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戒烟后仍从单系统形式进展为多系统形式的肺朗格汉斯细胞组织细胞增生症。

Pulmonary Langerhans Cell Histiocytosis That Progressed from a Single-system to a Multisystem Form despite Smoking Cessation.

机构信息

Department of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Japan.

Department of Pathology, Nagasaki University Graduate School of Biomedical Sciences, Japan.

出版信息

Intern Med. 2023 Mar 15;62(6):877-880. doi: 10.2169/internalmedicine.0139-22. Epub 2022 Aug 10.

DOI:10.2169/internalmedicine.0139-22
PMID:35945010
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10076126/
Abstract

A 36-year-old Japanese man presented with cavities and nodular shadows in the lower lobes of his lungs and osteolytic lesions in the thoracic spine. He was diagnosed with multisystem Langerhans cell histiocytosis (LCH). Three years earlier, he had been noted to have small cavities and granular lesions noted in the upper lobes of his lungs, which later improved with smoking cessation. It was likely that his single-system pulmonary LCH (PLCH) progressed to multisystem LCH despite smoking cessation. Relapse or progression may occur in cases where PLCH lesions improve after smoking cessation. Thus, close follow-up is vital.

摘要

一位 36 岁的日本男性因肺部下叶的空洞和结节状阴影以及胸腰椎的溶骨性病变就诊。他被诊断为多系统朗格汉斯细胞组织细胞增生症(LCH)。三年前,他曾被发现肺部上叶有小空洞和颗粒状病变,后来戒烟后有所改善。尽管他已经戒烟,但他的单系统肺朗格汉斯细胞组织细胞增生症(PLCH)仍有可能进展为多系统 LCH。在戒烟后 PLCH 病变改善的情况下,可能会出现复发或进展。因此,密切随访至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32fc/10076126/43428acbe1cf/1349-7235-62-0877-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32fc/10076126/4f00604a34e3/1349-7235-62-0877-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32fc/10076126/d755c7810f1d/1349-7235-62-0877-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32fc/10076126/43428acbe1cf/1349-7235-62-0877-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32fc/10076126/4f00604a34e3/1349-7235-62-0877-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32fc/10076126/d755c7810f1d/1349-7235-62-0877-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32fc/10076126/43428acbe1cf/1349-7235-62-0877-g003.jpg

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本文引用的文献

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International expert consensus recommendations for the diagnosis and treatment of Langerhans cell histiocytosis in adults.国际专家共识建议:成人朗格汉斯细胞组织细胞增生症的诊断与治疗。
Blood. 2022 Apr 28;139(17):2601-2621. doi: 10.1182/blood.2021014343.
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Langerhans cell histiocytosis with lung involvement in isolation and multisystem disease: Staging, natural history, and comparative survival.孤立性肺受累与多系统疾病的朗格汉斯细胞组织细胞增生症:分期、自然病程和比较生存。
Am J Hematol. 2021 Dec 1;96(12):1604-1610. doi: 10.1002/ajh.26355. Epub 2021 Oct 8.
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Langerhans cell histiocytosis.
朗格汉斯细胞组织细胞增生症。
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Eur Respir J. 2020 Feb 27;55(2). doi: 10.1183/13993003.01190-2019. Print 2020 Feb.
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How I manage pulmonary Langerhans cell histiocytosis.我如何治疗肺朗格汉斯细胞组织细胞增多症。
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Orphanet J Rare Dis. 2015 Mar 14;10:30. doi: 10.1186/s13023-015-0249-2.
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A prospective clinical multicentre study on adult pulmonary Langerhans' cell histiocytosis.一项关于成人肺部朗格汉斯细胞组织细胞增多症的前瞻性临床多中心研究。
Sarcoidosis Vasc Diffuse Lung Dis. 2012 Oct;29(2):132-8.
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