Pulmonary Type B Niemann-Pick Disease Successfully Treated with Lung Transplantation

Background. Niemann-Pick Disease (NPD) type B is a rare autosomal recessive disease characterised by hepatosplenomegaly and pulmonary disease, highlighted by preserved volumes and diminished diffusion capacity of the lung for carbon monoxide (DLCO) on pulmonary function tests (PFTs). There is no cur...

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Main Authors: R. S. O’Neill, N. Belousova, M. A. Malouf
Format: Article
Language:English
Published: Hindawi Limited 2019-01-01
Series:Case Reports in Transplantation
Online Access:http://dx.doi.org/10.1155/2019/9431751
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spelling doaj-28018ae663aa49d791aaeb78e57cdd402020-11-24T21:32:49ZengHindawi LimitedCase Reports in Transplantation2090-69432090-69512019-01-01201910.1155/2019/94317519431751Pulmonary Type B Niemann-Pick Disease Successfully Treated with Lung TransplantationR. S. O’Neill0N. Belousova1M. A. Malouf2St Vincent’s Hospital Department of Lung Transplant, Sydney, NSW, AustraliaSt Vincent’s Hospital Department of Lung Transplant, Sydney, NSW, AustraliaSt Vincent’s Hospital Department of Lung Transplant, Sydney, NSW, AustraliaBackground. Niemann-Pick Disease (NPD) type B is a rare autosomal recessive disease characterised by hepatosplenomegaly and pulmonary disease, highlighted by preserved volumes and diminished diffusion capacity of the lung for carbon monoxide (DLCO) on pulmonary function tests (PFTs). There is no current accepted treatment for the disease. We present a case of a successful bilateral lung transplant in a patient with a DLCO of 14%, and significant pulmonary changes attributable to NPD type B on computed tomography (CT) chest, and both microscopic and macroscopic assessment of the lung explant. To the author’s knowledge this is only the third case of lung transplantation in a patient with NPD type B and is one of two current living patients post lung transplantation for NPD type B. Case Report. A 64-year-old male patient underwent bilateral lung transplantation for NPD type B. Preoperative PFTs demonstrated preserved volumes with significantly decreased DLCO, with imaging showing a diffuse reticular interstitial pattern, typical of chronic fibrotic lung disease. The patient suffered from primary graft dysfunction type 3 in the postoperative period as well as rejection managed with methylprednisolone and intravenous immunoglobulin. The patient improved steadily and was discharged 80 days post-transplantation. Conclusions. This case is only the third reported case of lung transplantation in a patient with NPD type B and the second case of a patient with NPD type B currently living post-transplantation, being at postoperative day (POD) 267 at the time of manuscript drafting. It demonstrates that lung transplantation, although hazardous, is a viable strategy for treatment in patients with NPD type B who have significant pulmonary involvement.http://dx.doi.org/10.1155/2019/9431751
collection DOAJ
language English
format Article
sources DOAJ
author R. S. O’Neill
N. Belousova
M. A. Malouf
spellingShingle R. S. O’Neill
N. Belousova
M. A. Malouf
Pulmonary Type B Niemann-Pick Disease Successfully Treated with Lung Transplantation
Case Reports in Transplantation
author_facet R. S. O’Neill
N. Belousova
M. A. Malouf
author_sort R. S. O’Neill
title Pulmonary Type B Niemann-Pick Disease Successfully Treated with Lung Transplantation
title_short Pulmonary Type B Niemann-Pick Disease Successfully Treated with Lung Transplantation
title_full Pulmonary Type B Niemann-Pick Disease Successfully Treated with Lung Transplantation
title_fullStr Pulmonary Type B Niemann-Pick Disease Successfully Treated with Lung Transplantation
title_full_unstemmed Pulmonary Type B Niemann-Pick Disease Successfully Treated with Lung Transplantation
title_sort pulmonary type b niemann-pick disease successfully treated with lung transplantation
publisher Hindawi Limited
series Case Reports in Transplantation
issn 2090-6943
2090-6951
publishDate 2019-01-01
description Background. Niemann-Pick Disease (NPD) type B is a rare autosomal recessive disease characterised by hepatosplenomegaly and pulmonary disease, highlighted by preserved volumes and diminished diffusion capacity of the lung for carbon monoxide (DLCO) on pulmonary function tests (PFTs). There is no current accepted treatment for the disease. We present a case of a successful bilateral lung transplant in a patient with a DLCO of 14%, and significant pulmonary changes attributable to NPD type B on computed tomography (CT) chest, and both microscopic and macroscopic assessment of the lung explant. To the author’s knowledge this is only the third case of lung transplantation in a patient with NPD type B and is one of two current living patients post lung transplantation for NPD type B. Case Report. A 64-year-old male patient underwent bilateral lung transplantation for NPD type B. Preoperative PFTs demonstrated preserved volumes with significantly decreased DLCO, with imaging showing a diffuse reticular interstitial pattern, typical of chronic fibrotic lung disease. The patient suffered from primary graft dysfunction type 3 in the postoperative period as well as rejection managed with methylprednisolone and intravenous immunoglobulin. The patient improved steadily and was discharged 80 days post-transplantation. Conclusions. This case is only the third reported case of lung transplantation in a patient with NPD type B and the second case of a patient with NPD type B currently living post-transplantation, being at postoperative day (POD) 267 at the time of manuscript drafting. It demonstrates that lung transplantation, although hazardous, is a viable strategy for treatment in patients with NPD type B who have significant pulmonary involvement.
url http://dx.doi.org/10.1155/2019/9431751
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