Takuo Hayashi

ORCID: 0000-0002-8544-9370 · 8 papers in corpus
other 2026
International journal of women's dermatology ·doi:10.1097/jw9.0000000000000295
other 2025
International journal of molecular sciences ·doi:10.3390/ijms26167676

High-grade sarcomas often lack typical morphological features and exhibit no clear differentiation, often leading to a diagnosis of undifferentiated sarcoma (US). Pleomorphic leiomyosarcoma (PLMS) is a high-grade sarcoma consisting of a typ…

review 2022
Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia ·doi:10.5761/atcs.cr.21-00005

We report a 33-year-old man who presented with recurrent right pneumothorax. Computed tomography (CT) showed the presence of a large bulla with a maximum diameter of 8 cm in the right middle lobe; he subsequently underwent bullectomy. Histo…

observational 2019
Nature communications ·doi:10.1038/s41467-019-13708-y

Uterine adenomyosis is a benign disorder that often co-occurs with endometriosis and/or leiomyoma, and impairs quality of life. The genomic features of adenomyosis are unknown. Here we apply next-generation sequencing to adenomyosis (70 ind…

case-report 2017
Respiratory medicine case reports ·doi:10.1016/j.rmcr.2017.06.011

Perivascular epithelioid cell tumors (PEComas) are mesenchymal neoplasms with immunoreactivity for both melanocytic and smooth muscle markers. PEComas occur at multiple sites, and malignant PEComas can undergo metastasis, recurrence and agg…

case-report 2017
Internal medicine (Tokyo, Japan) ·doi:10.2169/internalmedicine.56.7769

This report describes two patients with sporadic lymphangioleiomyomatosis complicated by protein-losing enteropathy (PLE). Imaging studies indicated retroperitoneal lymphangioleiomyomas and abnormalities of the adjacent digestive tract. End…

case-report 2012
Human pathology ·doi:10.1016/j.humpath.2012.03.020

A 41-year-old woman carrying a germline tuberous sclerosis complex 2 (TSC2) mutation, whose regular medical follow-up for tuberous sclerosis complex and tuberous sclerosis complex-associated lymphangioleiomyomatosis had continued for 2 year…

1999
·doi:10.1007/s101470050075