了少见的原发性上睑上皮淋巴瘤伴垂体机能减退。病例介绍一名26岁妇女出现闭经,溢乳和神经系统疾病。另外,实验室检查发现局部垂体功能低下。头部的磁共振成像显示超鞍肿块。作出肉芽肿过程的推定诊断,并对患者进行了类固醇治疗。反复进行脑部MRI检查发现大脑上新的病变,伴鞍上肿块消退。脑室旁病变的立体定向活检显示B细胞淋巴瘤的诊断。结论本病例报告报告了垂体功能低下的罕见原因。原发性鞍上淋巴瘤极为罕见,代表了真正的诊断挑战。此外,超囊肿的病因各不相同,可能给放射科医生带来诊断问题。另外,由于PCNSL的发生率增加,在鉴别上鞍区域病变时必须牢记淋巴瘤。

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