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手术切除的原发性食管绒毛膜癌伴巴雷特腺癌:一例报告。

Surgically resected primary esophageal choriocarcinoma accompanied with Barrett's adenocarcinoma: a case report.

作者信息

Fujiwara Yuta, Okamoto Koichi, Ninomiya Itasu, Saito Hiroto, Yamaguchi Takahisa, Terai Shiro, Kinoshita Jun, Makino Isamu, Nakamura Keishi, Fushida Sachio, Ikeda Hiroko, Ohta Tetsuo

机构信息

Department of Gastroenterological Surgery, Kanazawa University, 13-1 Takara-Machi, Kanazawa, Ishikawa, 920-8641, Japan.

Department of Diagnostic Pathology, Kanazawa University, 13-1 Takara-Machi, Kanazawa, Ishikawa, 920-8641, Japan.

出版信息

Surg Case Rep. 2020 Sep 29;6(1):227. doi: 10.1186/s40792-020-00990-y.

Abstract

BACKGROUND

Choriocarcinomas are usually classified as either gestational or non-gestational. Primary choriocarcinomas in the gastrointestinal tract, especially primary choriocarcinomas in the esophagus, are extremely rare. We report a case of a rare primary esophageal choriocarcinoma mixed with squamous cell carcinoma-like components in association with Barrett's adenocarcinoma.

CASE PRESENTATION

A 58-year-old man visited the hospital, complaining of hematemesis and tarry stools. In emergency upper gastrointestinal endoscopy, a bleeding esophageal tumor was observed. Additionally, a contrast computed tomography (CT) scan showed a large hypervascular tumor 4.8 cm in diameter in the left kidney. He came to our institution for further examination and treatment of the esophageal tumor and kidney lesion. The patient had an easy bleeding elevated tumor 2 cm in diameter at the left wall of the middle thoracic esophagus and a left renal carcinoma. Histopathological diagnosis of the biopsy specimen of the esophageal tumor was a poorly differentiated carcinoma. However, a precise histological type diagnosis could not be obtained. In June 2016, mediastinoscopic transhiatal esophagectomy and posterior mediastinal gastric tube reconstruction were performed to treat his esophageal tumor. Histopathologically, most of the tumor comprised hCG-positive syncytiotrophoblasts. Therefore, we confirmed it as a primary esophageal choriocarcinoma. Furthermore, the tumor contained a poorly differentiated squamous cell carcinoma-like component that was also diagnosed as a choriocarcinoma using immunohistochemical staining and there was a small Barrett's esophageal adenocarcinoma lesion in the Barrett's epithelium near the tumor. Three months after surgery, a CT scan demonstrated multiple lung metastatic nodules and multiple intrahepatic masses. Needle biopsy from the lung nodule showed a choriocarcinoma. Despite chemotherapy, the metastatic choriocarcinoma regrew rapidly and multiple bone metastases appeared. He died because of his esophageal choriocarcinoma 13 months after primary resection.

CONCLUSIONS

We encountered an extremely rare case of esophageal choriocarcinoma combined with squamous cell carcinoma-like components in association with a simultaneous Barrett's adenocarcinoma that we followed for the entire course of his disease, from resection to end of life. Esophageal choriocarcinomas are rare with peculiar characteristics and very poor prognoses. Additional cases are needed to establish an appropriate future treatment.

摘要

背景

绒毛膜癌通常分为妊娠性或非妊娠性。胃肠道原发性绒毛膜癌,尤其是食管原发性绒毛膜癌极为罕见。我们报告一例罕见的原发性食管绒毛膜癌,其伴有鳞状细胞癌样成分,并与巴雷特腺癌相关。

病例介绍

一名58岁男性因呕血和柏油样便前来就诊。急诊上消化道内镜检查发现食管肿瘤出血。此外,对比增强计算机断层扫描(CT)显示左肾有一个直径4.8厘米的大血管丰富肿瘤。他前来我院进一步检查和治疗食管肿瘤及肾脏病变。患者在胸段食管中段左壁有一个直径2厘米、易出血的隆起肿瘤,同时患有左肾癌。食管肿瘤活检标本的组织病理学诊断为低分化癌。然而,无法获得精确的组织学类型诊断。2016年6月,为治疗其食管肿瘤,进行了纵隔镜辅助经裂孔食管切除术及后纵隔胃管重建术。组织病理学检查显示,大部分肿瘤由人绒毛膜促性腺激素(hCG)阳性的合体滋养层细胞组成。因此,我们确诊其为原发性食管绒毛膜癌。此外,肿瘤还含有低分化鳞状细胞癌样成分,经免疫组化染色也诊断为绒毛膜癌,且在肿瘤附近的巴雷特上皮中有一个小的巴雷特食管腺癌病灶。术后3个月,CT扫描显示肺部有多个转移结节和多个肝内肿块。肺结节穿刺活检显示为绒毛膜癌。尽管进行了化疗,转移性绒毛膜癌仍迅速复发,并出现多处骨转移。患者在初次切除术后13个月因食管绒毛膜癌死亡。

结论

我们遇到了一例极为罕见的食管绒毛膜癌,其合并鳞状细胞癌样成分,并同时伴有巴雷特腺癌,我们对其疾病的整个过程,从切除到生命终结进行了全程跟踪。食管绒毛膜癌罕见,具有独特特征,预后极差。需要更多病例以确立合适的未来治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2821/7524915/40fd46236aa5/40792_2020_990_Fig1_HTML.jpg

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