Allogeneic hematopoietic stem cell transplantation for treating severe lung involvement in Gaucher disease
To provide strategies for monitoring and treating severe lung involvement in Gaucher disease. We reviewed the chart of a 5-year-old boy who developed rapidly progressive, severe infiltrative lung involvement of Gaucher disease (GD) and improved after allogeneic hematopoietic stem cell transplant (HS...
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Published in | Molecular genetics and metabolism reports Vol. 25; p. 100652 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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01.12.2020
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Abstract | To provide strategies for monitoring and treating severe lung involvement in Gaucher disease.
We reviewed the chart of a 5-year-old boy who developed rapidly progressive, severe infiltrative lung involvement of Gaucher disease (GD) and improved after allogeneic hematopoietic stem cell transplant (HSCT), along with other case studies reported before December 2019. He was diagnosed with GD (homozygous mutation at c.1448 T > C, p.L483P), and started receiving enzyme replacement therapy (ERT) at 17 months old. He developed respiratory distress symptoms after 45 months of ERT; chest imaging reported diffuse interstitial infiltration of the bilateral lungs and consolidations at the right lungs. Allogeneic HSCT using cells from a matched unrelated donor was performed four months upon progressive respiratory symptoms.
His respiratory symptoms subsided in one month; chest imaging improvement, pulmonary function test improvement, and normalized activity of β-glucocerebrosidase were reported in three months.
This is the first report of a patient who received early and regular ERT but developed severe infiltrative lung involvement and recovered after allogeneic HSCT. Based on study results, we suggest regular chest imaging, even for asymptomatic patients. For patients with severe lung involvement, rapid deterioration, and unresponsive to higher ERT dosages, allogeneic HSCT should be considered. |
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AbstractList | Objective: To provide strategies for monitoring and treating severe lung involvement in Gaucher disease. Study design: We reviewed the chart of a 5-year-old boy who developed rapidly progressive, severe infiltrative lung involvement of Gaucher disease (GD) and improved after allogeneic hematopoietic stem cell transplant (HSCT), along with other case studies reported before December 2019. He was diagnosed with GD (homozygous mutation at c.1448 T > C, p.L483P), and started receiving enzyme replacement therapy (ERT) at 17 months old. He developed respiratory distress symptoms after 45 months of ERT; chest imaging reported diffuse interstitial infiltration of the bilateral lungs and consolidations at the right lungs. Allogeneic HSCT using cells from a matched unrelated donor was performed four months upon progressive respiratory symptoms. Results: His respiratory symptoms subsided in one month; chest imaging improvement, pulmonary function test improvement, and normalized activity of β-glucocerebrosidase were reported in three months. Conclusion: This is the first report of a patient who received early and regular ERT but developed severe infiltrative lung involvement and recovered after allogeneic HSCT. Based on study results, we suggest regular chest imaging, even for asymptomatic patients. For patients with severe lung involvement, rapid deterioration, and unresponsive to higher ERT dosages, allogeneic HSCT should be considered. To provide strategies for monitoring and treating severe lung involvement in Gaucher disease. We reviewed the chart of a 5-year-old boy who developed rapidly progressive, severe infiltrative lung involvement of Gaucher disease (GD) and improved after allogeneic hematopoietic stem cell transplant (HSCT), along with other case studies reported before December 2019. He was diagnosed with GD (homozygous mutation at c.1448 T > C, p.L483P), and started receiving enzyme replacement therapy (ERT) at 17 months old. He developed respiratory distress symptoms after 45 months of ERT; chest imaging reported diffuse interstitial infiltration of the bilateral lungs and consolidations at the right lungs. Allogeneic HSCT using cells from a matched unrelated donor was performed four months upon progressive respiratory symptoms. His respiratory symptoms subsided in one month; chest imaging improvement, pulmonary function test improvement, and normalized activity of β-glucocerebrosidase were reported in three months. This is the first report of a patient who received early and regular ERT but developed severe infiltrative lung involvement and recovered after allogeneic HSCT. Based on study results, we suggest regular chest imaging, even for asymptomatic patients. For patients with severe lung involvement, rapid deterioration, and unresponsive to higher ERT dosages, allogeneic HSCT should be considered. OBJECTIVETo provide strategies for monitoring and treating severe lung involvement in Gaucher disease. STUDY DESIGNWe reviewed the chart of a 5-year-old boy who developed rapidly progressive, severe infiltrative lung involvement of Gaucher disease (GD) and improved after allogeneic hematopoietic stem cell transplant (HSCT), along with other case studies reported before December 2019. He was diagnosed with GD (homozygous mutation at c.1448 T > C, p.L483P), and started receiving enzyme replacement therapy (ERT) at 17 months old. He developed respiratory distress symptoms after 45 months of ERT; chest imaging reported diffuse interstitial infiltration of the bilateral lungs and consolidations at the right lungs. Allogeneic HSCT using cells from a matched unrelated donor was performed four months upon progressive respiratory symptoms. RESULTSHis respiratory symptoms subsided in one month; chest imaging improvement, pulmonary function test improvement, and normalized activity of β-glucocerebrosidase were reported in three months. CONCLUSIONThis is the first report of a patient who received early and regular ERT but developed severe infiltrative lung involvement and recovered after allogeneic HSCT. Based on study results, we suggest regular chest imaging, even for asymptomatic patients. For patients with severe lung involvement, rapid deterioration, and unresponsive to higher ERT dosages, allogeneic HSCT should be considered. |
ArticleNumber | 100652 |
Author | Yen, Hsiu-Ju Chang, Sheng-Kai Yang, Chia-Feng Niu, Dau-Ming Yeh, Yi-Chen Hung, Giun-Yi Lee, Chih-Ying Chen, Paul Chih-Hsueh Lee, Fu-Shiuan |
Author_xml | – sequence: 1 givenname: Fu-Shiuan surname: Lee fullname: Lee, Fu-Shiuan organization: Department of Pediatrics, Taipei Veterans General Hospital, Taipei, Taiwan – sequence: 2 givenname: Hsiu-Ju surname: Yen fullname: Yen, Hsiu-Ju organization: Department of Pediatrics, Taipei Veterans General Hospital, Taipei, Taiwan – sequence: 3 givenname: Dau-Ming surname: Niu fullname: Niu, Dau-Ming organization: Department of Pediatrics, Taipei Veterans General Hospital, Taipei, Taiwan – sequence: 4 givenname: Giun-Yi surname: Hung fullname: Hung, Giun-Yi organization: Department of Pediatrics, Taipei Veterans General Hospital, Taipei, Taiwan – sequence: 5 givenname: Chih-Ying surname: Lee fullname: Lee, Chih-Ying organization: Department of Pediatrics, Taipei Veterans General Hospital, Taipei, Taiwan – sequence: 6 givenname: Yi-Chen surname: Yeh fullname: Yeh, Yi-Chen organization: School of Medicine, National Yang-Ming University, Taipei, Taiwan – sequence: 7 givenname: Paul Chih-Hsueh surname: Chen fullname: Chen, Paul Chih-Hsueh organization: School of Medicine, National Yang-Ming University, Taipei, Taiwan – sequence: 8 givenname: Sheng-Kai surname: Chang fullname: Chang, Sheng-Kai organization: Department of Pediatrics, Taipei Veterans General Hospital, Taipei, Taiwan – sequence: 9 givenname: Chia-Feng surname: Yang fullname: Yang, Chia-Feng email: pum_chia@yahoo.com.tw organization: Department of Pediatrics, Taipei Veterans General Hospital, Taipei, Taiwan |
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Keywords | PEF Glucocerebrosidase FVC ERT FEV FEF HRCT Lysosomal storage disease CXR Infiltrative lung disease GD HSCT GD, Gaucher disease PEF, Peak expiratory flow CXR, Chest X-ray FEF, Forced expiratory flow ERT, Enzyme replacement therapy FEV, Forced expiratory volume HSCT, Allogeneic hematopoietic stem cell transplant HRCT, High-resolution computed tomography FVC, Forced vital capacity |
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Snippet | To provide strategies for monitoring and treating severe lung involvement in Gaucher disease.
We reviewed the chart of a 5-year-old boy who developed rapidly... OBJECTIVETo provide strategies for monitoring and treating severe lung involvement in Gaucher disease. STUDY DESIGNWe reviewed the chart of a 5-year-old boy... Objective: To provide strategies for monitoring and treating severe lung involvement in Gaucher disease. Study design: We reviewed the chart of a 5-year-old... |
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SubjectTerms | Glucocerebrosidase Infiltrative lung disease Lysosomal storage disease Short Communication |
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Title | Allogeneic hematopoietic stem cell transplantation for treating severe lung involvement in Gaucher disease |
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