認識史帝芬強生症候群-高點醫護網
高點醫護網

篇名
認識史帝芬強生症候群
說明
觀念剖析
  史帝芬-強生症候群是一種皮膚與黏膜嚴重過敏反應,引起全身表皮細胞死亡,導致真皮與表皮分離的一種致命性疾病;容易引起面部、軀幹出現靶心狀病灶、口腔潰瘍、眼結膜紅腫、會陰部糜爛。
前言
  史帝芬-強生症候群(Stevens-Johnson syndrome,SJS)是一種皮膚與黏膜嚴重過敏反應(an immune-complex–mediated hypersensitivity complex that typically involves the skin and the mucous membranes),引起全身表皮細胞死亡,導致真皮與表皮分離(detachment)的一種致命性疾病;累及全身黏膜組織,包括眼、鼻、口、陰道、尿道、胃腸道、下呼吸道等處(significant involvement of oral, nasal, eye, vaginal, urethral, GI, and lower respiratory tract mucous membranes)。引起原因是藥物、感染。史帝芬-強生氏徵候群屬於多型紅斑的一種嚴重型(several investigators propose that Stevens-Johnson syndrome and toxic epidermal necrolysis (TEN) represent the same disease at different levels of severity),或中毒性表皮壞死症候群(TEN)的一個較輕微的形式。目前多將由藥物引起者稱史帝芬-強生氏徵候群,由病毒引起者稱多型性紅斑。
【註】 患病部位若超過體表面積(BSA) 30%以上,則稱中毒性表皮壞死症候群(Toxic epidermal necrolysis,TEN)。
  1. Stevens-Johnson syndrome:A "minor form of TEN," with less than 10% body surface area (BSA) detachment
  2. Overlapping Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN):Detachment of 10-30% BSA
  3. Toxic epidermal necrolysis Detachment of more than 30% BSA
歷史介紹
  史帝芬-強生氏症候群由兩位美國兒科醫生Albert Mason Stevens及Frank Chambliss Johnson描述,他們在1922年觀察2位7~8歲小朋友皆有發熱、皮疹、頰膜炎症、嚴重結膜炎等表現(an extraordinary, generalized eruption with continued fever, inflamed buccal mucosa, and severe purulent conjunctivitis),因此而被命名。當時兩位小朋友被誤診為hemorrhagic measles。
流行病學
  史帝芬-強生氏症候群每年大約有3/1,000,000。成人較兒童多見,女性:男性=3:2。
病因
  病因大致包括Infectious(常見於Pediatric cases)、Drug-induced與Malignancy- related (adults and elderly persons)、Idiopathic(25-50%) factors等四部分。
  1. 感染:一些病毒性疾病(如Herpes simplex virus、AIDS、Coxsackie viral infections、Influenza、Hepatitis、Mumps、Epstein-Barr virus and enteroviruses);細菌性疾病(Group A beta-hemolytic streptococci、Diphtheria、Brucellosis、Lymphogranuloma venereum、Mycobacteria、Mycoplasma pneumoniae、Rickettsial infections、Tularemia);真菌感染(如coccidioidomycosis, dermatophytosis, and histoplasmosis)。
  2. 藥物:抗生素(如penicillins and sulfa drugs are prominent; ciprofloxacin)、巴比妥鹽(Phenytoin、Carbamazepine、Valproic acid、Barbiturates)、抗癲癇藥物(psychoepileptics)、NSAIDs、抗痛風藥(如Allopurinol)、TNF-α antagonists (如infliximab、etanercept、adalimumab)、古柯鹼(Cocaine)、nevirapine及Indinavir。
  3. 遺傳:
    HLA-B1502 in patients of southeastern Asian ethnicity before starting treatment with carbamazepine
    HLA-B5801 HLA-B5801confers a risk of allopurinol-related reactions
    HLA-B44 Whites with HLA-B44 appear to be more susceptible to develop Stevens-Johnson syndrome
    HLA-A29、HLA-B12、HLA-DR7 associated with sulfonamide-induced Stevens-Johnson syndrome
    HLA-A2 encountered in Stevens-Johnson syndrome induced by NSAIDs
    HLA-A0206、HLA-DQB10601 strongly associated with Stevens-Johnson syndrome with ocular disease
症狀
  史帝芬-強生氏症候群會先出現類似流感的前驅症狀(Typical prodromal symptoms),包括咳嗽多痰、乏力、頭痛、關節痛(Cough productive of a thick purulent sputum、Headache、Malaise、Arthralgia),接著在面部與軀幹上半部位皮膚出現對稱性皮疹burning rash that begins symmetrically on the face and the upper part of the torso)---靶心狀病灶(target lesions),面積逐漸擴大,隨後出現水皰,可同時伴有眼的症狀(如Red eye、Tearing、Dry eye、Pain、Blepharospasm、Itching、Grittiness、Heavy eyelid、Foreign body sensation、Decreased vision、Burn sensation、Photophobia、Diplopia)。
 
(圖片來自考選部醫師專技)

  除在皮膚出現臨床表現外, 史帝芬-強生氏症候群上可累及身體各個部分 Oral mucosa、Esophagus、Pharynx and Larynx、Anus、Trachea、Vagina、Urethra 而出現相應器官表現。
併發症
  1. 嚴重眼部疾病(27-50%):Chronic cicatrizing conjunctivitis、Corneal epithelial defects、Corneal stromal ulcers、Corneal perforation、Endophthalmitis、Blindness);
  2. 胃腸道:如Esophageal strictures;
  3. 泌尿生殖道:如Renal tubular necrosis, renal failure, penile scarring, vaginal stenosis;
  4. 呼吸道:如Tracheobronchial shedding with resultant respiratory failure;
  5. 表皮:Scarring and cosmetic deformity, recurrences of infection through slow-healing ulcerations;
治療
  大部分是對症治療(most patients are treated symptomatically)。由藥物所以起的則必須停用引起過敏的藥物(Withdrawal of the suspected offending agent is critically important),並且靜脈補充水份。必要時可使用類固醇,但可能造成繼發性感染;近來有專家提出化學藥物治療,但有爭議(Immunomodulatory treatment is controversial);如有眼部疾病,應眼科醫生會診。
預後
  史帝芬-強生氏症候群約5%的致死率,史可爾登指數(SCORTEN scale)可以去評估SJS及TEN風險死亡率(The SCORTEN score calculates the risk for death in both SJS and TEN on the basis of the following variables):
1 Age >40 years 每一項目 1 分:死亡率計分如下:
  1. 0-1 points:≧3.2%
  2. 2 points:≧12.1%
  3. 3 points:≧35.3%
  4. 4 points:≧58.3%
  5. 5 or more points:≧90%
2 Malignancy
3 Heart rate >120
4 Initial percentage of epidermal detachment >10%
5 Serum glucose level >14 mmol/L
6 Blood BUN level >10 mmol/L
7 Bicarbonate level < 20 mmol/L
8 Persistent neutropenia lasting more than 5 days
9 Hypoalbuminemia < 2 g/dL
10 Persistent azotemia
關鍵詞
史帝芬強生症候群、過敏反應、多型紅斑、中毒性表皮壞死症候群、黏膜組織、對稱性皮疹、臨床醫學資訊館
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