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十二指肠假性脂肪肥厚症。一种非常罕见的发现的文献复习及病例报告。

Duodenal pseudolipomatosis. Literature review and case report of a very unusual finding.

机构信息

Pathology, Hospital Universitario Reina Sofía, España.

Pathology, Hospital Universitario Reina Sofía.

出版信息

Rev Esp Enferm Dig. 2024 Oct;116(10):562-563. doi: 10.17235/reed.2024.10673/2024.

Abstract

Pseudolipomatosis (PL) is a rare, benign, iatrogenic condition first described in colorectal mucosa. This condition is thought to arise from gas penetration into the mucosa due to mechanical or chemical injury during endoscopy. Despite these associations and its characteristic appearence, the definitive pathogenesis remains unclear and it continues to be underrecognized by some pathologists and endoscopists, which is crucial to avoid any further unnecessary treatments. Immunohistochemistry techniques play a role in differentiating PL from similar conditions such as cystic intestinal pneumatosis, intestinal lipomatosis, or lymphangiectasia. A 70-year-old man with a family history of colon adenocarcinoma was diagnosed with duodenal pseudolipomatosis after a routine endoscopic assessment. To the best of our knowledge, there have been only two reports of PL diagnosed in the duodenum. A review of over 500 duodenal biopsies at our centre revealed that no other instances were identified, emphasizing the unusual occurrence of this particular location.

摘要

假性脂肪肥厚症(PL)是一种罕见的良性医源性疾病,最初在结直肠黏膜中描述。这种情况被认为是由于内镜检查过程中机械或化学损伤导致气体穿透黏膜引起的。尽管存在这些关联及其特征性表现,但确切的发病机制仍不清楚,一些病理学家和内镜医生对此认识不足,这对于避免任何不必要的进一步治疗至关重要。免疫组织化学技术在将 PL 与类似疾病(如囊性肠气肿、肠脂肪肥厚症或淋巴管扩张症)区分开来方面发挥着作用。一名 70 岁男性,有结直肠癌家族史,在常规内镜评估后被诊断为十二指肠假性脂肪肥厚症。据我们所知,仅有两例 PL 被诊断为十二指肠病变。我们中心对超过 500 例十二指肠活检的回顾显示,没有发现其他病例,这强调了这种特定部位的罕见性。

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