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提高胸腔子宫内膜异位症的诊断识别:聚焦新的组织形态学指标。

Improving the diagnostic recognition of thoracic endometriosis: Spotlight on a new histo-morphological indicator.

机构信息

Department of Morbid Anatomy, University of Nigeria Teaching Hospital, Ituku/Ozalla, Enugu State, Nigeria.

Division of Cardiothoracic Surgery, National Cardiothoracic Centre, University of Nigeria Teaching Hospital, Ituku/Ozalla, Enugu State, Nigeria.

出版信息

PLoS One. 2021 May 13;16(5):e0251385. doi: 10.1371/journal.pone.0251385. eCollection 2021.

DOI:10.1371/journal.pone.0251385
PMID:33984033
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8118331/
Abstract

The diagnosis of thoracic endometriosis (TE) is challenging, hence resulting in under-diagnosis as well as long delays before arriving at a correct definitive diagnosis. Our aim is to review the histopathological findings in TE, summarise the diagnostic features, identify any major histo-morphological indicator(s) hitherto unrecognised as such, suggest diagnostic criteria; all with the aim of improving the diagnostic capacity and reducing observer error even where the clinical suspicion is low. A case-control study in which a search in the pathology archives of a referral hospital over a 10-year period was conducted. Twenty-six cases of TE were identified, reviewed, and compared with a control population of 48 cases taken from common benign thoracic diseases. Nine notable histological features were identified in varying permutations in the test group, namely: endometrioid glands, lymphoid clusters, ceroid macrophages, siderophages, cholesterol crystals, capillary congestion, multinucleated giant cells, smooth muscle bundles and fibrosis. The first 6 features were frequent; each being present in over 13 (13/26; 50%) test cases. The first 8 features showed significant association with TE by the Chi-squared test (P<0.05). In this group, the strength of association is high for the first 4 features (Cramér's V≥0.5). The presence of ceroid macrophages is shown to be a novel key feature, previously unrecognised as such, for the identification of TE. The presence of any three of four features including endometrioid glands, lymphoid clusters, ceroid macrophages and siderophages is a suggested criterion for the definitive diagnosis of TE.

摘要

胸子宫内膜异位症(TE)的诊断具有挑战性,因此导致诊断不足以及在得出正确明确诊断之前的长时间延迟。我们的目的是回顾 TE 的组织病理学发现,总结诊断特征,识别迄今为止尚未被识别为这种特征的任何主要组织形态学指标,并提出诊断标准;所有这些都是为了提高诊断能力并减少观察者的错误,即使临床怀疑很低。这是一项病例对照研究,其中对一家转诊医院的病理档案进行了为期 10 年的搜索。确定了 26 例 TE 病例,进行了回顾,并与从常见良性胸科疾病中抽取的 48 例对照组进行了比较。在实验组中发现了 9 种不同排列的显著组织学特征,即:子宫内膜样腺体、淋巴簇、类脂质巨噬细胞、含铁血黄素巨噬细胞、胆固醇晶体、毛细血管充血、多核巨细胞、平滑肌束和纤维化。前 6 种特征较为常见;每种特征均存在于超过 13 例(26/26;50%)实验组病例中。前 8 种特征通过卡方检验与 TE 具有显著相关性(P<0.05)。在该组中,前 4 种特征的关联强度较高(Cramér's V≥0.5)。类脂质巨噬细胞的存在被证明是识别 TE 的一个新的关键特征,以前尚未被识别为这种特征。存在任何三种或四种特征,包括子宫内膜样腺体、淋巴簇、类脂质巨噬细胞和含铁血黄素巨噬细胞,是 TE 明确诊断的建议标准。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a8d/8118331/4233088653a2/pone.0251385.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a8d/8118331/336a73277d5d/pone.0251385.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a8d/8118331/1b9496754bf9/pone.0251385.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a8d/8118331/b47b4c38295c/pone.0251385.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a8d/8118331/35ef0664631c/pone.0251385.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a8d/8118331/4233088653a2/pone.0251385.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a8d/8118331/336a73277d5d/pone.0251385.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a8d/8118331/1b9496754bf9/pone.0251385.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a8d/8118331/b47b4c38295c/pone.0251385.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a8d/8118331/35ef0664631c/pone.0251385.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a8d/8118331/4233088653a2/pone.0251385.g005.jpg

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Diagnosis of thoracic endometriosis with immunohistochemistry.免疫组织化学法诊断胸段子宫内膜异位症
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Catamenial pneumothorax caused by thoracic endometriosis.由胸腔子宫内膜异位症引起的经期气胸。
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Catamenial pneumothorax revealing diaphragmatic endometriosis: a case report and revue of literature.月经性气胸揭示膈肌子宫内膜异位症:一例报告及文献综述
Pan Afr Med J. 2017 Jun 14;27:112. doi: 10.11604/pamj.2017.27.112.8007. eCollection 2017.
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