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内脏利什曼病酷似自身免疫性肝炎、原发性胆汁性肝硬化和系统性红斑狼疮重叠综合征。

Visceral leishmaniasis mimicking autoimmune hepatitis, primary biliary cirrhosis, and systemic lupus erythematosus overlap.

作者信息

Tunccan Ozlem Guzel, Tufan Abdurrahman, Telli Gülçin, Akyürek Nalan, Pamukçuoğlu Merve, Yılmaz Güldal, Hızel Kenan

机构信息

Department of Clinical Microbiology and Infectious Diseases, Gazi University Hospital Besevler, 06500 Ankara, Turkey.

出版信息

Korean J Parasitol. 2012 Jun;50(2):133-6. doi: 10.3347/kjp.2012.50.2.133. Epub 2012 May 24.


DOI:10.3347/kjp.2012.50.2.133
PMID:22711924
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3375451/
Abstract

Visceral leishmaniasis (VL) is a life-threatening infection caused by Leishmania species. In addition to typical clinical findings as fever, hepatosplenomegaly, and cachexia, VL is associated with autoimmune phenomena. To date, VL mimicking or exacerbating various autoimmune diseases have been described, including systemic lupus erythematosus (SLE), rheumatoid arthritis, and autoimmune hepatitis (AIH). Herein, we presented a patient with VL who had overlapping clinical features with SLE, AIH, as well as antimitochondrial antibody (AMA-M2) positive primary biliary cirrhosis.

摘要

内脏利什曼病(VL)是由利什曼原虫属引起的一种危及生命的感染。除了发热、肝脾肿大和恶病质等典型临床症状外,VL还与自身免疫现象有关。迄今为止,已经描述了VL模仿或加重各种自身免疫性疾病,包括系统性红斑狼疮(SLE)、类风湿性关节炎和自身免疫性肝炎(AIH)。在此,我们报告了一名患有VL的患者,其具有与SLE、AIH以及抗线粒体抗体(AMA-M2)阳性的原发性胆汁性肝硬化重叠的临床特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3689/3375451/4881731b6520/kjp-50-133-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3689/3375451/7bb30724ff73/kjp-50-133-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3689/3375451/5e0b09e93980/kjp-50-133-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3689/3375451/4881731b6520/kjp-50-133-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3689/3375451/7bb30724ff73/kjp-50-133-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3689/3375451/5e0b09e93980/kjp-50-133-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3689/3375451/4881731b6520/kjp-50-133-g003.jpg

相似文献

[1]
Visceral leishmaniasis mimicking autoimmune hepatitis, primary biliary cirrhosis, and systemic lupus erythematosus overlap.

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[4]
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[5]
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Mediterr J Hematol Infect Dis. 2017-9-1

[6]
Autoantibodies in a Three-Year-Old Girl with Visceral Leishmaniasis: A Potential Diagnostic Pitfall.

Case Rep Infect Dis. 2016

[7]
Clinical Characteristics of Concomitant Systemic Lupus Erythematosus and Primary Biliary Cirrhosis: A Literature Review.

J Immunol Res. 2015

[8]
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Ann Saudi Med. 2014

[9]
Visceral leishmaniasis without fever in an 11-month-old infant: a rare clinical feature of Kala-azar.

Korean J Parasitol. 2014-4

本文引用的文献

[1]
Visceral leishmaniasis mimicking systemic lupus erythematosus.

J Clin Rheumatol. 2010-6

[2]
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Euro Surveill. 2010-3-11

[3]
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Turkiye Parazitol Derg. 2008

[4]
Immunological features of visceral leishmaniasis may mimic systemic lupus erythematosus.

Clin Biochem. 2008-1

[5]
Visceral leishmaniasis presented with Evans syndrome: a case report.

Am J Hematol. 2007-11

[6]
Serum markers of rheumatoid arthritis in visceral leishmaniasis: rheumatoid factor and anti-cyclic citrullinated peptide antibody.

J Autoimmun. 2007-2

[7]
Liposomal amphotericin B for the treatment of visceral leishmaniasis.

Clin Infect Dis. 2006-10-1

[8]
A case of visceral leishmaniasis misdiagnosed as autoimmune hepatitis.

Turk J Gastroenterol. 2005-3

[9]
Kala-azar associated with coombs-positive autoimmune hemolytic anemia in the patients coming from the endemic area of this disease and successful treatment of these patients with liposomal amphotericin B.

Pediatr Hematol Oncol. 2005

[10]
Visceral leishmaniasis resembling systemic lupus erythematosus.

Ann Rheum Dis. 2004-10

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