Suppr超能文献

肺结节病晚期。

The late stages of pulmonary sarcoidosis.

作者信息

Scadding J G

出版信息

Postgrad Med J. 1970 Aug;46(538):530-6. doi: 10.1136/pgmj.46.538.530.

Abstract

Pulmonary sarcoidosis is frequently preceded by bilateral hilar lymph-node enlargement (BHL). Although it is normally difficult to be certain in a patient without BHL that a stage of BHL has not in fact occurred in the past but been missed, there is good evidence that some cases of pulmonary sarcoidosis arise without preceding BHL. Although a prefibrotic infiltration of the lungs will usually show signs either of resolution or of developing fibrosis within 2 years, such an infiltration may remain apparently non-progressive, producing little functional defect, for much longer than this, and in such a case, substantial resolution remains possible. A high proportion of those who develop fibrosis show a characteristic pattern of strand-like fibrosis in the middle zones and lower part of the upper zones of the lungs, with emphysematous changes above and below. In densely fibrotic parts of the lungs, cavities may appear, probably from necrosis at the centres of large masses of hyaline fibrosis. A rare complication is the development of a ‘fungus ball’ due to the growth of in such a cavity. Occasionally, fine focal fibrosis develops without distortion of lung architecture, but with severe disability. A rare but important event is the development of bronchial stenoses. These may affect main, segmental or subsegmental bronchi, more especially the proximal parts of segmental or subsegmental bronchi. Calcification has been observed to develop in a characteristic symmetrical fashion in the hilar lymphnodes and occasionally in small foci in the lungs in about 5% of patients with pulmonary sarcoidosis who initially had BHL, followed for periods ranging from 5 to 20 years. In the late stages of sarcoid fibrosis of the lungs, the specific granuloma may be no longer convincingly demonstrable.

摘要

肺结节病常常先出现双侧肺门淋巴结肿大(BHL)。虽然对于没有BHL的患者,通常很难确定实际上过去未曾发生过BHL阶段而只是被漏诊,但有充分证据表明,一些肺结节病病例在没有先前BHL的情况下就会出现。尽管肺部的纤维化前期浸润通常会在2年内显示出消退或发展为纤维化的迹象,但这种浸润可能在更长时间内保持明显无进展状态,产生很少的功能缺陷,在这种情况下,仍有可能出现实质性消退。很大一部分发生纤维化的患者在肺上叶中部和下部呈现出特征性的条索状纤维化模式,其上方和下方有肺气肿改变。在肺部纤维化致密的部位,可能会出现空洞,这可能是由于大量透明样纤维化中心的坏死所致。一种罕见的并发症是由于这种空洞内真菌生长而形成“真菌球”。偶尔,会出现微小局灶性纤维化,而肺结构无扭曲,但伴有严重残疾。一种罕见但重要的情况是出现支气管狭窄。这些狭窄可能影响主支气管、段支气管或亚段支气管,尤其是段支气管或亚段支气管的近端部分。在最初有BHL且随访5至20年的约5%的肺结节病患者中,已观察到肺门淋巴结以特征性的对称方式发生钙化,偶尔肺部也会出现小的钙化灶。在肺结节病纤维化的晚期,可能不再能令人信服地显示出特异性肉芽肿。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e631/2467273/d96d1e66f632/postmedj00356-0078-a.jpg

引用本文的文献

2
Establishing a Diagnosis of Pulmonary Sarcoidosis.确立肺结节病的诊断
J Clin Med. 2023 Nov 2;12(21):6898. doi: 10.3390/jcm12216898.
4
Immune mechanisms in fibrotic pulmonary sarcoidosis.纤维化性肺结节病中的免疫机制。
Eur Respir Rev. 2022 Dec 21;31(166). doi: 10.1183/16000617.0178-2022. Print 2022 Dec 31.

本文引用的文献

1
Calcification in sarcoidosis.结节病中的钙化
Tubercle. 1961 Jun;42:121-35. doi: 10.1016/s0041-3879(61)80088-3.
3
A 'burnt-out' case of sarcoidosis.一例结节病“耗竭型”病例。
Postgrad Med J. 1968 Jan;44(507):105-8. doi: 10.1136/pgmj.44.507.105.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验