A case of adult-onset tubulointerstitial nephritis and uveitis syndrome presenting with granulomatous panuveitis

The tubulointerstitial nephritis and uveitis (TINU) syndrome is a rare disorder that is probably underdiagnosed in clinical practice. Ocular involvement in TINU syndrome not only presents with the nongranulomatous anterior uveitis in 80% of patients but also manifests as intermediate, posterior, or...

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Main Authors: Kemal Tekin, Yasemin Ozdamar Erol, Olcay Kurtulan, Dilek Ertoy Baydar
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-01-01
Series:Taiwan Journal of Ophthalmology
Subjects:
Online Access:http://www.e-tjo.org/article.asp?issn=2211-5056;year=2020;volume=10;issue=1;spage=66;epage=70;aulast=Tekin
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spelling doaj-1ba649c4ec1f48a5adbcbaf070eecd152020-11-25T00:37:33ZengWolters Kluwer Medknow PublicationsTaiwan Journal of Ophthalmology2211-50562211-50722020-01-01101667010.4103/tjo.tjo_33_18A case of adult-onset tubulointerstitial nephritis and uveitis syndrome presenting with granulomatous panuveitisKemal TekinYasemin Ozdamar ErolOlcay KurtulanDilek Ertoy BaydarThe tubulointerstitial nephritis and uveitis (TINU) syndrome is a rare disorder that is probably underdiagnosed in clinical practice. Ocular involvement in TINU syndrome not only presents with the nongranulomatous anterior uveitis in 80% of patients but also manifests as intermediate, posterior, or panuveitis. This case report mentions an adult male patient who presented with granulomatous iridocyclitis with panuveitis and mild renal insufficiency. Workup for connective tissue and infectious diseases was negative for the patient. He was diagnosed with TINU syndrome based on the findings of renal biopsy. Both the uveitis and nephritis promptly responded well to steroid treatment, and there was no recurrence during the follow-up of 24 months.http://www.e-tjo.org/article.asp?issn=2211-5056;year=2020;volume=10;issue=1;spage=66;epage=70;aulast=Tekingranulomatous iridocyclitistubulointerstitial nephritisuveitis
collection DOAJ
language English
format Article
sources DOAJ
author Kemal Tekin
Yasemin Ozdamar Erol
Olcay Kurtulan
Dilek Ertoy Baydar
spellingShingle Kemal Tekin
Yasemin Ozdamar Erol
Olcay Kurtulan
Dilek Ertoy Baydar
A case of adult-onset tubulointerstitial nephritis and uveitis syndrome presenting with granulomatous panuveitis
Taiwan Journal of Ophthalmology
granulomatous iridocyclitis
tubulointerstitial nephritis
uveitis
author_facet Kemal Tekin
Yasemin Ozdamar Erol
Olcay Kurtulan
Dilek Ertoy Baydar
author_sort Kemal Tekin
title A case of adult-onset tubulointerstitial nephritis and uveitis syndrome presenting with granulomatous panuveitis
title_short A case of adult-onset tubulointerstitial nephritis and uveitis syndrome presenting with granulomatous panuveitis
title_full A case of adult-onset tubulointerstitial nephritis and uveitis syndrome presenting with granulomatous panuveitis
title_fullStr A case of adult-onset tubulointerstitial nephritis and uveitis syndrome presenting with granulomatous panuveitis
title_full_unstemmed A case of adult-onset tubulointerstitial nephritis and uveitis syndrome presenting with granulomatous panuveitis
title_sort case of adult-onset tubulointerstitial nephritis and uveitis syndrome presenting with granulomatous panuveitis
publisher Wolters Kluwer Medknow Publications
series Taiwan Journal of Ophthalmology
issn 2211-5056
2211-5072
publishDate 2020-01-01
description The tubulointerstitial nephritis and uveitis (TINU) syndrome is a rare disorder that is probably underdiagnosed in clinical practice. Ocular involvement in TINU syndrome not only presents with the nongranulomatous anterior uveitis in 80% of patients but also manifests as intermediate, posterior, or panuveitis. This case report mentions an adult male patient who presented with granulomatous iridocyclitis with panuveitis and mild renal insufficiency. Workup for connective tissue and infectious diseases was negative for the patient. He was diagnosed with TINU syndrome based on the findings of renal biopsy. Both the uveitis and nephritis promptly responded well to steroid treatment, and there was no recurrence during the follow-up of 24 months.
topic granulomatous iridocyclitis
tubulointerstitial nephritis
uveitis
url http://www.e-tjo.org/article.asp?issn=2211-5056;year=2020;volume=10;issue=1;spage=66;epage=70;aulast=Tekin
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