Barbu Laurenţiu Augustus, Vasile Liviu, Mogoş Gabriel Florin Răzvan, Şurlin Valeriu, Vîlcea Ionică Daniel, Cercelaru Liliana, Mogoantă Stelian Ştefăniţă, Mărgăritescu Nicolae Dragoş, Ţenea-Cojan Tiberiu Ştefăniţă
Department of Surgery, University of Medicine and Pharmacy of Craiova, Romania;
Rom J Morphol Embryol. 2025 Apr-Jun;66(2):313-321. doi: 10.47162/RJME.66.2.04.
Background∕Objectives: Malakoplakia is an uncommon clinicopathological entity defined by the accumulation of dysfunctional macrophages containing undigested bacterial remnants and pathognomonic Michaelis-Gutmann bodies. Although it most frequently involves the gastrointestinal tract, particularly the colon, rectum, and rectosigmoid junction, appendiceal involvement remains rare. This case represents only the fourth reported occurrence of appendiceal malakoplakia in a young, immunocompetent adult without notable comorbidities, underscoring its exceptional clinical presentation. Study selection for review: A PubMed search was performed to explore the current understanding of malakoplakia, with emphasis on its etiopathogenesis, diagnostic criteria, and therapeutic strategies. Case presentation: A 25-year-old immunocompetent male presented with a periappendicular abscess mimicking a tumor, ultimately requiring right hemicolectomy. Histopathological (HP) evaluation confirmed intestinal-appendicular malakoplakia and granulomatous lymphadenitis, with no evidence of tuberculosis, underscoring the diagnostic challenge and the need for further investigation into its etiopathogenesis in young, otherwise healthy individuals. Conclusions: This case illustrates a rare instance of appendicular malakoplakia in a young adult, emphasizing the importance of HP evaluation for accurate diagnosis and the need to consider this entity in the differential diagnosis of appendiceal masses to avoid mismanagement.
背景∕目的:软斑病是一种罕见的临床病理实体,其特征是功能失调的巨噬细胞积聚,这些巨噬细胞含有未消化的细菌残余物和具有病理特征的迈克尔is-古特曼小体。虽然它最常累及胃肠道,特别是结肠、直肠和直肠乙状结肠交界处,但阑尾受累仍然罕见。该病例是第四例报道的年轻、免疫功能正常且无明显合并症的成年人阑尾软斑病,突出了其特殊的临床表现。综述的研究选择:进行了PubMed检索,以探索目前对软斑病的认识,重点是其病因发病机制、诊断标准和治疗策略。病例报告:一名25岁免疫功能正常的男性因疑似肿瘤的阑尾周围脓肿就诊,最终需要进行右半结肠切除术。组织病理学(HP)评估证实为肠-阑尾软斑病和肉芽肿性淋巴结炎,无结核病证据,突出了诊断挑战以及对年轻、健康个体其病因发病机制进行进一步研究的必要性。结论:该病例说明了年轻成年人阑尾软斑病的罕见情况,强调了HP评估对准确诊断的重要性,以及在阑尾肿块的鉴别诊断中考虑这一实体以避免管理不当的必要性。