Lamotrigine-induced tubulointerstitial nephritis and uveitis-atypical Cogan syndrome

被引:13
作者
Kolomeyer, Anton M. [1 ]
Kodat, Shyam [1 ]
机构
[1] Univ Pittsburgh, Dept Ophthalmol, Pittsburgh, PA 15213 USA
关键词
Atypical Cogan syndrome; Lamotrigine; TINU; Tubulointerstitial nephritis and uveitis;
D O I
10.5301/ejo.5000674
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To report a case of lamotrigine-induced tubulointerstitial nephritis and uveitis (TINU)-atypical Cogan syndrome. Methods: Case report. Results: A 16-year-old boy with traumatic brain injury and seizures presented to the emergency department with facial swelling, rash, and back pain several days after increasing lamotrigine dose secondary to a breakthrough seizure. Creatinine, urine beta 2 microglobulin, and eosinophils were elevated. Antinuclear antibodies, antineutrophil cytoplasmic antibodies, angiotensin-converting enzyme, and complement were normal. Renal biopsy showed acute granulomatous tubulointerstitial nephritis. Lamotrigine was discontinued, intravenous steroids were initiated, and the patient was discharged on Ativan and prednisone. Subsequently, he was diagnosed with bilateral anterior uveitis (vision 20/30 bilaterally) and started on prednisolone and cyclopentolate. Two months later, he developed a branch retinal artery occlusion in the right eye (vision 20/70) and bilateral ocular hypertension for which timolol-brimonidine and dorzolamide were added. Neuroimaging and hypercoagulability workup was unremarkable. Vision and intraocular pressure improved, while uveitis remained recalcitrant. Several months later, the patient developed central serous retinopathy in the right eye (vision 20/30). Prednisone was stopped but restarted due to methotrexate intolerance. A month later, he reported dizziness and was diagnosed with severe bilateral sensorineural hearing loss. Brain magnetic resonance imaging showed foci of perivascular, subcortical, and cochlear enhancement. Transtympanic Decadron injections and infliximab infusions were initiated. At the final visit, vision remained at 20/30 with trace anterior chamber reaction bilaterally while on timolol-brimonidine, dorzolamide, and prednisolone. Conclusions: An idiosyncratic drug reaction should be considered in the differential diagnosis of TINU-atypical Cogan syndrome.
引用
收藏
页码:E14 / E16
页数:3
相关论文
共 7 条
[1]   Antiepileptic drugs and adverse skin reactions: An update [J].
Blaszczyk, Barbara ;
Lason, Wladyslaw ;
Czuczwar, Stanislaw Jerzy .
PHARMACOLOGICAL REPORTS, 2015, 67 (03) :426-434
[2]   Tubulointerstitial nephritis, uveitis, hearing loss and vestibular failure: TINU-atypical Cogan's overlap syndrome [J].
Brogan, Kerr ;
Eleftheriou, Despina ;
Rajput, Kaukab ;
Edelsten, Clive ;
Sebire, Neil J. ;
Brogan, Paul A. .
RHEUMATOLOGY, 2012, 51 (05) :950-952
[3]   Cogan's Syndrome and Other Ocular Vasculitides [J].
Espinoza, Gabriela M. ;
Prost, Angela .
CURRENT RHEUMATOLOGY REPORTS, 2015, 17 (04)
[4]  
Fervenza FC, 2000, AM J KIDNEY DIS, V36, P1034
[5]   Typical and atypical Cogan's syndrome:: 32 cases and review of the literature [J].
Grasland, A ;
Pouchot, J ;
Hachulla, E ;
Blétry, O ;
Papo, T ;
Vinceneux, P .
RHEUMATOLOGY, 2004, 43 (08) :1007-1015
[6]   The tubulointerstitial nephritis and uveitis syndrome [J].
Mandeville, JTH ;
Levinson, RD ;
Holland, GN .
SURVEY OF OPHTHALMOLOGY, 2001, 46 (03) :195-208
[7]   Idiopathic acute interstitial nephritis and uveitis associated with deafness [J].
Navarro, JF ;
Gallego, E ;
Gil, J ;
Perera, A ;
Garcia, J .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1997, 12 (04) :781-784