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Articles 991 - 1020 of 1257
Full-Text Articles in Hematology
Adequacy Of Platelet Counting By Automated Haematology Analyzers: An Insight On Current Methodologies, Muhammad Shariq Shaikh, Noor Rahman Khan, Zeeshan Ansar Ahmed
Adequacy Of Platelet Counting By Automated Haematology Analyzers: An Insight On Current Methodologies, Muhammad Shariq Shaikh, Noor Rahman Khan, Zeeshan Ansar Ahmed
Department of Pathology and Laboratory Medicine
No abstract provided.
Comorbidities In Aging Patients With Sickle Cell Disease., Samir K. Ballas
Comorbidities In Aging Patients With Sickle Cell Disease., Samir K. Ballas
Cardeza Foundation for Hematologic Research
Sickle cell disease (SCD) in general and sickle cell anemia in particular is a highly complex disorder both at the molecular and clinical levels. Although the molecular lesion is a single-point mutation, the sickle gene is pleiotropic in nature causing multiple phenotypic expressions that constitute the various complications of the disease. Moreover, despite the fact that SCD is a chronic malady, its manifestations are both acute and chronic. The former include, among other things, the recurrent vaso-occlusive crises (its hallmark) and acute chest syndrome. The chronic complications include most commonly avascular necrosis and leg ulcers. Currently, survival of patients with …
Sickle Cell Disease: Classification Of Clinical Complications And Approaches To Preventive And Therapeutic Management., Samir K. Ballas
Sickle Cell Disease: Classification Of Clinical Complications And Approaches To Preventive And Therapeutic Management., Samir K. Ballas
Department of Medicine Faculty Papers
Sickle cell disease (SCD) is an inherited disorder of hemoglobin structure that has no established cure in adult patients. Cure has been achieved in selected children with sickle cell anemia (SCA) using allogeneic bone marrow transplantation or cord blood transplantation. SCD is essentially a triumvirate of (1) pain syndromes, (2) anemia and its sequelae and (3) organ failure, including infection. Pain, however, is the hallmark of SCD and dominates its clinical picture throughout the life of the patients. The prevalence of these complications varies with age from infancy through adult life. However, pain, infections and anemia requiring blood transfusion occur …
Blood Rheological Abnormalities In Sickle Cell Anemia., Philippe Connes, Céline Renoux, Marc Romana, Manouk Abkarian, Philippe Joly, Cyril Martin, Marie-Dominique Hardy-Dessources, Samir K. Ballas
Blood Rheological Abnormalities In Sickle Cell Anemia., Philippe Connes, Céline Renoux, Marc Romana, Manouk Abkarian, Philippe Joly, Cyril Martin, Marie-Dominique Hardy-Dessources, Samir K. Ballas
Department of Medicine Faculty Papers
This review focuses on the contribution of abnormal blood rheology in the pathophysiology of sickle cell anemia (SCA). SCA is characterized by a reduction of red blood cell (RBC) deformability but this reduction is very heterogeneous among patients. Recent works have shown that patients with the lowest RBC deformability (measured by ektacytometry) have enhanced hemolysis and would be more prone to develop several complications such as priapism, leg ulcers and glomerulopathy. In contrast, patients with the highest deformability, and not under hydroxyurea therapy, seem to develop more frequently vaso-occlusive like events. Although less studied, RBC aggregation properties are very different …
Cough, Hemoptysis And Hair Expectoration: An Intrapulmonary Teratoma, Shanila Ahmed, Habib Kibzai, Talha Shahzad, Saulat Fatimi, Madiha Bilal L Qureshi
Cough, Hemoptysis And Hair Expectoration: An Intrapulmonary Teratoma, Shanila Ahmed, Habib Kibzai, Talha Shahzad, Saulat Fatimi, Madiha Bilal L Qureshi
Section of Haematology/Oncology
Teratomas can be found in different organs of the body and may involve gonads, saccrococcygeal region, mediastinum and other sites. Intrathoracic teratomas always occur in mediastinum and less often arise within the lung. As teratomas mostly involve sex organs (gonads), they rarely occur as extra-gonadal tumors accounting for only 3% of all the cases and very small percentage of such tumors occur in mediastinum.We reported an interesting case of middle aged male who presented to us with symptoms of cough, hemoptysis and trichoptysis (hair expectoration).We found that patient had intrapulmonary teratoma that was initially being treated as case of pulmonary …
Clinical Audit To Assess Delays In Chemotherapy Administration At Daycare Oncology Center At A Tertiary Care Hospital In Karachi, Pakistan, Arifa Aziz, Zarka Samoon, Mohammad Khurshid, Afsheen Feroz, Nadia Ayoub, Safia Awan, Madhia Beg
Clinical Audit To Assess Delays In Chemotherapy Administration At Daycare Oncology Center At A Tertiary Care Hospital In Karachi, Pakistan, Arifa Aziz, Zarka Samoon, Mohammad Khurshid, Afsheen Feroz, Nadia Ayoub, Safia Awan, Madhia Beg
Section of Haematology/Oncology
Aim: There were delays reported by patients in chemotherapy administration in daycare oncology. Therefore, we decided to audit all processes which are involved in chemotherapy administration. The objective was to improve our service by decreasing the time between admission and initiation of chemotherapy and identify the reasons for delays.
Materials and Methods: The audit was conducted in three parts. In Review I, audit tool was developed and information documented of 109 patients receiving chemotherapy at daycare center from April 14 to May 13, 2015. Five processes were assessed out of which delay in initial assessment by the nurse was the …
Cold Agglutinins In Peripheral Blood With Atypical Cells With An Owl-Eye Appearance In Bone Trephine, Ayesha Majeed Memon, Farheen Karim
Cold Agglutinins In Peripheral Blood With Atypical Cells With An Owl-Eye Appearance In Bone Trephine, Ayesha Majeed Memon, Farheen Karim
Department of Pathology and Laboratory Medicine
Autoimmune hemolytic anemia (AIHA) is a form of hemolytic anemia in which red cells lysis occurs due to presence of an autoantibody. Association of AIHA is well known with lymphoproliferative disorders, especially with non-Hodgkin's lymphoma. However, AIHA in association with Hodgkin's lymphoma is seen occasionally. Of the AIHA associated with Hodgkin's lymphoma, most are of warm type or mixed type. Cold AIHA, as seen in our case, is very rare in Hodgkin's lymphoma.
Targeting Cdk6 And Bcl2 Exploits The "Myb Addiction" Of Ph+ Acute Lymphoblastic Leukemia, Marco De Dominici, Patrizia Porazzi, Angela Rachele Soliera, Samanta A. Mariani, Sankar Addya, Paolo Fortina, Luke F. Peterson, Orietta Spinelli, Alessandro Rambaldi, Giovanni Martinelli, Anna Ferrari, Ilaria Iacobucci, Bruno Calabretta
Targeting Cdk6 And Bcl2 Exploits The "Myb Addiction" Of Ph+ Acute Lymphoblastic Leukemia, Marco De Dominici, Patrizia Porazzi, Angela Rachele Soliera, Samanta A. Mariani, Sankar Addya, Paolo Fortina, Luke F. Peterson, Orietta Spinelli, Alessandro Rambaldi, Giovanni Martinelli, Anna Ferrari, Ilaria Iacobucci, Bruno Calabretta
Department of Cancer Biology Faculty Papers
Philadelphia chromosome–positive acute lymphoblastic leukemia (Phþ ALL) is currently treated with BCR-ABL1 tyrosine kinase inhibitors (TKI) in combination with chemotherapy. However, most patients develop resistance to TKI through BCR-ABL1–dependent and –independent mechanisms. Newly developed TKI can target Phþ ALL cells with BCR-ABL1–dependent resistance; however, overcoming BCR-ABL1–independent mechanisms of resistance remains challenging because transcription factors, which are difficult to inhibit, are often involved. We show here that (i) the growth of Phþ ALL cell lines and primary cells is highly dependent on MYB-mediated transcriptional upregulation of CDK6, cyclin D3, and BCL2, and (ii) restoring their expression in MYB-silenced …
Cd20 Expression And Effects On Outcome Of Relapsed/ Refractory Diffuse Large B Cell Lymphoma After Treatment With Rituximab, Afshan Asghar Rasheed, Adeel Samad, Ahmed Raheem, Samina Ismail Hirani, Shabbir Shabbir- Moosajee
Cd20 Expression And Effects On Outcome Of Relapsed/ Refractory Diffuse Large B Cell Lymphoma After Treatment With Rituximab, Afshan Asghar Rasheed, Adeel Samad, Ahmed Raheem, Samina Ismail Hirani, Shabbir Shabbir- Moosajee
Section of Haematology/Oncology
Introduction: Down regulation of CD20 expression has been reported in diffuse large B cell lymphoma (DLBCL)). Therefore, it is important to determine whether chemotherapy with rituximab induces CD20 down regulation and effects survival. Objectives: To determine the incidence of down regulation of CD20 expression in relapsed DLBCL after treatment with rituximab and to compare outcomes and assess pattern of relapse between CD20 negative and CD20 positive cases. Methodology: We retrospectively reviewed patients with relapsed DLBCL who received rituximab in the first line setting at Aga Khan University Hospital between January 2007 and December 2014. Data were recorded on predesigned questionnaires, …
Cabot Rings And Marked Anisopoikilocytosis In Imerslund-Gräsbeck Syndrome., Derrick L. Goubeaux, Weijie Li
Cabot Rings And Marked Anisopoikilocytosis In Imerslund-Gräsbeck Syndrome., Derrick L. Goubeaux, Weijie Li
Manuscripts, Articles, Book Chapters and Other Papers
No abstract provided.
Primary Cns Burkitt Lymphoma: A Case Report Of A 55-Year-Old Cerebral Palsy Patient, Kathryn Bower, Nilay Shah
Primary Cns Burkitt Lymphoma: A Case Report Of A 55-Year-Old Cerebral Palsy Patient, Kathryn Bower, Nilay Shah
Faculty & Staff Scholarship
With primary central nervous system lymphoma (PCNSL) being a rare disease, the subtype of Burkitt lymphoma (BL) presenting as a sole CNS lesion is an even more exceptional diagnosis. A case of coexistent primary CNS Burkitt lymphoma (PCNSBL) with cerebral palsy (CP) is presented. A 55-year-old Caucasian male presented with increasing bilateral lower extremity weakness above his baseline in addition to signs of increased intracranial pressure. Four abnormal enhancing masses were detected on MRI with biopsy results consistent with Burkitt lymphoma. Complete staging workup was completed with no evidence of extra- CNS disease noted on PET/CT, bone marrow biopsy, or …
Venous Thromboembolism Risk Stratification Via Electronic Medical Record Classification, Shannon L. Carpenter, Laura Miller-Smith, Brittney Hunter, Ashley Duty, Justin Sheets, Yuri Tupa, Kate Gibbs
Venous Thromboembolism Risk Stratification Via Electronic Medical Record Classification, Shannon L. Carpenter, Laura Miller-Smith, Brittney Hunter, Ashley Duty, Justin Sheets, Yuri Tupa, Kate Gibbs
Posters
No abstract provided.
การใช้ไมโครพาติเคิลจากเม็ดเลือดแดงเป็นตัวบ่งชี้ทางชีวภาพชนิดใหม่สำหรับวินิจฉัยภาวะปัสสาวะเป็นเลือดจากความผิดปกติของโกลเมอรูลัส, อวิรุทธ์ เจริญสรรพกิจ
การใช้ไมโครพาติเคิลจากเม็ดเลือดแดงเป็นตัวบ่งชี้ทางชีวภาพชนิดใหม่สำหรับวินิจฉัยภาวะปัสสาวะเป็นเลือดจากความผิดปกติของโกลเมอรูลัส, อวิรุทธ์ เจริญสรรพกิจ
Chulalongkorn University Theses and Dissertations (Chula ETD)
การจัดจำแนกภาวะปัสสาวะเป็นเลือดจากสาเหตุความผิดปกติของโกลเมอรูลัสเป็นปัญหาที่พบได้บ่อยในการตรวจพิสูจน์ทางไต และการตรวจนับปริมาณเม็ดเลือดแดงชนิดดิสมอร์ฟิก (dysmorphic red blood cell: DRBC) ในปัสสาวะเป็นวิธีการที่ใช้ในการจัดจำแนกอยู่ในปัจจุบัน แต่ขีดจำกัดของการตรวจนับด้วยวิธีนี้มีอยู่หลายประการ เช่น ผู้ปฏิบัติงาน และมีความไวต่ำ โดยการตรวจนับปริมาณของเม็ดเลือดแดงที่มีการแสดงออกของฟอสฟาติดิลซีรีน (phosphatidylserine exposing RBC: PS-RBC) และไมโครพาติเคิลจากเม็ดเลือดแดง (RBC derived microparticle: RMP) ซึ่งเป็นตัวบ่งชี้ถึงการบาดเจ็บของเม็ดเลือดแดงด้วยเทคนิคโฟลไซโตมิทรี (flow cytometry) กลับยังไม่เคยมีมาก่อน ในงานวิจัยนี้มีวัตถุประสงค์เพื่อ (1) เพื่อเปรียบเทียบปริมาณ RMP และ PS-RBC ในปัสสาวะระหว่างผู้ป่วยที่ภาวะปัสสาวะเป็นเลือดจากความผิดปกติของโกลเมอรูลัส (glomerular hematuria: GH) ผู้ป่วยที่ภาวะปัสสาวะเป็นเลือดจากสาเหตุที่ไม่ใช่โกลเมอรูลัส (non-glomerular hematuria: NGH) (2) เพื่อเปรียบความสามารถของการใช้ตัวบ่งชี้ทางชีวภาพจากเทคนิคflow cytometry และร้อยละของ DRBC ในการวินิจฉัยภาวะ GH (3) เพื่อศึกษาการเกิด DRBC, PS-RBC และการปลดปล่อย RMP จากการเปลี่ยนแปลงทางกายภายและเคมีในท่อของท่อหน่วยไตจำลองในหลอดทดลอง ปัสสาวะจะถูกเก็บมาจากผู้ป่วยที่ภาวะ GH, ผู้ป่วยที่ภาวะ NGH และอาสาสมัครที่ไม่มีภาวะปัสสาวะเป็นเลือด โดยปัสสาวะจะถูกนำมาตรวจตะกอนปัสสาวะภายใต้กล้องจุลทรรศน์เพื่อตรวจนับปริมาณ DRBC และวิเคราะห์ด้วยเทคนิค flow cytometry เพื่อตรวจนับปริมาณของ PS-RBC และ RMP โดยผู้ป่วยที่ภาวะ GH จะถูกยืนยันโรคของโกลเมอรูลัสภายใน 3 เดือน และผู้ป่วยที่ภาวะ NGH ต้องรู้สาเหตุของภาวะปัสสาวะเป็นเลือดที่แน่นอน โดยข้อมูลทั้งหมดจะถูกปกปิดไม่ให้ผู้ปฏิบัติงานรับทราบ และกราฟ ROC จะถูกใช้เพื่อพิสูจน์ความสามารถในการวินิจฉัยภาวะ GH ของตัวบ่งชี้ทางชีวภาพต่าง ๆ ผลการวิจัยพบว่ากลุ่มตัวอย่างในงานวิจัย ประกอบด้วย ผู้ป่วยภาวะ GH จำนวน 29 ราย, ผู้ป่วยภาวะ NGH จำนวน 29 ราย และอาสาสมัครที่ไม่มีภาวะปัสสาวะเป็นเลือดจำนวน 20 ราย โดยสาเหตุปัสสาวะเป็นเลือดหลักของผู้ป่วยภาวะ GH …
ฤทธิ์ของน้ำคะน้าจีนในการยับยั้งการเจริญของเซลล์ และเหนี่ยวนำการตายแบบอะพอพโทซิสในเซลล์มะเร็งเม็ดเลือดขาวเพาะเลี้ยงผ่านการเพิ่มการแสดงออกโปรตีนแคสเปส 3, ศิริพร พึ่งพวก
Chulalongkorn University Theses and Dissertations (Chula ETD)
ผักคะน้าจีนถูกนิยมนำมาใช้เป็นส่วนผสมในอาหารเอเชียตะวันออก ผักชนิดนี้จัดอยู่ในตระกูลกะหล่ำ ซึ่งผักในตระกูลนี้มีองค์ประกอบของสารต่อต้านอนุมูลอิสระสูง โดยเฉพาะอย่างยิ่งสารกลุ่มกลูโคซิโนเลตและไอโซไธโอซัยยาเนตซึ่งเป็นสารที่พบเฉพาะในผักตระกูลกะหล่ำ การศึกษาจำนวนมากแสดงให้เห็นว่าสารสกัดจากพืชตระกูลกะหล่ำมีฤทธิ์ต้านมะเร็ง อย่างไรก็ตามผู้คนส่วนใหญ่นิยมรับประทานผักคะน้าจีนด้วยการปรุงสุก โดยในงานวิจัยนี้มีวัตถุประสงค์เพื่อประเมินฤทธิ์ของน้ำผักคะน้าจีนต่ออัตราการมีชีวิตรอดและการเพิ่มจำนวนของเซลล์เม็ดเลือดขาว เซลล์ U937 ถูกเลี้ยงด้วยน้ำผักคะน้าแบบจีนแบบสดและที่ผ่านความร้อน ซึ่งถูกเตรียมโดยวิธีการนึ่ง (0.625, 1.25, 2.5 และ 5 %v/v) เพื่อเปรียบเทียบฤทธิ์ในการต้านมะเร็ง อัตราการมีชีวิตรอดมีชีวิตและการเพิ่มจำนวนของเซลล์ถูกทดสอบด้วยการใช้สีย้อมและวิธี XTT ที่ 24, 48 และ 72 ชั่วโมง ผลการวิจัยพบว่าที่ 72 ชม. การบ่มด้วยน้ำผักคะน้าจีนสด 5 %v/v ลดอัตราการมีชีวิตรอดของเซลล์ถึง 13 ± 11.9 % ในขณะที่การรักษาด้วยน้ำผักคะน้าจีนที่ผ่านความร้อน 5 %v/v ลดอัตราการมีชีวิตรอดของเซลล์ได้ 49 ± 8.3 % จำนวนเซลล์และการทดสอบ XTT แสดงให้เห็นว่าน้ำผักคะน้าจีนทั้งแบบสดและที่ผ่านความร้อนสามารถลดการเพิ่มจำนวนเซลล์ได้ตามระดับความเข้มข้นและเวลา วัฏจักรของเซลล์และการตายของเซลล์ที่เลี้ยงร่วมกับน้ำผักคะน้าจีนถูกวิเคราะห์โดยโฟลซัยโตมิตรี พบว่ามีประชากรของเซลล์เพิ่มขึ้นที่ระยะ sub G1 และเซลล์มีการตายแบบ apoptosis เพิ่มขึ้น โดยเฉพาะอย่างยิ่งที่ความเข้มข้นสูงและระยะเวลาที่มากขึ้น เมื่อเปรียบเทียบกับตัวควบคุม นอกจากนี้การวิเคราะห์ด้วยวิธี Western blot แสดงให้เห็นว่าการเกิดอะพอพโตซิสที่ถูกเหนี่ยวนำโดยน้ำผักคะน้าจีนนั้นเกี่ยวข้องกับการเพิ่มขึ้นของโปรตีน caspase 3 โดยรวมแล้วผลการวิจัยพบว่าน้ำผักคะน้าจีนสดมีประสิทธิภาพมากกว่าน้ำผักคะน้าจีนที่ผ่านความร้อนในการต้านมะเร็งเม็ดเลือดขาว อย่างไรก็ตามผักคะน้าจีนทั้งสองรูปแบบถูกใช้เป็นอาหารเสริมที่มีฤทธิ์ต้านมะเร็งเม็ดเลือดขาวได้
A Healthcare Improvement Initiative To Increase Multidisciplinary Pain Management Referrals Of Youth With Sickle Cell Disease, Rae Ann Kingsley, Gail Robertson, Lynne Covitz, Areli Ramphal
A Healthcare Improvement Initiative To Increase Multidisciplinary Pain Management Referrals Of Youth With Sickle Cell Disease, Rae Ann Kingsley, Gail Robertson, Lynne Covitz, Areli Ramphal
Posters
No abstract provided.
Medication Timeliness In Emergency Department In Pediatric Sickle Cell Disease Population Presenting With Vaso-Occlusive Episode, Derrick Goubeaux, Kaitlyn Hoch, Gerald Woods, Julie Routhieaux, Maureen Guignon, Valerie Mcdougall Kestner
Medication Timeliness In Emergency Department In Pediatric Sickle Cell Disease Population Presenting With Vaso-Occlusive Episode, Derrick Goubeaux, Kaitlyn Hoch, Gerald Woods, Julie Routhieaux, Maureen Guignon, Valerie Mcdougall Kestner
Posters
No abstract provided.
Mortality In Children, Adolescents And Adults With Sickle Cell Anemia In Rio De Janeiro, Brazil., Clarisse Lopes De Castro Lobo, Emilia Matos Do Nascimento, Leonardo José Carvalho De Jesus, Thiago Gotelip De Freitas, Jocemir Ronaldo Lugon, Samir K. Ballas
Mortality In Children, Adolescents And Adults With Sickle Cell Anemia In Rio De Janeiro, Brazil., Clarisse Lopes De Castro Lobo, Emilia Matos Do Nascimento, Leonardo José Carvalho De Jesus, Thiago Gotelip De Freitas, Jocemir Ronaldo Lugon, Samir K. Ballas
Cardeza Foundation for Hematologic Research
OBJECTIVE: To determine the mortality rate of children, adolescents and adults with sickle cell anemia in Rio de Janeiro, Brazil.
METHODS: The number of deaths, the mortality rate and the causes of deaths in patients with sickle cell anemia who were treated and followed up at our institution for 15 years were determined and compared to data available for the Brazilian population.
RESULTS: The overall number of deaths was 281 patients with a mortality rate of 16.77%. Survival probability was significantly higher in females. The number of deaths and the mortality rate were age-specific with a significant increase in the …
The Evaluation Of Mefloquine Drug Repurposing On Acute Myeloid Leukemia, Jessica L. Phan, Bhavuk Garg, Hrishikesh Mehta, Seth Corey
The Evaluation Of Mefloquine Drug Repurposing On Acute Myeloid Leukemia, Jessica L. Phan, Bhavuk Garg, Hrishikesh Mehta, Seth Corey
UROP Posters
The aim of this study is to observe cell proliferation, cell viability, apoptosis, and autophagy on acute myeloid leukemia (AML) cell lines, NB4 and U937, with the drug repurposing of mefloquine (MQ). Methods such as the 3-(4,5-Dimethylthiazol-2-Yl)-2,5-Diphenyltetrazolium Bromide (MTT) assay and trypan blue staining have shown a decrease in live cells with high concentrations of mefloquine. Using their average perspective IC50 values of MQ concentration, Western blotting was applied by means of apoptosis and autophagy markers to determine if the induction of apoptosis and inhibition of autophagy was present in MQ-treated AML cells. The experiment will be continued with more …
Evaluation And Adaptation Of Live-Cell Interferometry For Applications In Basic, Translational, And Clinical Research, Kevin A. Leslie
Evaluation And Adaptation Of Live-Cell Interferometry For Applications In Basic, Translational, And Clinical Research, Kevin A. Leslie
Theses and Dissertations
Cell mass is an important indicator of cell health and status. A diverse set of techniques have been developed to precisely measure the masses of single cells, with varying degrees of technical complexity and throughput. Here, the development of a non-invasive, label-free optical technique, termed Live-Cell Interferometry (LCI), is described. Several applications are presented, including an evaluation of LCI’s utility for assessing drug response heterogeneity in patient-derived melanoma lines and the measurement of CD3+ T cell kinetics during hematopoietic stem cell transplantation. The characterization of mast cells during degranulation, the measurement of viral reactivation kinetics in Kaposi’s Sarcoma, and drug …
The Changes Of Immunoglobulin G N-Glycosylation In Blood Lipids And Dyslipidaemia, Di Liu, Xi Chu, Hao Wang, Jing Dong, Si-Qi Ge, Zhong-Yao Zhao, Hong-Li Peng, Ming Sun, Li-Juan Wu, Man-Shu Song, Xiu-Hua Guo, Qun Meng, You-Xin Wang, Gordan Lauc, Wei Wang
The Changes Of Immunoglobulin G N-Glycosylation In Blood Lipids And Dyslipidaemia, Di Liu, Xi Chu, Hao Wang, Jing Dong, Si-Qi Ge, Zhong-Yao Zhao, Hong-Li Peng, Ming Sun, Li-Juan Wu, Man-Shu Song, Xiu-Hua Guo, Qun Meng, You-Xin Wang, Gordan Lauc, Wei Wang
Research outputs 2014 to 2021
Background
Alternative N-glycosylation has significant structural and functional consequences on immunoglobulin G (IgG) and can affect immune responses, acting as a switch between pro- and anti-inflammatory IgG functionality. Studies have demonstrated that IgG N-glycosylation is associated with ageing, body mass index, type 2 diabetes and hypertension.
Methods
Herein, we have demonstrated patterns of IgG glycosylation that are associated with blood lipids in a cross-sectional study including 598 Han Chinese aged 20–68 years. The IgG glycome composition was analysed by ultra-performance liquid chromatography.
Results
Blood lipids were positively correlated with glycan peak GP6, whereas they were negatively correlated with …
Ectopic Enterobius Vermicularis Iinfestation; An Extremely Rare Cause Of Mesenteric Lymphadenopathy Mimicking Tuberculous Lymphadenitis, Summaya Zafar, Muhammad Usman, Zubair Ahmad
Ectopic Enterobius Vermicularis Iinfestation; An Extremely Rare Cause Of Mesenteric Lymphadenopathy Mimicking Tuberculous Lymphadenitis, Summaya Zafar, Muhammad Usman, Zubair Ahmad
Department of Pathology and Laboratory Medicine
Enterobius vermicularis (EV) is a pinworm which commonly resides in the lumen of the intestinal tract and lays eggs on the perianal skin. However, rarely the worm can infest various other sites in the body and cases with infestation of such ectopic sites have been reported in literature. Rare cases of mesenteric lymph node involvement have also been reported. We report a case in a young male who presented with signs and symptoms of acute appendicitis. During surgery, enlarged mesenteric lymph nodes were identified. Histological examination revealed adult worm in the appendiceal lumen. Histological examination of mesenteric lymph node revealed …
Hematopoietic Stem Cell Transplantation In Pakistan – Country Report, Parvez Ahmed, Tahir Sultan Shamsi, Salman Adil, Tariq Mahmood Satti, Qamar Un Nisa Chaudhry, Tahir Sultan Shamsi, Syed Kamran Mahmood, Saqib Ansari, Natasha Bahadur Ali, Tariq Ghafoor
Hematopoietic Stem Cell Transplantation In Pakistan – Country Report, Parvez Ahmed, Tahir Sultan Shamsi, Salman Adil, Tariq Mahmood Satti, Qamar Un Nisa Chaudhry, Tahir Sultan Shamsi, Syed Kamran Mahmood, Saqib Ansari, Natasha Bahadur Ali, Tariq Ghafoor
Department of Pathology and Laboratory Medicine
No abstract provided.
Cost And Quality Issues In Establishing Hematopoietic Cell Transplant Program In Developing Countries, Shahrukh K. Hashmi, Alok Srivastava, Walid Rasheed, Salman Adil, Tong Wu, Madan Jagasia, Amr Nassar, William Y. K. Hwang, Amir Ali Hamidieh, Hildegard T. Greinix
Cost And Quality Issues In Establishing Hematopoietic Cell Transplant Program In Developing Countries, Shahrukh K. Hashmi, Alok Srivastava, Walid Rasheed, Salman Adil, Tong Wu, Madan Jagasia, Amr Nassar, William Y. K. Hwang, Amir Ali Hamidieh, Hildegard T. Greinix
Section of Haematology/Oncology
The hematopoietic cell transplant (HCT) activity has grown significantly over the past two decades in both developing and developed countries. Many challenges arise in establishing new HCT programs in developing countries, due to scarcity of resources and manpower in expertise in HCT. While cost issues can potentially hinder establishment of new HCT programs in certain regions, the focus on quality and value should be included in the general vision of leadership before establishing an HCT program. The main challenge in most developing countries is the lack of trained/qualified personnel, enormous start-up costs for a tertiary care center, and quality maintenance. …
Dynamic Assessment Of Nk Cell Interactions With Pediatric Tumor Cells To Predict Response To Immunotherapy, Arianexys Aquino Lopez
Dynamic Assessment Of Nk Cell Interactions With Pediatric Tumor Cells To Predict Response To Immunotherapy, Arianexys Aquino Lopez
Dissertations and Theses (Open Access)
Due to Natural Killer (NK) cells’ capacity to target tumor cells without prior sensitization, adoptive NK cell therapy represents a promising immunotherapy approach for pediatric cancer patients. Our laboratory has developed an NK cell expansion protocol that generates large quantities of NK cells for therapeutic infusion. Given that NK cells are heterogeneous, with variable receptor expression and potential to target tumor cells, the purpose of my study was to determine whether subpopulations of NK cells with enhanced anti-tumor potential could be identified for increased potency of the NK cell infusion product. In addition, we previously showed that our expanded NK …
Clinical Risks And Healthcare Utilization Of Hematopoietic Cell Transplantation For Sickle Cell Disease In The Usa Using Merged Databases., Staci D Arnold, Ruta Brazauskas, Naya He, Yimei Li, Richard Aplenc, Zhezhen Jin, Allistair Abraham, +Several Additional Authors
Clinical Risks And Healthcare Utilization Of Hematopoietic Cell Transplantation For Sickle Cell Disease In The Usa Using Merged Databases., Staci D Arnold, Ruta Brazauskas, Naya He, Yimei Li, Richard Aplenc, Zhezhen Jin, Allistair Abraham, +Several Additional Authors
Pediatrics Faculty Publications
Advances in allogeneic hematopoietic cell transplantation for sickle cell disease have improved outcomes, but there is limited analysis of healthcare utilization in this setting. We hypothesized that, compared to late transplantation, early transplantation (at age <10 >years) improves outcomes and decreases healthcare utilization. We performed a retrospective study of children transplanted for sickle cell disease in the USA during 2000-2013 using two large databases. Univariate and Cox models were used to estimate associations of demographics, sickle cell disease severity, and transplant-related variables with mortality and chronic graft-versus-host disease, while Wilcoxon, Kruskal-Wallis, or linear trend tests were applied for the estimates of …10>
Bk Polyomavirus Virus Hemorrhagic Cystitis Following Allogeneic Bone Marrow Transplant With Haploidentical Related Donor: Case Reports From Two Patients, Danish Shakeel, Natasha Bahadur Ali, Mohammad Usman Shaikh, Salman Adil
Bk Polyomavirus Virus Hemorrhagic Cystitis Following Allogeneic Bone Marrow Transplant With Haploidentical Related Donor: Case Reports From Two Patients, Danish Shakeel, Natasha Bahadur Ali, Mohammad Usman Shaikh, Salman Adil
Section of Haematology/Oncology
BK virus is well known to be associated with allograft failure in renal transplant recipients due to polyomavirus-associated nephropathy (PVAN). BK viruses are increasingly recognized an important cause of hemorrhagic cystitis during hematopoietic stem cell transplantation (HSCT). Here we describe two patients with acute lymphoblastic leukemia who received a haplo identical match related donor hematopoietic stem cell transplant after myeloablative conditioning and post-transplant cyclophosphamide. They developed cytology proven BK Virus cystitis. Both were treated with Leflunomide. Treatment was effective in alleviating the symptoms temporarily but eventually the symptoms progressed and resulted in mortality of both patients.
Primary Pulmonary Carcinoid Tumors: A Single Institution Retrospective Review: Topic: Medical Oncology, Samuel Adediran Md, Eliot L. Friedman Md, Ranjit R. Nair Md
Primary Pulmonary Carcinoid Tumors: A Single Institution Retrospective Review: Topic: Medical Oncology, Samuel Adediran Md, Eliot L. Friedman Md, Ranjit R. Nair Md
Department of Medicine
No abstract provided.
Hydroxyurea Lowers The Frequency Of Sickle Cell Vaso-Occlusive Crises, Corey S. Macrander
Hydroxyurea Lowers The Frequency Of Sickle Cell Vaso-Occlusive Crises, Corey S. Macrander
Clinical Research in Practice: The Journal of Team Hippocrates
A critical appraisal and clinical application of Charache S, Terrin ML, Moore RD, et al. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. N Engl J Med 1995;(332):1317-1322 doi: 10.1056/nejm199505183322001
Multimodality Therapy Improves Survival In Intramedullary Spinal Cord Metastasis Of Lung Primary, Hayder Saeed, Reema Patel, Jigisha Thakkar, Lames Hamoodi, Li Chen, John L. Villano
Multimodality Therapy Improves Survival In Intramedullary Spinal Cord Metastasis Of Lung Primary, Hayder Saeed, Reema Patel, Jigisha Thakkar, Lames Hamoodi, Li Chen, John L. Villano
Internal Medicine Faculty Publications
Background: Most metastatic spinal cord lesions are located either in the intradural, extramedullary, or in the epidural compartments. Intramedullary spinal cord metastasis (ISCM) is a rare central nervous system spread of cancer. The aim of this report was to evaluate ISCM in the published literature.
Methods: A literature review of PubMed from 1960 to 2016 was undertaken for the publications having demographic, clinical, histological, and outcome data.
Results: A total of 59 relevant papers were identified, showing 128 cases of intramedullary metastasis from lung cancer. The incidence of lung cancer as the primary malignancy with intramedullary metastasis was 56%. The …
Cerebral Venous Sinus Thrombosis In A Patient With Undiagnosed Factor Vii Deficiency, Hira Qadir, Anila Rashid, Salman Naseem Adil
Cerebral Venous Sinus Thrombosis In A Patient With Undiagnosed Factor Vii Deficiency, Hira Qadir, Anila Rashid, Salman Naseem Adil
Department of Pathology and Laboratory Medicine
Factor VII (FVII) deficiency is one of the rare inherited bleeding disorders. Thrombosis has been occasionally described in inherited FVII deficiency. Here, we report a young female with undiagnosed FVII deficiency who presented with cerebral venous sinus thrombosis (CVST). Oral contraceptive pill was found to be prothrombotic risk factor. The CVSToccurred in spite of the congenital FVII deficiency indicating that no definitive antithrombotic protection is assured by this defect. Low molecular weight heparin and anti-Xa assay were found to be safe choice of anticoagulation and monitoring, respectively, in this patient