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Primary epithelioid angiosarcoma of right hip joint: A case report and literature review

机译:右髋关节原发性上皮样血管肉瘤1例并文献复习

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Rationale: Epithelioid angiosarcoma (EA) is a rare, highly invasive tumor. The histopathological features of EA are not distinct and less reported in the literature, and most of the medical records are incomplete. Patient concerns: A 61-year-old woman who came to the hospital because of pain in her right hip. This patient had had surgery for right hip tuberculosis 30 years ago. Diagnoses: The present study reports a case of primary EA of bone with aneurysmal bone cyst (ABC) that was diagnosed by 3 experienced pathologists. Interventions: The patients had undergone 2 surgeries; however, an early recurrence of the tumor was caused the death of the patient. Outcomes: Ten EA cases from other literature were reviewed in this article; all the symptoms were found in different parts of bone , and the case data were relatively complete. The primary clinical features and nonspecific histopathological morphology of the disease were summarized from the 11 cases mentioned in the literature, and the main immunohistochemistry characteristics and diagnostic traps of EA were reviewed. Lessons: Because the tumor has no characteristic diagnostic index in imaging and laboratory examination, the histopathologic features are not typical, especially in the case of obvious secondary lesions. It is easy to miss and misdiagnose. If possible, the diagnosis should be combined with immunohistochemical results.
机译:理由:上皮样血管肉瘤(EA)是一种罕见的高度浸润性肿瘤。 EA的组织病理学特征尚不明确,文献中报道较少,而且大多数病历不完整。患者担心:一名61岁的女士因右臀部疼痛而来医院。该患者30年前曾接受过右髋结核手术。诊断:本研究报告了由3名经验丰富的病理学家诊断出的伴有动脉瘤性骨囊肿(ABC)的原发性EA病例。干预措施:患者接受了两次手术;但是,肿瘤的早期复发导致患者死亡。结果:本文回顾了其他文献中的10例EA病例;所有症状均在骨骼的不同部位发现,病例资料比较完整。从文献中提到的11例病例中总结出该病的主要临床特征和非特异性组织病理学形态,并综述了EA的主要免疫组化特征和诊断陷阱。经验教训:由于肿瘤在影像学和实验室检查中没有特征性的诊断指标,因此组织病理学特征并不典型,特别是在明显的继发性病变的情况下。很容易错过和误诊。如果可能,诊断应与免疫组化结果相结合。

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