Andargie Ephrem Adane, Belay Suleiman Ayalew, Negussie Michael A, Afework Hiwot Tesfaselassie, Kassie Melaku Tessema, Gebresellassie Hewan Fiseha
Department of Medicine, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.
School of Medicine, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.
Int J Surg Case Rep. 2025 Feb;127:110856. doi: 10.1016/j.ijscr.2025.110856. Epub 2025 Jan 6.
Amyand's hernia is a rare condition defined by the presence of the vermiform appendix within an inguinal hernia sac. The occurrence of Amyand's hernia with testicular necrosis is particularly uncommon, further complicating its clinical presentation and management.
A 50-year-old male presented with a two-year history of progressive right scrotal swelling, acutely worsened over four days with pain and fever. Examination revealed a firm, tender, irreducible right scrotal mass with overlying erythema. Laboratory tests showed leukocytosis. Imaging confirmed an inflamed appendix within the hernial sac, consistent with Amyand's hernia complicated by abscess formation. Emergency surgery revealed a gangrenous appendix, scrotal abscess, and necrotic right testicular tissue. The patient underwent appendectomy, orchiectomy, hernia repair, and abscess drainage. He recovered uneventfully, with symptom resolution and no recurrence at follow-up.
The progression of Amyand's hernia to appendicitis and subsequent perforation, as seen in our case, can result in severe complications, including abscess formation and testicular necrosis. The Losanoff and Basson classification categorizes Amyand's hernia based on the appendix's condition and associated complications, ranging from a normal appendix (Type 1) to severe extra-sac pathology such as gangrene or malignancy (Type 4). Our case aligns with Type 4, involving a perforated appendix with gangrene and a scrotal abscess, necessitating extensive surgical intervention.
This case highlights the rarity and complexity of Amyand's hernia in adults, emphasizing the need for prompt recognition and tailored management to achieve favorable outcomes.
艾米安德疝是一种罕见病症,定义为腹股沟疝囊内存在阑尾。艾米安德疝合并睾丸坏死的情况尤为罕见,这使其临床表现和治疗更加复杂。
一名50岁男性,有两年渐进性右侧阴囊肿胀病史,在四天内急性加重,伴有疼痛和发热。检查发现右侧阴囊有一个坚硬、压痛、不可复性肿块,表面有红斑。实验室检查显示白细胞增多。影像学检查证实疝囊内有发炎的阑尾,符合合并脓肿形成的艾米安德疝。急诊手术发现阑尾坏疽、阴囊脓肿和右侧睾丸组织坏死。患者接受了阑尾切除术、睾丸切除术、疝修补术和脓肿引流术。他恢复顺利,症状消失,随访无复发。
如我们病例中所见,艾米安德疝发展为阑尾炎并随后穿孔,可导致严重并发症,包括脓肿形成和睾丸坏死。洛萨诺夫和巴森分类法根据阑尾状况和相关并发症对艾米安德疝进行分类,从正常阑尾(1型)到严重的囊外病变如坏疽或恶性肿瘤(4型)。我们的病例符合4型,涉及穿孔坏疽阑尾和阴囊脓肿,需要广泛的手术干预。
本病例突出了成人艾米安德疝的罕见性和复杂性,强调需要及时识别并进行针对性治疗以取得良好效果。