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Profil bibliographique

R. Yoshiyuki Osamura

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

428Publications signalées
9776Citations signalées
4Affiliations récentes

Les institutions déclarées

Les domaines associés

Pituitary Gland Disorders and TreatmentsGrowth Hormone and Insulin-like Growth FactorsNeuroendocrine Tumor Research AdvancesNeuroblastoma Research and TreatmentsHER2/EGFR in Cancer Research

Les publications récentes

Accès ouvert 2026 article OpenAlex

Combination therapy of pasireotide and pegvisomant for aggressive acromegaly with an immature PIT1-lineage PitNET

Keiko Tomiyama, Izumi Fukuda, Shigeyuki Tahara, Chie Inomoto et autres

Summary: A 29-year-old male presented with central scotoma and was suspected of having acromegaly based on enlargement of facial features and extremities. Serum growth hormone (GH) and insulin-like growth factor 1 (IGF-1) levels were elevated to 10.14 ng/mL and 571 ng/mL (74.8 …

jp (code pays fourni par la source)

1 citation Endocrinology Diabetes and Metabolism Case Reports
Accès ouvert 2026 article OpenAlex

What do you mean by PitNETs in WHO Classification 2022?

R. Yoshiyuki Osamura, Chie Inomoto, Shigeyuki Tahara, Kenichi Oyama et autres

This review is aimed at clarifying the background and the meaning of new terminology "pituitary neuroendocrine tumours" (PitNETs) in WHO Classification 2022. The PitNETs share the unique structures of secretory granules (SG) with other neuroendocrine tumors, the good example of which is …

jp (code pays fourni par la source)

0 citations Endocrine Journal
Accès ouvert 2025 article OpenAlex

Coexistence Tumor of Craniopharyngioma and Pituitary Neuroendocrine Tumor: A Case Report and Literature Review

Yohei Nounaka, Fumihiro Matano, K Isayama, K. Tomiyama et autres

Acromegaly most commonly results from excess growth hormone (GH) produced by pituitary neuroendocrine tumors (PitNETs). Craniopharyngioma (CP) is an uncommon suprasellar tumor characterized by cystic change and calcification. The true coexistence of PitNET and CP is rare and poses diagnostic and operative …

jp (code pays fourni par la source)

0 citations Cureus
2025 preprint OpenAlex

Clinical-grade autonomous cytopathology via whole-slide edge tomography

Nao Nitta, Yuko Sugiyama, Takeaki Sugimura, Takahiko Ito et autres

ABSTRACT Cytopathology plays a central role in the early detection of cancers such as cervical, lung, and bladder cancer due to its speed, simplicity, and minimally invasive nature. However, its effectiveness is limited by variability in diagnostic accuracy stemming from subjective visual …

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0 citations medRxiv
Accès ouvert 2024 article OpenAlex

Insulinoma with suspected mutant somatostatin receptor expression according to histological examination

S. Onish, Aki Takada‐Watanabe, R. Yoshiyuki Osamura, Takayuki Shiomi et autres

Key Clinical Message This case highlights the possibility of an insulinoma expressing an aberrant form of SSTRs resulting in a discrepancy between the preoperative octreotide assessment and postoperative SSTR expression. Abstract Insulinoma is a pancreatic disease that causes hyperinsulinemic hypoglycemia. The first‐line …

jp (code pays fourni par la source)

0 citations Clinical Case Reports
Accès ouvert 2024 article OpenAlex

Global Study on the Accuracy of Human Epidermal Growth Factor Receptor 2-Low Diagnosis in Breast Cancer

Josef Rüschoff, Alexander Penner, Ian O. Ellis, M. Elizabeth Hammond et autres

CONTEXT.—: Recently, a new type of antibody-drug conjugate, trastuzumab-deruxtecan (T-DXd), has been approved for the treatment of metastatic breast cancer with low level of human epidermal growth factor receptor 2 (HER2) gene expression. Thereby, eligibility relies on an accurate diagnosis of HER2-low …

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30 citations Archives of Pathology & Laboratory Medicine
Accès ouvert 2023 article OpenAlex

Lung adenocarcinoma metastasis within a pituitary neuroendocrine tumor: a case report with review of literature

Koji Suzuki, Shigeyuki Tahara, Yujiro Hattori, Shinichiro Teramoto et autres

Collision tumors involving the metastasis of malignant neoplasms to pituitary neuroendocrine tumors (PitNETs) are extremely rare. We herein report a case involving a patient with lung adenocarcinoma metastasis within a PitNET who exhibited relatively rapid progression of neurological symptoms. A 75-year-old man …

jp (code pays fourni par la source)

5 citations Endocrine Journal
Accès ouvert 2023 article OpenAlex

Immunohistochemical Analyses of Mammalian Target of Rapamycin (mTOR) Expression in Pituitary Neuroendocrine Tumors (PitNETs): mTOR as a Therapeutic Target for Functional PitNETs

Ichiro Nakazato, Takayuki Shiomi, Kenichi Oyama, Akira Matsuno et autres

Current therapeutic modalities for pituitary neuroendocrine tumors (PitNETs) include medication, surgery, and radiotherapy. Some patients have tumors that are refractory to current modalities. Therefore, novel treatment options are needed for patients with intractable diseases. Consequently, we examined the pathological data of PitNETs …

jp (code pays fourni par la source)

0 citations ACTA HISTOCHEMICA ET CYTOCHEMICA
Accès ouvert 2023 article OpenAlex

Analysis of Insulinoma-Associated Protein 1 Expression in Pituitary Neuroendocrine Tumors

Yu Hirokawa, Chie Inomoto, Kenichi Oyama, Shigeyuki Tahara et autres

Insulinoma-associated protein 1 (INSM1) is a representative diagnostic marker of neuroendocrine neoplasms (NENs); however, it has not yet been used to diagnose pituitary neuroendocrine tumors (PitNETs), according to the 2022 World Health Organization (WHO) classification of pituitary tumors. This study aimed to …

jp, us (code pays fourni par la source)

2 citations ACTA HISTOCHEMICA ET CYTOCHEMICA
Accès ouvert 2023 conference-abstract OpenAlex

ED-1 PITUITARY TUMORS IN 5TH WHO CLASSIFICATION 2022: WHAT DO YOU MEAN BY PITNET?

R. Yoshiyuki Osamura

Abstract It has been well known that the terminology has been changed from pituitary adenoma(4th WHO) which means benign epithelial tumors to pituitary neuroendocrine tumor(5th WHO 2022). It is apparent that the anterior pituitary cells and derived tumors contain intracytoplasmic neurosecretory granules …

jp (code pays fourni par la source)

0 citations Neuro-Oncology Advances
Accès ouvert 2023 article OpenAlex

Concurrent IgG4-related hypophysitis and clinically nonfunctioning gonadotroph pituitary neuroendocrine tumor

Shigeyuki Tahara, R. Yoshiyuki Osamura, Yujiro Hattori, Eitaro Ishisaka et autres

BACKGROUND: Some patients develop immunoglobulin G4 (IgG4)-related hypophysitis associated with systemic diseases. More than 30 cases of IgG4-related hypophysitis have been reported. However, biopsy has rarely been performed in these patients, and none have had an associated pituitary neuroendocrine tumor (PitNET). We …

jp (code pays fourni par la source)

2 citations BMC Endocrine Disorders

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