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福尼尔坏疽揭示急性动脉闭塞:一例报告。

Fournier's gangrene revealing an acute arterial occlusion: A case report.

作者信息

Blaiech Walid, Othmen Mouna Ben, Ouahchi Ines, Hamida Mourad Ben, Hmida Wissem, Jaidane Mehdi

机构信息

Department of Urology, Sahloul University Hospital, Sousse, Tunisia.

Department of Urology, Sahloul University Hospital, Sousse, Tunisia.

出版信息

Int J Surg Case Rep. 2024 Mar;116:109471. doi: 10.1016/j.ijscr.2024.109471. Epub 2024 Feb 29.

Abstract

INTRODUCTION AND IMPORTANCE

Fournier gangrene (FG) is a rare form of necrotizing fasciitis that affects both the deep and superficial layers of the perineal genital region. When left untreated, Fournier gangrene can rapidly advance, leading to substantial morbidity and mortality. Herein, we present a case of Fournier's gangrene, which revealed acute arterial occlusion. To the best of our knowledge, few cases of Fournier's gangrene secondary to arterial occlusion have been reported.

CASE PRESENTATION

We report the case of a 37-year-old man with no known medical history who presented with fever and painful swelling of the scrotum. Physical examination revealed a large black spot on the scrotum surrounded by erythema, suggestive of Fournier's gangrene. We performed an extended debridement of the scrotal area. Three days later, the patient complained of severe pain in the left foot accompanied by numbness. Lower limb computed tomographic angiography (CTA) revealed multiple arterial occlusions. Thrombectomy and anticoagulation therapy were crucial in managing the vascular thrombosis and preventing the further extension of the gangrene.

CLINICAL DISCUSSION

This case underscores the importance of recognizing diverse etiologies of Fournier's gangrene, including vascular involvement, and emphasizes the need for a multidisciplinary approach. Early identification, aggressive surgical debridement, and broad-spectrum antibiotics remain the cornerstone of management, with the added consideration of anticoagulation in cases involving vascular thrombosis.

CONCLUSION

FG is a rare yet potentially life-threatening condition. Its multifaceted etiologies, including vascular factors, underscore the complexity of its presentation and challenges for timely diagnosis. The recognition of vascular involvement as a potential etiology of FG warrants further in-depth exploration.

摘要

引言与重要性

福尼尔坏疽(FG)是一种罕见的坏死性筋膜炎,累及会阴生殖器区域的深层和浅层。若不治疗,福尼尔坏疽会迅速发展,导致严重的发病率和死亡率。在此,我们报告一例福尼尔坏疽病例,该病例显示存在急性动脉闭塞。据我们所知,继发于动脉闭塞的福尼尔坏疽病例报道较少。

病例介绍

我们报告一例37岁男性,无已知病史,表现为发热和阴囊疼痛性肿胀。体格检查发现阴囊上有一个大的黑点,周围有红斑,提示福尼尔坏疽。我们对阴囊区域进行了广泛的清创术。三天后,患者抱怨左脚剧痛并伴有麻木。下肢计算机断层血管造影(CTA)显示多处动脉闭塞。血栓切除术和抗凝治疗对于处理血管血栓形成和防止坏疽进一步扩展至关重要。

临床讨论

该病例强调了认识福尼尔坏疽多种病因(包括血管受累)的重要性,并强调了多学科方法的必要性。早期识别、积极的手术清创和广谱抗生素仍然是治疗的基石,对于涉及血管血栓形成的病例还需考虑抗凝治疗。

结论

福尼尔坏疽是一种罕见但可能危及生命的疾病。其多方面的病因,包括血管因素,突显了其临床表现的复杂性以及及时诊断的挑战。认识到血管受累是福尼尔坏疽的潜在病因值得进一步深入探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06a8/10944086/71e2ea45ae6d/gr1.jpg

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