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 inMolecular genetics and metabolism reports Vol. 25; p. 100652
Main Authors Lee, Fu-Shiuan, Yen, Hsiu-Ju, Niu, Dau-Ming, Hung, Giun-Yi, Lee, Chih-Ying, Yeh, Yi-Chen, Chen, Paul Chih-Hsueh, Chang, Sheng-Kai, Yang, Chia-Feng
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Published United States Elsevier Inc 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.
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
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  surname: Yang
  fullname: Yang, Chia-Feng
  email: pum_chia@yahoo.com.tw
  organization: Department of Pediatrics, Taipei Veterans General Hospital, Taipei, Taiwan
BackLink https://www.ncbi.nlm.nih.gov/pubmed/33101978$$D View this record in MEDLINE/PubMed
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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
Language English
License This is an open access article under the CC BY-NC-ND license.
2020 The Authors.
This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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SSID ssj0001125324
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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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StartPage 100652
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
URI https://dx.doi.org/10.1016/j.ymgmr.2020.100652
https://www.ncbi.nlm.nih.gov/pubmed/33101978
https://search.proquest.com/docview/2454411711
https://pubmed.ncbi.nlm.nih.gov/PMC7576510
https://doaj.org/article/7d0c48e7a2914dac87bf2baec12f3342
Volume 25
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