一例输入性婴儿利什曼原虫皮肤利什曼病;旅行19年后出现的罕见病例。
A case of imported Leishmania infantum cutaneous leishmaniasis; an unusual presentation occurring 19 years after travel.
作者信息
Crowe Amy, Slavin John, Stark Damien, Aboltins Craig
机构信息
Department of Infectious Diseases, St Vincent's Hospital, Melbourne, Australia.
Department of Pathology, St Vincent's Hospital, Melbourne, Australia.
出版信息
BMC Infect Dis. 2014 Nov 27;14:597. doi: 10.1186/s12879-014-0597-x.
BACKGROUND
Leishmania infantum is a flagellated protozoan parasite that is able to parasitize blood and tissue. Leishmania species cause a spectrum of clinical disease with cutaneous, visceral or mucosal involvement. L. infantum is recognised as a cause of visceral leishmaniasis (VL) and is less commonly reported as a cause of cutaneous leishmaniasis (CL) from countries around the Mediterranean basin. This is the first report of imported L. infantum CL to Australia and is remarkable for a 19 year period between the patient's exposure to an endemic region, and the manifestation of symptoms.
CASE PRESENTATION
A 76 year old Italian-born man presented to our institution with a non-healing lesion over his upper lip, abutting his nasal mucosa. The patient had travelled to Italy, an endemic area for L. infantum 19 years earlier but had resided in Australia, a non-endemic area since. Histopathology performed on a biopsy of the lesion demonstrated findings consistent with CL. A species specific polymerase chain reaction (PCR) performed on the tissue detected L. infantum. The patient had complete clinical recovery following treatment with Liposomal amphotericin B at a dose of 3 mg/kg for five days followed by a subsequent 3 mg/kg dose at day ten.
CONCLUSIONS
L. infantum should be recognised as a cause of imported CL in returned travellers from the Mediterranean. In this case, the incubation period for L. infantum CL was at least 19 years. This case adds to the described spectrum of clinical presentations of leishmaniasis and supports the theory of parasite persistence underlying natural immunity and recurrence of disease. Clinicians should consider L. infantum CL in the differential diagnosis of a non-healing skin lesion in any patient who reports travel to the Mediterranean, even when travel occurred several years before clinical presentation.
背景
婴儿利什曼原虫是一种能够寄生于血液和组织中的有鞭毛原生动物寄生虫。利什曼原虫属可引发一系列临床疾病,累及皮肤、内脏或黏膜。婴儿利什曼原虫被认为是内脏利什曼病(VL)的病因,在地中海盆地周边国家,其作为皮肤利什曼病(CL)病因的报道较少。这是澳大利亚首例输入性婴儿利什曼原虫所致CL的报告,值得注意的是,患者从接触流行地区到症状出现间隔了19年。
病例介绍
一名76岁出生于意大利的男性因上唇靠近鼻黏膜处有一不愈合病灶前来我院就诊。该患者19年前前往意大利,该地是婴儿利什曼原虫的流行区,此后一直居住在澳大利亚,这是一个非流行区。对病灶活检进行的组织病理学检查结果与CL一致。对组织进行的物种特异性聚合酶链反应(PCR)检测到了婴儿利什曼原虫。患者接受脂质体两性霉素B治疗,剂量为3mg/kg,连用5天,第10天再给予3mg/kg剂量,治疗后临床完全康复。
结论
婴儿利什曼原虫应被视为来自地中海地区回国旅行者输入性CL的病因。在本病例中,婴儿利什曼原虫所致CL的潜伏期至少为19年。该病例增加了利什曼病所描述的临床症状谱,并支持了寄生虫持续存在是自然免疫和疾病复发基础的理论。临床医生在对任何有地中海地区旅行史的患者出现不愈合皮肤病变进行鉴别诊断时,都应考虑婴儿利什曼原虫所致CL,即使旅行发生在临床表现出现前数年。