Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Download full-text PDF

Source

Publication Analysis

Top Keywords

radiology case
4
case month
4
month developmental
4
developmental delay
4
delay agenesis
4
agenesis corpus
4
corpus callosum
4
radiology
1
month
1
developmental
1

Similar Publications

Coronary periarteritis in IgG4-RD: A case series.

Clin Rheumatol

September 2025

Division of Rheumatology, Department of Internal Medicine, Mayo Clinic, 200 First St SW, Rochester, MN, 55906, USA.

Objectives: IgG4-related disease (IgG4-RD) can affect multiple organ systems, with coronary artery involvement being rare. Coronary periarteritis may lead to complications such as myocardial infarction and ischemic cardiomyopathy. This case series characterizes the clinical and radiological features, complications, and treatment strategies in patients with IgG4-RD-associated coronary periarteritis.

View Article and Find Full Text PDF

Reverse slipped capital femoral epiphysis.

BMJ Case Rep

September 2025

Radiology, Children's Health Ireland at Temple Street, Dublin, Leinster, Ireland.

Slipped capital femoral epiphysis (SCFE) is a rare occurrence in the paediatric hip. Diagnosis is challenging. It may have an insidious onset.

View Article and Find Full Text PDF

Background: Despite the high prevalence of violence among transgender and gender-diverse individuals, injury disparities remain understudied and are often attributed to underreporting. To address this limitation, we analysed radiology reports to objectively compare the prevalence and patterns of injuries between transgender women and cisgender women.

Methods: We used the Research Patient Data Registry at a level 1 trauma centre in the USA to identify 263 transgender women and 525 age-matched, race-matched and ethnicity-matched cisgender women.

View Article and Find Full Text PDF

Background: Pheochromocytomas and paragangliomas (PPGLs) are rare catecholamine-secreting neuroendocrine tumors originating from the embryonic neural crest. Approximately 30% of PPGLs are hereditary and are frequently associated with genetic syndromes, including neurofibromatosis type 1 (NF1). Composite PPGLs, which include components of both PPGLs and related tumors such as ganglioneuromas, are extremely rare in NF1 patients.

View Article and Find Full Text PDF