From the Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California
From the Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California.
AJNR Am J Neuroradiol. 2022 Sep;43(9):1341-1345. doi: 10.3174/ajnr.A7618. Epub 2022 Aug 25.
Granulomatous hypophysitis is a rare inflammatory condition of the pituitary gland with an imaging appearance that can overlap with that of pituitary adenoma. Differentiating the two before surgical resection can have important treatment implications. The purpose of our study was to determine whether it was possible to differentiate between granulomatous hypophysitis and pituitary adenoma on the basis of diffuse enhancing infrasellar basisphenoid bone marrow.
We present 3 cases, initially thought to be pituitary adenomas, that were pathology-proved granulomatous hypophysitis. The preoperative MR images were reviewed for diffuse, enhancing infrasellar basisphenoid bone marrow. For comparison, we reviewed 100 cases of pathology-proved pituitary adenoma for the same finding. Additionally, imaging findings including the sphenoid sinus pneumatization pattern, clinical history, laboratory values, and pathology results were reviewed.
All 3 cases of granulomatous hypophysitis had diffuse enhancing infrasellar basisphenoid bone marrow. Conversely, this was not seen in any of the 100 pituitary adenomas. The patients with granulomatous hypophysitis were all women. Two patients had idiopathic granulomatous hypophysitis, and 1 had secondary granulomatous hypophysitis with sarcoidosis. Of the 100 patients with pituitary adenomas, 67 were women. The basisphenoid pneumatization patterns was as follows: 15 (type 2), 40 (type 3), and 45 (type 4).
We present 3 cases of granulomatous hypophysitis with diffuse enhancement of the infrasellar basisphenoid bone marrow that was not seen in our 100 cases of pituitary adenomas. This imaging feature may be valuable for suggesting a diagnosis of granulomatous hypophysitis and avoiding surgical resection of what might otherwise be misdiagnosed as a pituitary adenoma.
垂体炎是一种罕见的垂体炎症性疾病,其影像学表现可与垂体腺瘤重叠。在手术切除前区分这两种疾病具有重要的治疗意义。本研究旨在确定基于弥漫性强化鞍底下骨骨髓是否有可能区分垂体炎和垂体腺瘤。
我们报告了 3 例最初被认为是垂体腺瘤的病例,这些病例经病理证实为垂体炎。回顾了术前磁共振成像(MRI)的弥散性、增强的鞍底下骨骨髓。为了进行比较,我们回顾了 100 例经病理证实的垂体腺瘤的相同发现。此外,还回顾了影像学表现,包括蝶窦气化模式、临床病史、实验室值和病理学结果。
所有 3 例垂体炎均有弥漫性强化的鞍底下骨骨髓。相反,在 100 例垂体腺瘤中均未见这种情况。患有垂体炎的患者均为女性。2 例为特发性垂体炎,1 例为伴有结节病的继发性垂体炎。在 100 例垂体腺瘤患者中,67 例为女性。蝶骨底气化模式如下:15 例(2 型),40 例(3 型)和 45 例(4 型)。
我们报告了 3 例垂体炎患者,其鞍底下骨骨髓弥漫性强化,而在我们的 100 例垂体腺瘤中未见这种情况。这种影像学特征可能有助于提示垂体炎的诊断,并避免对可能误诊为垂体腺瘤的患者进行手术切除。