Autoimmune Hemolytic Anemia During Pregnancy With Hemolytic Disease in the Newborn
نویسندگان
چکیده
منابع مشابه
Kawasaki disease with autoimmune hemolytic anemia.
BACKGROUND Association of autoimmune haemolytic anaemia has been seldom reported with Kawasaki disease. CASE CHARACTERISTICS A 7-month-old boy, presented with prolonged fever, erythematous rash, severe pallor and hepatosplenomegaly. OBSERVATIONS Positive Direct Coombs test and coronary artery aneurysm on echocardiography. He was managed with steroids along with intravenous immunoglobulins a...
متن کاملThymoma with Autoimmune Hemolytic Anemia
A 38-year-old Japanese male was referred to our hospital with abnormal chest X-ray results and severe Coombs-positive hemolytic anemia. He was diagnosed with a stage IV, WHO type A thymoma and was treated with oral prednisolone (1 mg/kg/day) and subsequent chemotherapy. After chemotherapy, the patient underwent surgical resection of the thymoma. Hemolysis rapidly disappeared and did not return ...
متن کاملAutoimmune hemolytic anemia in multicentric Castleman's disease.
We report on a patient affected by multicentric Castleman's disease who developed an acute immunohemolytic anemia due to warm antibody. The clinical course was characterized by refractoriness to the steroidal treatment and by a dramatic improvement of the hematological and objective picture following combination chemotherapy (CHOP regimen). The possible existence of a link between the lymphopro...
متن کاملPregnancy-induced hemophagocytic lymphohistiocytosis combined with autoimmune hemolytic anemia.
Hemophagocytic lymphohistiocytosis (HLH), presenting with fever, cytopenia, liver dysfunction, hepatosplenomegaly, hypertriglyceridemia, and hyperferritinemia, is associated with various etiologies, including infections, collagen vascular diseases, and malignancies. The present report describes a 28-year-old woman who developed HLH combined with autoimmune hemolytic anemia (AIHA) at 23 weeks of...
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ژورنال
عنوان ژورنال: Blood
سال: 1973
ISSN: 0006-4971,1528-0020
DOI: 10.1182/blood.v41.2.293.293