Multifocal Stevens-Johnson syndrome after concurrent phenytoin and cranial and thoracic radiation treatment, a case report
© Kandil et al; licensee BioMed Central Ltd. 2010
Received: 25 December 2009
Accepted: 4 June 2010
Published: 4 June 2010
A 46 year old male patient with metastatic prostate cancer developed Stevens-Johnson syndrome (SJS), initially in three well-demarcated areas on his scalp, chest and back, corresponding to ports of radiation therapy while on phenytoin. The rash spread from these locations and became more generalized and associated with pain and sloughing in the mucous lining of the mouth. There is a documented association between phenytoin administration with concurrent cranial radiation therapy and development of SJS. Erythema multiforme (EM) associated with phenytoin and cranial radiation therapy (EMPACT) is the term that describes this reaction. However, this term may not cover the full spectrum of the disease since it describes EM associated with phenytoin and only cranial radiation therapy. This case report presents evidence that SJS may be induced by radiation to other parts of the body in addition to the cranium while phenytoin is administered concomitantly. With increasing evidence that phenytoin and levetiracetam are equally efficacious for seizure treatment and prophylaxis, and since there is no link identified so far of an association between levetiracetam and SJS, we believe that levetiracetam is a better option for patients who need anticonvulsant medication(s) while undergoing radiation therapy, especially cranial irradiation.
Patients with symptomatic metastases to osseous or soft tissues are frequently offered short courses of palliative external beam radiation. In the United States, fractionation schedules of 8 Gy in 1 fraction to 37.5 Gy delivered in 15 fractions is commonly used . These treatments are generally well tolerated. The most common toxicity experienced by patients is a mild and reversible irritation of cutaneous and mucosal surfaces. Patients in need of palliative radiation are often treated concurrently with glucocorticoid steroids, anti-emetic, and/or anti-epileptic drugs (AED) for relief of symptoms associated with the underlying disease process.
Phenytoin is one of the most frequently used AEDs in adult patients. Ninety percent of the drug is protein bound and it is metabolized mostly by the liver . It is in the category of enzyme inducing anti-epileptic drugs (EIAED) which include carbamazepine, oxcarbazepine, fosphenytoin, phenobarbital and primidone.
Stevens-Johnson syndrome (SJS) is a rare, but severe cutaneous, cell-mediated hypersensitivity reaction that is usually induced by medication or a virus [3, 4]. Historically, SJS was considered to be part of a spectrum of erythema multiforme (EM), but now it is considered clinically distinct from EM, and is part of the SJS-toxic epidermal necrolysis (SJS-TEN) spectrum. It is characterized by heterogeneous cutaneous bullous eruptions and can result in sloughing of the epidermis . Early in the disease process, the epidermis becomes infiltrated with CD8 T-lymphocytes and macrophages, while the dermis shows CD4 predominance cells. It is postulated that the lymphocytes release cytokines, which mediate the inflammatory reaction and apoptosis of epithelial cells. Patients often present with a prodrome of fever, malaise, and with mucous membrane involvement . Patients with 10-30% epidermal detachment are considered to have transitional SJS-TEN . Patients with more than 30% epidermal detachment are classified as TEN . The most frequent complications include infection (24%) and gastrointestinal bleeding (18%) . Several AEDs have been associated with increased risk of developing SJS which include phenytoin, carbamazepine, lamotrigine and phenobarbital [7, 8]. Certain human leukocyte antigen (HLA) types are sometimes associated with increased risk of SJS, including HLA B1502 .
A 46 year-old Caucasian man with a history of metastatic prostate cancer presented with erythema, pruritis, vesicles and skin sloughing in three well-demarcated areas on the head, chest and back. Mucous lining in the oral cavity also exhibited sloughing and was painful. He was admitted to the hospital for observation and pain management.
In December, 2006, he was diagnosed with diffuse, bony metastatic prostate cancer (Gleason score 9/10). He had received palliative radiation therapy (20 Gy in 5 fractions) to his right hip without complications. Seven months later, he was treated with palliative radiation therapy (8 Gy in 1 fraction) to his right ribs, again without complications. On August 1, 2007, he had a craniotomy for excision of a dural based mass with pathological diagnosis of metastatic prostate cancer. On September 18, 2007, a second resection for local recurrence of cranial metastatic prostate cancer was performed. Because of pial involvement of the tumor he was started on phenytoin for seizure prophylaxis on the day of surgery. He tolerated phenytoin well, and had experienced no anticonvulsant hypersensitivity syndrome or any other side effects. While on phenytoin, he received spinal radiation (T6-11 for T7-10 metastases with mild cord compression at T8-9) from October 1 to October 17, 2007 (36 Gy) and simultaneous whole brain radiation therapy from October 3 to October 19, 2007 (36 Gy). He also started dexamethasone 4 mg TID on the first day of radiation therapy for 11 days. The dexamethasone was increased to 8 mg TID for 7 days before a taper was initiated after completion of radiation therapy. He reported a pain level of 8 out of 10 on a pain scale at the start of radiation therapy. He started transdermal fentanyl patch 200 mcg per hour in addition to oral hydromorphone 4 mg every 4 hours for break-through pain. His pain subsided to a rating of 3 out of 10.
We performed a literature review searching for links between 1) EM, SJS, TEN and phenytoin and radiation therapy of all body systems except cranium and 2) EM, SJS, TEN and levetiracetam with radiation therapy of all body systems including cranium in PubMed and OVID MEDLINE databases. There is no article found in either link. However, there was one case report of SJS development at multiple sites of previously irradiated areas 2 weeks after lumbosacral radiation therapy while phenobarbital was administered concomitantly . The patient received sequential localized radiation therapy at sacrum, cranium, thorax and lumbosacral areas at 6 months, 4 months, 1 month and 2 weeks prior to the eruption of SJS, respectively. He also received both phenytoin and phenobarbital about 3 months earlier for seizure treatment, but phenytoin was discontinued 42 days before the rash eruption.
The patient reported here had tolerated two previous radiation therapy treatments without development of skin toxicity. He also tolerated phenytoin treatment alone without any toxicity prior to starting the combined brain and spine radiation therapies. Since the eruptions occurred first in areas corresponding to the radiation treatment fields, it is likely that the SJS development is due to concurrent exposure to phenytoin and radiation treatments of brain and spine. The weaning of dexamethasone may contribute to the development of SJS as well. EM-SJS-TEN syndrome is well described in patients receiving concurrent phenytoin and cranial irradiation treatments, although there appears to be some confusion in the published literature whether it is erythema multiforme or SJS [11–13]. Ahmed and colleagues suggested an acronym "EMPACT" (Erythema Multiforme associated with Phenytoin And Cranial Radiation Therapy) to describe this reaction . The case presented here demonstrates that the rash erupted in the patient's cranial radiation field and in the thoracic spinal irradiated areas, suggesting that phenytoin not only sensitizes for cranial radiation therapy, but also for radiation therapy received elsewhere in the body. It is possible that the combination of cranial radiation and phenytoin exposure triggered the sensitization and subsequent eruption of SJS on the scalp and on the skin of thoracic radiation fields. Combining the case reported by Duncan et al. , we believe that the EMPACT acronym may not cover the full spectrum of the syndrome because it suggests the syndrome is associated only with cranial irradiation with concurrent phenytoin administration.
It is believed that phenytoin induces cytochrome P450 3A and produces oxidative reactive intermediates that are involved in the hypersensitivity reaction . Additionally, it is thought that the aromatic chain in the chemical structure of phenytoin and other agents undergo a detoxification pathway mediated by epoxide hydrolases . Anticonvulsants that do not commonly cause SJS are metabolized differently. Since carbamazepine, valproic acid and barbiturates have shown cross-sensitivity with phenytoin, gabapentin was recommended as a substitute AED for a suspected sensitive patient while undergoing radiation treatment . Gabapentin related SJS reactions, however, have been reported in the literature . Nonetheless, they are rare events. Another alternative, levetiracetam, is increasingly being used as a phenytoin replacement . Depending on the seizure types, there are many new AEDs with lower rate of rash formation used alone or with radiation which include valproic acid, topiramate and zonisamide [8, 18, 19]. Levetiracetam is not known to produce SJS, EM or TEN when administered alone or with concurrent radiation therapy. A search in PubMed and OVID MEDLINE for a link between the levetiracetam, radiation therapy and EM, SJS or TEN yielded no positive results. Furthermore, there is preliminary data that levetiracetam may be effective when used as a monotherapy of AED [20, 21]. Therefore, for patients requiring AED who require radiation therapy, levetiracetam may be the preferred anticonvulsant, if there is no other contra-indication.
We have described a case of SJS erupted in the fields of cranial and thoracic irradiation while receiving concomitant phenytoin therapy. This case demonstrates that SJS can occur in other areas of the body in addition to the cranium where radiation was delivered. For patients who need whole brain radiation and require anticonvulsant, phenytoin should be avoided. We suggest levetiracetam as a better substitute.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
Erythema Multiforme associated with Phenytoin And Cranial Radiation Therapy
Toxic Epidermal Necrolysis.
We would like to thank Dr. Harty Ashby-Richardson for providing the photograph of hematoxylin and eosin stained specimen from the palmar skin biopsy.
- Hartsell WF, Santosh Y: Palliation of Bone Metastases,. In Principles and Practice of Radiation Oncology. 5th edition. Edited by: Halperin EC, Perez CA, Brady LW. Philadelphia: Lippincott, Williams & Wilkins; 2008:1992-1996.Google Scholar
- Browne TR: Pharmacokinetics of antiepileptic drugs. Neurology 1998,51(5 Suppl 4):S2-7.View ArticlePubMedGoogle Scholar
- Roujeau JC, Kelly JP, Naldi L, Rzany B, Stern RS, Anderson T, Auquier A, Bastuji-Garin S, Correia O, Locati F, Mockenhaupt M, Paoletti C, Shapiro S, Shear N, Schopf E, Kaufman D: Medication use and the risk of Stevens-Johnson syndrome or toxic epidermal necrolysis. N Engl J Med 1995, 333: 1600-1607. 10.1056/NEJM199512143332404View ArticlePubMedGoogle Scholar
- Fine JD: Management of acquired bullous skin diseases. N Engl J Med 1995, 333: 1475-1484. 10.1056/NEJM199511303332207View ArticlePubMedGoogle Scholar
- Garcia-Doval I, LeCleach L, Bocquet H, Otero XL, Roujeau JC: Toxic epidermal necrolysis and Stevens-Johnson syndrome: does early withdrawal of causative drugs decrease the risk of death? Arch Dermatol 2000, 136: 323-327. 10.1001/archderm.136.3.323View ArticlePubMedGoogle Scholar
- Phoon WH, Chan MO, Rajan VS, Tan KJ, Thirumoorthy T, Goh CL: Stevens-Johnson syndrome associated with occupational exposure to trichloroethylene. Contact Dermatitis 1984, 10: 270-276. 10.1111/j.1600-0536.1984.tb00145.xView ArticlePubMedGoogle Scholar
- Mockenhaupt M, Messenheimer J, Tennis P, Schlingmann J: Risk of Stevens-Johnson syndrome and toxic epidermal necrolysis in new users of antiepileptics. Neurology 2005, 64: 1134-1138.View ArticlePubMedGoogle Scholar
- Arif H, Buchsbaum R, Weintraub D, Koyfman S, Salas-Humara C, Bazil CW, Resor SR Jr, Hirsch LJ: Comparison and predictors of rash associated with 15 antiepileptic drugs. Neurology 2007, 68: 1701-1709. 10.1212/01.wnl.0000261917.83337.dbView ArticlePubMedGoogle Scholar
- Man CB, Kwan P, Baum L, Yu E, Lau KM, Cheng AS, Ng MH: Association between HLA-B*1502 allele and antiepileptic drug-induced cutaneous reactions in Han Chinese. Epilepsia 2007, 48: 1015-1018. 10.1111/j.1528-1167.2007.01022.xView ArticlePubMedGoogle Scholar
- Duncan KO, Tigelaar RE, Bolognia JL: Stevens-Johnson syndrome limited to multiple sites of radiation therapy in a patient receiving phenobarbital. J Am Acad Dermatol 1999, 40: 493-496. 10.1016/S0190-9622(99)70508-6View ArticlePubMedGoogle Scholar
- Ahmed I, Reichenberg J, Lucas A, Shehan JM: Erythema multiforme associated with phenytoin and cranial radiation therapy: a report of three patients and review of the literature. Int J Dermatol 2004, 43: 67-73. 10.1111/j.1365-4632.2004.01934.xView ArticlePubMedGoogle Scholar
- Cockey GH, Amann ST, Reents SB, Lynch JW Jr: Stevens-Johnson syndrome resulting from whole-brain radiation and phenytoin. Am J Clin Oncol 1996, 19: 32-34. 10.1097/00000421-199602000-00007View ArticlePubMedGoogle Scholar
- Aydin F, Cokluk C, Senturk N, Aydin K, Canturk MT, Turanli AY: Stevens-Johnson syndrome in two patients treated with cranial irradiation and phenytoin. European Academy of Dermatology and Venereology 2006, 20: 588-590. 10.1111/j.1468-3083.2006.01510.xView ArticleGoogle Scholar
- Micali G, Linthicum K, Han N, West DP: Increased risk of erythema multiforme major with combination anticonvulsant and radiation therapies. Pharmacotherapy 1999, 19: 223-227. 10.1592/phco.18.104.22.168917View ArticlePubMedGoogle Scholar
- Barbosa LA, Teixeira CR: Erythema multiforme associated with prophylactic use of phenytoin during cranial radiation therapy. American Journal of Health-System Pharmacy 2008, 65: 1048-1050. 10.2146/ajhp060580View ArticlePubMedGoogle Scholar
- Gonzalez-Sicilia L, Cano A, Serrano M, Hernandez J: Stevens-Johnson syndrome associated with gabapentin. American Journal of Medicine 1998, 105: 455.View ArticlePubMedGoogle Scholar
- Lim DA, Tarapore P, Chang E, Burt M, Chakalian L, Barbaro N, Chang S, Lamborn KR, McDermott MW: Safety and feasibility of switching from phenytoin to levetiracetam monotherapy for glioma-related seizure control following craniotomy: a randomized phase II pilot study. J. Neuro-Onco 2009, 93: 349-354. 10.1007/s11060-008-9781-4View ArticleGoogle Scholar
- French JA, Kanner AM, Bautista J, Abou-Khalil B, Browne T, Harden CL, Theodore WH, Bazil C, Stern J, Schachter SC, Bergen D, Hirtz D, Montouris GD, Nespeca M, Gidal B, Marks WJ Jr, Turk WR, Fischer JH, Bourgeois B, Wilner A, Faught RE Jr, Sachdeo RC, Beydoun A, Glauser TA: Efficacy and tolerability of the new antiepileptic drugs I: Treatment of new onset epilepsy: Report of the Therapeutics and Technology Assessment Subcommittee and Quality Standards Subcommittee of the American Academy of Neurology and the American Epilepsy Society. Neurology 2004, 62: 1252-1260.View ArticlePubMedGoogle Scholar
- French JA, Kanner AM, Bautista J, Abou-Khalil B, Browne T, Harden CL, Theodore WH, Bazil C, Stern J, Schachter SC, Bergen D, Hirtz D, Montouris GD, Nespeca M, Gidal B, Marks WJ Jr, Turk WR, Fischer JH, Bourgeois B, Wilner A, Faught RE Jr, Sachdeo RC, Beydoun A, Glauser TA: Efficacy and tolerability of the new antiepileptic drugs II: treatment of refractory epilepsy: report of the Therapeutics and Technology Assessment Subcommittee and Quality Standards Subcommittee of the American Academy of Neurology and the American Epilepsy Society. Neurology 2004, 62: 1261-1273.View ArticlePubMedGoogle Scholar
- Berkovic SF, Knowlton RC, Leroy RF, Schiemann J, Falter U, On behalf of the Levetiracetam N01057 Study Group: Placebo-controlled study of levetiracetam in idiopathic generalized epilepsy. Neurology 2007, 69: 1751-1760. 10.1212/01.wnl.0000268699.34614.d3View ArticlePubMedGoogle Scholar
- Jones KE, Puccio AM, Harshman KJ, Falcione B, Benedict N, Jankowitz BT, Stippler M, Fischer M, Sauber-Schatz EK, Fabio A, Darby JM, Okonkwo DO: Levetiracetam versus phenytoin for seizure prophylaxis in severe traumatic brain injury. Neurosurgical Focus 2008, 25: E3. 10.3171/FOC.2008.25.10.E3PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.