Publications by authors named "Kojima F"

Background: Limited data is available to evaluate the burden of device associated healthcare infections (HAI) [central line associated bloodstream infection (CLABSI), catheter associated urinary tract infection (CAUTI), and ventilator associated pneumonia (VAP)] in low and-middle-income countries. Our aim is to investigate the population attributable mortality fraction and the absolute mortality difference of HAI in a broad population of critically ill patients from Brazil.

Methods: Multicenter cohort study from September 2019 to December 2023 with prospective individual patient data collection.

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Itch is an unpleasant sensation that induces a desire to scratch. Chronic itch is accompanied by inflammatory skin diseases and causes repetitive scratching leading to tissue damage. The thyrotropin-releasing hormone analog taltirelin exerts analgesic effects on acute and chronic pain by activating the descending inhibitory systems.

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Microsomal prostaglandin E synthase-1 (mPGES-1) is an isozyme of the prostaglandin (PG) E synthase that acts downstream of cyclooxygenase and catalyzes the conversion of PGH to PGE. The impact of genetic deletion of mPGES-1 on the development of 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitis, a well-established model of inflammatory bowel disease (IBD), was investigated in this study. After administration of TNBS, mice deficient in mPGES-1 (mPGES-1 mice) showed more severe colitis than did wild-type (WT) mice.

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A 62-year-old man had bilateral eyelid swelling for 4 months. Two months before admission, he developed fatigue and lost 5 kg of body weight. Further examination revealed elevated serum C-reactive protein, normal angiotensin-converting enzyme, elevated proteinase-3 antineutrophil cytoplasmic antibody (PR3-ANCA), and normal immunoglobulin (Ig)G4 concentration.

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  • This study focuses on the challenge of diagnosing gastrointestinal stromal tumors (GISTs), particularly those that are smaller than 20 mm, which are often categorized as subepithelial lesions (SELs).
  • Researchers employed various endoscopic ultrasound techniques—specifically EUS elastography and contrast-enhanced harmonic EUS—to evaluate their effectiveness in distinguishing GISTs from other SELs.
  • The results showed that combining EUS strain elastography with CH-EUS enhanced diagnostic accuracy, making these methods promising tools for the early identification of GISTs.
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  • A 56-year-old woman experienced exertional shortness of breath and had elevated left diaphragm observed in chest X-rays, indicating unilateral diaphragmatic eventration.
  • Dynamic MRI revealed abnormal movement of the diaphragm, leading to surgical intervention.
  • Diaphragmatic plication was successfully performed using a minimally invasive technique, resulting in significant immediate symptom relief that lasted for six months post-surgery.
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Primary familial brain calcification (PFBC) is a genetic neurological disorder characterized by symmetric brain calcifications that manifest with variable neurological symptoms. This study aimed to explore the genetic basis of PFBC and elucidate the underlying pathophysiological mechanisms. Six patients from four pedigrees with brain calcification were enrolled.

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Recent research in urothelial carcinoma (UC) has focused on coding mutations, leaving the significance of non-coding mutations unexplored. This study aims to evaluate non-coding DNA mutation frequencies compared to coding regions in normal urothelium and flat lesions, exploring their implications for tumor biology. Using targeted next-generation sequencing with UC-related gene panel, we analyzed non-coding and coding DNA mutation frequencies across 119 samples of flat urothelium encompassing various lesion types.

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Pulmonary sclerosing pneumocytoma (PSP) is a rare, benign tumor. Given the challenges of a bronchoscopic diagnosis, surgery is performed during the early stages of the disease. Therefore, little is known about the growth pattern of PSP.

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  • The study investigates the genetic variants KMT2C and TSC2 in acquired cystic disease-associated renal cell carcinomas (ACD-RCCs) and their potential role in tumor development.
  • Researchers analyzed a total of 39 samples, including ACD-RCCs and related cysts, using DNA-targeted sequencing and immunohistochemistry.
  • Findings revealed that while KMT2C and TSC2 variants were present in several ACD-RCC samples, they are not likely the main contributors to tumor formation in this specific type of cancer.
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  • * Researchers screened 1555 Japanese IPN patients for CGG repeat expansions using advanced techniques, finding 44 cases with this genetic marker, making it a common cause of the condition.
  • * The findings underscore the importance of tailored screening strategies in clinical settings, particularly for identifying Charcot-Marie-Tooth disease (CMT) cases linked to CGG repeat expansions.
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Histological assessment of centroblasts is an important evaluation in the diagnosis of follicular lymphoma, but there is substantial observer variation in assessment among hematopathologists. We aimed to perform quantitative morphological analysis of centroblasts in follicular lymphoma using new artificial intelligence technology in relation to the clinical prognosis. Hematoxylin and eosin slides of lesions were prepared from 36 cases of follicular lymphoma before initial chemotherapy.

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The standard treatment for resectable non-small cell lung cancer (NSCLC) located in the superior sulcus is neoadjuvant chemoradiotherapy followed by highly invasive resection. Based on the results of the CheckMate 816 trial, which showed a marked improvement in the efficacy of neoadjuvant chemo-immunotherapy, we report a case of minimally invasive resection after neoadjuvant nivolumab plus chemotherapy for superior sulcus NSCLC, resulting in a pathologic complete response. The patient was a 76-year-old man with a 65-mm right superior sulcus tumour diagnosed as squamous cell carcinoma with 95% PD-L1.

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  • Diagnosing mediastinal tumors using low-dose CT (LDCT) for lung cancer screening is complex, often requiring invasive tests, highlighting a need for better diagnostic methods.
  • This study developed a hybrid transformer model combining LDCT features with clinical data to aid surgical planning for patients with incidental mediastinal tumors.
  • The model outperformed traditional methods, achieving an AUC of 0.90 compared to lower scores for models that didn't include clinical data, indicating significant improvement in decision-making for surgical options.
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Refractory pneumothorax associated with interstitial lung disease (ILD) remains a challenging condition due to the patient's tolerability and lung compliance that restrict the feasibility of aggressive interventions. Additionally, many cases recur after improvement with treatment, and reports of successful management for this complicated condition are limited. Herein, we report the case of a 60-year-old man with ILD, utilizing home oxygen therapy, who experienced a successful recovery from a surgical intervention under local anaesthesia for pneumothorax.

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The patient, a 40-year-old woman, was diagnosed as having a functional right vagal paraganglioma (PGL) 15 years after undergoing resection for a retroperitoneal PGL. I-MIBG scintigraphy showed no accumulation, but as the blood noradrenaline and urinary normetanephrine concentrations were elevated, the tumor was judged as being functional, and surgery was scheduled. The patient was started on doxazosin infusion and embolization of the tumor feeding vessel was performed before the surgery.

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Background: Early chest tube removal should be considered to enhance recovery after surgery. The current study aimed to provide a predictive algorithm for air leak episodes (ALE) and to create a knowledge base for early chest tube removal.

Methods: This retrospective study enrolled patients who underwent thoracoscopic anatomical pulmonary resections in our unit.

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There is limited contemporary prospective real-world evidence of patients with chronic arterial disease in Latin America. The Network to control atherothrombosis (NEAT) registry is a national prospective observational study of patients with known coronary (CAD) and/or peripheral arterial disease (PAD) in Brazil. A total of 2,005 patients were enrolled among 25 sites from September 2020 to March 2022.

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Proteins containing DM9 motifs, which were originally identified in the Drosophila melanogaster genome, are widely distributed in various organisms and are assumed to be involved in their innate immune response. In this study, we produced a recombinant protein of CG13321 (rCG13321) from D. melanogaster, which consists of four DM9 motifs, in Escherichia coli cells.

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Biallelic variants of 4-hydroxyphenylpyruvate dioxygenase-like (HPDL) gene have been linked to neurodegenerative disorders ranging from severe neonatal encephalopathy to early-onset spastic paraplegia. We identified a novel homozygous variant, c.340G > T (p.

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Background: Extramural venous invasion (EMVI) is a prognostic factor in rectal cancer. There are two types: EMVI detected by magnetic resonance imaging (MRI) (mr-EMVI) and EMVI detected by pathology (p-EMVI). They have been separately evaluated, but they have not yet been concurrently evaluated.

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Papillary thyroid carcinoma (PTC) is the most common type of thyroid carcinoma and has characteristic nuclear features. Genetic abnormalities of PTC affect recent molecular target therapeutic strategy towards RET-altered cases, and they affect clinical prognosis and progression. However, there has been insufficient objective analysis of the correlation between genetic abnormalities and nuclear features.

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Importance: Readmissions after an index heart failure (HF) hospitalization are a major contemporary health care problem.

Objective: To evaluate the feasibility and efficacy of an intensive telemonitoring strategy in the vulnerable period after an HF hospitalization.

Design, Setting, And Participants: This randomized clinical trial was conducted in 30 HF clinics in Brazil.

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Minute pulmonary meningothelial-like nodules (MPMNs) are benign lesions characterized by the appearance of ground-glass nodules (GGN) on computed tomography (CT). In the present case, an MPMN gradually developed into a substantial component during chest CT follow-up, and the GGN gradually transformed into a part-solid nodule. The imaging course described in this case is quite unique.

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Article Synopsis
  • - The study focuses on rare renal cell carcinomas (RCCs) that show features similar to haemangioblastomas, with a specific look at their clinicopathological characteristics and VHL gene alterations, comparing them to clear cell renal cell carcinomas (CCRCCs) that also exhibit these features.
  • - The identified RCCs with haemangioblastoma-like features are generally indolent, have a distinct appearance with a thick capsule, and specific immunohistochemical profiles, but do not show typical VHL mutations, indicating a different molecular behavior.
  • - Findings suggest these RCCs can be differentiated from CCRCCs, as they exhibit unique features in terms of blood vessel and cell structure, as well as differences in genetic mutations
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