Giant natal cleft epidermal inclusion cyst surgically excised in a young male in Australia.

IF 0.5 Q4 SURGERY Journal of Surgical Case Reports Pub Date : 2025-03-18 eCollection Date: 2025-03-01 DOI:10.1093/jscr/rjaf141
William Layt, Brielle Williams, Richard Maguire
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Abstract

Epidermal inclusion cysts are benign lesions commonly found in hair-bearing areas. Giant epidermal inclusion cysts (GEICs), those exceeding 5 cm in diameter, are rare and may pose diagnostic challenges, especially in atypical locations. We report the case of a 29-year-old male with a 7-8 cm swelling in the natal cleft, diagnosed as a GEIC after imaging studies, including ultrasound, CT, and MRI. Surgical excision was performed with careful dissection to preserve surrounding structures. The patient had an uneventful recovery. This case highlights the diagnostic and surgical challenges of GEICs in the natal cleft and emphasizes the importance of pre-operative imaging and meticulous surgical technique to avoid complications.

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巨大的先天性裂表皮包涵囊肿手术切除的年轻男性在澳大利亚。
表皮包涵体囊肿是一种良性病变,常见于生发部位。直径超过 5 厘米的巨型表皮包涵体囊肿(GEIC)非常罕见,可能会给诊断带来困难,尤其是在不典型的部位。我们报告了一例 29 岁男性的病例,他的产道裂隙处有一个 7-8 厘米的肿物,经过超声波、CT 和核磁共振成像等影像学检查,诊断为巨表皮包涵体囊肿。手术切除时仔细剥离以保留周围结构。患者恢复顺利。该病例凸显了产道裂中 GEIC 在诊断和手术方面的挑战,并强调了术前成像和精细手术技术对避免并发症的重要性。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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