A5102712068- Hematopoietic Stem Cell Transplantation
- Acute Lymphoblastic Leukemia research
- Chronic Lymphocytic Leukemia Research
- Chronic Myeloid Leukemia Treatments
- Hemoglobinopathies and Related Disorders
- Polyomavirus and related diseases
- Renal Transplantation Outcomes and Treatments
- Platelet Disorders and Treatments
- Acute Myeloid Leukemia Research
- Myeloproliferative Neoplasms: Diagnosis and Treatment
- Viral-associated cancers and disorders
- Blood groups and transfusion
- Prenatal Screening and Diagnostics
- Lymphoma Diagnosis and Treatment
- Drug-Induced Adverse Reactions
- T-cell and B-cell Immunology
- Reproductive Biology and Fertility
- Mesenchymal stem cell research
- Blood Coagulation and Thrombosis Mechanisms
- Autoimmune Bullous Skin Diseases
- Hepatitis B Virus Studies
- CNS Lymphoma Diagnosis and Treatment
- Multiple Myeloma Research and Treatments
- Renal Diseases and Glomerulopathies
- Blood properties and coagulation
King Faisal Specialist Hospital & Research Centre
2015-2024
King Fahd Security College
2015-2017
Henry Ford Hospital
2005-2012
Henry Ford Health System
2006-2011
Inherited dysfibrinogenemia is a rare disorder caused by mutations in the fibrinogen gene, described approximately 400 families to date. We present case of 20-year-old woman at 7 weeks pregnancy with history two first-trimester spontaneous abortions and family thrombotic events. Her testing revealed evidence dysfibrinogenemia, necessitating multidisciplinary management planning including Hematology, OB-GYN, Maternal-Fetal Medicine, Blood Bank Services Anesthesia. Antenatal care included...
Journal Article Fatal hypersensitivity reaction to gemtuzumab ozogamicin associated with platelet transfusion Get access Amr Hanbali, M.D., M.D. Fellow Department of Hematology and Oncology; Address correspondence Dr. Hanbali at the Oncology, Henry Ford Hospital, 2799 West Grand Boulevard, Detroit, MI 48202 (ahanbal1@hfhs.org). Search for other works by this author on: Oxford Academic Google Scholar Ira Wollner, Program Director Klodiana Neme, Pharm.D., Pharm.D. Pharmacist Cynthia Ulreich,...
A42-year-old female presented with fever and shortness of breath, was diagnosed community acquired pneumonia. On presentation she found to have a white cell count 13 · 10/L, hemoglobin 7.1 g/dL platelets 51 10/L. Peripheral blood smear showed left shift many cells hairy projections (56%) (See Fig. 1) that were positive for CD38 CD138 by peripheral flow cytometry. Other laboratory findings included B-2 microglobulin 15.3 mg/L normal creatinine calcium levels. Serum protein electrophoresis...
A 50-year-old female with no medical history presented B-symptoms for 2 weeks including generalized weakness, fevers, fatigue, and night sweats. Physical exam revealed diffuse cervical axillary lymphadenopathy splenomegaly. Initial laboratories showed Coombs-negative hemolytic anemia agglutination of red blood cells moderate thrombocytopenia. Some tear drop were also seen pointing toward the presence bone marrow infiltration. Computed tomography (CT) body a mediastinal mass widespread Bone...
Plasma cell leukemia (PCL) is defined by the presence of more than 2 × 109/L PCs in peripheral blood. It a very rare type with poor outcome. In this case, we report PCL case blood morphology hairy leukemia. We describe clinical and pathological presentation 44-year-old woman who found to have abnormal lymphoid looking cells confirmed be lambda specific plasma leukemic flow cytometry. Eventually, patient managed autologous stem transplantation after conformation such diagnosis five cycles VCD...
The recommended therapy for severe aplastic anemia (SAA) in younger patients with a matched sibling donor (MSD) is allogeneic hematopoietic cell transplantation (allo-HCT). A number of conditioning regimens and protocols have been used these patients. Here we report homogeneous cohort SAA receiving uniform protocol. This study retrospective analysis 82 consecutive who underwent MSD allo-HCT at single center. median duration follow-up survivors was 100 months, the 10-year overall survival...
Acquired hemophilia is a severe bleeding diathesis that affects both males and females. It caused by suddenly appearing autoantibodies interfere with the coagulation factor VIII activity. This disorder characterized spontaneous post-traumatic subcutaneous bleeds massive mucosal hemorrhages. We report case of postpartum-acquired compartment syndrome right (Rt.) forearm in 29-year-old woman. Hemostatic tests indicated prolonged activated partial thromboplastin time (APTT) to 99 s (normal...