First Report of Lamotrigine-Induced Drug Rash with Eosinophilia and Systemic Symptoms Syndrome with Pancreatitis

Author:

Roquin Guillaume1,Peres Marine2,Lerolle Nicolas3,Dib Nina4,Mercat Alain5,Croue Anne6,Augusto Jean-François7

Affiliation:

1. Resident in Gastroenterology, Service d'Hépato-Gastro-Entérologie, CHU Angers, Angers, France

2. Anesthesiology, Service de Réanimation Médicale et Médecine Hyperbare, CHU Angers; Faculté de Médecine, Université d'Angers, Angers

3. Intensive Care Medicine and Nephrology, Service de Réanimation Médicale et Médecine Hyperbare; Faculté de Médecine, Université d'Angers

4. Gastroenterology, Service d'Hépato-Gastro-Entérologie

5. Intensive Care Medicine and Pneumology, Service de Réanimation Médicale et Médecine Hyperbare; Faculté de Médecine, Université d'Angers

6. Anatomopathology, Département de Pathologie, Cellulaire et Tissulaire, CHU Angers

7. Nephrology and Intensive Care Medicine, Service de Néphrologie-Dialyse-Transplantation, CHU Angers; Faculté de Médecine, Université d'Angers

Abstract

Objective: To report a case of lamotrigine-induced drug rash with eosinophilia and systemic symptoms (DRESS) syndrome with pancreatitis as the initial visceral involvement. Case Summary: A 75-year-old man was admitted to the local hospital for generalized tonic-clonic seizures. Results of the clinical examination and neurologic investigations were unremarkable. Lamotrigine treatment was initiated and the patient was discharged a few days later. Forty days after lamotrigine initiation, he developed an exanthematous maculopapular rash with fever, peripheral lymphadenopathies, and hypereosinophilia. Lamotrigine hypersensitivity was suspected and the drug was suspended on day 45. On day 47, the patient presented with acute abdominal pain with an elevated lipase level. Acute pancreatitis was confirmed on computed tomography scan. The patient's condition worsened and he was transferred to the intensive care unit with multiorgan failure. The diagnosis of lamotrigine-induced DRESS syndrome was confirmed by a compatible skin histology and concomitant human herpesvirus-6 infection. Discussion: This observation has 2 points of interest. First, pancreatic toxicity of lamotrigine has been rarely reported in the literature. Secondly, pancreatitis is uncommon at the early stage of DRESS syndrome. Only 1 other case of DRESS syndrome, secondary to allopurinol, reports pancreatitis along with an Epstein-Barr virus infection. The Naranjo probability scale indicated a probable causality between lamotrigine and DRESS syndrome in this patient. Conclusions: This is the first reported case of lamotrigine-induced DRESS syndrome with pancreatitis as the initial visceral involvement. Clinicians should be aware of this mode of presentation of DRESS syndrome.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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