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Value of diffusion‐weighted imaging in diagnosis and therapy response assessment of hepatic fungal infection in patients with acute leukemia

OBJECTIVE: To investigate the role of diffusion‐weighted imaging (DWI) for diagnosis and posttreatment assessment of hepatic fungal infection in patients with acute leukemia. METHODS: Patients with acute leukemia and highly suspected hepatic fungal infection were collected in the study. All the pati...

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Autores principales: Wang, Haoyu, Yu, Haitao, Bai, Dong, Yao, Dan, Han, Yongjun, Shi, Yichao, Wang, Zhiqun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132180/
https://www.ncbi.nlm.nih.gov/pubmed/37102666
http://dx.doi.org/10.1002/iid3.843
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author Wang, Haoyu
Yu, Haitao
Bai, Dong
Yao, Dan
Han, Yongjun
Shi, Yichao
Wang, Zhiqun
author_facet Wang, Haoyu
Yu, Haitao
Bai, Dong
Yao, Dan
Han, Yongjun
Shi, Yichao
Wang, Zhiqun
author_sort Wang, Haoyu
collection PubMed
description OBJECTIVE: To investigate the role of diffusion‐weighted imaging (DWI) for diagnosis and posttreatment assessment of hepatic fungal infection in patients with acute leukemia. METHODS: Patients with acute leukemia and highly suspected hepatic fungal infection were collected in the study. All the patients underwent MRI examination, including initial and follow‐up DWI. The apparent diffusion coefficient (ADC) values of the lesions and the normal liver parenchyma were compared using Student's t‐test. The ADC values of the hepatic fungal lesions of pretreatment and posttreatment were compared using paired t‐test. RESULTS: A total of 13 patients with hepatic fungal infections have enrolled this study. Hepatic lesions were rounded or oval shaped, measured from 0.3 to 3 cm in diameter. The lesions showed significantly hyperintense signal on DWI and markedly hypointense signal on the ADC map, reflecting a marked restricted diffusion. The mean ADC values of the lesions were significantly lower than those of normal liver parenchyma (1.08 ± 0.34 × 10(−3) vs. 1.98 ± 0.12 × 10(−3) mm(2)/s, p < 0.001). After treatment, the mean ADC values of the lesions were significantly increased when comparing with those of pretreatment (1.39 ± 0.29 × 10(−3) vs. 1.06 ± 0.10 × 10(−3) mm(2)/s, p = .016). CONCLUSION: DWI can provide diffusion information of hepatic fungal infection in patients with acute leukemia, which could be taken as a valuable tool for diagnosis and therapy response assessment of these patients.
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spelling pubmed-101321802023-04-27 Value of diffusion‐weighted imaging in diagnosis and therapy response assessment of hepatic fungal infection in patients with acute leukemia Wang, Haoyu Yu, Haitao Bai, Dong Yao, Dan Han, Yongjun Shi, Yichao Wang, Zhiqun Immun Inflamm Dis Original Articles OBJECTIVE: To investigate the role of diffusion‐weighted imaging (DWI) for diagnosis and posttreatment assessment of hepatic fungal infection in patients with acute leukemia. METHODS: Patients with acute leukemia and highly suspected hepatic fungal infection were collected in the study. All the patients underwent MRI examination, including initial and follow‐up DWI. The apparent diffusion coefficient (ADC) values of the lesions and the normal liver parenchyma were compared using Student's t‐test. The ADC values of the hepatic fungal lesions of pretreatment and posttreatment were compared using paired t‐test. RESULTS: A total of 13 patients with hepatic fungal infections have enrolled this study. Hepatic lesions were rounded or oval shaped, measured from 0.3 to 3 cm in diameter. The lesions showed significantly hyperintense signal on DWI and markedly hypointense signal on the ADC map, reflecting a marked restricted diffusion. The mean ADC values of the lesions were significantly lower than those of normal liver parenchyma (1.08 ± 0.34 × 10(−3) vs. 1.98 ± 0.12 × 10(−3) mm(2)/s, p < 0.001). After treatment, the mean ADC values of the lesions were significantly increased when comparing with those of pretreatment (1.39 ± 0.29 × 10(−3) vs. 1.06 ± 0.10 × 10(−3) mm(2)/s, p = .016). CONCLUSION: DWI can provide diffusion information of hepatic fungal infection in patients with acute leukemia, which could be taken as a valuable tool for diagnosis and therapy response assessment of these patients. John Wiley and Sons Inc. 2023-04-26 /pmc/articles/PMC10132180/ /pubmed/37102666 http://dx.doi.org/10.1002/iid3.843 Text en © 2023 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Wang, Haoyu
Yu, Haitao
Bai, Dong
Yao, Dan
Han, Yongjun
Shi, Yichao
Wang, Zhiqun
Value of diffusion‐weighted imaging in diagnosis and therapy response assessment of hepatic fungal infection in patients with acute leukemia
title Value of diffusion‐weighted imaging in diagnosis and therapy response assessment of hepatic fungal infection in patients with acute leukemia
title_full Value of diffusion‐weighted imaging in diagnosis and therapy response assessment of hepatic fungal infection in patients with acute leukemia
title_fullStr Value of diffusion‐weighted imaging in diagnosis and therapy response assessment of hepatic fungal infection in patients with acute leukemia
title_full_unstemmed Value of diffusion‐weighted imaging in diagnosis and therapy response assessment of hepatic fungal infection in patients with acute leukemia
title_short Value of diffusion‐weighted imaging in diagnosis and therapy response assessment of hepatic fungal infection in patients with acute leukemia
title_sort value of diffusion‐weighted imaging in diagnosis and therapy response assessment of hepatic fungal infection in patients with acute leukemia
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132180/
https://www.ncbi.nlm.nih.gov/pubmed/37102666
http://dx.doi.org/10.1002/iid3.843
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