Cargando…
Tubulointerstitial nephritis and uveitis syndrome following meningitis and systemic lymphadenopathy with persistent Toxoplasma immunoglobulin M: a case report
BACKGROUND: Tubulointerstitial nephritis and uveitis syndrome is a rare lymphocyte-related oculorenal inflammatory disease presumed to be associated with drug use and infectious agents. Toxoplasma gondii is one of such pathogens that could exhibit encephalitis, meningitis, and uveitis in immunocompr...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461971/ https://www.ncbi.nlm.nih.gov/pubmed/34556154 http://dx.doi.org/10.1186/s13256-021-02909-z |
_version_ | 1784572100895309824 |
---|---|
author | Oya, Yoshihiro Futami, Hidekazu Nakazawa, Takuya Ishijima, Kazuyuki Umemiya, Keiko Takizawa, Fumiyoshi Imai, Naoki Kitamura, Hiroshi Matsumura, Ryutaro |
author_facet | Oya, Yoshihiro Futami, Hidekazu Nakazawa, Takuya Ishijima, Kazuyuki Umemiya, Keiko Takizawa, Fumiyoshi Imai, Naoki Kitamura, Hiroshi Matsumura, Ryutaro |
author_sort | Oya, Yoshihiro |
collection | PubMed |
description | BACKGROUND: Tubulointerstitial nephritis and uveitis syndrome is a rare lymphocyte-related oculorenal inflammatory disease presumed to be associated with drug use and infectious agents. Toxoplasma gondii is one of such pathogens that could exhibit encephalitis, meningitis, and uveitis in immunocompromised or in some immunocompetent individuals. If the immunoglobulin M of Toxoplasma is positive on screening, the interpretation of the result is not simple, especially when immunoglobulin M stays positive persistently. CASE PRESENTATION: A 34-year-old Asian male developed fever, headache, and lymphadenopathy with tenderness, which was initially diagnosed as meningitis. Antibiotics were started, and diclofenac sodium was used for the fever. Although his symptoms were alleviated in a week by the treatment, gradual decline in renal function was noted, prompting a renal biopsy that indicated acute granulomatous interstitial nephritis. A week later, tenderness in both eyes with blurred vision appeared and revealed iritis and keratic precipitations in both eyes; hence, the diagnosis of acute tubulointerstitial nephritis and bilateral uveitis syndrome was made. Toxoplasma gondii-specific immunoglobulin G and immunoglobulin M titers were both positive. Although we could not rule out recent infection of Toxoplasma gondii, which may cause uveitis initially, Toxoplasma immunoglobulin G avidity test indicated a distant infection, which allowed us to rule out meningitis and uveitis as responsible for the complication of recent Toxoplasma gondii infection. Drug-induced lymphocyte stimulation test, or lymphocyte transformation test of diclofenac sodium, was solely positive among the tested drugs. Uveitis was alleviated only with ophthalmic steroid, and renal function returned to normal without administration of systemic steroid. CONCLUSIONS: We experienced a case of diclofenac-induced tubulointerstitial nephritis and uveitis syndrome. In ruling out infections, Toxoplasma immunoglobulin M was persistently positive, and Toxoplasma immunoglobulin G avidity test indicated a “distant” infection. From these two results, we ruled out recent infection. However, it should be noted that “distant” infection indicated by commercial immunoglobulin G avidity is still a multiplex profile consisting of reinfection, reactivation, and latent infection. Narrowing down the infection profile of Toxoplasma is challenging in some cases. Therefore, careful diagnosis and extended follow-up of such patients are needed. |
format | Online Article Text |
id | pubmed-8461971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84619712021-09-24 Tubulointerstitial nephritis and uveitis syndrome following meningitis and systemic lymphadenopathy with persistent Toxoplasma immunoglobulin M: a case report Oya, Yoshihiro Futami, Hidekazu Nakazawa, Takuya Ishijima, Kazuyuki Umemiya, Keiko Takizawa, Fumiyoshi Imai, Naoki Kitamura, Hiroshi Matsumura, Ryutaro J Med Case Rep Case Report BACKGROUND: Tubulointerstitial nephritis and uveitis syndrome is a rare lymphocyte-related oculorenal inflammatory disease presumed to be associated with drug use and infectious agents. Toxoplasma gondii is one of such pathogens that could exhibit encephalitis, meningitis, and uveitis in immunocompromised or in some immunocompetent individuals. If the immunoglobulin M of Toxoplasma is positive on screening, the interpretation of the result is not simple, especially when immunoglobulin M stays positive persistently. CASE PRESENTATION: A 34-year-old Asian male developed fever, headache, and lymphadenopathy with tenderness, which was initially diagnosed as meningitis. Antibiotics were started, and diclofenac sodium was used for the fever. Although his symptoms were alleviated in a week by the treatment, gradual decline in renal function was noted, prompting a renal biopsy that indicated acute granulomatous interstitial nephritis. A week later, tenderness in both eyes with blurred vision appeared and revealed iritis and keratic precipitations in both eyes; hence, the diagnosis of acute tubulointerstitial nephritis and bilateral uveitis syndrome was made. Toxoplasma gondii-specific immunoglobulin G and immunoglobulin M titers were both positive. Although we could not rule out recent infection of Toxoplasma gondii, which may cause uveitis initially, Toxoplasma immunoglobulin G avidity test indicated a distant infection, which allowed us to rule out meningitis and uveitis as responsible for the complication of recent Toxoplasma gondii infection. Drug-induced lymphocyte stimulation test, or lymphocyte transformation test of diclofenac sodium, was solely positive among the tested drugs. Uveitis was alleviated only with ophthalmic steroid, and renal function returned to normal without administration of systemic steroid. CONCLUSIONS: We experienced a case of diclofenac-induced tubulointerstitial nephritis and uveitis syndrome. In ruling out infections, Toxoplasma immunoglobulin M was persistently positive, and Toxoplasma immunoglobulin G avidity test indicated a “distant” infection. From these two results, we ruled out recent infection. However, it should be noted that “distant” infection indicated by commercial immunoglobulin G avidity is still a multiplex profile consisting of reinfection, reactivation, and latent infection. Narrowing down the infection profile of Toxoplasma is challenging in some cases. Therefore, careful diagnosis and extended follow-up of such patients are needed. BioMed Central 2021-09-23 /pmc/articles/PMC8461971/ /pubmed/34556154 http://dx.doi.org/10.1186/s13256-021-02909-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Oya, Yoshihiro Futami, Hidekazu Nakazawa, Takuya Ishijima, Kazuyuki Umemiya, Keiko Takizawa, Fumiyoshi Imai, Naoki Kitamura, Hiroshi Matsumura, Ryutaro Tubulointerstitial nephritis and uveitis syndrome following meningitis and systemic lymphadenopathy with persistent Toxoplasma immunoglobulin M: a case report |
title | Tubulointerstitial nephritis and uveitis syndrome following meningitis and systemic lymphadenopathy with persistent Toxoplasma immunoglobulin M: a case report |
title_full | Tubulointerstitial nephritis and uveitis syndrome following meningitis and systemic lymphadenopathy with persistent Toxoplasma immunoglobulin M: a case report |
title_fullStr | Tubulointerstitial nephritis and uveitis syndrome following meningitis and systemic lymphadenopathy with persistent Toxoplasma immunoglobulin M: a case report |
title_full_unstemmed | Tubulointerstitial nephritis and uveitis syndrome following meningitis and systemic lymphadenopathy with persistent Toxoplasma immunoglobulin M: a case report |
title_short | Tubulointerstitial nephritis and uveitis syndrome following meningitis and systemic lymphadenopathy with persistent Toxoplasma immunoglobulin M: a case report |
title_sort | tubulointerstitial nephritis and uveitis syndrome following meningitis and systemic lymphadenopathy with persistent toxoplasma immunoglobulin m: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461971/ https://www.ncbi.nlm.nih.gov/pubmed/34556154 http://dx.doi.org/10.1186/s13256-021-02909-z |
work_keys_str_mv | AT oyayoshihiro tubulointerstitialnephritisanduveitissyndromefollowingmeningitisandsystemiclymphadenopathywithpersistenttoxoplasmaimmunoglobulinmacasereport AT futamihidekazu tubulointerstitialnephritisanduveitissyndromefollowingmeningitisandsystemiclymphadenopathywithpersistenttoxoplasmaimmunoglobulinmacasereport AT nakazawatakuya tubulointerstitialnephritisanduveitissyndromefollowingmeningitisandsystemiclymphadenopathywithpersistenttoxoplasmaimmunoglobulinmacasereport AT ishijimakazuyuki tubulointerstitialnephritisanduveitissyndromefollowingmeningitisandsystemiclymphadenopathywithpersistenttoxoplasmaimmunoglobulinmacasereport AT umemiyakeiko tubulointerstitialnephritisanduveitissyndromefollowingmeningitisandsystemiclymphadenopathywithpersistenttoxoplasmaimmunoglobulinmacasereport AT takizawafumiyoshi tubulointerstitialnephritisanduveitissyndromefollowingmeningitisandsystemiclymphadenopathywithpersistenttoxoplasmaimmunoglobulinmacasereport AT imainaoki tubulointerstitialnephritisanduveitissyndromefollowingmeningitisandsystemiclymphadenopathywithpersistenttoxoplasmaimmunoglobulinmacasereport AT kitamurahiroshi tubulointerstitialnephritisanduveitissyndromefollowingmeningitisandsystemiclymphadenopathywithpersistenttoxoplasmaimmunoglobulinmacasereport AT matsumuraryutaro tubulointerstitialnephritisanduveitissyndromefollowingmeningitisandsystemiclymphadenopathywithpersistenttoxoplasmaimmunoglobulinmacasereport |