Indian Journal of Private Psychiatry

Register      Login

VOLUME 17 , ISSUE 1 ( January-June, 2023 ) > List of Articles

CASE REPORT

Nail Hyperpigmentation Following Valproic Acid Use: A Rare Case Report

Jitendriya Biswal, Antara Kunwar

Keywords : Hyperpigmentation, Nail, Valproic acid

Citation Information : Biswal J, Kunwar A. Nail Hyperpigmentation Following Valproic Acid Use: A Rare Case Report. Ind J Priv Psychiatry 2023; 17 (1):45-46.

DOI: 10.5005/jp-journals-10067-0137

License: CC BY-NC 4.0

Published Online: 10-02-2023

Copyright Statement:  Copyright © 2023; The Author(s).


Abstract

Aim and background: Valproic acid (N-dipropylacetic acid) is a widely accepted anticonvulsant. Apart from its use in seizure treatment, it is also prescribed for various psychiatric disorders like bipolar disorder. The common side effects include gastrointestinal distress, tremors, weight gain, transient alopecia, exanthemas, and low platelets. Very few cases have been reported of nail and nail bed hyperpigmentation. We aim to report and highlight a case of hyperpigmentation of fingernails and toenails of both the upper limb and lower limb following use of valproic acid. Case description: A 22-year-old male presented with acute manic symptoms characterized by overtalkativeness, tall claims, being irritable, and aggression. He was hospitalized in view of being unmanageable at home. All the baseline investigations were within the normal range. The patient tested negative for HIV, hepatitis, and syphilis. Oral second generation antipsychotic, tablet riseperidone (4 mg/day) and valproic acid (1gm/day) was prescribed. The patient showed significant improvement with the above treatment and was discharged after 20 days of hospitalization. During the first follow-up, after a period of 4 weeks following discharge, tablet risperidone was gradually tapered-off in view of improvement of symptoms. On the second follow-up after 2-months duration, he reported a “brownish-yellow discoloration of all finer nails and toenails”. The patient had no other systemic disease and denied any other concomitant drug use or misuse. The potassium hydroxide (KOH) study was negative for any fungal infection, and the histopathological report was negative for any pigment incontinence melanophages/increased melanocytes. Discontinuation of valproic acid for about a month resulted in the clearing of brownish-yellow pigmentation. Conclusion: Valproic acid rarely causes nail and nail bed discoloration due to deposition of a drug (drug metabolite) or deposition of iron following blood vessel damage. These proinflammatory changes can be reversed if identified earlier with subsequent stoppage of valproic acid. Clinical significance: To provide prompt management, both general practitioners and specialists must be aware that medications may cause hyperpigmentation.


HTML PDF Share
  1. Lewis JR. Valproic acid (Depakene): A new anticonvulsant agent. JAMA 1978;240(20):2190–2192. DOI: 10.1001/jama.1978.03290200068031.
  2. Nanau RM, Neuman MG. Adverse drug reactions induced by valproic acid. Clin Biochem 2013;46(15):1323–1338. DOI: 10.1016/j.clinbiochem.2013.06.012.
  3. Alsdorf R, Wyszynski DF. Teratogenicity of sodium valproate. Expert Opin Drug Saf 2005;4(2):345–353. DOI: 10.1517/14740338.4.2.345.
  4. Gerstner T, Lipinski C, Longin E, et al. Valproate-induced change in hair color. J Am Acad Dermatol 2008;58(2 Suppl):S63–S64. DOI: 10.1016/j.jaad.2006.06.045.
  5. Gücüyener K, Türktaş I, Serdaroglu A, et al. Suspected allergy to lamotrigine. Allergy Eur J Allergy Clin Immunol 1999;54(7):767–768. DOI: 10.1034/j.1398-9995.1999.00178.x.
  6. Piraccini BM, Iorizzo M, Starace M, et al. Drug-induced nail diseases. Dermatol Clin 2006;24(3):387–391. DOI: 10.1016/j.det.2006.03.004.
  7. Poretti A, Lips U, Belvedere M, et al. Onychomadesis: A rare side-effect of valproic acid medication? Pediatr Dermatol 2009;26. DOI: 10.1111/j.1525-1470.2009.00867.x.
  8. Giménez-García R, Carrasco-Molina S, Zambrano-Centeno B. Valproic acid-induced hyperpigmentation. ARC J Dermatol 2017;2(1):16–18. DOI: 10.20431/2456-0022.0201003.
PDF Share
PDF Share

© Jaypee Brothers Medical Publishers (P) LTD.