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pro vyhledávání: '"Darcie Deaver"'
Autor:
Darcie Deaver
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 6, Iss 1, Pp e2014023-e2014023 (2014)
Due to a layout error, in the title Unites must be canged on United. At the first row of the abstract histiocytic lymphadenitis must be canged on histiocytic necrotizing lymphadenitis.
Externí odkaz:
https://doaj.org/article/4f6f802b9851479e85ee2e431e7f88af
Publikováno v:
Cancer Control. 21:313-321
Background: Kikuchi–Fujimoto disease (KFD) is a rare lymphohistiocytic disorder with an unknown etiopathogenesis. This disease is misdiagnosed as malignant lymphoma in up to one-third of cases and is associated with the development of systemic lupu
Autor:
L. Frank Glass, Lynn C. Moscinski, Pedro Horna, Darcie Deaver, Lubomir Sokol, Dahui Qin, Eduardo M. Sotomayor
Publikováno v:
Journal of Clinical Pathology. 67:431-436
Aims Assessment of peripheral blood tumour burden for staging of cutaneous T cells lymphoma is most often accomplished by flow cytometry (FC) using various non-standarised strategies. We report the results of calculating absolute Sezary cell counts (
Publikováno v:
Journal of the American Academy of Dermatology. 70:1058-1060
Background Mycosis fungoides (MF) is the most common type of cutaneous T-cell lymphoma, which typically presents as a patch or plaque in early-stage disease. Phototherapy including psoralen plus ultraviolet A and ultraviolet B are well-established tr
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 6, Iss 1, Pp e2014001-e2014001 (2013)
Mediterranean Journal of Hematology and Infectious Diseases
Mediterranean Journal of Hematology and Infectious Diseases
Kikuchi-Fujimoto Disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a benign, self-limiting disease that manifests primarily as cervical lymphadenopathy but may include low-grade fever, headache, and fatigue. There is a higher inc
Autor:
Darcie Deaver
Publikováno v:
Clinical journal of oncology nursing. 12(2)
Autor:
Darcie Deaver, Lynn C. Moscinski, Frank Glass, Eduardo M. Sotomayor, Pedro Horna, Lubomir Sokol
Publikováno v:
American Journal of Clinical Pathology. 140:A216-A216
Erythrodermic cutaneous T-cell lymphoma (eCTCL) is currently considered as stage III disease and indicative of an unfavorable outcome. Further risk stratification depends on convened criteria for stage IV, based on tumor burden assessment on peripher
Publikováno v:
Blood. 120:5085-5085
Abstract 5085 Background: Sezary syndrome is a rare leukemic subtype of cutaneous T cell lymphoma with aggressive clinical behavior and poor prognosis compare to the most common type of CTCL, mycosis fungoides. Hematologic criteria for the diagnosis
Autor:
Salvador Bruno, Darcie Deaver, Lubomir Sokol, Eduardo M. Sotomayor, Celeste M. Bello, Kenneth S. Zuckerman
Publikováno v:
Blood. 118:4956-4956
Abstract 4956 Background: The incidence of ocular adnexal lymphoma (OAL) is rare and usually presents in the setting of central nervous system (CNS) involvement. There are no rigid guidelines for the treatment of OAL, most probably because of the var
Publikováno v:
Blood. 118:4990-4990
Abstract 4990 Background: Mycosis fungoides is the most common type of cutaneous T-cell lymphoma. Early stage disease is effectively managed with skin directed therapies such as UV light and topical steroids. Excimer laser (EL) delivers monochromatic