نتایج جستجو برای: cytopenia

تعداد نتایج: 953  

Journal: :Pediatric Hematology Oncology Journal 2021

2017
G. Bruce Copley A. Robert Schnatter Thomas W. Armstrong Richard D. Irons Min Chen Xiao Qin Wang Patrick Kerzic

OBJECTIVE Due to the sparse data on benzene exposure and myelodysplastic syndrome (MDS) subtypes, we studied this relationship in patients from 29 hospitals in Shanghai, China. METHODS We recruited 604 cases of MDS and 1193 controls matched on age, sex, and admission date. We interviewed subjects for information on workplace and lifestyle exposures, and developed semi-quantitative exposure es...

Journal: :Journal of pediatric hematology/oncology 2014
Taly Glaubach Lisa J Robinson Seth J Corey

One of the most common hematologic malignancies in adults, myelodysplastic syndrome (MDS) is a heterogenous group of clonal disorders characterized by peripheral cytopenia(s) and normal or hypercellular bone marrow with dysplasia in ≥1 blood cell lineages. MDS frequently evolves to secondary acute myeloid leukemia with poor prognosis. Although uncommon among pediatric hematologic malignancies, ...

Journal: :Cancer research and treatment : official journal of Korean Cancer Association 2016
Jin Lim Ki Hwan Kim Koung Jin Suh Kyung Ah Yoh Jin Young Moon Ji Eun Kim Eun Youn Roh In Sil Choi Jin-Soo Kim Jin Hyun Park

Erdheim-Chester disease is a rare non-Langerhans-cell histiocytosis with bone and organ involvement. A 76-year-old man presented with low back pain and a history of visits for exertional dyspnea. We diagnosed him with anemia of chronic disease, cytopenia related to chronic illness, chronic renal failure due to hypertension, and hypothyroidism. However, we could not determine a definite cause or...

2015
Maryam Mobini Ramin Shekarriz Reza Ali Mohammad Pour Shahrzad Zakeri

BACKGROUND The aim of this study was to determine the prevalence and characteristics of rheumatologic manifestations associated with MDS. METHODS Eighty patients with MDS were evaluated by history and physical examination for inflammatory rheumatologic disorders from Jan 2013 to May 2014. Patients who had any signs or symptoms of rheumatologic disorders underwent evaluation by laboratory test...

Journal: :Iranian Journal of Blood and Cancer 2022

Due to the neoplastic nature of myelodysplastic syndromes (MDS), they have been renamed as neoplasms in World Health Organization (WHO) 2022 classification. These are heterogeneous groups myeloid disorders characterized by dysplasia bone marrow cells, ineffective hematopoiesis, increased apoptosis, peripheral blood cytopenia, and risk progression acute leukemia (AML). The recent progress unders...

Journal: :Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology 2012
Lian Huat Tan Lucy Chai See Lum Sharifah Faridah Syed Omar Foong Kee Kan

Hemophagocytic syndrome is a potentially fatal disorder. It is being increasingly reported but remained under-recognized in dengue. Most reported cases were in association with plasma leakage and shock but multi-organ impairment was also observed. We describe the time-lines of 6 cases of confirmed dengue with varying severities of hemophagocytosis. All had persistent fever, cytopenia and elevat...

Journal: :International journal of clinical and experimental pathology 2014
Mitsuaki Ishida Hiroko Okuno Miyuki Yoshii Akiko Horinouchi Ayaka Shirakawa Ayumi Harada Muneo Iwai Keiko Yoshida Akiko Kagotani Takashi Yoshida Hidetoshi Okabe

Myelodysplastic syndrome (MDS) is a clonal hematopoietic stem cell disease characterized by cytopenia, dysplasia in one or more of the major myeloid cell lines, ineffective hematopoiesis, and increased risk of development of acute myeloid leukemia [1]. The majority of patients with MDS present with symptoms related to cytopenia [1]. However, cutaneous manifestations have also been reported in p...

2016
Su Han Lum John D Grainger

Aplastic anemia (AA) is a potential life-threatening hematopoietic stem cell (HSC) disorder resulting in cytopenia. The mainstays of treatment for AA are definitive therapy to restore HSCs and supportive measures to ameliorate cytopenia-related complications. The standard definitive therapy is HSC transplantation for young and medically fit patients with suitable donors and immunosuppressive th...

Journal: :international journal of pediatrics 0
amitabh singh senior research associate, department of pediatrics, aiims, new delhi-110029, india. anirban mandal senior resident, department of pediatrics, aiims, new delhi-110029, india. rachna seth additional professor, department of pediatrics, aiims, new delhi-110029, india.

autoimmune lymphoproliferative syndrome (alps) is a rare, inherited disorder of immune dysregulation secondary to defective lymphocyte apoptosis. this leads to uninhibited proliferation of lymphoid tissue manifesting with lymphadenopathy, hepatosplenomegaly, autoimmune cytopenia, and an increased risk of lymphoid malignancy. we report a 2 year old boy with fever, generalized lymphadenopathy, he...

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