کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
10088652 | 1606117 | 2005 | 4 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Persistent cervical lymphadenopathy in an adolescent with Epstein-Barr induced hemophagocytic syndrome: Manifestations of a rare but often fatal disease
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کلمات کلیدی
موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
بیماری های گوش و جراحی پلاستیک صورت
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![عکس صفحه اول مقاله: Persistent cervical lymphadenopathy in an adolescent with Epstein-Barr induced hemophagocytic syndrome: Manifestations of a rare but often fatal disease Persistent cervical lymphadenopathy in an adolescent with Epstein-Barr induced hemophagocytic syndrome: Manifestations of a rare but often fatal disease](/preview/png/10088652.png)
چکیده انگلیسی
Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis (EBV-HLH) is a non-malignant proliferative disorder characterized by histiocytic proliferation and hemophagocytosis following Epstein-Barr virus infection. Though quite rare, this condition represents an often fatal disease primarily affecting the pediatric population. We discuss the case of an adolescent female who presented initially with persistent cervical lymphadenopathy and the typical findings of tonsillar hypertrophy, pharyngitis, and splenomegaly associated with infectious mononucleosis. This case study outlines the pathogenesis, common clinical findings, diagnostic criteria, and a review of the HLH-94 treatment protocol. Early recognition and treatment is emphasized because of the fulminant course of the disorder.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Journal of Pediatric Otorhinolaryngology - Volume 69, Issue 7, July 2005, Pages 1011-1014
Journal: International Journal of Pediatric Otorhinolaryngology - Volume 69, Issue 7, July 2005, Pages 1011-1014
نویسندگان
Timothy L. Lindemann, J. Scott Greene,