Suppr超能文献

导致严重肺功能受限的慢性胸膜炎:德戈斯病的一种罕见并发症。

Chronic pleuritis leading to severe pulmonary restriction: a rare complication of Degos disease.

作者信息

Saha Biplab Kumar, Beegle Scott

机构信息

Pulmonary and Critical Care Medicine, Albany Medical Center Hospital, Albany, New York, USA

Pulmonary and Critical Care Medicine, Albany Medical Center Hospital, Albany, New York, USA.

出版信息

BMJ Case Rep. 2019 Dec 8;12(12):e232759. doi: 10.1136/bcr-2019-232759.

Abstract

This case demonstrates chronic fibrosing pleuritis, as a rare pulmonary aetiology for mortality in patients with Degos disease or malignant atrophic papulosis (MAP). Knowledge of this unusual complication will help physicians identify this entity early and provide appropriate treatment.Patients with MAP die from gastrointestinal and brain involvement within 2-3 years of diagnosis. This case is unique as the patient survived for 9 years and died secondary to respiratory failure, which had not been reported before. Our patient was a young man, diagnosed with MAP at the age of 17. His skin and gastrointestinal disease were controlled with eculizumab and parenteral treprostinil. The patient developed severe restrictive pulmonary disease, required ventilatory support, and died from respiratory failure. An autopsy revealed chronic fibrosis pleuritis. Longer surviving patients with MAP might suffer from significant respiratory disease. Pulmonary function test should be obtained to identify subclinical respiratory limitation.

摘要

本病例显示了慢性纤维化胸膜炎,这是德戈斯病或恶性萎缩性丘疹病(MAP)患者罕见的肺部死亡病因。了解这种不寻常的并发症将有助于医生早期识别该病症并提供适当治疗。MAP患者在诊断后2至3年内死于胃肠道和脑部受累。该病例独特之处在于患者存活了9年,死于呼吸衰竭,此前未见报道。我们的患者是一名年轻男性,17岁时被诊断为MAP。他的皮肤和胃肠道疾病通过依库珠单抗和肠外曲前列尼尔得到控制。患者出现严重的限制性肺病,需要通气支持,最终死于呼吸衰竭。尸检显示慢性纤维化胸膜炎。存活时间较长的MAP患者可能患有严重的呼吸系统疾病。应进行肺功能测试以识别亚临床呼吸受限。

相似文献

1
Chronic pleuritis leading to severe pulmonary restriction: a rare complication of Degos disease.
BMJ Case Rep. 2019 Dec 8;12(12):e232759. doi: 10.1136/bcr-2019-232759.
4
Pediatric Malignant Atrophic Papulosis.
Pediatrics. 2018 Apr;141(Suppl 5):S481-S484. doi: 10.1542/peds.2016-4206.
5
Exploring the pathophysiologic basis of constrictive pericarditis of Kohlmeier Degos disease: A case series and review of the literature.
Ann Diagn Pathol. 2022 Aug;59:151943. doi: 10.1016/j.anndiagpath.2022.151943. Epub 2022 Mar 28.
6
Diffuse atrophic papules and plaques, intermittent abdominal pain, paresthesias, and cardiac abnormalities in a 55-year-old woman.
J Am Acad Dermatol. 2016 Dec;75(6):1274-1277. doi: 10.1016/j.jaad.2016.09.015. Epub 2016 Oct 4.
7
The effects of Eculizumab on the pathology of malignant atrophic papulosis.
Orphanet J Rare Dis. 2013 Nov 26;8:185. doi: 10.1186/1750-1172-8-185.
8
A fatal case of malignant atrophic papulosis in a pediatric patient.
Pediatr Dermatol. 2022 Jan;39(1):112-114. doi: 10.1111/pde.14878. Epub 2021 Dec 21.

引用本文的文献

1
Gastrointestinal Kohlmeier-Degos disease: a narrative review.
Orphanet J Rare Dis. 2022 Apr 20;17(1):172. doi: 10.1186/s13023-022-02322-9.

本文引用的文献

1
The effects of Eculizumab on the pathology of malignant atrophic papulosis.
Orphanet J Rare Dis. 2013 Nov 26;8:185. doi: 10.1186/1750-1172-8-185.
3
Malignant atrophic papulosis (Köhlmeier-Degos disease) - a review.
Orphanet J Rare Dis. 2013 Jan 14;8:10. doi: 10.1186/1750-1172-8-10.
4
Systemic diseases and the pleura.
Arch Bronconeumol. 2011 Jul;47(7):361-70. doi: 10.1016/j.arbres.2011.02.010. Epub 2011 Apr 17.
5
Degos disease: a C5b-9/interferon-α-mediated endotheliopathy syndrome.
Am J Clin Pathol. 2011 Apr;135(4):599-610. doi: 10.1309/AJCP66QIMFARLZKI.
10
Lesions resembling malignant atrophic papulosis in a patient with dermatomyositis.
J Am Acad Dermatol. 1997 Feb;36(2 Pt 2):317-9. doi: 10.1016/s0190-9622(97)80407-0.

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