نتایج جستجو برای: pancytopenia

تعداد نتایج: 3009  

Journal: :Journal of Pathology of Nepal 1970

Journal: :Archives of Disease in Childhood 1986

2016
Nicolò Binello Antonio Gasbarrini Eleonora Gaetani

Rendu-Osler-Weber syndrome, or hereditary hemorrhagic teleangiectasia (HHT), is a rare autosomal dominant vascular disorder, characterized by multiple mucocutaneous teleangiectases with recurrent nasal and gastrointestinal bleedings and/or solid-organ arteriovenous shunts. We describe the first case to our knowledge of pancytopenia in a 53-year-old patient, with a known history of HHT and recur...

2015
Magdalena Sarah Volz Mani Nassir Christoph Treese Moritz von Winterfeld Ursula Plöckinger Hans-Jörg Epple Britta Siegmund

BACKGROUND Inflammatory bowel disease (IBD)-like conditions in glycogen storage disease (GSD) type Ib have been predominantly described in children. Signs and symptoms of GSD type Ib are hypoglycemia, pancytopenia and hepatosplenomegaly. Based on few published cases, there is evidence that granulocyte-colony stimulating factor (G-CSF) in patients with glycogenosis-related pancytopenia might ame...

2011

Objective: To report pancytopenia caused by temozolomide, a second-generation alkylating agent. Clinical Presentation and Intervention: A 22-year-old patient presenting with seizures and confusion was seen in the emergency room. Cranial magnetic resonance imaging revealed a mass. After surgery, the patient was diagnosed with glioblastoma multiforme and was given temozolomide at 150 mg/m 2 on da...

2010
Tariq Aziz Liaquat Ali Tahir Ansari Hammad Bin Liaquat Shahnaz Shah Jamal Ara

Objectives: To find out the frequency of the different causes of Pancytopenia and also to specifically detect the percentage of vitamin B12 deficieny amongst these patients. Methodology: It is a prospective study carried out in Medical Unit I (Ward 5) of Jinnah Postgraduate Medical Centre Karachi from March to August 2007. A total of 88 patients were included after a detailed history and examin...

Journal: :Journal of Medical Case Reports 2008
Kathryn Chan Eric Behling David S Strayer William S Kocher Scott K Dessain

INTRODUCTION Hemophagocytic lymphohistiocytosis is an immune-mediated syndrome that typically has a rapidly progressive course that can result in pancytopenia, coagulopathy, multi-system organ failure and death. CASE PRESENTATION A 57-year-old Caucasian woman was referred in fulminant hemophagocytic lymphohistiocytosis, with fever, pancytopenia, splenomegaly, mental status changes and respira...

2016
Katharina Knoll Florian Anzengruber Antonio Cozzio Lars E. French Carla Murer Alexander A. Navarini

Methotrexate (MTX) is an antifolic drug used in the treatment of immune-mediated and neoplastic diseases. Initiation or dosage changes in MTX therapy can cause mucositis and bone marrow suppression. Skin lesions due to acute MTX toxicity are rare, but they serve as a herald for later-onset pancytopenia. Therefore, identification of those cutaneous lesions might help to initiate rescue strategie...

Journal: :iranian journal of medical sciences 0
akbar safaei department of pathology, school of medicine, shiraz university of medical sciences, shiraz, iran mansoureh shokripour department of pathology, school of medicine, shiraz university of medical sciences, shiraz, iran navid omidifar department of pathology, school of medicine, shiraz university of medical sciences, shiraz, iran

background: pancytopenia is a manifestation of a wide range of disorders. the main prognostic factor for predicting outcome and response to treatment is based on the underlying cause. to detect the root cause of this problem, depending on other accompanied signs or symptoms, the need for bone marrow examination and other advanced work ups is different at least at the practical level. this study...

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