Cargando…

Graves’ disease associated with HIV disease and late immune reconstitution inflammatory syndrome following the initiation of antiretroviral therapy

SUMMARY: Both human immunodeficiency virus (HIV) and antiretroviral therapy (ART) are associated with endocrine dysfunction (1). The term 'immune reconstitution inflammatory syndrome' (IRIS) describes an array of inflammatory conditions that occur during the return of cell-mediated immunit...

Descripción completa

Detalles Bibliográficos
Autores principales: Ludgate, S, Connolly, S P, Fennell, D, Muhamad, M F, Welaratne, I, Cotter, A, McQuaid, S E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8558905/
https://www.ncbi.nlm.nih.gov/pubmed/34612207
http://dx.doi.org/10.1530/EDM-21-0094
_version_ 1784592660799946752
author Ludgate, S
Connolly, S P
Fennell, D
Muhamad, M F
Welaratne, I
Cotter, A
McQuaid, S E
author_facet Ludgate, S
Connolly, S P
Fennell, D
Muhamad, M F
Welaratne, I
Cotter, A
McQuaid, S E
author_sort Ludgate, S
collection PubMed
description SUMMARY: Both human immunodeficiency virus (HIV) and antiretroviral therapy (ART) are associated with endocrine dysfunction (1). The term 'immune reconstitution inflammatory syndrome' (IRIS) describes an array of inflammatory conditions that occur during the return of cell-mediated immunity following ART. Graves’ disease (GD) occurs rarely as an IRIS following ART. In this study, we describe the case of a 40-year-old Brazilian female who was diagnosed with HIV following admission with cryptococcal meningitis and salmonellosis. At this time, she was also diagnosed with adrenal insufficiency. Her CD4 count at diagnosis was 17 cells/µL which rose to 256 cells/µL over the first 3 months of ART. Her HIV viral load, however, consistently remained detectable. When viral suppression was finally achieved 21 months post diagnosis, an incremental CD4 count of 407 cells/µL over the following 6 months ensued. Subsequently, she was diagnosed with a late IRIS to cryptococcus 32 months following initial ART treatment, which manifested as non-resolving lymphadenitis and resolved with high-dose steroids. Following the initiation of ART for 45 months, she developed symptomatic Graves’ hyperthyroidism. At this time, her CD4 count had risen to 941 cells/µL. She has been rendered euthyroid on carbimazole. This case serves to remind us that GD can occur as an IRIS post ART and typically has a delayed presentation. LEARNING POINTS: Endocrinologists should be aware of the endocrine manifestations of HIV disease, in particular, thyroid pathology. Endocrinologists should be aware that IRIS can occur following the initiation of ART. Thyroid dysfunction can occur post ART of which Graves' disease (GD) is the most common thyroid manifestation. GD as a manifestation of ART-induced IRIS can have a delayed presentation. Infectious disease physicians should be aware of endocrine manifestations associated with HIV and ART.
format Online
Article
Text
id pubmed-8558905
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Bioscientifica Ltd
record_format MEDLINE/PubMed
spelling pubmed-85589052021-11-03 Graves’ disease associated with HIV disease and late immune reconstitution inflammatory syndrome following the initiation of antiretroviral therapy Ludgate, S Connolly, S P Fennell, D Muhamad, M F Welaratne, I Cotter, A McQuaid, S E Endocrinol Diabetes Metab Case Rep Unusual Effects of Medical Treatment SUMMARY: Both human immunodeficiency virus (HIV) and antiretroviral therapy (ART) are associated with endocrine dysfunction (1). The term 'immune reconstitution inflammatory syndrome' (IRIS) describes an array of inflammatory conditions that occur during the return of cell-mediated immunity following ART. Graves’ disease (GD) occurs rarely as an IRIS following ART. In this study, we describe the case of a 40-year-old Brazilian female who was diagnosed with HIV following admission with cryptococcal meningitis and salmonellosis. At this time, she was also diagnosed with adrenal insufficiency. Her CD4 count at diagnosis was 17 cells/µL which rose to 256 cells/µL over the first 3 months of ART. Her HIV viral load, however, consistently remained detectable. When viral suppression was finally achieved 21 months post diagnosis, an incremental CD4 count of 407 cells/µL over the following 6 months ensued. Subsequently, she was diagnosed with a late IRIS to cryptococcus 32 months following initial ART treatment, which manifested as non-resolving lymphadenitis and resolved with high-dose steroids. Following the initiation of ART for 45 months, she developed symptomatic Graves’ hyperthyroidism. At this time, her CD4 count had risen to 941 cells/µL. She has been rendered euthyroid on carbimazole. This case serves to remind us that GD can occur as an IRIS post ART and typically has a delayed presentation. LEARNING POINTS: Endocrinologists should be aware of the endocrine manifestations of HIV disease, in particular, thyroid pathology. Endocrinologists should be aware that IRIS can occur following the initiation of ART. Thyroid dysfunction can occur post ART of which Graves' disease (GD) is the most common thyroid manifestation. GD as a manifestation of ART-induced IRIS can have a delayed presentation. Infectious disease physicians should be aware of endocrine manifestations associated with HIV and ART. Bioscientifica Ltd 2021-09-14 /pmc/articles/PMC8558905/ /pubmed/34612207 http://dx.doi.org/10.1530/EDM-21-0094 Text en © The authors https://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Unusual Effects of Medical Treatment
Ludgate, S
Connolly, S P
Fennell, D
Muhamad, M F
Welaratne, I
Cotter, A
McQuaid, S E
Graves’ disease associated with HIV disease and late immune reconstitution inflammatory syndrome following the initiation of antiretroviral therapy
title Graves’ disease associated with HIV disease and late immune reconstitution inflammatory syndrome following the initiation of antiretroviral therapy
title_full Graves’ disease associated with HIV disease and late immune reconstitution inflammatory syndrome following the initiation of antiretroviral therapy
title_fullStr Graves’ disease associated with HIV disease and late immune reconstitution inflammatory syndrome following the initiation of antiretroviral therapy
title_full_unstemmed Graves’ disease associated with HIV disease and late immune reconstitution inflammatory syndrome following the initiation of antiretroviral therapy
title_short Graves’ disease associated with HIV disease and late immune reconstitution inflammatory syndrome following the initiation of antiretroviral therapy
title_sort graves’ disease associated with hiv disease and late immune reconstitution inflammatory syndrome following the initiation of antiretroviral therapy
topic Unusual Effects of Medical Treatment
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8558905/
https://www.ncbi.nlm.nih.gov/pubmed/34612207
http://dx.doi.org/10.1530/EDM-21-0094
work_keys_str_mv AT ludgates gravesdiseaseassociatedwithhivdiseaseandlateimmunereconstitutioninflammatorysyndromefollowingtheinitiationofantiretroviraltherapy
AT connollysp gravesdiseaseassociatedwithhivdiseaseandlateimmunereconstitutioninflammatorysyndromefollowingtheinitiationofantiretroviraltherapy
AT fennelld gravesdiseaseassociatedwithhivdiseaseandlateimmunereconstitutioninflammatorysyndromefollowingtheinitiationofantiretroviraltherapy
AT muhamadmf gravesdiseaseassociatedwithhivdiseaseandlateimmunereconstitutioninflammatorysyndromefollowingtheinitiationofantiretroviraltherapy
AT welaratnei gravesdiseaseassociatedwithhivdiseaseandlateimmunereconstitutioninflammatorysyndromefollowingtheinitiationofantiretroviraltherapy
AT cottera gravesdiseaseassociatedwithhivdiseaseandlateimmunereconstitutioninflammatorysyndromefollowingtheinitiationofantiretroviraltherapy
AT mcquaidse gravesdiseaseassociatedwithhivdiseaseandlateimmunereconstitutioninflammatorysyndromefollowingtheinitiationofantiretroviraltherapy