TY - JOUR
T1 - Proximal Renal Tubular Acidosis (Fanconi Syndrome) Induced by Apremilast
T2 - A Case Report
AU - Perrone, Dana
AU - Afridi, Faraz
AU - King-Morris, Kelli
AU - Komarla, Ashwini
AU - Kar, Pran
N1 - Publisher Copyright:
© 2017 National Kidney Foundation, Inc.
PY - 2017/11
Y1 - 2017/11
N2 - Apremilast is a recently developed phosphodiesterase 4–inhibitory medication approved for use to treat psoriasis and psoriatic arthritis. We report a case of Fanconi syndrome and proximal renal tubular acidosis that was associated with this medication. Our patient was started on treatment with apremilast 2 weeks before his admission. On arrival, laboratory test results were significant for hypokalemia, hyperchloremic metabolic acidosis, low uric acid concentration, positive urine anion gap, and proteinuria, which resolved on discontinuation of the drug. Two months after the hospitalization, he was restarted on apremilast therapy; 17 days after resumption, the patient was admitted for similar laboratory values, which again improved when apremilast treatment was discontinued. After discharge, laboratory values remained normal without long-term electrolyte repletion. Proximal renal tubular acidosis (Fanconi syndrome) with quick correction of electrolyte concentrations on discontinuation of the drug was diagnosed. Our patient lacked evidence of other causes. Our patient fulfilled criteria associated with this disease and responded well off treatment with the offending agent. Literature review did not reveal prior cases associated with this medication.
AB - Apremilast is a recently developed phosphodiesterase 4–inhibitory medication approved for use to treat psoriasis and psoriatic arthritis. We report a case of Fanconi syndrome and proximal renal tubular acidosis that was associated with this medication. Our patient was started on treatment with apremilast 2 weeks before his admission. On arrival, laboratory test results were significant for hypokalemia, hyperchloremic metabolic acidosis, low uric acid concentration, positive urine anion gap, and proteinuria, which resolved on discontinuation of the drug. Two months after the hospitalization, he was restarted on apremilast therapy; 17 days after resumption, the patient was admitted for similar laboratory values, which again improved when apremilast treatment was discontinued. After discharge, laboratory values remained normal without long-term electrolyte repletion. Proximal renal tubular acidosis (Fanconi syndrome) with quick correction of electrolyte concentrations on discontinuation of the drug was diagnosed. Our patient lacked evidence of other causes. Our patient fulfilled criteria associated with this disease and responded well off treatment with the offending agent. Literature review did not reveal prior cases associated with this medication.
KW - adverse event
KW - Apremilast
KW - case report
KW - drug safety
KW - electrolyte derangement
KW - Fanconi syndrome
KW - Otezla
KW - proximal renal tubular acidosis
KW - RTA type II
UR - http://www.scopus.com/inward/record.url?scp=85027531731&partnerID=8YFLogxK
U2 - 10.1053/j.ajkd.2017.06.021
DO - 10.1053/j.ajkd.2017.06.021
M3 - Article
C2 - 28823583
AN - SCOPUS:85027531731
SN - 0272-6386
VL - 70
SP - 729
EP - 731
JO - American Journal of Kidney Diseases
JF - American Journal of Kidney Diseases
IS - 5
ER -