New York University School of Medicine, New York, New York 10016, USA.
J Am Acad Dermatol. 2011 May;64(5):950-4. doi: 10.1016/j.jaad.2010.01.049. Epub 2011 Feb 3.
The diagnosis of pyoderma gangrenosum (PG) can be exceedingly difficult, and misdiagnosis can potentially yield serious consequences. Clinical criteria for establishing a reliable diagnosis have been previously proposed, but a consensus in their application has yet to be reached.
We sought to review recent trends in diagnosing PG and compare them with previously suggested diagnostic criteria.
Data for this article were obtained by searching the PubMed database using the key words "pyoderma gangrenosum." Our search was limited to adult case reports that appeared in the English-language literature and received a final diagnosis of PG. The full text of the latest published 30 case reports that fulfilled these search criteria was reviewed. The articles spanned the years 2008 and 2009. Clinical features that appeared in the case descriptions were summarized and compared with the diagnostic criteria for the disease that were previously proposed.
Of the 30 case reports, 16 described ulcers involving one or both legs, whereas only one case had peristomal involvement. Although 8 cases were associated with inflammatory bowel disease, 11 of the 30 patients did not have a systemic comorbidity. Fifteen lesions were noted to manifest at sites of trauma, which ranged from surgical incision sites to prolonged seatbelt compression. Nine case reports mentioned an undermined border in their clinical description, whereas only 5 authors commented on pustules and 6 described a purulent discharge. Only two authors commented on cribriform scarring.
We only reviewed the latest published 30 case reports. Case series, which may have shown more typical cases, were excluded.
Currently, there is an underemphasis of clinical features in the diagnosis of PG, which can potentially lead to overdiagnosis. Establishing firm clinical criteria for diagnosing PG will ensure that case reports describe the same disease. This has implications in optimizing treatment strategies and improving patient outcomes.
坏疽性脓皮病(PG)的诊断极为困难,误诊可能会产生严重后果。之前已经提出了用于确立可靠诊断的临床标准,但尚未达成对其应用的共识。
我们旨在回顾 PG 的诊断近期趋势,并将其与之前提出的诊断标准进行比较。
本文的数据是通过在 PubMed 数据库中使用关键词“pyoderma gangrenosum”进行搜索获得的。我们的搜索仅限于在英语文献中发表的、最终诊断为 PG 的成人病例报告。对符合这些搜索标准的最新发表的 30 例病例报告的全文进行了回顾。这些文章的时间跨度为 2008 年至 2009 年。总结了病例描述中出现的临床特征,并与之前提出的疾病诊断标准进行了比较。
在 30 例病例报告中,有 16 例描述了累及一条或两条腿的溃疡,而仅有 1 例涉及造口周围。虽然有 8 例与炎症性肠病有关,但 30 例患者中有 11 例没有系统性合并症。15 处病变发生在创伤部位,范围从手术切口到长时间安全带压迫。9 份病例报告在其临床描述中提到了边缘潜行,而只有 5 位作者提到了脓疱,6 位作者描述了脓性分泌物。只有 2 位作者提到了筛状瘢痕。
我们仅回顾了最新发表的 30 例病例报告。排除了可能显示更典型病例的病例系列。
目前,PG 的诊断中对临床特征的重视不足,这可能导致过度诊断。确立 PG 诊断的明确临床标准将确保病例报告描述的是同一种疾病。这对优化治疗策略和改善患者结局具有重要意义。