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[皮肤利什曼病——一例来自伯利兹的输入病例]

[Cutaneous leishmaniasis--an import from Belize].

作者信息

Schnedl Jakob, Auer Herbert, Fischer Marcellus, Tomaso Herbert, Pustelnik Tom, Mooseder Gerhard

机构信息

Heeresspital Wien, Dermatologische Abteilung, Wien, Osterreich.

出版信息

Wien Klin Wochenschr. 2007;119(19-20 Suppl 3):102-5. doi: 10.1007/s00508-007-0871-7.

Abstract

Cutaneous leishmaniasis of the New World, in particular when caused by Leishmania (L.) braziliensis, harbours the risk of lymphogenic as well as hematogenic dissemination. This may result in mucocutaneous leishmaniasis causing severe destruction of orofacial structures. Dissemination may occur years after the disappearance of the skin lesions. In contrast, cutaneous leishmaniasis of the old world, is typically restricted to the site of inoculation. Therefore, a conservative diagnostic and therapeutic approach is usually sufficient. Infections acquired in the new world should be treated systemically, if infection with Leishmania (Viannia) braziliensis complex cannot be excluded. Here we report on three Austrian soldiers, who, weeks after having participated in an international jungle patrol course in Belize, presented themselves with multiple ulcers on the upper limbs. Diagnosis of cutaneous leishmaniasis was made based upon histological evaluation of biopsies taken from several ulcers revealing the presence of leishmanial bodies, and detection of amastigote leishmania in smears of material obtained from the ulcers. As species phenotyping could not be performed, infection with L. brasiliensis as well as progression into a mucocutaneous form were possible, demanding systemic therapy. Several treatment options including local cryotherapy with liquid nitrogen, paromomycin (Humatis Pulvis, Parke-Davis) 15% topically or oral fluconazole (Diflucan, Pfizer) 200 mg/d were applied, but showed no effect. Hence, a systemic therapy with intravenous pentamidine (Pentacarinat, Gerot), three times in total, 3-4 mg/kg body weight each, led to a complete regression of the lesions within four weeks.

摘要

新大陆的皮肤利什曼病,尤其是由巴西利什曼原虫(Leishmania (L.) braziliensis)引起的,存在淋巴管性及血源性播散的风险。这可能导致黏膜皮肤利什曼病,造成口腔面部结构的严重破坏。播散可能在皮肤病变消失数年之后发生。相比之下,旧大陆的皮肤利什曼病通常局限于接种部位。因此,保守的诊断和治疗方法通常就足够了。如果不能排除感染巴西利什曼原虫(Leishmania (Viannia) braziliensis)复合体,在新大陆获得的感染应进行全身治疗。在此,我们报告三名奥地利士兵,他们在参加了在伯利兹举行的国际丛林巡逻课程数周后,上肢出现多处溃疡。基于对取自多个溃疡的活检组织进行组织学评估发现利什曼小体,以及在从溃疡获取的材料涂片检测到无鞭毛体利什曼原虫,从而诊断为皮肤利什曼病。由于无法进行种属表型分析,感染巴西利什曼原虫以及进展为黏膜皮肤型均有可能,因此需要全身治疗。应用了多种治疗方案,包括液氮局部冷冻疗法、15%的局部用巴龙霉素(Humatis Pulvis,Parke-Davis)或口服氟康唑(Diflucan,Pfizer)200mg/d,但均无效果。因此,采用静脉注射喷他脒(Pentacarinat,Gerot)进行全身治疗,共三次,每次3 - 4mg/kg体重,使病变在四周内完全消退。

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