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Articles by Ho Cheol
Case Report: Concurrent breast myeloid sarcoma and ductal carcinoma in situ —multimodality imaging findings and differential treatment response
Abstract Myeloid sarcoma (MS) is an uncommon extramedullary manifestation of myeloid neoplasms, and breast involvement is rare. We report concurrent breast MS and ductal carcinoma in situ (DCIS) in a 49-year-old woman who was referred for evaluation of cervical lymphadenopathy and subsequently underwent breast imaging for a rapidly enlarging palpable left breast mass.
The potential clinical implications of slow vital capacity in patients with idiopathic pulmonary fibrosis - Respiratory Research
References Kim HJ, Perlman D, Tomic R. Natural history of idiopathic pulmonary fibrosis. Respir Med. 2015;109:661–70. Article PubMed Google Scholar Raghu G, Ghazipura M, Fleming TR, Aronson KI, Behr J, Brown KK, Flaherty KR, Kazerooni EA, Maher TM, Richeldi L et al. Meaningful Endpoints for Idiopathic Pulmonary Fibrosis (IPF) Clinical Trials: Emphasis on ‘Feels, Functions, Survives’.
Incidence and clinical impact of coronary artery disease confirmed by coronary CT angiography in patients with interstitial lung disease - BMC Pulmonary Medicine
References Maher TM. Interstitial lung disease: a review. JAMA. 2024;331:1655–65. Article CAS PubMed Google Scholar Collins BF, Raghu G. Antifibrotic therapy for fibrotic lung disease beyond idiopathic pulmonary fibrosis. Eur Respir Rev. 2019;28. Khor YH, Ng Y, Barnes H, Goh NSL, McDonald CF, Holland AE. Prognosis of idiopathic pulmonary fibrosis without anti-fibrotic therapy: a systematic review. Eur Respir Rev. 2020;29. Rajan SK, Cottin V, Dhar R, Danoff S, Flaherty KR, Brown KK et al.
Clinical characteristics and outcome of lung cancer in patients with fibrosing interstitial lung disease - BMC Pulmonary Medicine
Among the 163 patients, 92 (56.4%) had IPF ILD and 71 (43.6%) had non-IPF ILD. The median follow-up period after LC diagnosis was 11 months. The shortest follow-up period was 1 month, and the longest duration was 64 months. The non-IPF group included patients with unclassified ILD (n = 54), CTD-ILD (n = 14), nonspecific interstitial pneumonia (n = 2), and chronic hypersensitivity pneumonitis (n = 1). The patients’ baseline characteristics at the time of LC diagnosis are summarized in Table 1.
Clinical impact of pre-existing acute exacerbation in patients with interstitial lung disease who underwent lung transplantation - Respiratory Research
This single-center, retrospective study analyzed the data of patients with ILD who underwent bilateral lung transplantation at Asan Medical Center, Seoul, Republic of Korea, from October 2008 to January 2022. Two patients who underwent heart–lung transplantation were excluded from the study. The study period was concluded on January 31, 2022, to ensure that all patients had at least 1 year of follow-up data after the transplantation.
Clinical impact of weight loss on mortality in patients with idiopathic pulmonary fibrosis: a retrospective cohort study
Scientific Reports, Apr 2023 This is a preview of a remote PDF: https://www.nature.com/articles/s41598-023-32843-7.pdf Lee, Ju Kwang, Chung, Chiwook, Kim, Jiwon, Cho, Hyo Sin, Kim, Ho Cheol. , Scientific Reports, DOI: 10.1038/s41598-023-32843-7
Epidemiology and comorbidities in idiopathic pulmonary fibrosis: a nationwide cohort study - BMC Pulmonary Medicine
References Raghu G, Remy-Jardin M, Myers JL, Richeldi L, Ryerson CJ, Lederer DJ, Behr J, Cottin V, Danoff SK, Morell F, et al. Diagnosis of idiopathic pulmonary fibrosis: an official ATS/ERS/JRS/ALAT clinical practice guideline. Am J Respir Crit Care Med. 2018;198(5):e44–68. Google Scholar Maher TM, Bendstrup E, Dron L, Langley J, Smith G, Khalid JM, Patel H, Kreuter M. Global incidence and prevalence of idiopathic pulmonary fibrosis. Respir Res. 2021;22(1):197.
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