颅内多形性恶性纤维组织细胞瘤伴系统性红斑狼疮1例

M. Tena-Suck, C. Sánchez-Garibay, Citlaltepelt Salinas-Lara
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引用次数: 0

摘要

背景:多形性恶性纤维组织细胞瘤(MFH)是一种罕见的软组织和骨骼肿瘤,由成纤维细胞和组织细胞成分组成,具有有丝分裂特征,核多形性和间变性。病例介绍:我们提出一个罕见的病例MFH在44岁的妇女与历史的系统性红斑狼疮和癫痫发作。用强的松治疗。大脑TAC显示有颞部肿块。开颅检查,活检样本显示一个巨大的,多形性和非典型细胞。免疫组化分析显示vimentin、CD68、fastin、溶酶酶阳性,mb -1标记指数为20%。诊断为多形性恶性纤维组织细胞瘤,累及上覆颞叶。我们报告一例成人左颞部MFH。讨论:神经影像学及术中诊断为脑膜瘤。组织病理学,病例研究Tena-Suck等;地球物理学报,21(9):1-8,2017;文章no.BJMMR。32743 2结合免疫组织化学评价和增殖标志物,证实了诊断。这是第五个病例报道PMFH相关的系统性红斑狼疮和不同的组织学模式。
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Intracranial Pleomorphic Malignant Fibrous Histiocytoma, Associated to Systemic Lupus Erythematous: A Case Report
Background: Pleomorphic Malignant Fibrous histiocytoma (MFH) is a rare neoplasms of the soft tissue and bone composed of fibroblastic and histiocytic components with mitosis figures, nuclear pleomorphism and anaplasia. Case Presentation: We presented a rare case of MFH in 44 year old woman with history of systemic erythematosus lupus and seizures. Treated with prednisone. The cerebral TAC showed a temporal mass. Craniotomy was performed and the examination of the biopsy sample revealed a giant, pleomorphic and atypical cells. Immunohistochemical analysis showed positivity for vimentin, CD68, Fascin, lysosyme and MIB-1 labeling index of 20%. Pleomorphic malignant fibrous histiocytoma was diagnosed, with involvement of the overlying temporal lobe. We report a case of MFH of the left temporal in adult. Discussion: The neuroimaging and intra-operative opinion were of a meningioma. Histopathology, Case Study Tena-Suck et al.; BJMMR, 21(9): 1-8, 2017; Article no.BJMMR.32743 2 in conjunction with immunohistochemical evaluation and proliferation marker, confirmed the diagnosis. This is the firth case reported of PMFH associated to systemic lupus erythematous and different histological patterns.
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