Keer Dipinder, Jeon Paul, Borganonkar Mark, Potoczny Stefan
Faculty of Medicine, Department of Medicine, Memorial University of Newfoundland, St John's, Newfoundland.
Can J Gastroenterol. 2010 Jun;24(6):355-8. doi: 10.1155/2010/530475.
Cavitating mesenteric lymph node syndrome (CMLNS) is a rare complication of celiac disease. Globally, only 36 cases of CMLNS have been reported to date. The present article reports an incidence of its unique pathology and possible complications of celiac disease, followed by a review of the syndrome. A case involving a 51-year-old man with celiac disease who was referred to hospital because of a nontender abdominal mass is described. Plain film x-ray of the abdomen revealed fine curvilinear calcifications in the left lower quadrant. A complex, cystic-appearing, lobulated mass with somewhat echogenic walls most consistent with calcifications was revealed on subsequent ultrasound (US) imaging. Colour Doppler imaging showed no evidence of vascularity within the lesion. Computed tomography (CT) imaging showed a thin rim of calcification in the walls of multiple cystic components. Enhanced magnetic resonance (MR) imaging revealed a mixed solid and cystic multiloculated mass, with fat-fluid layers originating from the root of the small bowel mesentery. A CT-guided biopsy was performed. The fine-needle aspirate revealed calcified matter with no associated cellular material. No malignant cells were seen; CMLNS was established as the diagnosis. To the authors' knowledge, there are no previous reports in the literature describing the finding of rim calcification on US or MR imaging in the setting of CMLNS. CMLNS is an important diagnosis to consider, particularly in patients with a history of celiac disease. The finding of rim calcification on US in the setting of cavitating mesenteric adenopathy should prompt further diagnostic imaging studies such as CT or MR imaging. These may lead to additional pathology studies such as a CT-guided biopsy to further characterize the lesion at the cellular level, to investigate potential malignancy and to further guide follow-up and patient management.
空化性肠系膜淋巴结综合征(CMLNS)是乳糜泻的一种罕见并发症。在全球范围内,迄今为止仅报告了36例CMLNS病例。本文报道了其独特的病理学发病率以及乳糜泻可能的并发症,随后对该综合征进行了综述。描述了一例涉及一名51岁乳糜泻男性患者的病例,该患者因腹部无痛性肿块被转诊至医院。腹部平片显示左下腹有细曲线状钙化。随后的超声(US)成像显示一个复杂的、呈囊性外观的分叶状肿块,其壁有点状回声,最符合钙化表现。彩色多普勒成像显示病变内无血管迹象。计算机断层扫描(CT)成像显示多个囊性成分的壁上有薄的钙化边缘。增强磁共振(MR)成像显示一个混合实性和囊性的多房肿块,有来自小肠系膜根部的脂肪 - 液平面。进行了CT引导下活检。细针穿刺吸出物显示为钙化物质,无相关细胞成分。未见恶性细胞;诊断为CMLNS。据作者所知,文献中以前没有报道在CMLNS情况下超声或MR成像发现边缘钙化。CMLNS是一个需要考虑的重要诊断,特别是对于有乳糜泻病史的患者。在空化性肠系膜腺病情况下超声发现边缘钙化应促使进行进一步的诊断性成像研究,如CT或MR成像。这些可能会导致进行额外的病理学研究,如CT引导下活检,以在细胞水平进一步表征病变,调查潜在的恶性肿瘤,并进一步指导随访和患者管理。