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非功能性垂体腺瘤伴慢性包裹性扩张性血肿。

Chronic encapsulated expanding hematoma in nonfunctioning pituitary adenoma.

机构信息

Department of Neurosurgery, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan.

出版信息

Neurosurg Rev. 2013 Jul;36(3):395-402. doi: 10.1007/s10143-013-0449-y. Epub 2013 Jan 24.

Abstract

The diagnosis and treatment of pituitary macroadenomas with entire hematoma fluid accumulation are problematic. Such lesions are often difficult to completely resect, and recurrence is not uncommon. We present five cases of pituitary macroadenomas entirely composed of hematoma fluid and investigated their histopathology to clarify the mechanism of the hematoma fluid accumulation. Five patients with pituitary adenoma and significant intra-tumor hematoma underwent transsphenoidal resection and were retrospectively reviewed for their clinical status, findings on magnetic resonance imaging (MRI), intraoperative findings, and histopathology. The specific surgical techniques used to address these cases were also reviewed. All patients were diagnosed with nonfunctioning pituitary adenomas by histopathological examination. MRI showed all tumors extended to the cavernous sinus. Histopathology showed tumor tissues were located between the thick granulation tissue and the pseudocapsule of the tumor. The thick granulation tissues were composed of collagenous layers, neovascular vessels, and necrotic red blood cells, indicating repeat hemorrhage from the granulation tissues. The boundary between adenoma and normal pituitary gland was identified during surgical removal in four patients and was not identified in the other patient who showed a recurrence 2 years later. Clinical and histopathological findings indicate hematoma fluid accumulation in the present cases is caused by repeat hemorrhage from the reactive granulation tissues and can be regarded as a chronic encapsulated expanding hematoma. In these cases, the boundary between adenoma and normal pituitary gland should be identified before puncturing the hematoma fluid to minimize the risk of tumor recurrence.

摘要

垂体大腺瘤伴全部积血的诊断和治疗存在问题。此类病变往往难以完全切除,且复发并不少见。我们报告了 5 例完全由积血组成的垂体大腺瘤,并对其组织病理学进行了研究,以阐明积血形成的机制。5 例垂体腺瘤伴明显瘤内血肿的患者接受了经蝶窦切除术,对其临床状况、磁共振成像(MRI)检查结果、术中所见和组织病理学进行了回顾性研究。还回顾了用于解决这些病例的具体手术技术。所有患者均通过组织病理学检查诊断为无功能垂体腺瘤。MRI 显示所有肿瘤均延伸至海绵窦。组织病理学显示肿瘤组织位于厚肉芽组织和肿瘤假包膜之间。厚的肉芽组织由胶原层、新生血管和坏死的红细胞组成,表明肉芽组织反复出血。4 例患者在手术切除过程中确定了腺瘤与正常垂体之间的边界,而另 1 例在 2 年后复发的患者未确定。临床和组织病理学发现表明,目前病例中的积血是由反应性肉芽组织反复出血引起的,可以视为慢性包裹性扩张性血肿。在这些情况下,在穿刺积血之前应确定腺瘤与正常垂体之间的边界,以最大程度降低肿瘤复发的风险。

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