Very Unusual Sellar/Suprasellar Region Masses: A Review

被引:17
|
作者
Abushamat, Layla A. [1 ]
Kerr, Janice M. [1 ]
Lopes, Beatriz S. [2 ]
Kleinschmidt-DeMasters, Bette K. [3 ,4 ,5 ]
机构
[1] Univ Colorado Denver, Univ Colorado, Hlth Sci Ctr, Dept Endocrinol, Anschutz Med Campus, Aurora, CO USA
[2] Univ Virginia, Dept Pathol Neuropathol & Neurol Surg, Charlottesville, VA USA
[3] Univ Colorado Denver, Dept Pathol, Anschutz Med Campus, Aurora, CO USA
[4] Univ Colorado Denver, Dept Neurol, Anschutz Med Campus, Aurora, CO USA
[5] Univ Colorado Denver, Dept Neurosurg, Anschutz Med Campus, Aurora, CO USA
关键词
Chronic lymphocytic leukemia; Diffuse large cell B cell lymphoma; Granulomatosis with polyangiitis; Malignant peripheral nerve sheath tumor; Neurosarcoidosis; NERVE SHEATH TUMOR; ATYPICAL TERATOID/RHABDOID TUMOR; CHRONIC LYMPHOCYTIC-LEUKEMIA; MIMICKING PITUITARY-ADENOMA; SOLITARY FIBROUS TUMOR; DIABETES-INSIPIDUS; SELLA TURCICA; WEGENERS-GRANULOMATOSIS; CAVERNOUS HEMANGIOMA; H3K27; TRIMETHYLATION;
D O I
10.1093/jnen/nlz044
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:673 / 684
页数:12
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