Radiology Department, Zhongda Hospital affiliated to Southeast University, Nanjing, 210009, China.
Br J Radiol. 2010 Sep;83(993):e188-91. doi: 10.1259/bjr/26883993.
Calcifying fibrous pseudotumour (CFPT) is a rare lesion that has only recently been reported in the literature. Usually, the lesion develops in subcutaneous tissue, deep soft tissues or viscera. It appears as a uniform, hypocellular and well-circumscribed mass without a capsule. Only nine cases of gastric CFPT have been reported in the literature so far. Here, we report a new case of gastric CFPT, which was, surprisingly, associated with an ulcer. To our knowledge, a gastric CFPT with an ulcer has not been previously reported in the literature. The patient (a healthy 49-year-old man) had vomited approximately 300 g brown liquid and developed syncope once. CT scan and gastroscopy revealed a polypoid mass at the great curvature of the gastric body with a larger ulcer on its top. The mass was removed by surgery. During a follow-up of 5 months, the patient was asymptomatic with no recurrence. We discuss the imaging findings, as well as the clinicopathological features of this unusual case and review the related literature.
钙化性纤维性假瘤(CFPT)是一种罕见的病变,最近才在文献中报道。通常,病变发生在皮下组织、深部软组织或内脏。它表现为均匀、低细胞和边界清楚的肿块,没有包膜。到目前为止,文献中仅报道了 9 例胃 CFPT。在这里,我们报告了一例新的胃 CFPT,令人惊讶的是,它与溃疡有关。据我们所知,以前文献中没有报道过胃 CFPT 合并溃疡。患者(健康的 49 岁男性)呕吐约 300 克棕色液体,并出现一次晕厥。CT 扫描和胃镜检查显示胃体大弯处有一个息肉样肿块,顶部有一个较大的溃疡。该肿块通过手术切除。在 5 个月的随访中,患者无症状,无复发。我们讨论了这个不寻常病例的影像学表现以及临床病理特征,并复习了相关文献。