Department of Dermatology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
Department of Cosmetic Applications and Management, Yuh Ying Junior College of Healthcare and Management, Kaohsiung, Taiwan.
J Eur Acad Dermatol Venereol. 2018 Sep;32(9):1575-1583. doi: 10.1111/jdv.14804. Epub 2018 Feb 12.
Protothecosis is an uncommon infection caused by the achlorophyllic algae found more commonly in tropical areas. Only a limited number of cases have been reported.
We aimed to evaluate the clinicopathological features and treatment outcomes of cutaneous protothecosis.
We retrospectively identified 20 pathology-confirmed cases of cutaneous protothecosis based on skin biopsies in two tertiary medical centres in Taiwan from 1997 to 2015.
The age of the patients at the time of diagnosis ranged from 48 to 85 years (mean age of 74 years). All lesions developed on the limbs. Twelve (60%) patients had adrenal insufficiency, but no patients had active malignancy at diagnosis. Interestingly, four (20%) patients had concurrent scabies infestation. Clinically, most lesions were erythematous plaques studded with punctate ulcers. Microscopically, the most common finding was granulomatous inflammation. Nineteen (95%) cases were successfully treated with itraconazole for 14-148 days with only one case of recurrence. Concomitant scabies should be suspected if pruritus is recalcitrant despite itraconazole treatment.
Despite its rarity, cutaneous protothecosis has become more significant due to an increased prevalence of immunocompromised individuals. Steroid overuse or iatrogenic adrenal insufficiency predisposes individuals to high-risk infections. Neglecting the disease leads to a chronic and incurable state. Protothecosis should be suspected in chronic eczematous and ulcerative plaques on the limbs refractory to conventional antibacterial and antiviral treatments, especially in patients with adrenal insufficiency. Clinical suspicion should be confirmed by skin biopsies, and confirmed cases can be successfully treated with itraconazole.
原藻病是一种由在热带地区更常见的无叶绿素藻类引起的罕见感染。仅有少数病例报告。
我们旨在评估皮肤原藻病的临床病理特征和治疗结果。
我们回顾性地在台湾的两个三级医疗中心,根据从 1997 年到 2015 年的皮肤活检,确定了 20 例经病理证实的皮肤原藻病病例。
患者在诊断时的年龄从 48 岁到 85 岁(平均年龄为 74 岁)不等。所有病变均发生在四肢。12 例(60%)患者有肾上腺功能不全,但无患者在诊断时患有活动性恶性肿瘤。有趣的是,有 4 例(20%)患者并发疥疮感染。临床上,大多数病变为红斑斑块,散布着点状溃疡。显微镜下,最常见的发现是肉芽肿性炎症。19 例(95%)患者成功地接受伊曲康唑治疗 14-148 天,仅 1 例复发。如果伊曲康唑治疗后瘙痒仍然顽固,应怀疑同时存在疥疮。
尽管罕见,但由于免疫功能低下人群的增加,皮肤原藻病的发病率越来越高。皮质类固醇的过度使用或医源性肾上腺功能不全使个体易患高危感染。忽视该疾病会导致慢性和不可治愈的状态。在对常规抗菌和抗病毒治疗反应不佳的四肢慢性湿疹性和溃疡性斑块中,应怀疑存在原藻病,特别是在有肾上腺功能不全的患者中。临床怀疑应通过皮肤活检确认,确诊病例可用伊曲康唑成功治疗。