Mita Akane, Nakakubo Sho, Nishimura Yusuke, Shima Hideki, Watanabe Masaaki, Shimamura Tsuyoshi, Konno Satoshi
Department of Respiratory Medicine, Faculty of Medicine, Hokkaido University, North 15 West 7, Kita-ku, Sapporo, 060-8638, Japan.
Department of Gastroenterology and Hepatology, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
BMC Infect Dis. 2025 Jan 25;25(1):120. doi: 10.1186/s12879-025-10488-3.
Mycobacterium avium complex (MAC) is a common pathogen causing non-tuberculous mycobacterial infections, primarily affecting the lungs. Disseminated MAC disease occurs mainly in immunocompromised individuals, such as those with acquired immunodeficiency syndrome, hematological malignancies, or those positive for anti-interferon-γ antibodies. However, its occurrence in solid organ transplant recipients is uncommon. Herein, we report a rare case of disseminated MAC disease following liver transplantation, which led to an obstructive mass in the intestinal tract that required differentiation from a malignant tumor.
A 76-year-old woman, who had undergone living-donor liver transplantation 15 years earlier for primary biliary cirrhosis, presented with persistent fever and vomiting three months before admission. She had a history of pulmonary MAC diagnosed five years earlier but remained untreated due to stable lung lesions. Abdominal computed tomography (CT) during her current illness revealed new thickening at the jejuno-jejunal anastomosis site and enlarged mesenteric lymph nodes. Positron emission tomography-CT indicated increased uptake at these sites, suggesting a possible malignancy. Endoscopy revealed an elevated lesion with circumferential ulcers, leading to a suspicion of primary malignant lymphoma. However, biopsies showed CD68-positive histiocyte-like cells with numerous acid-fast bacilli, confirming disseminated MAC infection. Despite ongoing antimicrobial therapy, the patient's intestinal lesions persisted, and she required prolonged hospitalization and interventions for bile drainage and enteral nutrition.
This case underscores the importance of considering disseminated MAC as a potential complication in solid organ transplant recipients, even when a long period has passed since transplantation. Disseminated MAC can mimic malignancy, presenting with significant lesions causing intestinal obstruction. Awareness and thorough differential diagnosis are essential for timely and accurate management in such complex cases. The patient's outcome emphasizes the need for vigilance in managing long-term immunosuppressed patients, particularly when they present with atypical infections.
鸟分枝杆菌复合群(MAC)是引起非结核分枝杆菌感染的常见病原体,主要影响肺部。播散性MAC病主要发生在免疫功能低下的个体,如获得性免疫缺陷综合征患者、血液系统恶性肿瘤患者或抗干扰素-γ抗体阳性者。然而,其在实体器官移植受者中的发生并不常见。在此,我们报告一例肝移植后罕见的播散性MAC病病例,该病导致肠道出现梗阻性肿块,需要与恶性肿瘤进行鉴别。
一名76岁女性,15年前因原发性胆汁性肝硬化接受了活体供肝肝移植,入院前3个月出现持续发热和呕吐。她5年前被诊断为肺部MAC,但由于肺部病变稳定而未接受治疗。此次患病期间的腹部计算机断层扫描(CT)显示空肠-空肠吻合部位出现新的增厚以及肠系膜淋巴结肿大。正电子发射断层扫描-CT显示这些部位摄取增加,表示可能存在恶性肿瘤。内镜检查发现一个隆起性病变,周围有溃疡,怀疑是原发性恶性淋巴瘤。然而,活检显示CD68阳性的组织细胞样细胞内有大量抗酸杆菌,证实为播散性MAC感染。尽管持续进行抗菌治疗,患者的肠道病变仍持续存在,她需要长期住院,并接受胆汁引流和肠内营养干预。
本病例强调了即使在移植后很长时间,也应将播散性MAC视为实体器官移植受者潜在并发症的重要性。播散性MAC可模仿恶性肿瘤,出现导致肠梗阻的显著病变。对于此类复杂病例,提高认识并进行全面的鉴别诊断对于及时、准确的管理至关重要。患者的结局强调了对长期免疫抑制患者进行监测的必要性,尤其是当他们出现非典型感染时。