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模仿转移性黑色素瘤的伊匹单抗囊性垂体炎。

Ipilimumab cystic hypophysitis mimicking metastatic melanoma.

作者信息

Wallace John, Krupa Martin, Brennan James, Mihlon Frank

机构信息

Department of Radiology, Eastern Virginia Medical School, 600 Gresham Dr, Norfolk, VA 23507, USA.

出版信息

Radiol Case Rep. 2018 May 21;13(3):740-742. doi: 10.1016/j.radcr.2018.03.011. eCollection 2018 Jun.

Abstract

Ipilimumab is an immunotherapeutic agent used in the treatment of metastatic melanoma, and is known to cause hypophysitis in some patients. Magnetic resonance imaging of ipilimumab-induced hypophysitis typically shows diffuse enlargement of the pituitary gland with variable enhancement or enlargement of the infundibulum. This often produces a diagnostic dilemma as melanoma not uncommonly metastasizes to the pituitary gland due to the rich vascular plexus of the hypophyseal portal system, and has a similar imaging appearance to autoimmune hypophysitis. We present a case of a 49-year-old man with a Clark level 4 melanoma of the left calf with inguinal nodal metastases that was treated with resection and 2 cycles of ipilimumab, and subsequently developed a "cystic" pituitary mass. To our knowledge, all of the described cases of ipilimumab-induced hypophysitis to date have shown solid enhancement on imaging. Because metastatic melanoma to the pituitary gland often has internal hemorrhage that produces a "cystic" appearance, and ipilimumab-induced hypophysitis is typically a solidly enhancing abnormality, this presented a significant diagnostic and therapeutic dilemma. Our patient's symptoms, although significant, did not necessitate immediate surgical intervention, and a conservative approach of withholding the ipilimumab and administering therapeutic corticosteroids was pursued. The patient's symptoms abated and follow-up magnetic resonance imaging 1 month later showed near complete resolution of the pituitary abnormalities. As such, this is a unique case of ipilimumab-induced hypophysitis presenting as a "cystic" pituitary mass.

摘要

伊匹木单抗是一种用于治疗转移性黑色素瘤的免疫治疗药物,已知在一些患者中会引起垂体炎。伊匹木单抗诱导的垂体炎的磁共振成像通常显示垂体弥漫性增大,伴有不同程度的强化或漏斗部增粗。这常常造成诊断上的两难局面,因为黑色素瘤由于垂体门脉系统丰富的血管丛而常转移至垂体,其影像学表现与自身免疫性垂体炎相似。我们报告一例49岁男性患者,左小腿Clark 4级黑色素瘤伴腹股沟淋巴结转移,接受了手术切除及2个周期的伊匹木单抗治疗,随后出现“囊性”垂体肿块。据我们所知,迄今为止所有描述过的伊匹木单抗诱导的垂体炎病例在影像学上均表现为实性强化。由于垂体转移瘤常伴有内部出血而呈现“囊性”表现,而伊匹木单抗诱导的垂体炎通常是实性强化的异常,这就带来了重大的诊断和治疗难题。我们患者的症状虽然严重,但并不需要立即进行手术干预,因此采取了停用伊匹木单抗并给予治疗性皮质类固醇的保守方法。患者症状减轻,1个月后的随访磁共振成像显示垂体异常几乎完全消退。因此,这是一例独特的伊匹木单抗诱导的垂体炎表现为“囊性”垂体肿块的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/505e/6026098/e66fa5b28da7/radcr494-fig-0001.jpg

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