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18941“…Patient: Female, 60-year-old Final Diagnosis: Amyloid light-chain amyloidosis • hepatic amyloidosis Symptoms: Abdominal pain • anemia • emesis Medication: — Clinical Procedure: Bone marrow biopsy • exploratory laparotomy • hepatectomy • stem cell transplant Specialty: Hematology • Oncology OBJECTIVE: Unusual clinical course BACKGROUND: Immunoglobulin light chain (AL) amyloidosis is a plasma cell disorder in which excess light chain deposits in tissues, resulting in organ dysfunction and damage. …”
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18942“…HbS polymerization in deoxygenated condition induces the sickling of red blood cells (RBCs), which become less deformable and more fragile, and thus prone to lysis. In addition to anemia, SCD patients may exhibit a plethora of clinical manifestations ranging from acute complications such as the frequent and debilitating painful vaso-occlusive crisis to chronic end organ damages. …”
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18943por Hama, Abdalla Hussein, Shakiba, Ebrahim, Rahimi, Zohreh, Karimi, Mehran, Mozafari, Hadi, Abdulkarim, Omed Adnan“…METHODS: In a case‐control study, 101 SCD patients including 61 sickle cell anemia (SCA), 39 S/β‐thalassemia, and 1 HbS/HbD (SD) along with 110 healthy individuals from Kurdistan of Iraq were studied. …”
Publicado 2021
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18944por Ugurel, Elif, Goksel, Evrim, Goktas, Polat, Cilek, Neslihan, Atar, Dila, Yalcin, Ozlem“…Supraphysiological shear stresses (SSs) induce irreversible impairments of red blood cell (RBC) deformability, overstretching of RBC membrane, or fragmentation of RBCs that causes free hemoglobin to be released into plasma, which may lead to anemia. The magnitude and exposure tisme of the SSs are two critical parameters that determine the hemolytic threshold of a healthy RBC. …”
Publicado 2021
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18945por Kim, J.H., Kim, S.H., Jeon, M.K., Kim, J.E., Kim, K.H., Yun, K.-H., Jeung, H.-C., Rha, S.Y., Ahn, J.-H., Kim, H.S.“…The most frequent treatment-related grade 3-4 toxicities included neutropenia (16.2%), anemia (13.5%), thrombocytopenia (13.5%), and fatigue (8.1%). …”
Publicado 2021
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18946por Jin, De, Zhang, Yuqin, Zhang, Yuehong, Duan, Liyun, Zhou, Rongrong, Duan, Yingyin, Sun, Yuting, Lian, Fengmei, Tong, Xiaolin“…Moreover, a few studies showed that alleviation of clinical phenotype such as reducing albuminuria, serum creatinine and renal anemia in DKD patients after application or consumption of Panax ginseng C.A.Mey.. …”
Publicado 2021
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18947por Maximiano, Cristiana, Silva, Andreia, Duro, Inês, Branco, Tiago, Correia-Costa, Liane, Teixeira, Ana, Rocha, Liliana, Costa, Teresa, Matos, Paula, Faria, Maria do Sameiro, Mota, Conceição, Afonso, Alberto Caldas“…INTRODUCTION: Atypical hemolytic uremic syndrome (aHUS) is a rare disorder characterized by the triad of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury, which primarily affects preschool-aged children. …”
Publicado 2021
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18948por Jun, Kang Woong, Cho, Jinbeom, Kim, Mi Hyeong, Hwang, Jeong Kye, Park, Sun Cheol, Moon, In Sung, Kim, Ji Il“…They also had pre-transplantation anemia, suggesting a concomitant bleeding diathesis. …”
Publicado 2021
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18949por Tan, Xinmei, Liang, Xueyan, Xi, Jiaxi, Guo, Sitong, Meng, Mingyu, Chen, Xiaoyu, Li, Yan“…Compared to PBC alone, HCS plus PBC improved the ORR, DCR, 1- and 2-year survival rates, and QOL and alleviated neutropenia, thrombocytopenia, nausea, vomiting, anemia, liver injury, renal injury, and alopecia. …”
Publicado 2021
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18950“…During treatment, fatigue and anemia developed, physical strength decreased, and a few petechiae were seen in the lower extremities. …”
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18951por Tian, Xi, Xu, Wen-Hao, Wu, Jun-Long, Gan, Hua-Lei, Wang, Hong-Kai, Gu, Wei-Jie, Qu, Yuan-Yuan, Zhang, Hai-Liang, Ye, Ding-Wei“…Germline mutation detection showed that nine variants associated with Fanconi anemia (VAFAs) pathway (FANCA, 6/18; FANCI, 3/18) were identified in 18 ccpRCC patients. …”
Publicado 2021
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18952por Brewer, Danielle, MacMillan, Margaret L., Schleiss, Mark R., Ayuthaya, Satja Issaranggoon Na, Young, Jo-Anne, Ebens, Christen L.“…CASE PRESENTATION: We describe the use of cerebrospinal fluid polymerase chain reaction and plasma cell-free DNA technologies to supplement neuroimaging in the diagnosis of cerebral toxoplasmosis in an immunocompromised pediatric patient following allogeneic hematopoietic cell transplantation for idiopathic severe aplastic anemia. Successful cerebral toxoplasmosis treatment included antibiotic therapy for 1 year following restoration of cellular immunity with an allogeneic stem cell boost. …”
Publicado 2021
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18953por Kodaira, Shota, Ehara, Jun, Takamizawa, Shigemasa, Ogita, Shin, Norisue, Yasuhiro, Nakama, Tatsuya, Hiraoka, Eiji“…Hematological adverse effects, including anemia, thrombocytopenia, and lymphocytopenia, have been reported. …”
Publicado 2021
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18954por Idrissi, Houda, Hakkour, Maryam, Duchateau, Luc, Zanatta, Renato, Kachani, Malika, Azrib, Rahma, Daminet, Sylvie, Kichou, Faouzi, El Asatey, Sabrine, Tazi, Noureddine, Sahibi, Hamid, El Hamiani Khatat, Sarah“…Lymphadenomegaly (81.2%), dermatological disorders (65.6%) (mostly exfoliative dermatitis), weight loss (59.3%), exercise intolerance (56.2%), anorexia (28.1%), hyporexia (15.6%), and ocular lesions (28.1%) were the most frequent clinical signs and complaints recorded. Anemia and hyperproteinemia due to hyperglobulinemia were observed in 68.7% and 72.7% of the cases, respectively. …”
Publicado 2021
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18955por Axling, Ulrika, Önning, Gunilla, Martinsson Niskanen, Titti, Larsson, Niklas, Hansson, Stefan R., Hulthén, Lena“…RESULTS: Intake of Lp attenuated the decrease in serum ferritin from baseline to week 28 (p = 0.003) and week 35 (p ˂ 0.001) and resulted in reduced prevalence of iron deficiency (59% vs 78%, p = 0.017) and iron deficiency anemia (7.4% vs 21%, p = 0.023) at week 35. Intake of Lp also resulted in beneficial effects on the soluble transferrin receptor (p = 0.011) and total body iron (p ˂ 0.001) at week 35. …”
Publicado 2021
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18956“…A year after the surgery, he was admitted again due to his somnolence but was diagnosed only with hypothyroidism and anemia. At the age of 7 years and 8 months, he was admitted to our department with ataxia and abnormal gait from the past year with instability and numerous falls. …”
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18957por Colella, Marina P., Orsi, Fernanda A., Alves, Elizio C. F., Delmoro, Gabriela de F., Yamaguti‐Hayakawa, Gabriela G., de Paula, Erich V., Annichino‐Bizzacchi, Joyce M.“…The main cause in these cases was hemolytic anemia and methemoglobinemia. Reductions in hemoglobin levels during the use of dapsone were seen in 94% of the patients. …”
Publicado 2021
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18958“…Transfusion helped reverse the imbalance in the frequencies of Tregs and Th17 cells and the Treg/Th17 ratio and especially contributed to a better outcome in HF patients with moderate-to-severe anemia. In conclusion, a higher frequency of peripheral blood Tregs and a higher Treg/Th17 ratio may be associated with unfavorable outcomes in HF patients, and blood transfusion may benefit moderate-to-severe HF patients rebalance their immune response.…”
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18959por Santander Ballestín, Sonia, Giménez Campos, Marta Isabel, Ballestín Ballestín, Jara, Luesma Bartolomé, María José“…Results: There are accepted interventions during pregnancy, such as folic acid supplementation to prevent congenital neural tube defects, potassium iodide supplementation to correct neurodevelopment, and oral iron supplementation during the second half of pregnancy to reduce the risk of maternal anemia and iron deficiency. A number of micronutrients have also been associated with pre-eclampsia, gestational diabetes mellitus, and nausea and vomiting in pregnancy. …”
Publicado 2021
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18960“…PATIENTS AND METHODS: This cross-sectional study collected data from 200 pairs of caregivers and children with asthma, anemia, and thalassemia aged 5 to 12 years after receiving treatment and follow-up in the pediatric outpatient department of the tertiary hospital, June to November 2020. …”
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