|Year : 2005 | Volume
| Issue : 4 | Page : 270-272
Simultaneous occurrence of toxic epidermal necrolysis and neuroleptic malignant syndrome
K Muhammed, P Raman
Department of Dermatology and Venereology, Government Medical College, Kozhikode, Kerala, India
Kunnummal house, Koroth School Road, Vatakara-1, 673101, Kozhikode, Kerala
Source of Support: None, Conflict of Interest: None
Toxic epidermal necrolysis (TEN) is an acute life-threatening blistering disease characterized by involvement of the skin, multiple mucous membranes and internal organs. It is most commonly precipitated by the administration of medications like anticonvulsants. Neuroleptic malignant syndrome (NMS) is a rare complication of neuroleptic therapy characterized by catatonic behavior, generalized muscular rigidity, hyperthermia and autonomic dysfunction. An 18-year-old girl presenting with simultaneous appearance of TEN and NMS following anti-psychotic drugs given for bipolar mood disorder, is reported for the rare association and her complete recovery.
Keywords: Toxic epidermal necrolysis, Neuroleptic malignant syndrome
|How to cite this article:|
Muhammed K, Raman P. Simultaneous occurrence of toxic epidermal necrolysis and neuroleptic malignant syndrome. Indian J Dermatol Venereol Leprol 2005;71:270-2
|How to cite this URL:|
Muhammed K, Raman P. Simultaneous occurrence of toxic epidermal necrolysis and neuroleptic malignant syndrome. Indian J Dermatol Venereol Leprol [serial online] 2005 [cited 2019 Aug 21];71:270-2. Available from: http://www.ijdvl.com/text.asp?2005/71/4/270/16621
| Introduction|| |
Toxic epidermal necrolysis (TEN) also known as Lyell's syndrome, is an uncommon but acute life-threatening idiosyncratic syndrome involving the skin and multiple mucous membranes. It is characterized by fever, systemic toxicity, skin tenderness, erythema and widespread epidermal detachment. Although Ruskin described this condition in 1948, it was Lyell in 1956, who reported four cases and proposed the name TEN. TEN is often fatal; mortality ranges from 20-30%. Death usually occurs due to septicemia or other systemic complications. Many etiological factors have been proposed. Although TEN is often idiopathic, it mostly represents an idiosyncratic drug-induced dose-independent reaction in about 77% cases. Frequently implicated are antiepileptic drugs (carbamazepine, phenytoin), sulfonamides and NSAIDs. TEN is known to affect women more than men. The incidence is high in HIV patients.
Neuroleptic malignant syndrome (NMS) is characterized by catatonic behavior, generalized muscular rigidity, hyperthermia and autonomic dysfunction. It can suddenly arise in patients treated with neuroleptic drugs and causes a high mortality rate even today. It was first described by Delay et al in 1960. The incidence is 0.02% to 3.23%. Virtually all classes of D2 dopamine receptor antagonists such as haloperidol and chlorpromazine have been associated with NMS. NMS is not the result of overdosage. Concomitant treatment with lithium or carbamazepine potentiates the risk. It usually occurs within 30 days of neuroleptic treatment and the reported mortality rate is 10-20%. Death results from cardiac or respiratory arrest.
The combination of these two severe complications of drug therapy in a patient and her complete recovery from these two is reported here. To the best of our knowledge, such an association has not been previously reported.
| Case report|| |
An 18-year-old girl was brought to our casualty in a comatose state with high-grade fever and generalized charred appearance with peeling of skin in sheets. There were a few bullous and target lesions. She had incontinence of urine, sialorrhea and diaphoresis. All these developed following administration of carbamazepine (100 mg tid) and chlorpromazine (100 mg bid) for her bipolar mood disorder, for two weeks. About 95% of her body was involved with denudation, including her scalp. Nikolsky sign was demonstrable. Oral, conjunctival and genital mucosae were involved with erosions. She had muscular rigidity of the lead pipe type. Her blood pressure was 150/100 mm of Hg. Her respiratory system and cardiovascular systems were normal except for tachypnea and tachycardia.
Baseline investigations showed leukocytosis with eosinophilia and hyperglycemia (fasting blood sugar 250 mg/dl). She was polyuric with glycosuria and no albuminuria. The serum creatinine phosphokinase (CPK) level was raised (294 units/L). Blood cultures were negative for organisms on repeated testing. Pus culture from cutaneous lesions showed growth of Staphylococcus aureus sensitive to ceftazidime and the patient was started on this drug.
As a burn care center was not available, we managed the patient in our intensive care unit (ICU). She was on parenteral nutrition and fluids with monitoring of all vital parameters. She was given systemic steroids starting from 8 mg/day of intravenous betamethasone, which was gradually tapered off over 3 weeks. Her skin lesions dried up and started epithelializing after a week. She started recovering from coma after 3 days of admission. She was discharged after 3 weeks on thioridazine after a psychiatry consultation for her mood disorder.
| Discussion|| |
Our patient had all the classical features of TEN and satisfied the criteria for the diagnosis of NMS as proposed by Caroff and Mann in 1991. She was on both carbamazepine and chlorpromazine. Invariably, chlorpromazine is a neuroleptic drug and it might have produced NMS. The simultaneous ingestion of carbamazepine might have potentiated the NMS. It is a form of drug-induced hyperthermia. All neuroleptics implicated in NMS share the property of central D2 dopamine receptor antagonism, particularly in nigro-striatal and hypothalamic pathways. Generalized rigidity (lead pipe type) is reported in 97% of cases. CPK from skeletal muscle is raised in 95% cases and myoglobinuria is seen in 67% of cases. Increased levels of serum and blister fluid CPK are reported in TEN patients also. Dopamine agonists such as bromocriptine and dantrolene are used as specific pharmacotherapeutic agents in the treatment of NMS. Electroconvulsive therapy can also be given. But once neuroleptics are stopped, NMS is self-limited, the mean recovery time being 9.6±9.1 days. Usually, 63% of patients recover by the end of one week. Our patient recovered following withdrawal of the drug and maintenance of the vital parameters under strict medical supervision without any specific antidote. Hyperglycemia is seen in some NMS cases as in our patient.
Both carbamazepine and chlorpromazine can induce TEN. But, in our experience, among these, the most probable cause is carbamazepine., The pathogenesis of TEN remains largely unknown. The cytotoxic lymphocyte-mediated immune reaction aimed at destruction of the keratinocytes expressing foreign (drug-related) antigens is proposed as the primary cause for the development of TEN. Histologically, TEN is characterized by extensive keratinocyte apoptosis, which is induced by a suicidal interaction between 'Fas' and 'Fas ligand' (Fas L), which are both expressed by keratinocytes.
TEN has been reported to be associated with a few other life-threatening conditions, most commonly adult respiratory distress syndrome (ARDS) and other pulmonary complications. Fulminant hepatitis has been noted with TEN due to nevirapine in AIDS patients and due to moxifloxacin. Recently, a novel manifestation of lupus with TEN has been reported. To the best of our knowledge, the co-occurrence of two life-threatening reactions, NMS and TEN has not been documented.
We treated the patient in our ICU, with a moderately high dose of systemic steroids under cover of antibiotics, even though the usefulness of corticosteroids is controversial. Her miraculous escape from both these rare life-threatening conditions is interesting.
| References|| |
|1.||Dowd PM, Champion RH. Disorders of blood vessels. In : Champion RH, Burton JL, Burns DA, Breathnach SM, editors. Textbook of dermatology. 6th edn. New York: Blackwell Science; 2000. p. 2087-9. |
|2.||Akosa AB, Elhag AB. Toxic epidermal necrolysis: A study of the sweat glands. J Cutan Pathol 1995;20:359-64. |
|3.||Caroff SN, Mann SC. Neuroleptic malignant syndrome. Medical Clin N Am 1993;77:185-202. [PUBMED] |
|4.||Caux F, Chosidow O, Philippon C, Roujeau JC, Revuz J. Increased serum and blister fluid levels of creatinine phosphokinase in patients with toxic epidermal necrolysis. Br J Dermatol 1994;130:337-41. [PUBMED] |
|5.||Friedman PS, Strickland I, Pirmohamed M, Park BK. Investigation of mechanism in toxic epidermal necrolysis induced by carbamazepine. Arch Dermatol 1994;130:598-604. |
|6.||Wallis C, McClymount W. Toxic epidermal necrolysis with adult respiratory distress syndrome. Anesthesia 1995;50:801-3. |
|7.||Kamata T, Sakamaki F, Fujitha H, Urana T, Mori M, Yamaguchi K, et al. Toxic epidermal necrolysis with tracheobronchial and pulmonary complications. Intern Med 1994;33:252-5. |
|8.||Claes P, Wintzen M, Allard S, Simons P, Deconick A. Nevirapine induced toxic epidermal necrolysis and toxic hepatitis treated successfully with a combination of intravenous immunoglobulins and N-acetyl cycteine. Eur J Intern Med 2004;15:255-58. |
|9.||Nori S, Nebesio C, Brasher R, Travers IB. Moxifloxacin associated drug hypersensitivity syndrome with toxic epidermal necrolysis and fulminant hepatic failure. Arch Dermatol 2004;140:1537-8. |
|10.||Mandelcorn R, Shear NH. Lupus-associated toxic epidermal necrolysis: A novel manifestation of lupus? J Am Acad Dermatol 2003;48:525-9. [PUBMED] [FULLTEXT] |
|This article has been cited by|
||Neuroleptic Malignant Syndrome in Children and Adolescents : A Review
| ||Young-Sook Kwack,Jae-Sung Ryu |
| ||Journal of korean Academy of Child and Adolescent Psychiatry. 2013; 24(1): 13 |
|[Pubmed] | [DOI]|
||Infections as complications of neuroleptic malignant syndrome
| ||Nikolaos Bilanakis,Vaios Peritogiannis,Georgios Kalampokis |
| ||The World Journal of Biological Psychiatry. 2009; 10(4-3): 973 |
|[Pubmed] | [DOI]|
|| Infections as complications of neuroleptic malignant syndrome
| ||Bilanakis, N., Peritogiannis, V., Kalampokis, G. |
| ||World Journal of Biological Psychiatry. 2009; 10(4 PART 3): 973-976 |