Publications by authors named "Yanagida E"

Article Synopsis
  • Peripheral T-cell lymphoma not otherwise specified (PTCL-NOS) can be divided into two main subtypes: PTCL-TBX21 and PTCL-GATA3, each exhibiting different characteristics.
  • In a study involving 100 Japanese patients, PTCL-TBX21 showed better treatment response and lower CD4 positivity compared to PTCL-GATA3, which also had worse overall survival rates.
  • The findings suggest that classifying PTCL-NOS based on these subtypes can help predict patient outcomes and tailor immune therapy.
View Article and Find Full Text PDF

NK-lymphoblastic leukemia/lymphoma (NK-LL) is an extremely rare hematopoietic tumor consisting of natural killer (NK) precursor cells, and their lineage overlaps with T-cells, making it challenging to diagnose. COVID-19 vaccination is recommended for people with a risk of aggravation such as cancer-bearing patients, including hematopoietic tumors. We present a 55-year-old man who had cervical lymph node swelling post vaccination for COVID-19.

View Article and Find Full Text PDF

Background/aim: Conversion surgery (CS) following atezolizumab plus bevacizumab (Atez+Bev) is a treatment strategy for unresectable hepatocellular carcinoma (UR-HCC). Herein, we report a case of CS after transcatheter arterial embolization (TAE) and Atez+Bev for primary HCC with peritoneal metastases and multiple liver metastasis after HCC rupture.

Case Report: A 75-year-old man with a suspected ruptured HCC in segment 4b was referred to the National Hospital Organization Kumamoto Medical Center.

View Article and Find Full Text PDF
Article Synopsis
  • CD37 is a protein linked to tumor survival in B-cell lymphomas, particularly in follicular lymphoma (FL), which originates from germinal center B cells.
  • A study examined 167 FL cases, finding that 60% were CD37-positive, with its expression associated with better overall survival in patients with high FLIPI scores.
  • While CD37 could be a potential therapeutic target due to its role in tumor progression, more research is necessary to fully understand its implications.
View Article and Find Full Text PDF

Follicular lymphoma (FL) is characterized by an indolent clinical course and a high relapse rate, and often exhibits a diffuse pattern beyond the follicular area. Our group previously reported that immune checkpoint (ICP) pathways, such as programmed cell death (PD-1) and programmed death ligand 1 (PD-L1), are poor prognostic factors for diffuse large B-cell lymphoma and adult T-cell leukemia/lymphoma. In this study, the association between the expression of multiple ICP molecules according to immunohistochemistry and clinicopathological features in FL was determined via immunostaining of 173 biopsy samples.

View Article and Find Full Text PDF

Myeloid sarcoma (MS) is defined as a tumour mass consisting of myeloid blasts that occurs at an anatomical site other than bone marrow. MS with megakaryocytic differentiation (MSmgk) is extremely rare and its clinicopathological features have not been well described. We reviewed 11 cases in 11 patients of extramedullary mass-forming malignant tumours composed of immature non-lymphoid haematopoietic cells expressing CD41 with or without concurrent bone marrow lesions.

View Article and Find Full Text PDF

Telomere length is maintained by the activation of telomerase, which causes continuous cell division and proliferation in many carcinomas. A catalytic reverse transcriptase protein (TERT) encoded by the TERT gene plays a critical role in the activation of telomerase. We performed a molecular and pathological analysis of the TERT against three different peripheral T-cell lymphoma (PTCL) subtypes: PTCL, not otherwise specified (PTCL-NOS), angioimmunoblastic T-cell lymphoma (AITL), and adult T-cell leukemia/lymphoma (ATLL).

View Article and Find Full Text PDF

This paper is concerned with a nonlinear optimization problem that naturally arises in population biology. We consider the population of a single species with logistic growth residing in a patchy environment and study the effects of dispersal and spatial heterogeneity of patches on the total population at equilibrium. Our objective is to maximize the total population by redistributing the resources among the patches under the constraint that the total amount of resources is limited.

View Article and Find Full Text PDF
Article Synopsis
  • Adult T-cell leukemia/lymphoma (ATLL) is linked to the human T-cell leukemia virus type 1 (HTLV-1), with key roles played by the HBZ and tax mRNA in its development.
  • A study analyzed 88 ATLL tissue samples and found that high HBZ and tax expression levels were associated with specific clinicopathological features, including increased skin lesions and tumor-infiltrating lymphocytes.
  • Patients with very high tax expression had lower HLA class I and β2M levels and significantly poorer overall survival rates, suggesting that treatment for ATLL should be approached cautiously in high tax expression cases.
View Article and Find Full Text PDF

Introduction: Adult T-cell leukemia/lymphoma (ATLL) is a malignant peripheral T-cell neoplasm associated with human T-cell leukemia virus type-1 (HTLV-1). The acute and lymphoma subtypes are regarded as aggressive ATLLs, and the overall survival (OS) of patients remains poor. Transforming acidic coiled-coil-containing protein 3 (TACC3) regulates microtubules, which are associated with cancer-related proteins overexpressed in various cancers.

View Article and Find Full Text PDF
Article Synopsis
  • Follicular T-cell lymphoma (FTCL) likely originates from follicular helper T-cells and is associated with RHOA G17V mutations, similar to other T-cell lymphomas like angioimmunoblastic T-cell lymphoma (AITL).
  • In a study of 16 FTCL cases, 9 showed RHOA mutations, with variations linked to different clinicopathological features, indicating a tendency for B-immunoblasts and AITL characteristics in mutation-positive cases.
  • While RHOA mutations may influence certain features of FTCL, there was no significant difference in overall survival between mutation-positive and mutation-negative groups, suggesting a need for further research on their role in the disease.
View Article and Find Full Text PDF

The interaction of CD47 and signal-regulatory protein alpha (SIRPα) induces "don't eat me signal", leading suppression of phagocytosis. This signal can affect the clinical course of malignant disease. Although CD47 and SIRPα expression are associated with clinicopathological features in several neoplasms, the investigation for adult T-cell leukemia/lymphoma (ATLL) has not been well-documented.

View Article and Find Full Text PDF

A pathological evaluation is one of the most important methods for the diagnosis of malignant lymphoma. A standardized diagnosis is occasionally difficult to achieve even by experienced hematopathologists. Therefore, established procedures including a computer-aided diagnosis are desired.

View Article and Find Full Text PDF

The interaction between CD47 and signal-regulatory protein-α (SIRPα) inhibits phagocytosis, thus affecting the clinical outcomes of neoplastic diseases. Although CD47 upregulation is associated with poor prognosis in several malignancies, the effect of SIRPα expression and its coexpression with CD47 remains unclear. This study aimed to investigate the clinicopathologic effect of CD47 and SIRPα expression in diffuse large B-cell lymphoma (DLBCL).

View Article and Find Full Text PDF

Acute or lymphomatous type adult T cell leukemia/lymphoma (ATLL) is an aggressive hematopoietic malignancy with poor prognosis. We previously reported that programmed cell death ligand 1 (PD-L1) expression could predict ATLL outcomes. However, the roles of other immune checkpoint molecules remain largely unknown in ATLL.

View Article and Find Full Text PDF

Primary splenic low-grade B-cell lymphoma of the red pulp comprises hairy cell leukemia (HCL) and splenic B-cell lymphoma/leukemia, unclassifiable (SPLL-U). SPLL-U is a rare disease that includes subtypes of a hairy cell leukemia-variant (HCL-v), splenic diffuse red pulp small B-cell lymphoma (SDRPL) and other types that are known as narrow sense SPLL-U (SPLL-U-NS). Notably, limited information is available regarding the BRAF mutation (V600E) and cyclin D3 expression in subtypes of SPLL-U.

View Article and Find Full Text PDF
Article Synopsis
  • - The study investigates in situ follicular neoplasm (ISFN), a rare condition previously seen as a precursor to follicular lymphoma, focusing on its features in Japan based on 19 biopsy samples.
  • - Two types of ISFN were identified: one with strong BCL-2 positivity and translocation, and another resembling follicular lymphoma without obvious translocation.
  • - Analysis revealed a significant occurrence of ISFN alongside other lymphomas, but molecular findings indicated that ISFN and follicular lymphoma lesions in the same lymph node exhibit different clonality.
View Article and Find Full Text PDF

Attenuated human leukocyte antigen (HLA) class I expression is implicated as a major immune escape mechanism in several types of tumor. We previously reported that HLA class I/β2 microglobulin and programmed death ligand-1 expression are prognostic factors in adult T-cell leukemia/lymphoma. A recent report suggested that HLA class II expression is also an important prognostic factor for the clinical outcome of programmed death-1 blockade therapy in recurrent/refractory Hodgkin lymphoma.

View Article and Find Full Text PDF

This study provides an overview of the epidemiology and secular trends of malignant lymphoma in Japan. Using data from clinics and hospitals throughout Japan, we analyzed 9426 cases of malignant lymphoma diagnosed in 2007-2014. We show that the proportion of follicular lymphoma and methotrexate-associated lymphoproliferative disorder increased during this time, as did the onset age for follicular lymphoma and diffuse large B-cell lymphoma.

View Article and Find Full Text PDF

Peripheral T-cell lymphoma, not otherwise specified (PTCL-NOS) is cytologically and phenotypically heterogeneous. Retinoic acid-related orphan receptor-γt (RORγt) is a transcription factor that regulates the differentiation of naïve CD4 helper T cells to Th17 cells. In the present study, we immunohistochemically confirmed the expression of RORγt in PTCL-NOS.

View Article and Find Full Text PDF

Pulmonary pleomorphic carcinoma (PPC) is a very rare type of primary lung cancer with an aggressive clinical course. Few reports have documented therapeutic options for PPC with EGFR mutations. Herein, we report a case of PPC with EGFR mutation treated with EGFR-tyrosine kinase inhibitors (TKIs).

View Article and Find Full Text PDF

Rates of childhood sexual abuse are unacceptably high, with potentially long-lasting consequences for those who have been victimized. Currently, there are a number of sexual violence prevention programs that have been developed to lower rates of victimization, increase awareness, and connect victims with resources. Within this area of research, there has been less focus on effective methods of program dissemination.

View Article and Find Full Text PDF

Histiocytic and dendritic cell neoplasms are rare and poorly studied. We report the clinical characteristics and prognostic factors in such cases in Japan. We investigated the clinical characteristics and survival in adult patients with histiocytic and dendritic cell neoplasms.

View Article and Find Full Text PDF

Extranodal NK/T-cell lymphoma, nasal type (ENKTL) is a subtype of non-Hodgkin lymphoma with a poor prognosis. Although first-line treatments for patients with localized ENKTL have been established, there is no gold standard treatment for patients with advanced ENKTL and refractory and/or relapsed disease. Anti-CD30 antibody-based therapy, including brentuximab vedotin (BV), has been shown to target malignant lymphomas with CD30 expression.

View Article and Find Full Text PDF