Hemophagocytic Lymphohistiocytosis Presenting with Nonimmune Hydrops Fetalis
نویسندگان
چکیده
منابع مشابه
Familial Hemophagocytic Lymphohistiocytosis Presenting as Hydrops Fetalis
Background Familial hemophagocytic lymphohistiocytosis (FLH) is an autosomal recessive disorder of immune regulation that leads to a hyperinflammatory syndrome. Fetal onset FHL is extremely rare and is considered to be the most severe form of FHL. Case We report a preterm case of FHL that presented as hydrops fetalis. The infant was treated with a chemotherapy regimen based on the HLH-2004 prot...
متن کاملThoracic Ganglioneuromas Resulting in Nonimmune Hydrops Fetalis
Introduction Most often, ganglioneuromas affect older pediatric and adult patients. They are typically slow growing tumors that remain clinically silent until they become large enough to cause symptoms by compression of adjacent structures. Case We report a case of a 22-year-old Hispanic gravida 2 para 1 female patient who was found to have massive hydrops fetalis at 20 completed gestational we...
متن کاملCongenital hypothyroidism and nonimmune hydrops fetalis: associated?
Hydrops fetalis (HF) consists of an abnormal accumulation of fluid in two or more fetal compartments, including ascites, pleural effusion, pericardial effusion, and skin edema. Almost all observed cases of HF are of the nonimmune type, the causes of which remain undetermined in 15% of patients. We report a newborn infant with nonimmune hydrops fetalis (NIHF) and congenital hypothyroidism. The i...
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Background Hereditary spherocytosis is the most common form of inherited hemolytic anemia and is characterized by a structural defect in the RBC membrane. The disorder is commonly inherited in an autosomal dominant fashion and leads to a mild to moderate anemia. The autosomal recessive form of hereditary spherocytosis is rarely reported in association with fetal anemia and hydrops fetalis. Ca...
متن کاملDisseminated Tuberculosis Presenting as Hemophagocytic Lymphohistiocytosis
Hemophagocytic lymphohistiocytosis (HLH) is an immune dysregulation syndrome which is characterized by widespread but ineffective activation of immune system of our body. This activation leads to release of a large pool of cytokines from the activated lymphocytes and macrophages. This hypercytokinemia leads to the development of characteristic features of HLH such as fever, cytopenias, hepatosp...
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ژورنال
عنوان ژورنال: Journal of Perinatology
سال: 2004
ISSN: 0743-8346,1476-5543
DOI: 10.1038/sj.jp.7211121