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Necrotizing fasciitis from perforated sigmoid diverticulitis with subsequent pyoderma gangrenosum: a case report

机译:从脓性斑霉菌肝炎的穿孔术憩室炎的坏死性筋膜炎:案例报告

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Postsurgical pyoderma gangrenosum is a very rare form of cutaneous ulceration that is poorly recognized outside of dermatology and in some circumstances has been mistaken for necrotizing fasciitis. Here, we present a rare case of sigmoid diverticulitis with left ureter obstruction that perforated and quickly progressed into necrotizing fasciitis of the left buttock and leg via retroperitoneal spread in an immunocompetent patient. Nearly a year after intense surgical therapy, the patient rapidly developed ulcerating lesions over the left hip which presented a diagnostic dilemma. These were initially thought to represent Marjolin’s ulcers, which would require aggressive local excision. Multiple diagnostic imaging tests and biopsies eventually confirmed pyoderma gangrenosum, which was successfully treated with immunosuppressive therapy. This case highlights the need for a very broad differential diagnosis and wide expertise consultation when managing unusual postsurgical complications, especially when treatment modality critically depends on the correct diagnosis.
机译:后晶的Pyoderma gangrenosum是一种非常罕见的皮肤溃疡形式,在皮肤科外部识别不足,在某些情况下被误认为坏死性筋膜炎。在这里,我们呈现了一种罕见的乙状病憩室炎,左输尿管梗阻,穿孔并迅速进展到左臀部和腿部的坏死性筋膜炎,通过腹膜腹膜扩散在免疫活性患者中。近一年在激烈的手术治疗后,患者在左髋髋上迅速发育溃疡病变,呈现诊断困境。这些最初被认为是Marjolin的溃疡,这将需要积极的地方切除。多种诊断成像测试和活组织检查最终确认了Pyoderma Gangrenosum,其用免疫抑制疗法成功处理。这种情况突出了在管理不寻常的后勤并发症时对非常广泛的差异诊断和广泛专业知识咨询的需求,特别是当治疗方式批判性地取决于正确的诊断时。

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