Publications by authors named "K Tomiyama"

Liver transplant (LT) for colorectal cancer liver metastases (CRLM) is increasingly popular, yet the ideal selection criteria remain unknown. Pretransplant positron emission tomography (PET) metabolic tumor volume (MTV) has been described as predicting recurrence, with a proposed cutoff of MTV ≥70 cm 3 . This approach has not been validated.

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We report a case of a 55-year-old male with intrahepatic cholangiocarcinoma (iCCA) who underwent living donor liver transplantation (LDLT) after complete radiographic response on second-line pemigatinib. LDLT for iCCA is controversial, but recent reports have cited the potential benefit for patients with unresectable disease, especially those with disease stability after 6 months of systemic therapy. Concomitantly, genomic profiling has identified potentially treatable oncologic targets in iCCA.

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Article Synopsis
  • This study aimed to evaluate the effectiveness of a mouthrinse with silver nanoparticles (AgNP) against polymicrobial biofilms in a lab setting.
  • Polymicrobial biofilms were created on glass slips, treated with various solutions, including the mouthrinse with AgNP, chlorhexidine, and xylitol, then analyzed for viable cell counts and lactic acid levels.
  • Results showed that the AgNP mouthrinse reduced viable cells in the biofilm similarly to or even better than 0.2% chlorhexidine, indicating its potential as an effective antimicrobial agent.
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Living donor liver transplantation (LDLT) is a treatment option for select patients with unresectable colorectal liver metastasis. We describe our center's experience of patient selection, insurance approval, and outcomes after LDLT after first referral in March 2019. Of the 206 evaluated patients, 23 underwent LDLT.

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Here, we report the identification of causative genes for limb-shortening in individuals repeatedly found in a population of severely immunodeficient NOG mice maintained via sibling mating. First, we conducted a pedigree survey to determine whether limb-shortening was a recessive genetic trait and then identified it using a crossing test. Simultaneously, the symptoms were identified in detail using pathological analysis.

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