Octavian Fodor Regional Institute of Gastroenterology and Hepatology, 19-21, Croitorilor Street, 400 162, Cluj-Napoca, Romania.
BMC Gastroenterol. 2013 Feb 11;13:26. doi: 10.1186/1471-230X-13-26.
The cavitating mesenteric lymph node syndrome (CMLNS) is a rare manifestation of celiac disease, with an estimated mortality rate of 50%. Specific infections and malignant lymphoma may complicate its clinical course and contribute to its poor prognosis. Diagnosing the underlying cause of CMLNS can be challenging. This is the first report on contrast enhanced ultrasound (CEUS) findings in enteropathy associated T-cell lymphoma (EATL) complicating CMLNS in a gluten-free compliant patient with persistent symptoms and poor outcome.
We present the case of a 51-year old Caucasian male patient, diagnosed with celiac disease and CMLNS. Despite his compliance to the gluten-free diet the symptoms persisted and we eventually considered the possible development of malignancy. No mucosal changes suggestive of lymphoma were identified with capsule endoscopy. Low attenuation mesenteric lymphadenopathy, without enlarged small bowel segments were seen on computed tomography. CEUS revealed arterial rim enhancement around the necrotic mesenteric lymph nodes, without venous wash-out. No malignant cells were identified on laparoscopic mesenteric lymph nodes biopsies. The patient died due to fulminant liver failure 14 months later; the histopathological examination revealed CD3/CD30-positive atypical T-cell lymphocytes in the liver, mesenteric tissue, spleen, gastric wall, kidney, lung and bone marrow samples; no malignant cells were present in the small bowel samples.
CEUS findings in EATL complicating CMLNS include arterial rim enhancement of the mesenteric tissue around the cavitating lymph nodes, without venous wash-out. This vascular pattern is not suggestive for neoangiogenesis, as arteriovenous shunts from malignant tissues are responsible for rapid venous wash-out of the contrast agent. CEUS failed to provide a diagnosis in this case.
空泡性肠系膜淋巴结综合征(CMLNS)是乳糜泻的一种罕见表现,其死亡率估计为 50%。特定感染和恶性淋巴瘤可能使临床病程复杂化,并导致其预后不良。诊断 CMLNS 的根本原因可能具有挑战性。这是首例关于空泡性肠系膜淋巴结综合征并发乳糜泻患者对比增强超声(CEUS)表现的报告,该患者在持续症状和不良预后的情况下,对 gluten-free 饮食依从性良好。
我们介绍了一位 51 岁的白种男性患者,他被诊断为乳糜泻和 CMLNS。尽管他对 gluten-free 饮食依从良好,但症状仍持续存在,我们最终考虑可能发生恶性肿瘤。胶囊内镜未发现提示淋巴瘤的黏膜变化。计算机断层扫描显示低衰减肠系膜淋巴结病,无肿大的小肠段。CEUS 显示坏死肠系膜淋巴结周围动脉边缘增强,无静脉洗脱。腹腔镜肠系膜淋巴结活检未发现恶性细胞。14 个月后,患者因暴发性肝衰竭死亡;组织病理学检查显示肝、肠系膜组织、脾、胃壁、肾、肺和骨髓样本中存在 CD3/CD30 阳性的非典型 T 细胞淋巴细胞;小肠样本中未发现恶性细胞。
EATL 并发 CMLNS 的 CEUS 表现包括围绕空泡性淋巴结的肠系膜组织的动脉边缘增强,无静脉洗脱。这种血管模式不提示新生血管形成,因为恶性组织的动静脉分流导致造影剂快速静脉洗脱。CEUS 在本例中未能提供诊断。