Primary Peritoneal Psammocarcinoma Misdiagnosed as an Heterotopic Ossification: A Case Report.

Q4 Medicine
Gayoung Jeon, Seo Young Park
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引用次数: 0

Abstract

Primary peritoneal psammocarcinoma is a rare type of serous carcinoma that is characterized by the massive formation of psammoma bodies and the invasion of adjacent organs. A 55-year-old female who previously underwent a hysterectomy presented to the emergency room with severe abdominal pain. Contrast-enhanced CT revealed an intra-abdominal calcific mass. Initially, it was thought to be a heterotopic ossification due to the previous pelvic surgery with intact ovaries. However, this was diagnosed as a primary peritoneal psammocarcinoma. Primary peritoneal psammocarcinoma is a very rare disease entity that should be considered a differential diagnosis in patients with normal ovaries, massive ossification in the pelvic cavity, and calcific peritoneal nodules.

Abstract Image

原发性腹膜沙粒癌误诊为异位骨化1例。
原发性腹膜沙粒癌是一种罕见的浆液性癌,其特征是大量形成沙粒体并侵犯邻近器官。一名55岁女性,曾接受子宫切除术,以严重腹痛就诊于急诊室。增强CT显示腹内钙化肿块。最初,它被认为是异位骨化,因为以前的骨盆手术和完整的卵巢。然而,这被诊断为原发性腹膜沙粒癌。原发性腹膜沙粒癌是一种非常罕见的疾病,在卵巢正常、盆腔大量骨化和腹膜钙化结节的患者中应考虑鉴别诊断。
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来源期刊
Journal of the Korean Society of Radiology
Journal of the Korean Society of Radiology Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
0.40
自引率
0.00%
发文量
98
审稿时长
16 weeks
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