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乳头型颅咽管瘤:48例临床病理研究

Papillary craniopharyngioma: a clinicopathological study of 48 cases.

作者信息

Crotty T B, Scheithauer B W, Young W F, Davis D H, Shaw E G, Miller G M, Burger P C

机构信息

Division of Anatomic Pathology, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

J Neurosurg. 1995 Aug;83(2):206-14. doi: 10.3171/jns.1995.83.2.0206.

Abstract

Two distinct clinicopathological variants of craniopharyngioma exist: the classic adamantinomatous type and a recently described papillary form that predominates in adults and reportedly behaves in a less aggressive manner. The present study describes the clinicopathological features of 48 patients with papillary craniopharyngioma treated at the Mayo Clinic between 1910 and 1994. An additional four tumors were found to have histological features of both adamantinomatous and papillary craniopharyngioma. Whereas adamantinomatous tumors typically occur in adolescent patients, the mean age of the 48 patients (23 males and 25 females) with papillary craniopharyngioma was 44.7 years (range 10 to 74 years). Presenting clinical features included visual impairment (84%), headache (68%), and pituitary insufficiency (anterior 42%; posterior 27%). Preoperative computerized tomography (CT) and magnetic resonance (MR) imaging in 17 patients typically revealed a noncalcified, partially cystic mass that enhanced peripherally and contained mural nodules (67%). Many (41%) of the lesions involved or extended into the third ventricle on imaging. At first surgery, gross total tumor removal was achieved in 17 patients (36%) and subtotal resection in 30 patients (64%) in whom tumor resection was attempted. Tumor recurrence was noted in two patients who underwent gross total removal. Tumor-free survival rates of 100% and 78% were obtained in patients who underwent gross total and subtotal resection at initial surgery, respectively. Postoperative radiation therapy was beneficial to patients having undergone a subtotal resection, with an increase in tumor-free survival from 26% to 86%. Aside from well-documented morphological distinctions, papillary craniopharyngiomas differ from adamantinomatous tumors in several important respects. These include the almost exclusive occurrence of papillary tumors in adulthood and their more uniform appearance on both CT and MR imaging. However, a preliminary analysis of our data suggests there are no significant differences between the two lesions with respect to resectability, efficacy of radiation therapy, and overall survival.

摘要

颅咽管瘤存在两种不同的临床病理变体

经典的造釉细胞瘤型和最近描述的乳头状型,后者在成人中占主导,据报道侵袭性较小。本研究描述了1910年至1994年间在梅奥诊所接受治疗的48例乳头状颅咽管瘤患者的临床病理特征。另外发现4例肿瘤具有造釉细胞瘤和乳头状颅咽管瘤的组织学特征。造釉细胞瘤通常发生在青少年患者中,而48例乳头状颅咽管瘤患者(23例男性和25例女性)的平均年龄为44.7岁(范围10至74岁)。呈现的临床特征包括视力障碍(84%)、头痛(68%)和垂体功能不全(前部42%;后部27%)。17例患者术前计算机断层扫描(CT)和磁共振(MR)成像通常显示为非钙化、部分囊性肿块,周边强化并含有壁结节(67%)。许多(41%)病变在影像学上累及或延伸至第三脑室。在首次手术时,17例患者(36%)实现了肿瘤全切,30例尝试肿瘤切除的患者(64%)实现了次全切除。在接受全切的2例患者中发现肿瘤复发。首次手术时接受全切和次全切除的患者无瘤生存率分别为100%和78%。术后放疗对接受次全切除的患者有益,无瘤生存率从26%提高到86%。除了有充分记录的形态学差异外,乳头状颅咽管瘤在几个重要方面与造釉细胞瘤不同。这些包括乳头状肿瘤几乎仅发生在成年期以及它们在CT和MR成像上外观更均匀。然而,对我们数据的初步分析表明,在可切除性、放疗疗效和总生存率方面,这两种病变之间没有显著差异。

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