Honda Manami, Iwamuro Masaya, Miyamoto Kazuya, Tanaka Takehiro, Otsuka Motoyuki
Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama, JPN.
Department of Pathology, Okayama University Hospital, Okayama, JPN.
Cureus. 2025 May 15;17(5):e84161. doi: 10.7759/cureus.84161. eCollection 2025 May.
We report a rare case of pseudoachalasia secondary to malignant pleural mesothelioma involving the esophagus. A 66-year-old man presented with progressive dysphagia, weight loss, and postprandial hiccups. Endoscopic examination showed esophageal dilation with luminal narrowing at the esophagogastric junction, but no mucosal abnormalities. Computed tomography revealed an irregular-shaped mass extending from the peri-esophagogastric junction to the retroperitoneum, accompanied by pleural effusion, right-sided hydronephrosis, and multiple hepatic lesions. Endoscopic ultrasound-guided fine-needle aspiration from the mass lesion through the esophageal lumen revealed epithelioid malignant mesothelioma. This case highlights the importance of considering malignant mesothelioma in the differential diagnosis of pseudoachalasia, particularly when imaging reveals extrinsic esophageal compression without mucosal lesions.
我们报告了一例罕见的继发于累及食管的恶性胸膜间皮瘤的假性贲门失弛缓症病例。一名66岁男性患者出现进行性吞咽困难、体重减轻和餐后呃逆。内镜检查显示食管扩张,食管胃交界处管腔狭窄,但无黏膜异常。计算机断层扫描显示一个不规则形肿块,从食管胃周围交界处延伸至腹膜后,伴有胸腔积液、右侧肾积水和多个肝脏病变。通过食管腔对肿块病变进行内镜超声引导下细针穿刺活检显示为上皮样恶性间皮瘤。该病例强调了在假性贲门失弛缓症的鉴别诊断中考虑恶性间皮瘤的重要性,尤其是当影像学显示食管外压而无黏膜病变时。