Abstract:
Background/Objectives: The infrequent occurrence of pyoderma gangrenosum (PG) during pregnancy and in postpartum, with its subsequent diagnostic intricacies, caused us to present the following case. Methods: This article describes a rare case of PG in postpartum in a patient without any prior pathology and a short review of the literature, aiming to identify similar rare instances. Results: We conducted a literature review to ascertain the prevalence of postpartum pyoderma gangrenosum, and we identified a total of 41 cases. Conclusions: Our article underlines again the importance of interdisciplinary collaboration for the prompt identification and commencement of necessary therapeutic interventions in postpartum women afflicted by pyoderma gangrenosum.
摘要:
背景/目标:在怀孕期间和产后不经常发生坏疽性脓皮病(PG),随着其随后的诊断复杂性,导致我们提出以下案例。方法:本文描述了一个罕见的PG在产后患者没有任何先前的病理和文献回顾,旨在识别类似的罕见情况。结果:我们进行了文献综述,以确定产后坏疽性脓皮病的患病率,我们确认了41例.结论:我们的文章再次强调了跨学科合作对于迅速识别和开始患有坏疽性脓皮病的产后妇女的必要治疗干预措施的重要性。