نتایج جستجو برای: atll
تعداد نتایج: 284 فیلتر نتایج به سال:
Abstract A 53 year old male with history of HTLV-1 infection associated myelopathy but unknown mode transmission, presented acute on chronic bilateral lower extremity weakness and numbness no other deficits. Examination revealed decreased strength (grade 1/5) in extremities normal bulk, tone sensations. Initial blood work hypercalcemia corrected Calcium 16.2mg/dl(8.5-11.5), Phosphorus 2.7mg/dl ...
It is critical to distinguish CD30+ T-cell LPDs from other CD30+ processes involving the skin that include: Systemic lymphomas (eg, systemic ALCL, ATLL, PTCL), Other cutaneous process such as other CD30+ skin lymphomas such as mycosis fungoides (MF), especially transformed MF, cytotoxic T-cell lymphomas, and Benign disorders such as lymphomatoid drug reactions, arthropod bites, viral infections...
Introduction The discovery in 1980 of the first human retrovirus (1), the human T-lymphotropic virus type 1 (HTLV-I), inaugurated a new era in human pathology. Two conditions were promptly associated with this retroviral infection (2): adult T-cell leukemia/lymphoma (ATLL) and tropical spastic paraparesis (TSP). Thus, this discovery solved a longlasting enigma in tropical medicine, the cause of...
TOPIC: Critical Care TYPE: Medical Student/Resident Case Reports INTRODUCTION: Human T-cell lymphotropic virus type 1 (HTLV-1) was the first human retrovirus to be discovered [1]. Its infection can lead adult leukemia/lymphoma (ATLL). Hemophagocytic lymphohistiocytosis (HLH) is a syndrome with mortality of 95% caused by overstimulation immune system [2,3,4]. This case report presents male HTLV-...
BACKGROUND Fanconi syndrome (FS) is a generalized transport defect in the proximal renal tubule leading to renal losses of phosphate, calcium, uric acid, bicarbonates as well as glucose, amino acids and other organic compounds. It is caused by inherited or acquired disorders including low mass or high mass multiple myeloma. OBJECTIVES To report the first case series of patients with lymphoma ...
We describe a new rat immunoglobulin M monoclonal antibody (CH-F42) that recognizes a subset (1.5% to 8%) of normal peripheral blood T lymphocytes. The phenotype of these cells was determined, using dual-color immunofluorescence, to be CD2+, CD3+, CD4+, CD5+, CD7-, CD8-. They do not express T-cell activation markers, and are positive for UCHL1 (CD45RO), but negative for 2H4 (CD45RA). The antige...
UNLABELLED The establishment of a latent reservoir by human tumor viruses is a vital step in initiating cellular transformation and represents a major shortcoming to current therapeutic strategies and the ability to eradicate virus-infected cells. Human T-cell leukemia virus type 1 (HTLV-1) establishes a lifelong infection and is linked to adult T-cell leukemia lymphoma (ATLL). Here, we demonst...
Human T-cell lymphotropic virus type I (HTLV-I) associated adult T-cell leukemia/lymphoma (ATLL) occurs endemically in southwestern Japan, the Caribbean, and West Africa, but occurs sporadically in most of the rest of the world. However, because ATLL and non-HTLV-I associated T-cell neoplasms share overlapping clinicopathologic features, the prevalence of ATLL in nonendemic regions is unknown. ...
PURPOSE Human T-cell leukemia virus type I (HTLV-I) can cause an adult T-cell leukemia/lymphoma (ATLL). Because ATLL is a life-threatening lymphoproliferative disorder and is resistant to chemotherapy, the establishment and enhancement of T-cell immunity to HTLV-I through the development of therapeutic vaccines could be of value. Thus, the identification of HTLV-I epitopes for both CD8(+) and C...
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