肠道钙化纤维瘤:病例报告

Gonzalo Nathaniel Cantú-Soriano , Álvaro Lezid Padilla-Rodríguez
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引用次数: 0

摘要

钙化纤维瘤(CFT)是一种罕见的间叶源性良性病变,其特征可能与其他更常见的肿瘤相似。我们报告了一例 36 岁女性空肠近端肿瘤患者的病例,她最初被怀疑是胃肠道间质瘤(GIST)。手术切除后发现,反肠管边界有一个界限清楚的结节,显微镜下具有典型的钙化纤维瘤特征。肿瘤细胞的 CD34 阳性,其他标记物阴性,可与其他肿瘤鉴别。钙化纤维性肿瘤因其外观可能与更常见的肿瘤相混淆,但通过免疫组化技术进行准确诊断至关重要。完全手术切除通常可以治愈。
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Tumor fibroso calcificante intestinal: reporte de caso

Calcifying fibrous tumor (CFT) is a rare benign lesion of mesenchymal origin that may present similar characteristics to other more common tumors. We present the case of a 36-year-old woman with a tumor in the proximal jejunum, initially suspected to be a gastrointestinal stromal tumor (GIST). Surgical resection was performed, revealing a well-demarcated nodule at the anti-mesenteric border with microscopic features typical of a calcifying fibrous tumor. The tumor cells were positive for CD34 and negative for other markers, differentiating it from other neoplasms. Calcifying fibrous tumors can be confused with more common tumors because of its appearance, but an accurate diagnosis supported by immunohistochemistry is essential. Complete surgical excision is usually curative.

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来源期刊
Revista Espanola de Patologia
Revista Espanola de Patologia Medicine-Pathology and Forensic Medicine
CiteScore
0.90
自引率
0.00%
发文量
53
审稿时长
34 days
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