Literature DB >> 31831514

Accelerated silicosis with bone marrow, hepatic and splenic involvement in a patient with lung transplantation.

M Cruz Carreño Hernández1, Sara Garrido Paniagua2, María Colomés Iess3, Mehdi Guemra4.   

Abstract

Chronic silicosis is an entity widely described in literature. However, other types such as accelerated, acute, complicated and extrapulmonary silicosis are little documented. We present a case of accelerated extrapulmonary silicosis in a lung transplant patient in whom the diagnosis of systemic silicosis was made incidental to non-respiratory complications that occurred during follow-up. The appearance of cytopenia and liver failure led to diagnostic tests that documented the presence of silicotic granulomas in those locations. Taking into account the intensity, time of exposure, onset and development of the disease, we found a highly atypical case of accelerated extrapulmonary silicosis in which inorganic particles (presumably silica) were documented inside granulomas and macrophages of the bone marrow. With these findings, we reflect on the lack of consideration of these entities within clinical practice, their probable under diagnosis and the need to study other pathophysiological mechanisms of acquisition and dissemination of silicosis. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  exposures; haematology (incl blood transfusion); interstitial lung disease; migration and health; pathology

Mesh:

Substances:

Year:  2019        PMID: 31831514      PMCID: PMC6936535          DOI: 10.1136/bcr-2019-230781

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  17 in total

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Review 1.  Early Identification, Accurate Diagnosis, and Treatment of Silicosis.

Authors:  Tian Li; Xinyu Yang; Hong Xu; Heliang Liu
Journal:  Can Respir J       Date:  2022-04-25       Impact factor: 2.130

  1 in total

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