Very Unusual Sellar/Suprasellar Region Masses: A Review. Issue 8 (20th May 2019)

• Record Type: Journal Article
• Authors: Abushamat, Layla A; Kerr, Janice M; Lopes, M Beatriz S; Kleinschmidt-DeMasters, Bette K
• Is Part Of: Journal of neuropathology and experimental neurology. Volume 78:Issue 8(2019)
• Page Start: 673
• Page End: 684
• Publication Date: 2019-05-20
• Subjects: Chronic lymphocytic leukemia -- Diffuse large cell B cell lymphoma -- Granulomatosis with polyangiitis -- Malignant peripheral nerve sheath tumor -- Neurosarcoidosis; Neurology -- Diseases -- Periodicals; Neurology -- Diseases -- Physiopathology -- Periodicals; 616.8047
• DOI: 10.1093/jnen/nlz044
• Languages: English
• ISSNs: 0022-3069

Abstract

Abstract: The cause of sellar region masses in large retrospective series is overwhelmingly pituitary adenomas (84.6%), followed by craniopharyngiomas (3.2%), cystic nonneoplastic lesions (2.8%), inflammatory lesions (1.1%), meningiomas (0.94%), metastases (0.6%), and chordomas (0.5%) (1 ). While other rare lesions were also identified (collectively 6.0%), single unusual entities in the above-cited series numbered <1–2 examples each out of the 4122 cases, underscoring their rarity. We searched our joint files for rare, often singular, sellar/suprasellar masses that we had encountered over the past several decades in our own specialty, tertiary care specialty pituitary center practices. Cases for this review were subjectively selected for their challenging clinical and/or histological features as well as teaching value based on the senior authors' (MBSL, BKD) collective experience with over 7000 examples. We excluded entities deemed to be already well-appreciated by neuropathologists such as mixed adenoma-gangliocytoma, posterior pituitary tumors, metastases, and hypophysitis. We identified examples that, in our judgment, were sufficiently unusual enough to warrant further reporting. Herein, we present 3 diffuse large cell B cell pituitary lymphomas confined to the sellar region with first presentation at that site, 2 sarcomas primary to sella in nonirradiated patients, and 1 case each of granulomatosis with polyangiitis and neurosarcoidosis with first presentations as a sellar/suprasellar mass. Other cases included 1 of chronic lymphocytic leukemia within a gonadotroph adenoma and 1 of ectopic nerve fascicles embedded within a somatotroph adenoma, neither of which impacted patient care. Our objective was to share these examples and review the relevant literature.