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急性淋巴细胞白血病治疗后的脑钙化性坏死

Calcified cerebral necrosis following ALL therapy.

作者信息

Müller K M, Menne R, Bachmann K D, Gröbe H

出版信息

J Cancer Res Clin Oncol. 1981;102(1):81-91. doi: 10.1007/BF00410537.

DOI:10.1007/BF00410537
PMID:6949906
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12252912/
Abstract

Calcified cerebral necrosis was an unusual finding at the autopsy of a 13-year-old girl who died after prolonged therapy for ALL. The patient had shown symptoms of progressive cerebral damage subsequent to a second cycle of prophylactic high-dose cytostatic therapy combined with cranial irradiation. Pathoanatomic examination revealed extensive florid recurrency of meningosis and leukemic encephalosis with scalloped calcified necroses measuring up to 5 cm, in the medullar layer of brain and cerebellum. Located predominantly near the ventricular area, encapsulated necroses showed many fibrous vessels with thickened walls and stenosed or obstructed lumina. The cerebral cortex remained largely unaffected by tissue destruction. Besides methotrexate toxicity and the enhancing effect of irradiation the vascular involvement was interpreted as a particularly important factor. Formal pathogenesis is attributed to combined chemo- and radiotherapy in parallel to leukemic infiltration of vascular walls and partial obstruction of lumina by tumor emboli. Wall damage, severe fibrosis, and consecutive nutritional defects result in the destruction of cerebral tissue. The preferential occurrence of necroses in cortex-adjacent medullar layers is explained by the relatively poor blood supply of this border zone between meningeal and intracerebral tissue, no safe conclusion can be drawn pathoanatomically with regard to the actually fatal factor, whether it is the leukemic infiltration of vascular walls, the effect of cytostatic agents, or that of irradiation. The proposed multifactorial pathogenesis of cerebral calcification may be supported by computed tomography (CT) intra vitam.

摘要

在一名13岁死于急性淋巴细胞白血病(ALL)长期治疗后的女孩尸检中,钙化性脑坏死是一项不寻常的发现。该患者在预防性高剂量细胞抑制疗法联合颅脑照射的第二个周期后,出现了进行性脑损伤症状。病理解剖检查显示,在脑和小脑的髓质层中,广泛存在明显的脑膜白血病复发和白血病性脑病,伴有长达5厘米的扇形钙化坏死灶。包囊状坏死灶主要位于脑室区域附近,可见许多纤维血管,其壁增厚,管腔狭窄或阻塞。大脑皮层在很大程度上未受组织破坏的影响。除了甲氨蝶呤毒性和照射的增强作用外,血管受累被认为是一个特别重要的因素。正式的发病机制归因于化疗和放疗联合作用,同时白血病浸润血管壁以及肿瘤栓子部分阻塞管腔。血管壁损伤、严重纤维化和连续的营养缺陷导致脑组织破坏。坏死灶优先出现在靠近皮层的髓质层,这是由于脑膜和脑内组织之间的这个边界区域血液供应相对较差所致,就实际的致命因素而言,无论是血管壁的白血病浸润、细胞抑制剂的作用还是照射的作用,从病理解剖学上都无法得出确切结论。所提出的脑钙化多因素发病机制可能在生前通过计算机断层扫描(CT)得到支持。

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引用本文的文献

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Asymptomatic cerebral calcification--a previously unrecognized feature.无症状性脑钙化——一个先前未被认识的特征。
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