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首页> 外文期刊>Revista chilena de pediatría >Dermatofibrosarcoma protuberans pigmentado: Descripción de un caso pediátrico
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Dermatofibrosarcoma protuberans pigmentado: Descripción de un caso pediátrico

机译:Dermatofibrosarcoma着色的普促蛋白:小儿案描述

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摘要

Introduction: Bednar tumor is a rare low-grade sarcoma considered the pigmented variant of dermatofibrosarco ma protuberans (DFSP). Objective: To describe the clinical and histopathological characteristics, treatment and evolution of this rare neoplasm. Clinical Case: A 9-year old female presented with a 2-year history of an indurated, asymptomatic papule on the back of her fourth left toe. The incisio nal biopsy was compatible with pigmented DFSP. The immunohistochemical study showed intense positivity for CD34 throughout the lesion, with negative factor XIIIa. We complemented the study with molecular cytogenetics (FISH) for PDGFB gene (22q13.1) which showed an abnormal pattern in tumor cells, but not in the melanocytes or the peritumoral skin. Delayed Mohs surgery and skin substitute dressing were performed without neoplastic recurrence at 5 years of follow up. Conclu sion: Pigmented DFSP is a low-grade sarcoma that is very rare in pediatric patients. The classical and pigmented variants should be suspected in the presence of a single papulonodular lesion of slow and progressive growth, with presence of spindle cells with storiform pattern in the biopsy and positive immunohistochemical study for CD34. It is an entity with good prognosis, with little risk of recurren ce and metastasis, if complete excision is achieved.
机译:介绍:卧脉肿瘤是一种罕见的低级肉瘤,被认为是DermatofibrosoSarco MA Protuberans(DFSP)的着色变体。目的:描述这种稀有肿瘤的临床和组织病理学特征,治疗和演化。临床案例:一位9岁女性介绍了她第四件左脚趾背面的2年迷住的无症状的丘疹历史。切除的NAL活组织检查与着色的DFSP相容。免疫组织化学研究表明整个病变中CD34的强烈阳性,具有负因子XIIIa。我们与PDGFB基因(22Q13.1)的分子细胞遗传学(FISH)与分子细胞遗传学(FISH)进行了补充,其在肿瘤细胞中显示出异常模式,但不在黑色细胞或腹膜皮肤中。延迟MOHS手术和皮肤替代敷料在5年后没有肿瘤复发的情况下进行。结论:色素沉着的DFSP是一种低级肉瘤,在儿科患者中非常罕见。应在慢性和逐渐生长的单个灭心菌病变存在下怀疑古典和着色的变体,在活组织检查和阳性免疫组化研究中存在梭形图案的主轴细胞。这是一个具有良好预后的实体,如果达到完全切除,则重复恢复的风险很小。

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