Allopurinol-induced toxic epidermal necrolysis featuring almost 60% skin detachment

被引:8
作者
Wang, Feifei [2 ]
Ma, Zhuo [1 ]
Wu, Xinan [2 ]
Liu, Lihong [1 ]
机构
[1] Capital Med Univ, Beijing Chao Yang Hosp, Pharm Dept, 8 GongrenTiyuchangNanlu, Beijing 100020, Peoples R China
[2] Hefei BOE Hosp, Pharm Dept, Hefei, Anhui, Peoples R China
关键词
toxic epidermal necrolysis; HLA genes; allopurinol; STEVENS-JOHNSON-SYNDROME;
D O I
10.1097/MD.0000000000016078
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale: Toxic epidermal necrolysis (TEN) is a life-threatening, immunologically mediated, and usually drug-induced disease. Rarely, clinical pharmacists participating in finding the etiology have been reported. Patients concerns: A 33-year-old male presented to the emergency department with a 1-day history of fever and rash. The patient, being newly diagnosed with gout 10 days ago, received allopurinol at a dose of 250 mg by mouth daily. After 10 days' exposure to allopurinol, the patient manifested with an "influenza-like" prodromal phase (fever of 38 degrees C, throat pains), which was treated with amoxicillin and nonsteroidal anti-inflammatory drugs of the oxicam type. The next day, he developed a worsening fever of 39.5 degrees C, accompanied by a pruriginous rash all over his body. Diagnosis: On physical examination, we observed coalescing dusky red macules over>60% of his body surface area, with blisters and detachment of large sheets of necrolytic epidermis all over his chest and face. The diagnosis of TEN was confirmed. Interventions: The patient recovered following treatment with short-term high-dose methylprednisolone sodium succinate, immunoglobulin therapy, topical medication, and supportive therapy. Outcomes: He showed a slow but progressive improvement both in symptoms and cutaneous manifestations. Reepithelization of the skin was achieved after 3 weeks. Lessons: Drug-induced-TEN is potentially fatal. This case underlines the necessity of asking medication history in detail and detecting related drug gene to correctly identify the cause of TEN.
引用
收藏
页数:4
相关论文
共 18 条
  • [1] Toxic epidermal necrolysis-like acute cutaneous lupus erythematosus in a patient with progressive systemic sclerosis
    Aiempanakit, K.
    Chiratikarnwong, K.
    Juthong, S.
    Auepemkiate, S.
    [J]. LUPUS, 2018, 27 (11) : 1860 - 1863
  • [2] Bloom R, 2017, AN BRAS DERMATOL, V92, P139
  • [3] Burn Center Care of Patients with Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis
    Cartotto, Robert
    [J]. CLINICS IN PLASTIC SURGERY, 2017, 44 (03) : 583 - +
  • [4] Chapman James, 2017, Clin Pract Cases Emerg Med, V1, P417, DOI 10.5811/cpcem.2017.6.34371
  • [5] Cost-effectiveness analysis of HLA-B*58:01 genetic testing before initiation of allopurinol therapy to prevent allopurinol-induced Stevens-Johnson syndrome/toxic epidermal necrolysis in a Malaysian population
    Chong, Huey Yi
    Lim, Yi Heng
    Prawjaeng, Juthamas
    Tassaneeyakul, Wichittra
    Mohamed, Zahurin
    Chaiyakunapruk, Nathorn
    [J]. PHARMACOGENETICS AND GENOMICS, 2018, 28 (02) : 56 - 67
  • [6] Toxic epidermal necrolysis: Review of pathogenesis and management
    Downey, Andrew
    Jackson, Chris
    Harun, Nadia
    Cooper, Alan
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2012, 66 (06) : 995 - 1003
  • [7] Fakoya Adegbenro Omotuyi John, 2018, Open Access Maced J Med Sci, V6, P730, DOI 10.3889/oamjms.2018.148
  • [8] HLA-B*58:01 is a risk factor for allopurinol-induced DRESS and Stevens-Johnson syndrome/toxic epidermal necrolysis in a Portuguese population
    Goncalo, M.
    Coutinho, I.
    Teixeira, V.
    Gameiro, A. R.
    Brites, M. M.
    Nunes, R.
    Martinho, A.
    [J]. BRITISH JOURNAL OF DERMATOLOGY, 2013, 169 (03) : 660 - 665
  • [9] A Review of the Active Treatments for Toxic Epidermal Necrolysis
    Kinoshita, Yuri
    Saeki, Hidehisa
    [J]. JOURNAL OF NIPPON MEDICAL SCHOOL, 2017, 84 (03) : 110 - 117
  • [10] Kinoshita Yuri, 2016, J Nippon Med Sch, V83, P216, DOI 10.1272/jnms.83.216