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间变性少突胶质细胞瘤骨髓转移潜伏17年后出现类白血病发作:一例尸检病例报告

Leukemia-like onset of bone marrow metastasis from anaplastic oligodendroglioma after 17 years of dormancy: an autopsy case report.

作者信息

Tanaka Yuko, Nobusawa Sumihito, Ikota Hayato, Yokoo Hideaki, Hirato Junko, Ito Hideaki, Saito Tatsuhiro, Ogura Hidemi, Nakazato Yoichi

机构信息

Department of Human Pathology, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma, 371-8511, Japan,

出版信息

Brain Tumor Pathol. 2014 Apr;31(2):131-6. doi: 10.1007/s10014-013-0156-y. Epub 2013 Jul 31.

Abstract

Extraneural metastases from primary brain tumors are extremely rare. We present an autopsy case that displayed a very late and unique pattern of metastasis from an anaplastic oligodendroglioma. The patient was a 74-year-old woman who was disease free for 17 years after resection of the primary oligodendroglioma. She was subsequently admitted to a hospital for heart failure where her bone marrow was found to be completely infiltrated with tumor cells, eventually resulting in disseminated intravascular coagulation. The onset was like leukemia, but the "blast-like" cells were different from leukemic cells, and the diagnosis was difficult until autopsy. After her death, a review of her past medical history and comprehensive analysis of her primary brain tumor and aspiration biopsy/autopsy bone marrow samples with glial immunohistochemical markers, fluorescence in situ hybridization examination, and immunohistochemical/sequencing analyses of mutant IDH1 revealed the accurate diagnosis. The metastatic tumor in her bone marrow was finally diagnosed as bone metastasis from the primary anaplastic oligodendroglioma. Although metastatic oligodendroglioma is very rare, it should be noted that this condition displays a propensity for bone and bone marrow and can present with features similar to those of leukemia after a long latency period.

摘要

原发性脑肿瘤的神经外转移极为罕见。我们报告一例尸检病例,该病例显示了间变性少突胶质细胞瘤极晚期且独特的转移模式。患者为一名74岁女性,在原发性少突胶质细胞瘤切除术后17年无疾病复发。随后她因心力衰竭入院,在那里发现其骨髓被肿瘤细胞完全浸润,最终导致弥散性血管内凝血。发病情况类似白血病,但“原始细胞样”细胞与白血病细胞不同,直至尸检时诊断仍很困难。她死后,回顾其既往病史,并对其原发性脑肿瘤以及骨髓穿刺活检/尸检样本进行综合分析,采用胶质细胞免疫组化标记、荧光原位杂交检查以及对突变型异柠檬酸脱氢酶1进行免疫组化/测序分析后,得出了准确诊断。她骨髓中的转移性肿瘤最终被诊断为原发性间变性少突胶质细胞瘤的骨转移。尽管转移性少突胶质细胞瘤非常罕见,但应注意这种情况易发生于骨骼和骨髓,并且在长时间潜伏期后可能表现出与白血病相似的特征。

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