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病例报告:原发性腹膜砂粒体状癌的偶然发现。

Case Report: Incidental discovery of primary peritoneal psammocarcinoma.

机构信息

Department of Pathology, Habib Thameur Hospital, Tunis, 1008, Tunisia.

Faculty of medicine of Tunis, Tunis El Manar University, Tunis, 1007, Tunisia.

出版信息

F1000Res. 2023 Oct 16;11:696. doi: 10.12688/f1000research.110362.2. eCollection 2022.

DOI:10.12688/f1000research.110362.2
PMID:39233872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11372342/
Abstract

Psammocarcinoma is an uncommon subtype of low-grade serous carcinoma. It is characterized by the presence of extensive psammoma bodies and can have either an ovarian or peritoneal origin. To our knowledge fewer than 30 cases of primary peritoneal psammocarcinoma (PPP) have been reported in the English literature. We report a rare case of  PPP in a 74-year-old female, discovered fortuitously within a laparotomy for gallbladder lithiasis. At laparotomy, multiple nodular implants involving the omentum, the peritoneum and a magma of intestinal loops in the right iliac fossa were noted. A biopsy from nodules was performed. Gross examination showed multiple nodules of different sizes in the fat tissue. Pathologic examination showed massive psammoma bodies representing more than 75% of the tumor. The final diagnosis was psammocarcinoma. Our patient was referred to the gynecologic department for further investigation and to ascertain whether the tumor arose from the ovaries or peritoneum. Hysterectomy, bilateral adnexectomy and omentectomy were performed. Macroscopic examination showed that both ovaries were intact having a normal size. No invasion of ovarian stroma was shown in microscopic examination. The patient died of SARS-CoV-2 (COVID-19) six days after the surgery. PPP is a rare type of  low-grade serous carcinoma. The behavior of this tumor is unclear, and the treatment is not standardized because of its rarity and lack of long-term follow-up. More cases need to be studied for better understanding and improvement of the management protocols.

摘要

砂粒体癌是一种罕见的低级别浆液性癌亚型。其特征为广泛存在砂粒体,并可能起源于卵巢或腹膜。据我们所知,英文文献中报道的原发性腹膜砂粒体癌(PPP)病例少于 30 例。我们报告了一例罕见的 74 岁女性 PPP 病例,该患者在因胆囊结石行剖腹手术时偶然发现。剖腹术中,发现多个腹膜和网膜的结节状植入物,以及右髂窝的多个肠袢。对结节进行了活检。大体检查显示脂肪组织中有多个大小不同的结节。病理检查显示大量砂粒体,占肿瘤的 75%以上。最终诊断为砂粒体癌。我们的患者被转至妇科进一步检查,以确定肿瘤是否来自卵巢或腹膜。行子宫切除术、双侧附件切除术和网膜切除术。大体检查显示双侧卵巢完整,大小正常。显微镜检查未见卵巢间质浸润。患者在手术后六天因 SARS-CoV-2(COVID-19)去世。PPP 是一种罕见的低级别浆液性癌。由于其罕见性和缺乏长期随访,该肿瘤的行为尚不清楚,治疗也未标准化。需要更多的病例来进行研究,以更好地了解和改进管理方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11372349/8d2241c6bac0/f1000research-11-157236-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11372349/f5d198245f64/f1000research-11-157236-g0000.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11372349/1e57d934b5a5/f1000research-11-157236-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11372349/6f3b2c6af878/f1000research-11-157236-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11372349/8d2241c6bac0/f1000research-11-157236-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11372349/f5d198245f64/f1000research-11-157236-g0000.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11372349/1e57d934b5a5/f1000research-11-157236-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11372349/6f3b2c6af878/f1000research-11-157236-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b751/11372349/8d2241c6bac0/f1000research-11-157236-g0003.jpg

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