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http://dx.doi.org/10.1016/j.jbspin.2022.105489 | DOI Listing |
Joint Bone Spine
March 2023
Department of Diabetes, Endocrinology and Clinical Immunology, Hyogo Medical University School of Medicine, 1-1, Mukogawa-cho, Hyogo 663-8501 Nishinomiya, Japan.
Yonsei Med J
March 2021
Department of Surgery, Ajou University School of Medicine, Suwon, Korea.
Hemophagocytic syndrome (HPS) is a rare but potentially life-threatening disease in kidney transplant recipients, and is caused by systemic proliferation of macrophages actively phagocytizing other blood cells in the bone marrow, lymph nodes, and the spleen. Here, we report a 40-year-old male kidney transplant recipient who presented with fever, bicytopenia, and elevated liver enzymes 2 months after transplantation. Given that cytomegalovirus antigenemia and real-time polymerase chain reaction tests were positive, liver biopsy was performed under an assumption of cytomegalovirus-induced hepatitis.
View Article and Find Full Text PDFCureus
October 2020
Diabetes and Endocrinology, Royal Hampshire County Hospital, Winchester, GBR.
Cytomegalovirus (CMV) infection generally causes asymptomatic infection in the majority of immunocompetent individuals. However, the presentation may be complicated by life-threatening conditions in immunocompromised patients. We report a case of a 23-year-old healthy Caucasian female with acute CMV infection and splenic infarction.
View Article and Find Full Text PDFAm J Med
March 2020
Department of Imaging, Laniado Hospital, Sanz Medical Center, Netanya, Jerusalem, Israel.
Thromb Res
August 2018
2nd Department of Internal Medicine, St. Stephen Hospital, Prato, Italy.
Introduction: Venous thromboembolic events (VTE) occur in more than 5% of hospitalized patients with acute CMV infection. In immunocompetent patients, splanchnic vein thrombosis (SVT) and splenic infarction have been suggested to represent approximately half of the published cases of CMV-associated VTE. We performed a systematic review of the literature with the aim to describe epidemiology, clinical characteristics, treatment, and natural history of CMV-associated SVT in immunocompetent patients.
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