Your browser doesn't support javascript.
loading
Epstein-Barr Virus Associated Hemophagocytic Syndrome after Scrub Typhus Infection / 감염과화학요법
Infection and Chemotherapy ; : 330-333, 2016.
Article in English | WPRIM (Western Pacific) | ID: wpr-26684
Responsible library: WPRO
ABSTRACT
There have been a small number of cases of scrub typhus-associated hemophagocytic syndrome (HPS), most of which were treated successfully using adequate antibiotics. Here, we report a case of Epstein-Barr virus (EBV)-associated HPS after scrub typhus infection that was not improved using antirickettsial treatment. A 73-year-old male who had been diagnosed with scrub typhus according to an eschar and a positive serology was transferred to our institution because of a persistent fever despite 7-day doxycycline therapy. Physical and laboratory data showed hepatosplenomegaly, bicytopenia, hyperferritinemia, and hypofibrinogenemia. A bone marrow examination (BM) revealed hypercellular marrow with hemophagocytosis and histiocyte infiltration. EBV was detected in BM aspirates using polymerase chain reaction. After a diagnosis of HPS was made, the patient was treated successfully using high-dose steroids.
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Main subject: Steroids / Bone Marrow / Bone Marrow Examination / Scrub Typhus / Polymerase Chain Reaction / Doxycycline / Herpesvirus 4, Human / Epstein-Barr Virus Infections / Diagnosis / Lymphohistiocytosis, Hemophagocytic Type of study: Diagnostic study Limits: Aged / Humans / Male Language: English Journal: Infection and Chemotherapy Year: 2016 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Steroids / Bone Marrow / Bone Marrow Examination / Scrub Typhus / Polymerase Chain Reaction / Doxycycline / Herpesvirus 4, Human / Epstein-Barr Virus Infections / Diagnosis / Lymphohistiocytosis, Hemophagocytic Type of study: Diagnostic study Limits: Aged / Humans / Male Language: English Journal: Infection and Chemotherapy Year: 2016 Document type: Article
...