Omry Ahmed, Ferjaoui Wael, Gaied Louay Ben, Messaoudi Houssem, Behi Hager, Khalifa Med Bachir
General Surgery Department, Military Hospital of Tunis, Mont Fleury-1008, Tunis, Tunisia; Faculty of Medicine of Tunis, 15, Djebel Lakhdhar Street - 1007 Bab Saadoun, Tunis, Tunisia.
General Surgery Department, Military Hospital of Tunis, Mont Fleury-1008, Tunis, Tunisia; Faculty of Medicine of Tunis, 15, Djebel Lakhdhar Street - 1007 Bab Saadoun, Tunis, Tunisia.
Int J Surg Case Rep. 2025 Jun;131:111401. doi: 10.1016/j.ijscr.2025.111401. Epub 2025 May 3.
Xanthogranulomatous cholecystitis (XGC) is a rare, aggressive gallbladder condition marked by chronic inflammation, fibrosis, and lipid-laden macrophages. It often mimics gallbladder carcinoma clinically and radiologically, complicating diagnosis and treatment. Early differentiation from malignancy is essential for proper management. This case emphasizes the diagnostic challenges of XGC and the need for a multidisciplinary approach.
A 61-year-old man presented with four months of intermittent right upper quadrant abdominal pain radiating to the back, without fever, jaundice, or weight loss. Examination revealed right hypochondrial tenderness, and labs showed elevated inflammatory markers. Imaging indicated gallstones, gallbladder wall thickening, and ill-defined liver boundaries, raising malignancy concerns. A biopsy confirmed xanthogranulomatous cholecystitis (XGC), ruling out carcinoma. He underwent successful laparoscopic cholecystectomy, with histopathology confirming XGC. Recovery was uneventful, and he remained symptom-free at six-month follow-up.
XGC is a diagnostic challenge due to its nonspecific symptoms and imaging findings that overlap with malignancy. Preoperative biopsy, as performed in this case, can be invaluable in guiding management. Laparoscopic cholecystectomy, though technically demanding due to dense adhesions and local invasion, is feasible in selected cases. Histopathology remains the gold standard for definitive diagnosis, revealing chronic inflammation and lipid-laden macrophages without malignancy.
This case underscores the importance of considering XGC in the differential diagnosis of gallbladder masses, particularly when imaging suggests local invasion. Preoperative biopsy and histopathology play pivotal roles in distinguishing XGC from malignancy. Successful laparoscopic management, despite its challenges, highlights the potential for minimally invasive surgery in carefully selected cases.
黄色肉芽肿性胆囊炎(XGC)是一种罕见的侵袭性胆囊疾病,其特征为慢性炎症、纤维化以及充满脂质的巨噬细胞。它在临床和影像学上常与胆囊癌相似,使诊断和治疗变得复杂。早期与恶性肿瘤鉴别对于正确的治疗管理至关重要。本病例强调了XGC的诊断挑战以及多学科方法的必要性。
一名61岁男性,出现右上腹间歇性腹痛4个月,疼痛放射至背部,无发热、黄疸或体重减轻。检查发现右季肋部压痛,实验室检查显示炎症标志物升高。影像学检查提示胆结石、胆囊壁增厚以及肝脏边界不清,引发了对恶性肿瘤的担忧。活检证实为黄色肉芽肿性胆囊炎(XGC),排除了癌症。他接受了成功的腹腔镜胆囊切除术,组织病理学证实为XGC。恢复过程顺利,6个月随访时无症状。
XGC因其非特异性症状和与恶性肿瘤重叠的影像学表现而成为诊断挑战。如本病例所进行的术前活检在指导治疗方面可能非常宝贵。腹腔镜胆囊切除术虽然由于致密粘连和局部侵犯在技术上要求较高,但在某些病例中是可行的。组织病理学仍然是明确诊断的金标准,显示为慢性炎症和充满脂质的巨噬细胞,无恶性肿瘤表现。
本病例强调了在胆囊肿物的鉴别诊断中考虑XGC的重要性,特别是当影像学提示局部侵犯时。术前活检和组织病理学在区分XGC与恶性肿瘤方面起着关键作用。尽管存在挑战,但成功的腹腔镜治疗突出了在精心挑选的病例中进行微创手术的潜力。