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Artykuły w czasopismach na temat „Stevens Johnson's syndrome”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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1

Comparin, Cristiane, Günter Hans Filho, Luiz Carlos Takita, Nayara de Castro Wiziack Costa, Roberta Ayres Ferreira do Nascimento, and Lidiane de Oliveira Costa Nanni. "Treatment of toxic epidermal necrolysis with intravenous immunoglobulin: a series of three cases." Anais Brasileiros de Dermatologia 87, no. 3 (2012): 477–81. http://dx.doi.org/10.1590/s0365-05962012000300022.

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Stevens-Johnson's syndrome (SJS) and toxic epidermal necrolysis (TEN) are life-threatening dermatoses, that lead to keratinocyte apoptosis induced by interactions between Fas (cell death receptor) and soluble Fas-ligand, present in serum of Stevens-Johnson's syndrome / toxic epidermal necrolysis patients. Anti-Fas antibodies in intravenous immunoglobulin (IVIG) would block the apoptosis cascade. Three cases of toxic epidermal necrolysis occurred in one male and two female patients, after use of allopurinol, leprosy multidrug therapy concomitant with dipyrone, and diclofenac. The cases were tre

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V.Vijaya, Prasad* P.Venkata Sravan Kumar Dr R. Siddarama. "DEATH DUE TO STEVENS JOHNSON SYNDROME; A RARE CASE REPORT." Indo American Journal of Pharmaceutical Sciences 04, no. 07 (2017): 2072–76. https://doi.org/10.5281/zenodo.835176.

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Stevens Johnson’s syndrome is a life threatening drug induced hypersensitivity reaction. The drugs that cause SJS commonly are antibacterials (sulfonamides), anticonvulsants (phenytoin, phenobarbital, and carbamazepine), non-steroidal anti-inflammatory drugs (oxicam derivatives) and oxide inhibitors (allopurinol).Clinical symptoms are urticarial skin eruptions, arthralgia or arthritis, lymphadenopathy and fever.Treatment of Stevens Johnsons Syndrome includes systemic steroids, cyclosporine, intravenous immunoglobulin’s and supportive therapy.A male patient of 58 years was admitted in cardiolog

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HAMADA, Yoshiki, Akiko HAMADA, Michihiko KINOSHITA, Norihiko TAKADA, and Kanichi SETO. "A case of Stevens-Johnson's syndrome attributed to Sulpyrine." Japanese Journal of Oral & Maxillofacial Surgery 41, no. 7 (1995): 659–61. http://dx.doi.org/10.5794/jjoms.41.659.

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Jensen, Søren. "A CASE OF STEVENS-JOHNSON'S SYNDROME FOLLOWING ANTIEPILEPTIC MEDICATION." Acta Ophthalmologica 45, no. 4 (2009): 576–81. http://dx.doi.org/10.1111/j.1755-3768.1967.tb06524.x.

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GOMI, Hiroko, Harumi MIMURA, Junko SHIOJIMA, et al. "A Case of Esophagitis Associated with Stevens‐Johnson's Syndrome." Digestive Endoscopy 9, no. 4 (1997): 309–13. http://dx.doi.org/10.1111/j.1443-1661.1997.tb00507.x.

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Tammiraju, Iragavarapu, B. Srinivas, K. Nirupama, and KPruthvi Naresh. "Recurrent cardiac tamponade with stevens–Johnson's syndrome – A rare deadly combo." JOURNAL OF INDIAN COLLEGE OF CARDIOLOGY 11, no. 2 (2021): 82. http://dx.doi.org/10.4103/jicc.jicc_20_20.

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Катилов, А. В. "Principles of diagnostics and intensive therapy of a Stevens-Johnson's syndrome at children." Pain, anesthesia and intensive care, no. 4(69) (December 21, 2014): 77–82. http://dx.doi.org/10.25284/2519-2078.4(69).2014.84670.

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NISHIGUCHI, Hiroaki, Hiroko HAGINO, Shinichi TSURUSAKO, Iwai TOHNAI, Takeshi USAMI, and Minoru UEDA. "A case of Stevens-Johnson's syndrome showing initial symptoms in the oral cavity." Japanese Journal of Oral & Maxillofacial Surgery 49, no. 1 (2003): 19–22. http://dx.doi.org/10.5794/jjoms.49.19.

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Ström, Justus. "OCULAR SYMPTOMS IN FEBRILE MUCOCUTANEOUS REACTIONS (ECTODERMOSIS EROSIVA PLURIORIFICIALIS, STEVENS-JOHNSON'S SYNDROME, MUCOCUTANEOUS-OCULAR SYNDROME ETC.)." Acta Ophthalmologica 44, no. 3 (2009): 411–14. http://dx.doi.org/10.1111/j.1755-3768.1966.tb08051.x.

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Dahake, Shubham, Bibin Kurian, and Archana Maurya. "A Rare Low-Grade Glioma with Stevens Jonson’s Syndrome - Case Report." International Journal of Neonatal Care and Pediatric Nursing 4, no. 2 (2023): 1–7. http://dx.doi.org/10.46610/ijncpn.2023.v04i02.001.

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Introduction: The brain has a complicated structure within the body, but the CNS develops during growth and development in three stages: cytogenesis, histogenesis, and organogenesis, which determine the CNS's final makeup and shape. Organogenesis occurs in children when neural and extra-neural tissues mingle, causing a growing lesion inside the skull. Nearly 20% of the second-most prevalent group of paediatric neoplasms after leukaemia either a benign or malignant primary brain tumour may exist. The majority of infratentorial and close-to-midline brain tumours result in hydrocephalus. Astrocyt

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11

DeToledo, John C., Alireza Minagar, Meredith R. Lowe, and R. Eugene Ramsay. "Skin Eruption with Gabapentin in a Patient with Repeated AED-Induced Stevens-Johnson's Syndrome." Therapeutic Drug Monitoring 21, no. 1 (1999): 137–38. http://dx.doi.org/10.1097/00007691-199902000-00022.

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Venkatesan, S. A., and S. M. Rajappa. "HLA-B*1502 genotyping in carbamazepine induced Stevens Johnson's syndrome and toxic epidermal necrolysis." Journal of the Neurological Sciences 333 (October 2013): e62. http://dx.doi.org/10.1016/j.jns.2013.07.220.

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Chirag, U. Nayee, and R. Kubavat Amita. "A case report of Steven Johnson's Syndrome (SJS) /Toxic Epidermal Necrolysis(TEN) overlap caused by Nimesulide." World Journal of Biology Pharmacy and Health Sciences 18, no. 2 (2024): 154–56. https://doi.org/10.5281/zenodo.13734318.

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<strong>Introduction</strong>: Stevens–Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN) are rare, acute and life-threatening mucocutaneous diseases that are nearly always drug-related. Incidence of SJS and TEN is 0.05 to 2 persons per million populations per year. In India, Nimesulide is easily available as an over the counter drug (OTC), different cutaneous reactions associated with, Nimesulide including angioedema, maculo-papular rash, severe urticaria, pityriasis rosea and worsening of preexisting psoriasis. <strong>Patient concern (Case summary):</strong> A 17 years o

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Mattsson, Ragnar, and Olof Carlberg. "EYE LESIONS AND THEIR TREATMENT IN THE SO-CALLED STEVENS-JOHNSON'S SYNDROME OR ECTODERMOSIS EROSIVA PLURIORIFICIALIS." Acta Ophthalmologica 31, no. 5 (2009): 469–83. http://dx.doi.org/10.1111/j.1755-3768.1953.tb07664.x.

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Barea‐Jiménez, Natalia, Javier Calero, Damaris Molina‐Negrón, and Lydia M. López Del‐Valle. "Treatment for oral lesions in pediatric patients with Stevens‐Johnson's syndrome: A case report and literature review." International Journal of Paediatric Dentistry 30, no. 4 (2020): 489–96. http://dx.doi.org/10.1111/ipd.12615.

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Dr., Prarthana Kishore, Raghavendra Kini Dr., Meghana HC Dr., et al. "Steven Johnsons Syndrome Induced by Carbamezapene." International Journal of Innovative Science and Research Technology 8, no. 4 (2023): 2007–10. https://doi.org/10.5281/zenodo.8020743.

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Stevens – Johnson syndrome (SJS) is characterized by rapidly spreading blisters which occur in the form of macules or target lesions which has clinical features which may be potentially fatal. It is usually associated with drugs such as anticonvulsants including carbamazepine, lamotarigine, phenobarbotal, phenytoin and valproic acid. This is a rare case report in which we describe a case of Steven Johnsons Syndrome induced by Carbamezapene that was prescribed to treat trigeminal neuralgia affecting the oro-facial region.

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Okonkwo, Sunday Nnamdi, Ernest Ikechukwu Ezeh, and Emmanuel Olu Megbelayin. "Bilateral Levator Aponeurosis Disinsertion Following Stevens – Johnson Syndrome: Case Report." Scholars Journal of Medical Case Reports 9, no. 6 (2021): 687–89. http://dx.doi.org/10.36347/sjmcr.2021.v09i06.020.

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Stevens–Johnson syndrome is complex immunological syndrome characterized by acute blistering of skin and mucous membrane. The disease frequently involves the eye and can cause blindness. Here we report an unusual occurrence of bilateral blepharoptosis due to bilateral levator aponeurosis dehiscence following Stevens –Johnson’s syndrome.

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18

Syedraja, K., U. Karthikeyan, and S. Tamilselvan. "A Case Report of Phenytoin-Induced Stevens-Johnson Syndrome." International Journal of Research and Review 10, no. 5 (2023): 202–5. http://dx.doi.org/10.52403/ijrr.20230523.

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Stevens-Johnson syndrome and Toxic epidermal necrosis are acute, self-limited diseases, rare but life-threatening adverse drug reactions. Anti-epileptic drug-induced Steven-Johnson syndrome is a severe cutaneous adverse reaction, among anti-epileptic drugs carbamazepine and phenytoin are the major culprit. We report here a case of Steven-Johnson syndrome due to phenytoin. A 22-year-old female reported the chief complaint of fever and multiple rashes all over the body with skin peeling, gradual onset, and progressive in nature. The reaction was evoked after intake of T. Phenytoin for 1 ½ months

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Chetan, Ramesh Sangati, and Kudari Ananda. "Steven's Johnson Syndrome: A Case Report and Application of Lydia E. Hall's Core, Care, Cure, Theory with Nursing Process Approach." Research & Review: Management of Emergency and Trauma Nursing 1, no. 2 (2019): 5–10. https://doi.org/10.5281/zenodo.3251676.

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Steven’s–Johnson syndrome is abbreviated as SJS and is also medically recognized or it is also known as Lyell's syndrome, toxic epidermal necrolysis, and Stevens-Johnson syndrome toxic epidermal necrolysis spectrum. It's usually due to the reaction of medication or an infection. Later, it begins with flu-like symptoms, like Fever, unexplained widespread skin pain, a red or purple skin rash that spreads, blisters on your skin and the mucous membranes. To find out the Steven’s-Johnson syndrome clinical systemic examination is must, in which skin biopsy is important diag

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Sah, Ranjit, Samikshya Neupane, Shusila Khadka, et al. "A Case Study of Stevens–Johnson Syndrome-Toxic Epidermal Necrolysis (SJS-TEN) Overlap in Mycoplasma pneumoniae-Associated Tracheobronchitis." Case Reports in Infectious Diseases 2019 (May 30, 2019): 1–5. http://dx.doi.org/10.1155/2019/5471765.

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Stevens–Johnson syndrome is a medical emergency which is characterized by skin and mucosal reaction to the use of certain drugs. Atypical Steven–Johnson syndrome can occur due to various microorganisms and Mycoplasma pneumoniae being one of them. We present a clinical course, diagnosis, and successful management of Steven–Johnson syndrome-toxic epidermal necrolysis (SJS-TEN) overlap due to Mycoplasma pneumoniae in a 17-year-old Nepalese female. In the resource-limiting country and hospitals where serology and PCR for M. pneumoniae is not easily accessible, a simple bedside cold agglutination t

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Chernysh, V. F., N. N. Haritonova, A. N. Kulikov, P. A. Kacherovich, and A. A. Kol'bin. "Current surgical treatment options for ocular complications of Stevens-Johnson and Lyell's syndromes." Russian Journal of Clinical Ophthalmology 23, no. 2 (2023): 99–106. http://dx.doi.org/10.32364/2311-7729-2023-23-2-99-106.

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Epidermolytic drug reactions (EDR) are severe acute drug-induced allergic disorders characterized by extensive lesions of the skin and mucous membranes. Drug-induced Stevens-Johnson and Lyell's syndromes manifested with acute skin and mucous membrane disorders and often leading to lethal outcome may affect eyelids and ocular surface with different levels of severity and thus can cause serious functional ocular complications. The authors present two clinical reports of patients with ocular EDR manifestations in acute and long-term time periods and review the currently available effective treatm

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McGouran, DCR, T. Petterson, JM McLaren, and MP Wolbinski. "Mucositis, Conjunctivitis but no rash – The “Atypical Stevens –Johnson syndrome”." Acute Medicine Journal 10, no. 2 (2011): 81–82. http://dx.doi.org/10.52964/amja.0473.

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The Stevens-Johnson syndrome (SJS) classically involves a rash, conjunctivitis and mucositis. We describe the case of a young adult male with isolated mucositis and conjunctivitis . Previous rare reports of severe SJS like syndromes without a rash are confined to children, usually with mycoplasma pnemoniae infection.1 Terminology for this syndrome includes – “Stevens-Johnson Syndrome without skin lesions”, or “Atypical Stevens – Johnson Syndrome”.2 This case highlights the importance of maintaining an open mind when a “full house” of clinical features is absent. It also illustrates the use of

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Oliveira, Alex Ferreira de, Ingrith do Socorro Neves da Silva, Lídia Pinheiro de Brito, et al. "Stevens-Johnson Syndrome, fisiopatológics aspects: A literature review." Revista Científica Multidisciplinar Núcleo do Conhecimento 06, no. 08 (2016): 40–51. http://dx.doi.org/10.32749/nucleodoconhecimento.com.br/health/syndrome-stevens-johnson.

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Mkhoyan, Anna, Md Foorquan Hashmi, Fiza Khan, Naira Gyulazyan, Vigen Asoyan, and Varsen Nersisyan. "Stevens-Johnson syndrome: a case report of possible cephalosporin-induced cutaneous adverse reaction." Journal of Infection in Developing Countries 17, no. 10 (2023): 1493–96. http://dx.doi.org/10.3855/jidc.18301.

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A severe medical condition known as Stevens-Johnson syndrome (SJS) is marked by a cutaneous and mucosal reaction from the use of specific medications. The prodromal illness is followed by severe mucocutaneous symptoms in this immune-mediated disease. We describe the clinical history of a 55-year-old Caucasian woman who was exposed to cephalosporins. In resource-constrained countries and hospitals where cutaneous biopsy is not readily available, it is not easy to diagnose Steven Johnson Syndrome. This is particularly true in countries where the incidence of infectious diseases such as scarlet f

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Rozenbajgier, Martyna, Justyna Wójcik-Grudzień, Paulina Pawłowska, and Alicja Ozga-Stachurska. "Stevens–Johnson Syndrome and Toxic Epidermal Necrolysis, A Review of Pathogenesis, Clinical Features, Diagnosis and Treatment." Journal of Education, Health and Sport 12, no. 9 (2022): 512–18. http://dx.doi.org/10.12775/jehs.2022.12.09.060.

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Stevens Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are rare, acute conditions, potentially life-threatening, immune-mediated and often unpredictable. Characteristic for SJS and TEN is acute necrosis of the epidermis and mucous membranes, caused by the extensive death of keratinocytes. These syndromes are considered hypersensitivity reactions. They are most often caused by drugs. There have also been reports of SJS / TEN being caused by infection, SJS/TEN disease is very rare and due to its rarity there is no specific pharmaceutical algorythm. Supportive care and tr

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Ghosh, Somdatta, and Supreeti Biswas Mondal. "Carbamazepine Induced Stevens Johnson Syndrome - A Case Report." International Journal of Science and Research (IJSR) 14, no. 2 (2025): 416–18. https://doi.org/10.21275/sr25206094227.

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Ramayanti, Sri. "MANIFESTASI ORAL DAN PENATALAKSANAAN PADA PENDERITA SINDROM STEVENS-JOHNSON." Majalah Kedokteran Andalas 35, no. 2 (2011): 91. http://dx.doi.org/10.22338/mka.v35.i2.p91-97.2011.

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AbstrakSindrom Stevens-Johnson adalah bentuk penyakit mukokutan dengan tanda dan gejala sistemik yang parah berupa lesi target dengan bentuk yang tidak teratur, disertai macula, vesikel, bula, dan purpura yang tersebar luas terutama pada rangka tubuh. Sindrom Stevens-Johnson mempunyai tiga gelaja yang khas yaitu kelainan pada mata berupa konjungtivitis, kelainan pada genital berupa balanitis dan vulvovaginitis, serta kelainan oral berupa stomatitis. Diagnosis sindrom Stevens-Johnson terutama berdasarkan atas anamnesis, pemeriksaan klinis dan pemeriksaan penunjang perawatan pada penderita sindr

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Lucero, Carmen León Rocha, Elizabeth Rodea Montellano Sarahí, del Rosario Escalona Arroyo María, Ramiro García Navarro Ángel, Méndez Carrasco Martha, and Fresnel Narcisse Alvarez Jahir. "Toxic Epidermal Necrolysis Induced by Allopurinol, One Case in a Million." INTERNATIONAL JOURNAL OF MEDICAL SCIENCE AND CLINICAL RESEARCH STUDIES 03, no. 12 (2023): 3123–28. https://doi.org/10.5281/zenodo.10409670.

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<strong>Background</strong>:Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are part of the spectrum of one of the most serious dermatological conditions that occur in the hospital setting, considered a dermatological emergency. Stevens-Johnson syndrome is called toxic epidermal necrolysis (TEN) when ≥30% of the body surface is affected, and it is the most serious form of the disease, with adverse drug reactions being the main etiology, up to 80%.   <strong>Clinical case:</strong>We present the clinical case of a 30-year-old male, with a history of systemic arterial

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Doležalová, Irena, Ivan Rektor, and Milan Brázdil. "Stevens-Johnson syndrome: complications as part of neurointensive care." Neurologie pro praxi 18, no. 5 (2017): 336–40. http://dx.doi.org/10.36290/neu.2019.049.

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Ruttkay-Nedecká, Anna, David Frejlach, Petra Gkalpakioti, and Jan David. "Stevens-Johnson syndrome as a rare complication of mycoplasma infection." Pediatrie pro praxi 26, no. 3 (2025): 179–82. https://doi.org/10.36290/ped.2025.035.

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Basak, Arpan Kumar, and Joya Debnath. "Stevens-Johnson Syndrome." KYAMC Journal 8, no. 2 (2018): 31–35. http://dx.doi.org/10.3329/kyamcj.v8i2.35702.

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Stevens-Johnson syndrome (SJS) is an immune complex mediated hypersensitivity complex that typically involves the skin and mucous membranes. While minor presentations may occur, significant involvement of oral, nasal, eye, vaginal, urethral, gastrointestinal, and lower respiratory mucous membranes may develop in the course of the illness. GI and respiratory involvement may progress to necrosis. Stevens-Johnson syndrome is a serious systemic disorder with the potential for severe morbidity and even death. The syndrome was first described in 1922, when the American pediatricians Albert Mason Ste

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Pathak, Dr Gargi H., Dr Anuya Chauhan, and Dr Dhriti Shukla. "Drug induced Stevens Johnsons Syndrome : a case report." International Journal Of Medical Science And Clinical Invention 5, no. 1 (2018): 3465–66. http://dx.doi.org/10.18535/ijmsci/v5i1.19.

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Stevens Johnson syndrome is an acute self limited disease presenting with severe mucosal erosions with widespread erythematous, cutaneous macules or atypical targets .The majority of cases are drug induced affecting oral and perioral region. A 3 year old male child presented with chief complaints of fever, cough, cold , breathlessness and extensive rashes on the skin of face , oral mucosa, neck, abdomen, erythema of conjunctiva , ulceration of eyelid and oral cavity. The reaction was evoked after consumption of tab oxcarbamezapine since 10 days . He was treated with corticosteroids , ant

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Olisova, O. Yu, O. V. Grabovskaya, N. P. Teplyuk, A. A. Lepekhova, D. V. Ignatiev, and Kseniya V. Ignatieva. "Stevens-Johnson syndrome." Russian Journal of Skin and Venereal Diseases 19, no. 4 (2016): 216–20. http://dx.doi.org/10.18821/1560-9588-2016-19-4-216-220.

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The literature review of the epidemiology, etiology and pathogenesis, clinical presentation and diagnosis of the syndrome of Stevens-Johnson severe life-threatening disease characterized by extensive lesions of the skin and mucous membranes, fever and bone and muscle aches, often induced by medication is presented. A review on the methods of treatment and prevention of this disease is presented. The clinical case of patient with the syndrome of Stevens-Johnson is described. The successful treatment of Syndrome Stevens-Johnson with high-dose systemic glucocorticoids was performed.

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Hasan, R., A. Abidi, A. Ahmad, K. Saxena, A. D. Rizvi, and A. Thadani. "ACECLOFENAC INDUCED STEVENS JOHNSON SYNDROME: A RARE CASE REPORT." Era's Journal of Medical Research 4, no. 1 (2017): 76–79. http://dx.doi.org/10.24041/ejmr2017.19.

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Arora, Surabhi, Afroz Abidi, Fariha Fatima, Roohana Hasan, Darakhshan Rizvi, and Anupriya Thadani. "METHOTREXATE INDUCED STEVENS JOHNSON SYNDROME: A RARE CASE REPORT." Era's Journal of Medical Research 5, no. 2 (2018): 197–99. http://dx.doi.org/10.24041/ejmr2018.95.

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Madhavi, CH Bindhu, K. Vineetha, Balaiah Sandyapakula, and T. Srinivasa Rao. "A Clinical Case Report on Stevens-Johnson Syndrome (SJS)." International Journal of Pharma Research and Health Sciences 7, no. 3 (2019): 2958–61. http://dx.doi.org/10.21276/ijprhs.2019.03.01.

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Stewart, Michael G., Newton O. Duncan, Daniel J. Franklin, Ellen M. Friedman, and Marcelle Sulek. "Head and Neck Manifestations of Erythema Multiforme in Children." Otolaryngology–Head and Neck Surgery 111, no. 3P1 (1994): 236–42. http://dx.doi.org/10.1177/01945998941113p112.

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Erythema multiforme, Stevens-Johnson syndrome, and toxic epidermal necrolysis are related disorders of skin and mucous membranes, which are typically associated with antecedent medication use or infection. We review 108 cases of erythema multiforme, Stevens-Johnson syndrome, and toxic epidermal necrolysis from Texas Children's Hospital, Houston, Texas, from 1981 to 1991, and illustrate the characteristic skin and mucosal lesions. In addition, we describe in detail two unusual cases requiring intensive airway management. Head and neck manifestations were present in 4 of 79 patients (5%) with er

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Laurencin, Cato T., Richard F. Horan, Patrick B. Senatus, Clara B. Wheeler, and Stephen J. Lipson. "Stevens-Johnson-Type Reaction with Vancomycin Treatment." Annals of Pharmacotherapy 26, no. 12 (1992): 1520–21. http://dx.doi.org/10.1177/106002809202601206.

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OBJECTIVE: To report a case of Stevens-Johnson syndrome caused by vancomycin. CASE SUMMARY: Stevens-Johnson syndrome is an acute mucocutaneous process characterized by epidermal and mucosal desquamation. Its pathogenesis is poorly understood. Mortality rates have ranged from 30 to 100 percent. We describe a case of Stevens-Johnson syndrome related to the use of vancomycin in a 71-year-old woman with rheumatoid arthritis receiving treatment for an infected cervical fusion site. Classic “target” lesions distributed throughout the trunk and extremities along with erosive lesions involving the ora

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Fitriany, Julia, and Fajri Alratisda. "STEVENS JOHNSON SYNDROME." AVERROUS: Jurnal Kedokteran dan Kesehatan Malikussaleh 5, no. 1 (2019): 94. http://dx.doi.org/10.29103/averrous.v5i1.1632.

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Stevens Johnson Syndrome (SJS) merupakan suatu sindroma atau kumpulan gejala yang mengenai kulit, selaput lendir, dan mata dengan keadaan umum yang bervariasi dari ringan sampai berat. Penyakit ini bersifat akut dan pada bentuk yang berat dapat menyebabkan kematian, oleh karena itu penyakit ini merupakan salah satu kegawatdaruratan penyakit kulit. Sindroma ini merupakan salah satu contoh immune-complex-mediated hypersensitivity, atau yang juga disebut reaksi hipersensitivitas tipe III, di mana kejadiaannya dapat diinduksi oleh paparan obat, infeksi, imunisasi, maupun akibat paparan fisik lain

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Nurtdinova, G. M., E. S. Galimova, O. I. Kucher, and V. K. Muslimova. "Stevens — Johnson syndrome." Russian Medical Review 4, no. 1 (2020): 52–57. http://dx.doi.org/10.32364/2587-6821-2020-4-1-52-57.

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Fein, Jordan D., and Kendal L. Hamann. "Stevens–Johnson Syndrome." New England Journal of Medicine 352, no. 16 (2005): 1696. http://dx.doi.org/10.1056/nejmicm031127.

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&NA;. "STEVENS-JOHNSON SYNDROME." Nursing 17, no. 6 (1987): 96–101. http://dx.doi.org/10.1097/00152193-198706000-00027.

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Bryant, Bobby G., and B. Lynn Mathews. "Stevens-Johnson Syndrome." Drug Intelligence & Clinical Pharmacy 20, no. 6 (1986): 489–93. http://dx.doi.org/10.1177/106002808602000612.

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Stevens-Johnson syndrome (SJS) is an acute inflammatory eruption of the skin and mucous membranes. Presented here is a case of an 18-month-old child admitted to the hospital with raised erythematous rash with some vesicular formation. The rash and associated symptomatology developed in a manner consistent with SJS. The child was treated for 27 days and was discharged in a much improved condition. This syndrome is reviewed in regard to incidence, etiology, clinical features, and management. Of particular emphasis are the drugs that may precipitate this syndrome.

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Starcher, Laura C., and Anne E. Braun. "Stevens-Johnson Syndrome." Dimensions Of Critical Care Nursing 4, no. 6 (1985): 330–34. http://dx.doi.org/10.1097/00003465-198511000-00003.

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Edwards, Robbie, and Marie Ridder. "Stevens-Johnson Syndrome." Dimensions Of Critical Care Nursing 4, no. 6 (1985): 335–48. http://dx.doi.org/10.1097/00003465-198511000-00004.

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Davis, Wesley D., and Phillip A. Schafer. "Stevens–Johnson Syndrome." Advanced Emergency Nursing Journal 40, no. 3 (2018): 176–82. http://dx.doi.org/10.1097/tme.0000000000000197.

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Dhannisa Ika Savitri and Mohammad Mimbar Topik. "Stevens-Johnson Syndrome." Detector: Jurnal Inovasi Riset Ilmu Kesehatan 2, no. 1 (2024): 217–26. http://dx.doi.org/10.55606/detector.v2i1.3335.

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Stevens-Johnson Syndrome (SJS) is an antibody-mediated disease characterized by prodromal symptoms followed by severe mucocutaneous manifestations. The more severe form of SJS is Toxic Epidermal Necrolysis (TEN), which causes an inflammatory response resulting in keratinocyte necrosis and perivascular lymphocyte infiltration. The incidence of SJS is said to be 1 - 6 per one million people per year, while the incidence of TEN is only 0.4 - 1.2 per one million people per year. So far, similar studies on SJS/TEN cases in Indonesia are minimal as this disease is one of the rare cases. SJS/TEN is a

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Ting, H. C., and B. A. Adam. "Stevens-Johnson Syndrome." International Journal of Dermatology 24, no. 1 (1985): 587–91. http://dx.doi.org/10.1111/j.1365-4362.1985.tb05580.x.

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Ting, H. C., and B. A. Adam. "Stevens-Johnson Syndrome." International Journal of Dermatology 24, no. 9 (1985): 587–91. http://dx.doi.org/10.1111/j.1365-4362.1985.tb05857.x.

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Lesh, Diane. "Stevens-Johnson Syndrome." Journal of the American Academy of Nurse Practitioners 7, no. 11 (1995): 549–51. http://dx.doi.org/10.1111/j.1745-7599.1995.tb01245.x.

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