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Báo cáo y học: Ocular pathology of uncommon hematologic malignancies: a case series
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Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài: Ocular pathology of uncommon hematologic malignancies: a case series...
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Báo cáo y học: "Ocular pathology of uncommon hematologic malignancies: a case series"Journal of Medical Case Reports BioMed Central Open AccessCase reportOcular pathology of uncommon hematologic malignancies: a caseseriesJames E Head1,2, Defen Shen1, Maribel Santiago-Maysonet1, Rachel J Bishop3and Chi-Chao Chan*1Address: 1Immunopathology Section, National Institutes of Health, Bethesda, MD, USA, 2Clinical Research Training Program, NIH, Bethesda, MD,USA and 3Consult Services Section National Eye Institute, National Institutes of Health, Bethesda, MD, USAEmail: James E Head - headj@od.nih.gov; Defen Shen - dshen@nei.nih.gov; Maribel Santiago-Maysonet - santiagom@nei.nih.gov;Rachel J Bishop - bishopra@nei.nih.gov; Chi-Chao Chan* - chanc@nei.nih.gov* Corresponding authorPublished: 28 November 2007 Received: 6 June 2007 Accepted: 28 November 2007Journal of Medical Case Reports 2007, 1:158 doi:10.1186/1752-1947-1-158This article is available from: http://www.jmedicalcasereports.com/content/1/1/158© 2007 Head et al; licensee BioMed Central Ltd.This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Introduction: In general, ocular complications of hematologic malignancies such as leukemia are well documented. However, reports of ocular involvement in such diseases as lymphomatoid granulomatosis and chronic myelomonocytic leukemia are uncommon. Here we present cases of these two relatively rare hematologic malignancies demonstrating clinical and subclinical ocular involvement. Case Presentation: In the first case, a 54-year-old man with a previous diagnosis of lymphomatoid granulomatosis presented with a new-onset conjunctival lesion while his systemic disease was thought to be in remission. A biopsy was taken that revealed heavy infiltrates of B and T cells at the site of the lesion. Molecular analysis confirmed that these cells were positive for both Epstein-Barr viral DNA and immunoglobulin heavy chain gene rearrangement, consistent with a manifestation of his systemic disease. In the second case, a 51-year-old man with chronic myelomonocytic leukemia died after a waxing and waning clinical course. Post-mortem studies revealed the presence of atypical monocytes in the choroidal and subretinal spaces, consistent with his previous diagnosis. Conclusion: While ocular involvement in hematologic malignancies is not uncommon, these two cases describe involvement of the eye by two relatively rare neoplasms. We herein emphasize novel findings in each case, including conjunctival involvement as the first sign of recurrent lymphomatoid granulomatosis and the combination of subretinal and choroidal myelomonocytic leukemic infiltration. With the evolution of new antineoplastic therapies that may prolong life, these cases exemplify the importance of eye care in patients diagnosed with hematologic malignancies. Page 1 of 4 (page number not for citation purposes)Journal of Medical Case Reports 2007, 1:158 http://www.jmedicalcasereports.com/content/1/1/158 ogy is consistent with the biopsy in this case, marked byIntroductionOcular complications of hematologic malignancies such the diffuse presence of B cells with an exuberant, attend-as leukemia are well documented. It is estimated that 50% ant T-cell response. Current research suggests that LYGor more of all leukemias manifest some form of ocular may be categorized as an EBV-related B-cell lymphomainvolvement [1,2]. Here we present the cases of two [5]. This conjunctival lesion, confirmed immunohisto-patients with relatively rare hematologic malignancies chemically and molecular ...
Nội dung trích xuất từ tài liệu:
Báo cáo y học: "Ocular pathology of uncommon hematologic malignancies: a case series"Journal of Medical Case Reports BioMed Central Open AccessCase reportOcular pathology of uncommon hematologic malignancies: a caseseriesJames E Head1,2, Defen Shen1, Maribel Santiago-Maysonet1, Rachel J Bishop3and Chi-Chao Chan*1Address: 1Immunopathology Section, National Institutes of Health, Bethesda, MD, USA, 2Clinical Research Training Program, NIH, Bethesda, MD,USA and 3Consult Services Section National Eye Institute, National Institutes of Health, Bethesda, MD, USAEmail: James E Head - headj@od.nih.gov; Defen Shen - dshen@nei.nih.gov; Maribel Santiago-Maysonet - santiagom@nei.nih.gov;Rachel J Bishop - bishopra@nei.nih.gov; Chi-Chao Chan* - chanc@nei.nih.gov* Corresponding authorPublished: 28 November 2007 Received: 6 June 2007 Accepted: 28 November 2007Journal of Medical Case Reports 2007, 1:158 doi:10.1186/1752-1947-1-158This article is available from: http://www.jmedicalcasereports.com/content/1/1/158© 2007 Head et al; licensee BioMed Central Ltd.This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Introduction: In general, ocular complications of hematologic malignancies such as leukemia are well documented. However, reports of ocular involvement in such diseases as lymphomatoid granulomatosis and chronic myelomonocytic leukemia are uncommon. Here we present cases of these two relatively rare hematologic malignancies demonstrating clinical and subclinical ocular involvement. Case Presentation: In the first case, a 54-year-old man with a previous diagnosis of lymphomatoid granulomatosis presented with a new-onset conjunctival lesion while his systemic disease was thought to be in remission. A biopsy was taken that revealed heavy infiltrates of B and T cells at the site of the lesion. Molecular analysis confirmed that these cells were positive for both Epstein-Barr viral DNA and immunoglobulin heavy chain gene rearrangement, consistent with a manifestation of his systemic disease. In the second case, a 51-year-old man with chronic myelomonocytic leukemia died after a waxing and waning clinical course. Post-mortem studies revealed the presence of atypical monocytes in the choroidal and subretinal spaces, consistent with his previous diagnosis. Conclusion: While ocular involvement in hematologic malignancies is not uncommon, these two cases describe involvement of the eye by two relatively rare neoplasms. We herein emphasize novel findings in each case, including conjunctival involvement as the first sign of recurrent lymphomatoid granulomatosis and the combination of subretinal and choroidal myelomonocytic leukemic infiltration. With the evolution of new antineoplastic therapies that may prolong life, these cases exemplify the importance of eye care in patients diagnosed with hematologic malignancies. Page 1 of 4 (page number not for citation purposes)Journal of Medical Case Reports 2007, 1:158 http://www.jmedicalcasereports.com/content/1/1/158 ogy is consistent with the biopsy in this case, marked byIntroductionOcular complications of hematologic malignancies such the diffuse presence of B cells with an exuberant, attend-as leukemia are well documented. It is estimated that 50% ant T-cell response. Current research suggests that LYGor more of all leukemias manifest some form of ocular may be categorized as an EBV-related B-cell lymphomainvolvement [1,2]. Here we present the cases of two [5]. This conjunctival lesion, confirmed immunohisto-patients with relatively rare hematologic malignancies chemically and molecular ...
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