Alkarem A, Hegazi A, Hassan A, Elhassan Y, Taha Mussab Mohjoub, Taha Sami Mahjoub
Faculty of Medicine, University of Nile Valley, Sudan.
Federal Ministry of Health, Sudan.
Int J Surg Case Rep. 2025 Jul 17;134:111696. doi: 10.1016/j.ijscr.2025.111696.
Schistosomiasis is the second most common endemic disease after malaria. This case highlights the rarity of adult S. haematobium worms in a sub-granuloma area and explores how they may reach this site.
A 25-year-old man presented with hematuria, dysuria, and urinary incontinence, with no prior history of schistosomiasis. Investigations revealed numerous RBCs, pus cells, and S. haematobium eggs in his urine. An abdominal ultrasound showed a thickened bladder wall with filling defects. Cystoscopy revealed two bladder tumors and sandy patches, where multiple mobile worms were found beneath granulomas. The granulomas and worms were completely removed (TURBT). Histopathology confirmed bilharzial granuloma and adult S. haematobium. The patient was treated by empirical regimen postoperatively and reported symptom improvement at follow-up.
Schistosomiasis is prevalent in tropical and subtropical regions, particularly in Africa, where over 90 % of cases occur in areas with inadequate sanitation. In Sudan, urinary schistosomiasis was first reported in 1919. The disease manifests in two forms: urogenital, caused by S. haematobium, and intestinal, caused by other species. Adult worms reside in the bladder, and their eggs lead to symptoms such as dysuria and "sandy patches." Praziquantel has been the gold standard treatment for over 30 years. Granulomas around adult worms are rare due to their location in the peri-vesical plexus and inability to migrate to bladder cavity. The presence of viable adult worms in uncommon sites may be explained by many possibilities such as angiogenesis in chronic inflammation or aberrant vascularity that early led the small adult worm to reach this site and to grow to this size.
This case mirroring rarity of the presence of adult S. haematobium in sub-granuloma area, it's also discuss the different possibilities of how this adult worm reach this rare site.
血吸虫病是仅次于疟疾的第二常见地方病。本病例突出了亚肉芽肿区域成人埃及血吸虫虫体的罕见性,并探讨了它们可能如何到达该部位。
一名25岁男性出现血尿、尿痛和尿失禁,既往无血吸虫病史。检查发现其尿液中有大量红细胞、脓细胞和埃及血吸虫卵。腹部超声显示膀胱壁增厚并有充盈缺损。膀胱镜检查发现两个膀胱肿瘤和沙斑,在肉芽肿下方发现多条活动的虫体。肉芽肿和虫体被完全切除(经尿道膀胱肿瘤切除术)。组织病理学证实为血吸虫性肉芽肿和成人埃及血吸虫。患者术后接受经验性治疗方案,随访时症状有所改善。
血吸虫病在热带和亚热带地区流行,尤其是在非洲,超过90%的病例发生在卫生条件差的地区。在苏丹,1919年首次报告了泌尿生殖系统血吸虫病。该疾病有两种表现形式:由埃及血吸虫引起的泌尿生殖系统型和由其他种类引起的肠道型。成虫寄生于膀胱,其虫卵导致尿痛和“沙斑”等症状。30多年来,吡喹酮一直是金标准治疗药物。由于成虫位于膀胱周围丛且无法迁移至膀胱腔,其周围的肉芽肿很少见。成虫出现在不常见部位可能有多种原因,比如慢性炎症中的血管生成或早期异常血管使小成虫到达该部位并生长到该大小。
本病例反映了亚肉芽肿区域成人埃及血吸虫存在的罕见性,同时也讨论了该成虫到达这个罕见部位的不同可能性。