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肺泡毛细血管发育不良诊断中的毛细血管贴附和密度

Capillary apposition and density in the diagnosis of alveolar capillary dysplasia.

作者信息

Melly L, Sebire N J, Malone M, Nicholson A G

机构信息

Department of Histopathology, Royal Free Hospital, London, UK.

出版信息

Histopathology. 2008 Oct;53(4):450-7. doi: 10.1111/j.1365-2559.2008.03134.x.

Abstract

AIM

Alveolar capillary dysplasia (ACD) is a rare disorder, typically presenting with persistent pulmonary hypertension of the newborn. The aim was to characterise further the histological features of patients suspected of having ACD and to correlate histopathological features with outcome.

METHODS AND RESULTS

Three pathologists retrospectively reviewed 21 surgical lung biopsy specimens (SLBx) where ACD entered the differential diagnosis. Semi-quantitative assessment showed that there was a spectrum of muscular arterial hypertrophy, capillary apposition to epithelium and capillary density within the interstitium, with the latter being more disordered in ACD. Misalignment of pulmonary vessels was also frequently seen. Four of 19 patients survived beyond the neonatal period, these having higher degrees of capillary apposition and density. Associated extrapulmonary abnormalities were common, most frequently with ACD.

CONCLUSION

Poor capillary apposition and density, allied with medial arterial hypertrophy and misalignment of pulmonary vessels are the strongest diagnostic features of ACD. Of the four patients alive, all had high capillary apposition and density, suggesting that these features may be of prognostic value. SLBx remains useful in such cases as it may help predict patients who survive the neonatal period and also identify patients with disorders that are not primarily vascular anomalies.

摘要

目的

肺泡毛细血管发育不良(ACD)是一种罕见疾病,通常表现为新生儿持续性肺动脉高压。目的是进一步描述疑似患有ACD患者的组织学特征,并将组织病理学特征与预后相关联。

方法与结果

三位病理学家回顾性分析了21例手术肺活检标本(SLBx),这些标本的鉴别诊断包括ACD。半定量评估显示,存在一系列肌性动脉肥大、毛细血管与上皮的贴附以及间质内的毛细血管密度情况,后者在ACD中更为紊乱。肺血管排列异常也很常见。19例患者中有4例存活至新生儿期以后,这些患者的毛细血管贴附和密度程度更高。肺外相关异常很常见,最常与ACD相关。

结论

毛细血管贴附和密度差,伴有肌性动脉肥大和肺血管排列异常是ACD最有力的诊断特征。在存活的4例患者中,所有患者的毛细血管贴附和密度都很高,这表明这些特征可能具有预后价值。SLBx在这类病例中仍然有用,因为它可能有助于预测存活至新生儿期的患者,并识别那些并非主要是血管异常疾病的患者。

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