Jonnakuty Catherine G, Mezitis Spyros G E
Department of Medicine, Lenox Hill Hospital, New York, New York, USA.
Endocr Pract. 2007 May-Jun;13(3):291-5. doi: 10.4158/EP.13.3.291.
To report a unique case of a peripherally located pulmonary atypical carcinoid tumor with metastatic involvement of the pituitary, manifesting with evidence of functional hypopituitarism and compressive symptoms of dysarthria, bitemporal loss of vision, and ataxia.
We present a case report, including detailed laboratory, radiologic, and pathologic findings in a 50-year-old woman with a peripherally located pulmonary atypical carcinoid tumor and a lesion metastatic to the pituitary gland. The pertinent literature is also reviewed.
A 50-year-old woman with a medical history of metastatic pulmonary atypical carcinoid tumor presented with symptoms of bitemporal hemianopia, ataxia, and dysarthria. Laboratory evaluation revealed functional hypopituitarism, and magnetic resonance imaging of the brain with use of gadolinium contrast demonstrated a pituitary lesion measuring 3.5 by 2.5 by 2.5 cm. Visual field testing revealed bitemporal superior quadrantanopia, consistent with a pituitary lesion of the chiasm. Computed tomographic angiography excluded the presence of an aneurysm of the internal carotid artery. Subsequently, the patient underwent subtotal transsphenoidal hypophysectomy. Findings on pathology examination were consistent with a lesion metastatic from the primary pulmonary atypical carcinoid tumor. The patient subsequently received monthly octreotide injections as well as chemotherapeutic regimens of capecitobine and temozolomide. At 18-month follow-up, disease had not recurred.
This case of metastatic involvement of the pituitary gland from a peripherally located pulmonary atypical carcinoid tumor manifesting with evidence of functional hypopituitarism is highly uncommon. To our knowledge, such a case has not been previously reported. The presentation of an advanced pituitary metastatic lesion can be particularly dramatic, and the course can be potentially complicated. Therefore, heightened awareness of the possibility of a pituitary lesion metastatic from a pulmonary atypical carcinoid tumor is important.
报告一例罕见的周围型肺非典型类癌肿瘤伴垂体转移的病例,该病例表现为功能性垂体功能减退的证据以及构音障碍、双颞侧视野缺损和共济失调等压迫症状。
我们报告一例病例,包括一名50岁患有周围型肺非典型类癌肿瘤及垂体转移瘤的女性患者的详细实验室、影像学和病理学检查结果。同时对相关文献进行综述。
一名有转移性肺非典型类癌肿瘤病史的50岁女性出现双颞侧偏盲、共济失调和构音障碍症状。实验室检查显示功能性垂体功能减退,使用钆对比剂的脑部磁共振成像显示垂体有一个大小为3.5×2.5×2.5厘米的病变。视野测试显示双颞侧上象限偏盲,与视交叉处的垂体病变一致。计算机断层血管造影排除了颈内动脉动脉瘤的存在。随后,患者接受了经蝶窦垂体次全切除术。病理检查结果与原发性肺非典型类癌肿瘤转移的病变一致。患者随后每月接受奥曲肽注射以及卡培他滨和替莫唑胺的化疗方案。在18个月的随访中,疾病未复发。
这种周围型肺非典型类癌肿瘤转移至垂体并表现出功能性垂体功能减退证据的病例非常罕见。据我们所知,此前尚未有此类病例报道。晚期垂体转移瘤的表现可能特别显著,病程可能会很复杂。因此,提高对肺非典型类癌肿瘤转移至垂体可能性的认识很重要。