单个肌纤维肉瘤的磁共振成像、组织病理学和 Ki-67 标记指数结果比较:病例报告。

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Journal of Medical Case Reports Pub Date : 2024-08-16 DOI:10.1186/s13256-024-04693-y
Ryusuke Tsujimura, Kenta Uto, Noriyuki Nakano, Yusuke Sato, Yuko Kobashi, Toshio Kojima, Hiroyuki Hao
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引用次数: 0

摘要

背景:肌纤维肉瘤是一种肌样软组织肉瘤,在磁共振成像中显示为 T2 高强度。然而,肌纤维肉瘤是一种异质性肉瘤,既有肌样部分,也有细胞部分。在一个肌纤维肉瘤的不同部位获得了磁共振成像结果,并将磁共振成像结果与组织学和 Ki-67 免疫组化特征进行了比较:磁共振成像观察结果与一名 50 岁日本女性肌纤维肉瘤的大体病理和显微镜检查结果进行了比较。比较了肿瘤不同部分的 Ki-67 标记指数,即肌样、细胞和组织学证实的浸润边缘部分(病理尾征)。T2 低强度区域的细胞数量多于 T2 高强度区域,而细胞部分的 Ki-67 指数明显高于肌样部分(p = 0.0313)。有病理尾征的部分的Ki-67标记指数明显高于无病理尾征的部分(p = 0.0313):结论:肌纤维肉瘤中细胞较多的部分与肿瘤中表现出侵袭性特征的区域相对应。此外,我们的数据还支持了肌纤维肉瘤的高侵袭性与病理尾征相关的假设。据我们所知,这是第一例对一个肌纤维肉瘤不同部位的成像结果、组织学特征和Ki-67免疫组化结果进行比较的病例报告。
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Comparisons of magnetic resonance imaging, histopathological and Ki-67 labeling index findings in a single myxofibrosarcoma: a case report.

Background: Myxofibrosarcoma is a myxoid soft tissue sarcoma showing T2 high intensity on magnetic resonance imaging. However, myxofibrosarcoma is a heterogeneous sarcoma with both myxoid and cellular portions. Magnetic resonance imaging findings were obtained MRI findings for comparison with histological and Ki-67 immunohistochemical features, in different portions of one myxofibrosarcoma.

Case presentation: Magnetic resonance imaging observations were compared with gross pathological and microscopic findings of a myxofibrosarcoma from a 50-year-old Japanese female. The Ki-67 labeling indices of different portions of the tumor, that is, the myxoid, cellular, and histologically confirmed infiltrative margin portions (pathological tail sign), were compared. The T2 low intensity area was more cellular than the T2 high intensity area, while the cellular portion had a significantly higher Ki-67 index than the myxoid portion (p = 0.0313). The portions with the pathological tail sign had a significantly higher Ki-67 labeling index than those without this sign (p = 0.0313).

Conclusions: More cellular portions of a myxofibrosarcoma correspond to more areas of the tumor showing aggressive features. Furthermore, our data also support the hypothesis of high aggressiveness being associated with the pathological tail sign in myxofibrosarcoma. To our knowledge, this is the first case report to describe comparisons among the imaging findings, histological features, and Ki-67 immunohistochemistry results for different portions of one myxofibrosarcoma.

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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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