Valeros Katherine A, Khoo Eric
Division of Endocrinology, Department of Medicine, National University Hospital Singapore, 1E Kent Ridge Road, NUHS Tower Block Level 10, Singapore 119228, Singapore.
Division of Endocrinology, Department of Medicine, National University Hospital Singapore, 1E Kent Ridge Road, NUHS Tower Block Level 10, Singapore 119228, Singapore.
J Clin Neurosci. 2014 Aug;21(8):1464-6. doi: 10.1016/j.jocn.2013.10.042. Epub 2014 Apr 16.
The most common presentation of metastases to the pituitary gland in systemic lymphoma is diabetes insipidus resulting from infiltration of the infundibulum/posterior lobe. We describe a 69-year-old man with diffuse large B-cell stage IV lymphoma who presented with anterior pituitary hypofunction, without features of posterior pituitary involvement. He presented with a few months of postural dizziness and hypotension, weight loss, fever, strabismus of right eye and a superficial abdominal wall mass. At this time he had no history of malignancy. Biochemically he had hypovolemic hyponatremia, secondary hypothyroidism and adrenal insufficiency. Further hormonal work-up revealed panhypopituitarism but no diabetes insipidus. Imaging of the brain, thorax and abdomen demonstrated diffuse intracranial pachymeningeal thickening and enhancement, multiple lymphadenopathies, a bulky right adrenal gland and a large left suprarenal mass, which were indicative of an infiltrative disease. Imaging of the pituitary showed heterogeneous enhancement of the anterior lobe with an unremarkable pituitary stalk and posterior lobe. Biopsy of the superficial abdominal wall mass revealed diffuse large B-cell lymphoma confirmed by bone marrow aspiration biopsy. Positron emission tomography (PET) scan confirmed diffuse systemic disease involving the right orbital apex, bilateral adrenal glands, bone and bone marrow, retroperitoneum and subcutaneous tissues; however, the pituitary gland, infundibulum and hypothalamus did not show any lesions on the PET scan. The patient was commenced on two cycles of chemotherapy but unfortunately died, thus recovery of pituitary function was not tested. Pure anterior pituitary hypofunction can uncommonly present in individuals with metastases to the pituitary gland, in contrast to the more common posterior pituitary/infundibulum involvement.
系统性淋巴瘤转移至垂体时最常见的表现是由于漏斗部/后叶受浸润导致的尿崩症。我们描述了一名69岁的男性,患有弥漫性大B细胞IV期淋巴瘤,表现为垂体前叶功能减退,无垂体后叶受累的特征。他出现了几个月的体位性头晕和低血压、体重减轻、发热、右眼斜视以及腹壁浅表肿块。此时他没有恶性肿瘤病史。生化检查显示他有低血容量性低钠血症、继发性甲状腺功能减退和肾上腺功能不全。进一步的激素检查发现全垂体功能减退但无尿崩症。脑部、胸部和腹部的影像学检查显示弥漫性颅内硬脑膜增厚和强化、多处淋巴结肿大、右侧肾上腺肿大和左侧肾上腺巨大肿块,提示为浸润性疾病。垂体的影像学检查显示垂体前叶不均匀强化,垂体柄和后叶无异常。腹壁浅表肿块活检显示为弥漫性大B细胞淋巴瘤,骨髓穿刺活检证实。正电子发射断层扫描(PET)显示弥漫性全身病变累及右侧眶尖、双侧肾上腺、骨骼和骨髓、腹膜后和皮下组织;然而,垂体、漏斗部和下丘脑在PET扫描上未显示任何病变。该患者开始接受两个周期的化疗,但不幸去世,因此未检测垂体功能的恢复情况。与更常见的垂体后叶/漏斗部受累不同,单纯垂体前叶功能减退在垂体转移患者中较少见。