Department of Pathology, University of Gondar College of Medicine and Health Sciences, Gondar, Ethiopia.
J Med Case Rep. 2023 Apr 6;17(1):123. doi: 10.1186/s13256-023-03852-x.
There are three main forms of leishmaniases: visceral (the most serious form because it is almost always fatal without treatment), cutaneous (the most common, usually causing skin ulcers), and mucocutaneous (affecting mouth, nose, and throat). Leishmaniasis is caused by protozoan parasites, which are transmitted by the bite of infected female phlebotomine sandflies. The disease affects some of the world's poorest people and is associated with malnutrition, population displacement, poor housing, a weak immune system, and lack of financial resources. An estimated 700,000 to 1 million new cases occur annually. Only a small fraction of those infected by parasites causing leishmaniasis will eventually develop the disease. We report a case of exclusive lymph node involvement in leishmaniasis, presenting as localized lymphadenopathies. The diagnosis of lymphatic leishmaniasis was confirmed by the presence of Leishmania donovani bodies in fine needle aspiration cytology, and positive anti-rK39 antibodies. The bone marrow aspiration was negative for Leishmania donovani bodies. Abdominal ultrasound was done and there was no organomegaly. Furthermore, localized lymphadenopathies may provide a diagnostic challenge by clinically mimicking a lymphoma or other causes of lymphadenopathy. Due to its rarity and its tendency to pose a clinical diagnostic challenge, we decided to report a case of lymphatic leishmaniasis.
A 12-year-old Amara male patient presented to the University of Gondar comprehensive specialized hospital, Northwestern Ethiopia, with six discrete right lateral cervical lymphadenopathies, the largest measuring 3 × 2 cm, with no cutaneous lesion. Fine needle aspiration cytology confirmed the diagnosis of leishmaniasis in lymph node, and he was put on sodium stibogluconate (20 mg/kg body weight/day) and paromomycin (15 mg/kg body weight/day) injections, which are given intramuscularly for 17 days. Having completed his medication at the University of Gondar comprehensive specialized hospital, he had a smooth course and was discharged with appointment scheduled for follow-up after 3 months.
In the clinical evaluation of a patient with isolated lymphadenopathies, leishmaniasis must be considered as a differential diagnosis in immunocompetent subjects in endemic areas for early diagnostic workup and management.
利什曼病有三种主要形式:内脏利什曼病(最严重的形式,因为如果不治疗几乎总是致命的)、皮肤利什曼病(最常见的,通常导致皮肤溃疡)和黏膜皮肤利什曼病(影响口腔、鼻子和喉咙)。利什曼病是由原生动物寄生虫引起的,通过受感染的雌性白蛉沙蝇叮咬传播。该疾病影响世界上一些最贫穷的人,与营养不良、人口流离失所、住房简陋、免疫系统薄弱和缺乏财政资源有关。据估计,每年有 70 万至 100 万例新发病例。只有一小部分感染利什曼原虫的人最终会患上这种疾病。我们报告了一例仅累及淋巴结的利什曼病,表现为局部淋巴结病。通过细针抽吸细胞学检查发现利什曼原虫体,以及抗 rK39 抗体阳性,确诊为淋巴利什曼病。骨髓抽吸物未发现利什曼原虫体。进行了腹部超声检查,未发现器官肿大。此外,局部淋巴结病可能通过临床模拟淋巴瘤或其他淋巴结病原因而带来诊断挑战。由于其罕见性及其倾向于构成临床诊断挑战,我们决定报告一例淋巴利什曼病。
一名 12 岁的 Amara 男性患者因六个离散的右侧颈外侧淋巴结肿大,最大者为 3×2cm,无皮肤病变,到埃塞俄比亚西北部贡德尔大学综合专科医院就诊。细针抽吸细胞学检查证实了淋巴结利什曼病的诊断,他接受了葡甲酸钠(20mg/kg 体重/天)和巴龙霉素(15mg/kg 体重/天)肌肉注射治疗,共 17 天。在贡德尔大学综合专科医院完成药物治疗后,他病情顺利,在预约 3 个月后进行随访后出院。
在对孤立性淋巴结病患者进行临床评估时,必须考虑在流行地区免疫功能正常的患者中,将利什曼病作为鉴别诊断,以便进行早期诊断检查和管理。