Cho Jake, Elyaman Selsabeel A, Avera Stephen A, Iyamu Kenneth
Graduate Medical Education, University of Central Florida College of Medicine, Orlando, FL, USA.
Internal Medicine Residency Program, HCA Ocala Regional Medical Center, Ocala, FL, USA.
Am J Case Rep. 2019 Sep 20;20:1387-1393. doi: 10.12659/AJCR.917427.
BACKGROUND Erythroderma is an exfoliative dermatitis that manifests as generalized erythema and scaling that involves 90% of the body surface. If untreated, erythroderma can be fatal because of its metabolic burden and risk of secondary infections. CASE REPORT The patient was a 56-year-old male with prior rash attributed to group A Streptococcal cellulitis and discharged on Augmentin, Clindamycin with hydrocortisone cream, and Bactrim, but he had been noncompliant. He was admitted again for rash involving the face, torso, and extremities characterized by diffuse, desquamative, dry scales in morbilliform pattern. The patient was septic with bacteremia and compromised skin barrier. He was started on vancomycin and switched to Cefazolin IV due to concern for drug reaction. Autoimmune workup included antibodies for anti-Jo-1, anti-dsDNA, anti-centromere, and ANCA. However, only antinuclear antibody and scleroderma antibody were positive. Given the unclear workup results and lack of response to antibiotics, the patient was started on prednisone 60 mg PO and topical Triamcinolone 0.1% cream. A skin biopsy revealed psoriasiform hyperplasia with atypical T cell infiltrate and eosinophils, but negative for T cell gene rearrangement. The rash resolved after day 12 of application of topical Triamcinolone. CONCLUSIONS This case is unique in terms of the rarity of erythroderma and the diagnostic challenge given confounding factors such as noncompliance and drug reaction. Serious causes, such as SLE and cutaneous T cell lymphoma, were ruled out. Fortunately, the rash responded well to steroids; however, given the adverse effects of long-term use of topical steroids, the patient will need follow up with Dermatology.
背景 红皮病是一种剥脱性皮炎,表现为全身性红斑和鳞屑,累及90%的体表。若不治疗,红皮病因其代谢负担和继发感染风险可能会致命。 病例报告 该患者为一名56岁男性,既往有皮疹,归因于A组链球菌蜂窝织炎,出院时使用阿莫西林克拉维酸钾、克林霉素加氢化可的松乳膏以及复方磺胺甲恶唑,但他未遵医嘱用药。他因面部、躯干和四肢出现皮疹再次入院,皮疹特征为麻疹样弥漫性、脱屑性、干燥鳞屑。患者因菌血症而发生脓毒症,皮肤屏障受损。因担心药物反应,起初给予万古霉素治疗,后改用头孢唑林静脉注射。自身免疫检查包括抗Jo-1、抗双链DNA、抗着丝点抗体和抗中性粒细胞胞浆抗体检测。然而,仅抗核抗体和硬皮病抗体呈阳性。鉴于检查结果不明确且对抗生素无反应,开始给予患者口服泼尼松60毫克及外用0.1%曲安奈德乳膏。皮肤活检显示银屑病样增生,伴有非典型T细胞浸润和嗜酸性粒细胞,但T细胞基因重排为阴性。外用曲安奈德12天后皮疹消退。 结论 就红皮病的罕见性以及诸如不遵医嘱和药物反应等混杂因素带来的诊断挑战而言,本病例较为独特。排除了诸如系统性红斑狼疮和皮肤T细胞淋巴瘤等严重病因。幸运的是,皮疹对类固醇反应良好;然而,鉴于长期使用外用类固醇的不良反应,患者需要皮肤科随访。