Publications by authors named "Kenichi Kohashi"

Objectives: Spread through air spaces (STAS) is considered a poor prognostic factor in patients with resected non-small lung cell cancer; however, the clinical significance of STAS extent remains unclear. We hypothesized that the further the tumour cells spread from the tumour edge, the worse the prognosis becomes.

Methods: This study retrospectively reviewed the data of 642 patients with completely resected pathological stage I-III non-small lung cell cancer between 2008 and 2018.

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To predict the therapeutic response of systemic therapy, comprehensive analyses of the tumor microenvironment in papillary renal cell carcinoma (pRCC) have been conducted previously using immunohistochemistry and RNA sequencing. This study aimed to evaluate the correlation between hematoxylin and eosin-based histological immunophenotypes and gene signatures employed in several clinical trials predicting responsiveness to immune checkpoint inhibitors and tyrosine kinase inhibitors, using data from the Cancer Genome Atlas (TCGA)-KIRP cohort (n = 254). Herein, we evaluated tumor-associated immune cells (TAICs) using three methodologies previously reported in clear cell RCC: a 3-tier immunophenotype (desert, excluded, and inflamed) based on the spatial distribution of TAICs; a 4-tier immunophenotype (cold, immune-low, excluded, and hot) considering both the location and degree of TAICs; and an inflammation score (score 0, 1, and 2) focusing only on the degree of TAICs.

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Mixed epithelial and stromal tumor of the kidney (MESTK) is a rare renal tumor characterized by both cystic and solid components. Although typically benign, its components can undergo malignant transformation, manifesting as a sarcomatous feature. Carcinomatous transformations are exceedingly rare.

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Background: Hepatoid adenocarcinoma of the stomach (HAS), a subtype of gastric cancer (GC), includes multiple tumor components, such as enteroblastic and tubular adenocarcinoma components. However, which component mostly contributes to the aggressive behavior of HAS remains unclear. Moreover, the role of tumor-associated macrophages (TAMs) has not been explored in HAS.

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Article Synopsis
  • - Malignant triton tumor (MTT) is a rare and aggressive nerve sheath tumor with a very low survival rate and no standard treatment options.
  • - A 16-year-old male diagnosed with MTT in his distal femur underwent chemotherapy followed by surgery and additional chemotherapy.
  • - After 1.5 years, the combined treatment successfully avoided recurrence, and he can walk without pain or any signs of metastasis.
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  • A new study aimed to create a standardized reporting system for bone and soft tissue tumor cytopathology, modifying an existing classification from the Milan System and comparing it to the upcoming WHO system.
  • The analysis of 285 cytology cases revealed a variety of categories, with malignancy risk ranging significantly across different classifications, including a high 100% in malignant cases.
  • The modified Milan and WHO systems showed high diagnostic reliability and effectiveness in identifying malignancy, suggesting they could be valuable tools for cytopathologic assessments.
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A 74-year-old man visited the urology clinic with the chief complaint of urinary retention in December 2014. Serum level of initial prostate specific antigen (PSA) was 50 ng/ml and he was diagnosed with Gleason Score 4+4 prostate adenocarcinoma with regional lymphadenopathy (cT3aN1M0). PSA level had declined after the treatment with combined androgen blockade.

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Dedifferentiated liposarcoma is a rare cancer with a poor prognosis. A 52-year-old man presented with a chief complaint of a mass in his left scrotum. He came with suspected testicular tumor, but all the measured tumor markers were negative.

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In papillary renal neoplasm with reverse polarity (PRNRP), the status of chromosomal copy number alterations, especially chromosomes 7/17 gain and chromosome Y loss, has remained controversial. In the literatures, there is a discrepancy among the results of chromosomal alteration in PRNRP depending on the analytical methods. Here, we comprehensively analyzed the status of chromosomal abnormalities in PRNRP.

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Epithelioid sarcoma (ES) is a rare aggressive sarcoma that, unlike most soft-tissue sarcomas, shows a tendency toward local recurrence and lymph node metastasis. Novel antitumor agents are needed for ES patients. Forkhead box transcription factor 1 (FOXM1) is a member of the Forkhead transcription factor family and is associated with multiple oncogenic functions; FOXM1 is known to be overexpressed and correlated with pathogenesis in various malignancies.

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Hepatoblastoma (HB) is the most common malignant liver tumor in childhood. Although pre-operative cisplatin (CDDP)-based chemotherapy is often used in cases of HB, about 20% of HB patients exhibit resistance to CDDP. Forkhead box protein M1 (FOXM1) and chromo-domain-helicase-DNA-binding protein 4 (CHD4) have been associated with CDDP resistance in various tumors.

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Isolated hypoganglionosis (IHG) is histologically characterized by small numbers of myenteric ganglion cells and small myenteric ganglia; however, no numerical diagnostic criteria for IHG have been established. Therefore, this study aimed to develop quantitative pathologic criteria for IHG. We evaluated 160 resected intestinal tissue specimens from 29 pediatric autopsies and 10 IHG cases.

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  • The study investigates the potential of nuclear morphology to predict the prognosis of myxoid liposarcoma (MLS) from primary biopsy specimens.
  • Two pathologists assessed nuclear shapes using established grading systems, finding that a significant portion of cases were classified as high nuclear grade.
  • Results showed that high nuclear grade is linked to worse disease-free and overall survival, suggesting that nuclear grading could be an effective tool for prognosis in MLS.
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Low-grade central osteosarcoma (LGCOS), which arises from the intramedullary cavity of the metaphysis of long bones, occasionally exhibits extraosseous spread. Approximately 10-30% of patients with LGCOS exhibit dedifferentiation, but it is rare to experience a primary tumor with a dedifferentiated component. A 38-year-old female patient presented with right knee pain for two months.

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Background: In gastric solid-type poorly differentiated adenocarcinoma (PDA), the role of microsatellite instability and immune escape mechanism remains unclear. The current study aimed to elucidate the clinical significance of mismatch repair (MMR) status, genome profile, C-X-C motif chemokine receptor 2 (CXCR2) expression, and myeloid-derived suppressor cell (MDSC) infiltration in solid-type PDA.

Methods: In total, 102 primary solid-type PDA cases were retrieved, and classified into 46 deficient-MMR (dMMR) and 56 proficient-MMR (pMMR) cases based on immunohistochemistry (IHC) and polymerase chain reaction-based molecular testing results.

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Article Synopsis
  • - Several cases of high-grade pleomorphic sarcomas have been provisionally classified as undifferentiated pleomorphic sarcoma (UPS), while some dedifferentiated liposarcoma (DDLS) cases may also fit into this classification due to certain genetic markers.
  • - A study reviewed 77 high-grade pleomorphic sarcoma cases, identifying 66 as UPS and 11 as DDLS, and conducted analyses to look for amplifications of the genes DDIT3 and MDM2 in these tumors.
  • - Findings suggested a potential reclassification of certain sarcomas with DDIT3 amplification, particularly those showing 5'-predominant amplification, which may indicate they should be considered separate from the UPS category due to
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Myxoid pleomorphic liposarcoma (MPLS) is an extremely rare tumor listed in the fifth edition of the WHO classification (2020). Histologically, it mainly comprises a mixture of myxoid and pleomorphic liposarcoma-like components. Genetically, it lacks fusion and amplification.

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A glomus tumor is a benign mesenchymal tumor comprised of cells that resemble the perivascular modified smooth muscle cells of the glomus body. Glomus tumors typically appear in the superficial lesions of the soft tissue in the extremities, such as the subungual region. However, their occurrence in the bone is rare, with only about 30 cases reported to date.

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Prognosis after neoadjuvant chemotherapy (NAC) for osteosarcoma is generally predicted using manual necrosis-rate assessments; however, necrosis rates obtained in these assessments are not reproducible and do not adequately reflect individual cell responses. We aimed to investigate whether viable tumor cell density assessed using a deep-learning model (DLM) reflects the prognosis of osteosarcoma. Seventy-one patients were included in this study.

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  • Scientists looked at a group of 214 patients with liver cancer who had a surgery called liver transplantation.
  • They discovered that a special protein called mTOR was found more often in tumor clusters that had a specific mark (VETC).
  • The study also found that patients with higher mTOR levels had more of another protein, Ang-2, and that their cancer was more likely to come back after surgery.
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  • Blastobotrys mokoenaii is a rare yeast linked to invasive fungal infections, especially in immunocompromised individuals, such as those with acute myeloid leukemia (AML).
  • A case study details a 46-year-old man with AML who developed a B. mokoenaii infection after a second stem cell transplant, leading to his death from multiorgan failure.
  • The yeast was misidentified in routine tests but confirmed through DNA sequencing, highlighting the importance of advanced diagnostic methods in recognizing rare fungal pathogens.
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Purpose: Transferrin receptor (TFR), a membrane protein that has a critical role in the transport of iron into cells, is known to be a ferroptosis-related marker. Although TFR is reported to be abundantly expressed in tumor cells, its relationship with ferroptosis inducers in hepatocellular carcinoma (HCC) remains unclear.

Methods: The authors performed immunohistochemical staining of TFR and divided 350 HCC patients into two groups according to its expression.

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Synovial sarcoma (SS) is a malignant soft tissue tumor that usually arises in the para-articular regions of the extremities. Only nine cases of SS in the mandible have been reported to date. The present study described a case of SS arising from the left mandible.

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