COMPLETE RESPONSE OF EXTRAMEDULLARY RELAPSE IN BREAST OF ACUTE T LYMPHOBLASTIC LEUKEMIA AFTER BONE MARROW TRANSPLANTATION TO CHEMORADIOTHERAPY: A CASE REPORT AND LITERATURE REVIEW
Tìm thấy 10,000 tài liệu liên quan tới tiêu đề "Complete response of extramedullary relapse in breast of acute T lymphoblastic leukemia after bone m...":
Complete response of extramedullary relapse in breast of acute T lymphoblastic leukemia after bone marrow transplantation to chemoradiotherapy: A case report and literature review
Relapse of acute lymphoblastic leukemia (ALL) occurring in the breast after allografting is extremely rare, with only 22 reported cases in the literature thus far. Further, the lack of a systemic analysis provides little information about this entity. We present a case of isolated extramedullary rel[r]
CHAPTER 061. DISORDERS OF GRANULOCYTES AND MONOCYTES (PART 12) PPTX
chemotherapy. Patients with chronic neutropenia with evidence of a good bone marrow reserve need not receive prophylactic antibiotics. Patients with chronic or cyclic neutrophil counts < 500/µL may benefit from prophylactic antibiotics and G-CSF during perio[r]
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Upregulation of the proto-oncogene Bmi-1 predicts a poor prognosis in pediatric acute lymphoblastic leukemia
Discussion
New biomarkers could be helpful in predicting treatment outcomes earlier and more precisely, which is of great interest to physicians and researchers in the field. This re- port describes for the first time that the proto-oncogene Bmi-1 is aberr[r]
New biomarkers could be helpful in predicting treatment outcomes earlier and more precisely, which is of great interest to physicians and researchers in the field. This re- port describes for the first time that the proto-oncogene Bmi-1 is aberr[r]
Coexisting of bone marrow fibrosis, dysplasia and an X chromosomal abnormality in chronic neutrophilic leukemia with CSF3R mutation: A case report and literature review
Discussion and conclusion
CNL is a rare aggressive myeloproliferative neoplasm, similar to other MPN, the clinical course of CNL is het- erogeneous. Clinical course of CNL is recognized by a chronic phase, an accelerated phase, and a blast ph[r]
CNL is a rare aggressive myeloproliferative neoplasm, similar to other MPN, the clinical course of CNL is het- erogeneous. Clinical course of CNL is recognized by a chronic phase, an accelerated phase, and a blast ph[r]
BÁO CÁO HÓA HỌC:" DIAGNOSTIC CHALLENGE: BILATERAL INFECTED LUMBAR FACET CYSTS - A RARE CAUSE OF ACUTE LUMBAR SPINAL STENOSIS AND BACK PAIN" PPTX
CAS E REP O R T Open AccessDiagnostic challenge: bilateral infected lumbarfacet cysts - a rare cause of acute lumbar spinalstenosis and back painBrett A Freedman, Tuan L Bui, S Timothy Yoon*AbstractSymptomatic synovial lumbar facet cysts are a relativ[r]
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BÁO CÁO HÓA HỌC:" LARGE ANEURYSMAL BONE CYST OF ILIAC BONE IN A FEMALE CHILD: A CASE REPORT" PPT
Agarwal et al. Journal of Orthopaedic Surgery and Research 2010, 5:24http://www.josr-online.com/content/5/1/24Open AccessCASE REPORTBioMed Central© 2010 Agarwal et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons[r]
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AGARWAL ET AL. JOURNAL OF ORTHOPAEDIC SURGERY AND RESEARCH 2010, 5:24 PPT
Agarwal et al. Journal of Orthopaedic Surgery and Research 2010, 5:24http://www.josr-online.com/content/5/1/24Open AccessCASE REPORTBioMed Central© 2010 Agarwal et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons[r]
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CHAPTER 108 HEMATOPOIETIC CELL TRANSPLANTATION PART 8
Chapter 108. Hematopoietic Cell Transplantation (Part 8) Aplastic Anemia Transplantation from matched siblings after a preparative regimen of high-dose cyclophosphamide and antithymocyte globulin can cure up to 90% of patients <40 years[r]
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Efficacy of T-DM1 for leptomeningeal and brain metastases in a HER2 positive metastatic breast cancer patient: New directions for systemic therapy - a case report and literature review
In August 2015, a 46-year-old Caucasian woman re- ferred to our Institution for a metastatic breast cancer. Three years before she had undergone a left quadran- tectomy and ipsilateral axillary nodal dissection for a pT1c pN3 M0 infiltrating du[r]
COMPARISON OF CHILD AND FAMILY REPORTS OF HEALTH-RELATED QUALITY OF LIFE IN PEDIATRIC ACUTE LYMPHOBLASTIC LEUKEMIA PATIENTS AFTER INDUCTION THERAPY
This study aims at determining the health-related quality of life (HRQOL) of children with acute lymphoblastic leukemia (ALL) after the induction therapy, assessing the agreement between child self-reports and family proxy-reports HRQOL, and determining the factors related to this agreement, especia[r]
POSSIBLE ROLES OF GENETIC VARIATIONS IN CHEMOTHERAPY RELATED CARDIOTOXICITY IN PEDIATRIC ACUTE LYMPHOBLASTIC LEUKEMIA AND OSTEOSARCOMA
The treatment of acute lymphoblastic leukemia (ALL) and osteosarcoma (OSC) is very effective: the vast majority of patients recover and survive for decades. However, they still need to face serious adverse effects of chemotherapy
CHAPTER 102. APLASTIC ANEMIA, MYELODYSPLASIA, AND RELATED BONE MARROW FAILURE SYNDROMES (PART 14) POTX
sideroblastic anemia to a few months in refractory anemia with excess blasts or severe pancytopenia associated with monosomy 7; an International Prognostic Scoring System (Table 102-6) assists in making predictions. Most patients die as a result of complicat[r]
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THE POTENTIAL PREDICTIVE VALUE OF DEK EXPRESSION FOR NEOADJUVANT CHEMORADIOTHERAPY RESPONSE IN LOCALLY ADVANCED RECTAL CANCER
Limited data are available regarding the ability of biomarkers to predict complete pathological response to neoadjuvant chemoradiotherapy in locally advanced rectal cancer. Complete response translates to better patient survival.
MAP3K7 IS RECURRENTLY DELETED IN PEDIATRIC T-LYMPHOBLASTIC LEUKEMIA AND AFFECTS CELL PROLIFERATION INDEPENDENTLY OF NF-ΚB
Deletions of 6q15–16.1 are recurrently found in pediatric T-cell acute lymphoblastic leukemia (T-ALL). This chromosomal region includes the mitogen-activated protein kinase kinase kinase 7 (MAP3K7) gene which has a crucial role in innate immune signaling and was observed to be functionally and progn[r]
IROQUOIS HOMEOBOX 2 SUPPRESSES CELLULAR MOTILITY AND CHEMOKINE EXPRESSION IN BREAST CANCER CELLS
Disseminated tumor cells (DTCs) can be detected using ultrasensitive immunocytochemical assays and their presence in the bone marrow can predict the subsequent occurrence of overt metastasis formation and metastatic relapse.
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BÁO CÁO HÓA HỌC:" HIGH CORRELATION OF THE PROTEOME PATTERNS IN BONE MARROW AND PERIPHERAL BLOOD BLAST CELLS IN PATIENTS WITH ACUTE MYELOID LEUKEMIA" POT
8. Hanash SM, Kuick R, Strahler J, Richardson B, Reaman G, Stoolman L,Hanson C, Nichols D, Tueche HJ: Identification of a cellularpolypeptide that distinguishes between acute lymphoblasticleukemia in infants and in older children. Blood 1989,73(2):527-532.9.[r]
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CHAPTER 099. DISORDERS OF HEMOGLOBIN (PART 14) DOCX
sustain HbF induction in the majority of patients with sickle cell disease. It is unclear whether butyrates will have similar activity in patients with β-thalassemia. Aplastic and Hypoplastic Crisis in Patients with Hemoglobinopathies Patients with hemolytic anemia[r]
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BÁO CÁO HÓA HỌC:" SMALL CELL OSTEOSARCOMA OF A TOE PHALANX: A CASE REPORT AND REVIEW OF LITERATURE" PPT
of patients [12]. Radiological findings include involve-ment of both medulla and cortex, with disruption of thelatter and the presence of a mass in the adjacent soft tis-sue. Histologically the production of osteoid is present inall tumo[r]
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INFLUENCE OF PRE-TRANSPLANT MINIMAL RESIDUAL DISEASE ON PROGNOSIS AFTER ALLO-SCT FOR PATIENTS WITH ACUTE LYMPHOBLASTIC LEUKEMIA: SYSTEMATIC REVIEW AND METAANALYSIS
This meta-analysis was performed to explore the impact of minimal residual disease (MRD) prior to transplantation on the prognosis for patients with acute lymphoblastic leukemia (ALL).
CHAPTER 105. MALIGNANCIES OF LYMPHOID CELLS (PART 20) DOCX
lymphoblastic lymphoma are also often treated with "leukemia-like" regimens. Patients who present with localized disease have an excellent prognosis. However, advanced age is an adverse prognostic factor. Adults with precursor T cell lymphoblastic lymphoma who present wit[r]
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