Publications by authors named "T Kamimaki"

Objectives: : To investigate the utility of shear wave elastography values (SWE) in differentiating IgG4-related submandibular sialadenitis (IgG4-RSS) from healthy individuals and in monitoring the response to glucocorticoid treatment.

Methods: : Patients with IgG4-RSS who underwent ultrasound between 2017 and 2023 were included. Gland size, border, internal echo pattern, vascularity, and SWE were measured.

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The incidence of non-obese non-alcoholic fatty liver disease (NAFLD), characterized by the presence of a fatty liver in individuals with a normal body mass index, is on the rise globally. Effective management strategies, including lifestyle interventions such as diet and exercise therapy, are urgently needed to address this growing public health concern. The aim of this study was to investigate the association between non-obese NAFLD, dietary habits, and physical activity levels.

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Juvenile xanthogranuloma (JXG) is a type of non-Langerhans cell histiocytosis that rarely involves other than the skin. Here, we present detailed ultrasound (US) findings, including a contrast study, of a rare JXD renal lesion. A 42-year-old woman with JXG had chronic kidney disease.

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A 26-year-old man presented with congenital left thumb macrodactyly. MRI showed diffuse enlargement of the left median nerve from the wrist to the digits, with particularly severe swelling of the thumb; US revealed the median nerve swelling comprised enlarged hypoechoic nerve bundles and increased hyperechoic areas around the nerve bundles. These typical cable-like and spaghetti-like appearances led to the diagnosis of fibrolipomatous hamartoma (FLH).

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Article Synopsis
  • Haploinsufficiency of the SHOX gene is a significant genetic cause of nonsyndromic short stature, with eight potential enhancer regions identified near its exons.
  • A study reported a deletion in a boy that was over 60kb downstream from these known enhancers, correlating with his moderate short stature and nonspecific skeletal changes; his father's height was normal but lower than expected.
  • The deletion overlaps with previously identified copy-number variations (CNVs) in other short stature patients, suggesting that this far-downstream area functions as a novel enhancer, contributing to varied short stature phenotypes and indicating genomic instability around the SHOX region.
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