دورية أكاديمية

Hemophagocytic lymphohistiocytosis and thrombotic microangiopathy after parvovirus B19 infection and renal transplantation: a case report

التفاصيل البيبلوغرافية
العنوان: Hemophagocytic lymphohistiocytosis and thrombotic microangiopathy after parvovirus B19 infection and renal transplantation: a case report
المؤلفون: C. J. Steffen, N. Koch, K. U. Eckardt, K. Amann, E. Seelow, A. Schreiber
المصدر: BMC Nephrology, Vol 22, Iss 1, Pp 1-6 (2021)
بيانات النشر: BMC, 2021.
سنة النشر: 2021
المجموعة: LCC:Diseases of the genitourinary system. Urology
مصطلحات موضوعية: Hemophagocytic Lymphohistiocytosis (HLH), Atypical hemorrhagic uremic syndrome (aHUS), Parvovirus B19, Case report, Diseases of the genitourinary system. Urology, RC870-923
الوصف: Abstract Background Hemophagocytic lymphohistiocytosis (HLH) is a rare and life-threatening disease characterized by hyperactivation of the immune system that causes hypercytokinemia and potentially multi organ failure. HLH can occur in patients with underlying rheumatic or autoinflammatory disorders. Additionally, HLH can develop in patients during infections or malignancies without a known genetic predisposition. Case presentation We herein report a patient, who presented with fever, both acute kidney and liver injury, anemia, thrombocytopenia and HSV stomatitis. HLH was diagnosed based on clinical criteria and qPCR revealed an acute parvovirus B19 infection as potential underlying infectious trigger. Treatment was started with both IVIG and dexamethasone. Subsequently, kidney biopsy demonstrated TMA. Conclusions In rare cases both HLH and aHUS can occur simultaneously in a patient as a consequence of viral infections. Insights from this unusual case might help physicians understand this complex symptom constellation.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1471-2369
Relation: https://doaj.org/toc/1471-2369
DOI: 10.1186/s12882-021-02538-0
URL الوصول: https://doaj.org/article/4c1d302e1c6e4de3bdbd7cf972fc8f4b
رقم الأكسشن: edsdoj.4c1d302e1c6e4de3bdbd7cf972fc8f4b
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14712369
DOI:10.1186/s12882-021-02538-0