中华皮肤科杂志
中華皮膚科雜誌
중화피부과잡지
Chinese Journal of Dermatology
2009年
2期
91-93
,共3页
郭一峰%姜嫒芳%唐黎%余红%祁怀山%姚志荣
郭一峰%薑嬡芳%唐黎%餘紅%祁懷山%姚誌榮
곽일봉%강애방%당려%여홍%기부산%요지영
外胚层发育不良症%免疫减弱宿主
外胚層髮育不良癥%免疫減弱宿主
외배층발육불량증%면역감약숙주
Ectodermal dysplasia%Immunocompromised host
患儿男,16个月.出生2个月后,反复出现不明原因发热,体温在38~40℃之间,敞开衣物并口服退热药后热退,发热及退热过程中皮肤始终干燥.7个月时行皮肤活检,诊断为无汗性外胚层发育不良.6个月起至今,反复发生上呼吸道感染或肺炎.20 d前,患儿出现舌部破溃糜烂,口周和双手红斑、水疱,伴高热.4 d前,皮疹加重,收入院.皮肤科检查示牙发育不全,仅见2颗门齿,呈上圆下尖的锥形;口唇周围、鼻腔、下颏和双下颌多处破溃糜烂,结厚血痂.臀部、阴囊和下肢见多处溃疡,部分溃疡周围有红斑基础上成簇水疱,中央有脐凹.双手暗紫红色肿胀,伴大量糜烂、结痂和渗出.实验室检查示白细胞和C反应蛋白显著增高,CD3、CD8和自然杀伤细胞降低,IgM降低.Ⅰ型单纯疱疹病毒IgM抗体阳性.诊断:无汗性外胚层发育不良伴免疫缺陷,播散性单纯疱疹病毒感染.入院后给予更昔洛韦抗病毒治疗和抗生素治疗,辅以营养支持和创面护理,治疗3周后皮疹愈合,痂皮脱落.
患兒男,16箇月.齣生2箇月後,反複齣現不明原因髮熱,體溫在38~40℃之間,敞開衣物併口服退熱藥後熱退,髮熱及退熱過程中皮膚始終榦燥.7箇月時行皮膚活檢,診斷為無汗性外胚層髮育不良.6箇月起至今,反複髮生上呼吸道感染或肺炎.20 d前,患兒齣現舌部破潰糜爛,口週和雙手紅斑、水皰,伴高熱.4 d前,皮疹加重,收入院.皮膚科檢查示牙髮育不全,僅見2顆門齒,呈上圓下尖的錐形;口脣週圍、鼻腔、下頦和雙下頜多處破潰糜爛,結厚血痂.臀部、陰囊和下肢見多處潰瘍,部分潰瘍週圍有紅斑基礎上成簇水皰,中央有臍凹.雙手暗紫紅色腫脹,伴大量糜爛、結痂和滲齣.實驗室檢查示白細胞和C反應蛋白顯著增高,CD3、CD8和自然殺傷細胞降低,IgM降低.Ⅰ型單純皰疹病毒IgM抗體暘性.診斷:無汗性外胚層髮育不良伴免疫缺陷,播散性單純皰疹病毒感染.入院後給予更昔洛韋抗病毒治療和抗生素治療,輔以營養支持和創麵護理,治療3週後皮疹愈閤,痂皮脫落.
환인남,16개월.출생2개월후,반복출현불명원인발열,체온재38~40℃지간,창개의물병구복퇴열약후열퇴,발열급퇴열과정중피부시종간조.7개월시행피부활검,진단위무한성외배층발육불량.6개월기지금,반복발생상호흡도감염혹폐염.20 d전,환인출현설부파궤미란,구주화쌍수홍반、수포,반고열.4 d전,피진가중,수입원.피부과검사시아발육불전,부견2과문치,정상원하첨적추형;구진주위、비강、하해화쌍하합다처파궤미란,결후혈가.둔부、음낭화하지견다처궤양,부분궤양주위유홍반기출상성족수포,중앙유제요.쌍수암자홍색종창,반대량미란、결가화삼출.실험실검사시백세포화C반응단백현저증고,CD3、CD8화자연살상세포강저,IgM강저.Ⅰ형단순포진병독IgM항체양성.진단:무한성외배층발육불량반면역결함,파산성단순포진병독감염.입원후급여경석락위항병독치료화항생소치료,보이영양지지화창면호리,치료3주후피진유합,가피탈락.
To report a case of 16-month-old boy with anhidrotic ectodermal dysplasia with immunodeficiency who experienced disseminated herpes simplex infection. From 2 months of age, the patient experienced multiple pyrexial episodes of undetermined origin, which responded well to anti-inflammatory agents after undressed. Abnormal sweat with dry skin was noted; therefore, the skin biopsy of right axilla was performed at 7 months of age, and suggested a diagnosis of anhidrotic ectodermal
dysplasia. Since 6 months of age, he developed recurrent upper respiratory infections and 2 episodes of pneumonia. Twenty days before, several glossal erosions occurred in the patient, supervened by painful and erosive eruptions and numerous blisters around the mouth and both hands with hyperpyrexia. Four days before, the patient was transferred to the department owing to skin lesion exacerbation. Cutaneous examination showed multiple crested or ulcerated plaques distributed eriorificially (mouth and nasal cavity) on the face. Several irregular, demarcated ulcers were scattered on the buttocks, scrotum and lower limbs, surrounded by grouped and umbilicated vesicles arising on erythema. Both hands were swelling, crusting and painful. Dentition was abnormal, and the patient had only 2 upper conical incisors. Routine investigation revealed that white cell count and C-reactive protein extremely elevated. Immunologic profile showed an abnormal distribution of lymphocyte subsets with decreased CD3+ T cells, CD8+ T cells and NK cells. Serum IgM level was slightly low. IgM antibodies to herpes simplex virus type 1 (HSV-1) were detected by serological testing. Based on the above-mentioned features, a diagnosis of anhidrotic ectodermal dysplasia with immunodeficiency and disseminated herpes simplex infection was confirmed. The patient was resolved favourahly after intravenous ganciclovir and antibiotics for 3 weeks without relapse of skin lesions.