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土耳其地中海地区南部儿童内脏利什曼病的鉴定

Identification of from Pediatric Visceral Leishmaniasis in Southern Mediterranean Region of Turkey.

作者信息

Alabaz Derya, Eroğlu Fadime, Elçi Hüseyin, Çay Ümmühan

机构信息

Department of Pediatrics, Pediatric Infectious Diseases, Faculty of Medicine, Cukurova University, Adana, Turkey.

Aksaray University, Basic Sciences Medical Parasitology Departman, Aksaray, Turkey.

出版信息

Mediterr J Hematol Infect Dis. 2022 Jul 1;14(1):e2022053. doi: 10.4084/MJHID.2022.053. eCollection 2022.

Abstract

BACKGROUND AND OBJECTIVE

Protozoa of the genus are obligate intracellular parasites, and species cause a spectrum of species-specific clinical symptoms known as cutaneous, mucocutaneous, and visceral leishmaniasis. For example, and cause cutaneous leishmaniasis, while and cause visceral leishmaniasis (VL). However, molecular studies in recent years have shown that species cause different clinical symptoms.

OBJECTIVES

Our aim was to evaluate the relationship between the clinical and molecular characterization of leishmania isolates in children with VL defined in Turkey, an intercontinental transitional region.

METHODS

The clinical diagnosis of VL was confirmed by detecting amastigotes in the bone marrow aspirate and/or the rK39 test and/or molecular methods (genus-specific PCR, Real-Time PCR, ITS1 PCR-RFLP, DNA sequencing).

RESULTS

Most of the VL patients were referred from the districts of Adana (53.3%) and others from neighboring provinces; Hatay (16.6%), Osmaniye (3%), Gaziantep (3%), Adıyaman (3%), and 20% case were Syrian immigrants A clinical diagnosis of VL was confirmed in 30 patients with different diagnostic methods. 93% was found positive with microscopic examination, 79.1% with rK39 dipstick test, and 60% with genus-specific PCR assay in clinical samples. The isolates were identified as (40%), (26.7%), and (23.3%) using Real-Time PCR, ITS1 PCR-RFLP, and DNA sequencing. There was no cutaneous finding in any case in clinical examination.The most common clinical findings were fever (93.3%) and splenomegaly (90%), followed by hepatomegaly (76.6%). The most common laboratory finding was thrombocytopenia (86.6%), followed by anemia (70%). In addition, hemophagocytic lymphohistiocytosis was detected in bone marrow aspiration in two of our patients. Since pentavalent antimony salts treatment initially failed in four patients, it was necessary to switch to Liposomal-Amphotericin B with treatment success.

CONCLUSIONS

The presence of in VL patients, despite the absence of cutaneous findings in any of the cases, shows that this strain can cause VL, contrary to conventional knowledge. In the Adana province, where this study was carried out, from CL cases in previous studies should be taken into account, and visceral spread in CL cases and accompanying cutaneous lesions in VL cases should be investigated in detail.

摘要

背景与目的

属原生动物为专性细胞内寄生虫,该属不同种会引发一系列种特异性临床症状,即皮肤利什曼病、黏膜皮肤利什曼病和内脏利什曼病。例如,和会引发皮肤利什曼病,而和会引发内脏利什曼病(VL)。然而,近年来的分子研究表明,种会引发不同的临床症状。

目的

我们的目的是评估在土耳其这个洲际过渡地区确诊为VL的儿童中,利什曼原虫分离株的临床特征与分子特征之间的关系。

方法

通过在骨髓穿刺物中检测无鞭毛体和/或rK39试验和/或分子方法(属特异性PCR、实时荧光定量PCR、ITS1 PCR-RFLP、DNA测序)来确诊VL的临床诊断。

结果

大多数VL患者来自阿达纳地区(53.3%),其他来自邻近省份;哈塔伊(16.6%)、奥斯曼尼耶(3%)、加济安泰普(3%)、阿迪雅曼(3%),20%的病例为叙利亚移民。通过不同诊断方法在30例患者中确诊为VL临床诊断。临床样本中,93%通过显微镜检查呈阳性,79.1%通过rK39试纸条试验呈阳性,60%通过属特异性PCR检测呈阳性。使用实时荧光定量PCR、ITS1 PCR-RFLP和DNA测序将分离株鉴定为(40%)、(26.7%)和(23.3%)。临床检查中任何病例均未发现皮肤表现。最常见的临床症状为发热(93.3%)和脾肿大(90%),其次是肝肿大(76.6%)。最常见的实验室检查结果为血小板减少(86.6%),其次是贫血(70%)。此外,我们的两名患者骨髓穿刺中检测到噬血细胞性淋巴组织细胞增生症。由于4例患者最初使用五价锑盐治疗失败,因此有必要改用脂质体两性霉素B并取得了治疗成功。

结论

VL患者中存在,尽管所有病例均未出现皮肤表现,但这表明该菌株可引发VL,这与传统认知相反。在开展本研究的阿达纳省,应考虑到先前研究中CL病例中的,并且应详细调查CL病例中的内脏播散情况以及VL病例中伴随的皮肤病变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a600/9266607/87085a98bdcf/mjhid-14-1-e2022053f1.jpg

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