191 results match your criteria: "Japanese Red Cross Narita Hospital.[Affiliation]"

We report two the cases of patients with imported Plasmodium falciparum malaria during the COVID-19 pandemic. One was coinfected with COVID-19 and the other was misdiagnosed with COVID-19; either way, the diagnosis of malaria was delayed. These cases suggest that physicians should beware of cognitive biases during pandemics and carefully evaluate febrile patients.

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Preoperative simulation using a three-dimensional printer is effective to perform safe surgery by knowing the range limit of drilling in the temporal bone. Moreover, simulations using models are thought to be useful for education of young surgeon.

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  • A study was conducted to evaluate the effectiveness of convalescent plasma therapy for COVID-19 in high-risk patients who showed symptoms within five days.
  • The trial involved 25 patients, with no significant difference in viral load changes between those receiving convalescent plasma and those receiving standard care over the first five days.
  • The results suggest that early convalescent plasma treatment does not reduce SARS-CoV-2 viral load compared to standard care alone within that timeframe.
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  • Laryngotracheoesophageal cleft (LTEC) is a rare congenital condition where the larynx and trachea are abnormally connected behind the esophagus, often linked with other gastrointestinal issues.
  • A case was reported where a male fetus had a gastric polypoid lesion detected via ultrasound, leading to frequent vomiting and respiratory problems after birth.
  • After examinations revealed LTEC type III, a partial gastrectomy showed that the tumor had characteristics similar to bronchial tissue, suggesting the gastric tissue abnormalities may stem from the same developmental issues causing LTEC.
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  • Germline genetic variants play a significant role in the development of pediatric B cell acute lymphoblastic leukemia (B-ALL), with genome-wide association studies identifying specific susceptibility loci.
  • The study focused on rare variants of a key transcription factor involved in B cell development and involved sequencing saliva DNA from 527 pediatric B-ALL patients in remission.
  • The analyses found a strong association between rare deleterious variants and pediatric B-ALL, particularly highlighting the variant rs372168347, which may influence B cell maturation and increase leukemia risk.
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  • Pulmonary tumor thrombotic microangiopathy is a severe condition where tumor cells block small blood vessels in the lungs, leading to symptoms like difficulty breathing and heart failure, often seen in advanced cancer cases.
  • A 68-year-old woman with non-small cell lung cancer, who was responding well to treatment, suddenly experienced worsening breathlessness and fatigue, despite no signs of tumor progression on imaging.
  • An autopsy revealed that while her primary tumor had shrunk, tumor clusters still caused significant blockage in lung vessels, highlighting that this condition can occur even with effective cancer treatment.
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Objective: We aimed to determine the prevalence and risk factors for osteonecrosis of the femoral head (ONFH) in a multicentre cohort of patients with antineutrophil cytoplasmic antibody-associated vasculitis (AAV).

Methods: One hundred and eighty-six AAV patients who underwent radiographs and MRI screening of bilateral hip joints at more than 6 months after initial remission induction therapy (RIT) were retrospectively assessed for the presence of ONFH.

Results: Among 186 AAV patients, 33 (18%) were diagnosed with ONFH.

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  • A multicenter study in Japan, HM-SCREEN-Japan 01, focused on detecting genetic mutations in acute myeloid leukemia (AML) patients using paraffin-embedded bone marrow clot samples, which is a less invasive method than using bone marrow fluid.* -
  • The study involved 188 patients and found actionable genetic mutations in 38% of them, which could guide treatment decisions, while also detecting a high rate of genetic alterations and fusion transcripts.* -
  • Key mutations, such as those in KIT and WT1, were linked to overall survival rates, highlighting the potential of comprehensive genomic profiling in identifying effective therapeutic targets for newly diagnosed and relapsed AML patients.*
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Mortality and morbidity of extremely low birth weight infants in Japan, 2015.

Pediatr Int

January 2023

The Committee on Neonatal Medicine, Japan Pediatric Society, Tokyo, Japan.

Background: In Japan, the mortality rate of extremely low birth weight (ELBW) infants is notably low in comparison with other developed countries, but the prevalence of chronic lung disease (CLD) and retinopathy of prematurity (ROP) is relatively high. This study aimed to estimate the mortality and morbidity of ELBW infants born in 2015 who were admitted to neonatal intensive care units (NICUs) in Japan and to examine the factors that affected the short-term outcomes of these infants. We also compared the mortality of ELBW infants born in 2005, 2010, and 2015.

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A 72-year-old man was presented with anemia and diagnosed with sigmoid colon cancer by colonoscopy. CT showed a soft tissue density around the retroperitoneum, leading to the diagnosis of retroperitoneal fibrosis. Stenosis of left ureter, inferior mesenteric artery, and left colic artery due to the soft tissues were detected.

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Methylmalonic acidemia (MMA) is a disorder of methylmalonic acid metabolism caused by impaired methylmalonyl CoA mutase. Neuroimaging shows symmetric hypodensity on CT, and T2 prolongation on MRI in the globus pallidus; however, there have been only a few reports on MR spectroscopy findings and no previous reports on arterial spin labeling (ASL), both of which could reflect neurochemical derangement in MMA. We herein report an 18-month-old Sri Lankan boy presented with severe acute exacerbation of MMA due to bacteremia of O7.

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Introduction: Cowden syndrome is a rare autosomal dominant disease characterized by the development of hamartomas and increased risks of other tumors, including breast, thyroid, and uterine cancers. Most patients with Cowden syndrome show mutations of the phosphatase and tensin homolog (PTEN) gene on chromosome 10; however, some patients with mutations do not show clinical symptoms, while patients with clinical symptoms may not have detectable PTEN mutations.

Case Presentation: A 39-year-old woman with macrocephaly had previously been diagnosed with Cowden syndrome at another hospital, when she presented with the onset of breast cancer.

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Comprehensive genomic profiling examinations (CGPs) have recently been developed, and a variety of tumor-agnostic mutations have been detected, leading to the development of new molecular-targetable therapies across solid tumors. In addition, the elucidation of hereditary tumors, such as breast and ovarian cancer, has pioneered a new age marked by the development of new treatments and lifetime management strategies required for patients with potential or presented hereditary cancers. In acute myeloid leukemia (AML), however, few tumor-agnostic or hereditary mutations have been the focus of investigation, with associated molecular-targeted therapies remaining poorly developed.

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Chronic myeloid leukemia (CML) is a myeloproliferative disorder caused by the BCR-ABL1 tyrosine kinase. Although ABL1-specific tyrosine kinase inhibitors (TKIs) including nilotinib have dramatically improved the prognosis of patients with CML, the TKI efficacy depends on the individual patient. In this work, we found that the patients with different nilotinib responses can be classified by using the estimated parameters of our simple dynamical model with two common laboratory findings.

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Basic practices for gastrointestinal ultrasound.

J Med Ultrason (2001)

July 2023

Department of Laboratory Medicine (Endoscopy and Ultrasound), Kawasaki Medical School Hospital, Okayama, Japan.

The standard diagnostic modalities for gastrointestinal (GI) diseases have long been endoscopy and barium enema. Recently, trans-sectional imaging modalities, such as computed tomography and magnetic resonance imaging, have become increasingly utilized in daily practice. In transabdominal ultrasonography (US), the bowel sometimes interferes with the observation of abdominal organs.

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Autologous stem cell transplantation (ASCT) remains an important therapeutic strategy for multiple myeloma; however, a proportion of patients fail to mobilize a sufficient number of peripheral blood stem cells (PBSCs) to proceed to ASCT. In the present study, we aimed to clarify the characteristics and outcomes of poor mobilizers. Clinical data on poorly mobilized patients who underwent PBSC harvest for almost 10 years were retrospectively collected from 44 institutions in the Japanese Society of Myeloma (JSM).

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Prolonged isolated thrombocytopenia (PIT) is a complication following allogeneic hematopoietic cell transplantation that results in prolonged transfusion dependence. Recently, the efficacy of a thrombopoietin receptor agonist (eltrombopag) against PIT has been reported in adults; however, there are few reports in children. A 4-year-old male pediatric patient diagnosed with congenital pure red cell aplasia underwent allogeneic hematopoietic cell transplantation.

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Inherited genetic variation is associated with 6-mercaptopurine (6-MP) dose reduction and frequent toxicities induced by 6-MP. However, the tolerable dose for 6-MP is not fully predicted by the known variation in NUDT15 and TPMT among Asian children with acute lymphoblastic leukaemia (ALL). We performed a genome-wide association study (GWAS) related to 6-MP dose among Japanese children with ALL.

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  • Anaplastic thyroid cancer (ATC) is a rare and aggressive type of cancer, and a study was conducted to evaluate the effectiveness and safety of a drug called lenvatinib in patients whose cancer could not be surgically removed.
  • The study involved 52 patients, with 42 being eligible for analysis, revealing a low 1-year overall survival rate of 11.9% and limited response rates; however, some patients did experience stable disease and durable responses.
  • Despite the high rate of adverse effects experienced by patients, the results suggest lenvatinib may still benefit a select group of patients, indicating the need for further research to identify who could be the best candidates for this treatment.
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The mortality of coronavirus disease 2019 (COVID-19) is strongly correlated with pulmonary vascular pathology accompanied by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection-triggered immune dysregulation and aberrant activation of platelets. We combined histological analyses using field emission scanning electron microscopy with energy-dispersive X-ray spectroscopy analyses of the lungs from autopsy samples and single-cell RNA sequencing of peripheral blood mononuclear cells to investigate the pathogenesis of vasculitis and immunothrombosis in COVID-19. We found that SARS-CoV-2 accumulated in the pulmonary vessels, causing exudative vasculitis accompanied by the emergence of thrombospondin-1-expressing noncanonical monocytes and the formation of myosin light chain 9 (Myl9)-containing microthrombi in the lung of COVID-19 patients with fatal disease.

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International medical evacuation, which is an option to receive better medical care for travelers with emergencies staying in low- and middle-income countries, has been more challenging during the coronavirus disease 2019 (COVID-19) pandemic. We herein discuss our experience with four Japanese patients with COVID-19 who required medical evacuation from Asian countries during the pandemic. Of these, none of the patients had received a COVID-19 vaccine; three patients needed oxygen therapy on admission to our hospital; and one patient died due to respiratory failure on day 50 after hospitalization.

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