Peters’ anomaly is a rare congenital eye condition characterized by anterior segment dysgenesis
and commonly presents as unilateral or bilateral corneal opacity in the early neonatal …

Phakomatoses, or neurocutaneous syndromes, are a heterogeneous group of rare genetic
disorders that predominantly affect structures arising from the embryonic ectoderm, namely …

Primary intracranial sarcoma, DICER1-mutant, is a rare, recently described entity in the fifth
edition of the WHO Classification of CNS Tumors. Given the entity’s rarity and recent …

Background and purpose Visualization of annular fissures on MRI is becoming increasingly
important but remains challenging. Our purpose was to test whether an image processing …

Langerhans Cell Histiocytosis (LCH) is a rare disorder characterized by neoplastic proliferation
of Langerhans-type dendritic cells. LCH is most frequently encountered in the pediatric …

Discussion Surgery and more recently laparoscopic surgery have been used to manage
adrenal metastases. Specifically for RCC, consolidative metastasectomy has been shown to be …

Recently, a distinct clinicoradiologic entity involving cerebellar, hippocampal, and basal
nuclei transient edema with restricted diffusion (CHANTER) on MR imaging was identified. …

Background and purpose Parathyroid carcinoma is the rarest endocrine neoplasm with very
few published data discussing its imaging appearance with primary focus on ultrasound …

With recent advancements in cancer therapy, especially immunotherapy, overall survival of
many cancers has increased and patient toxicity has been reduced. However, many …

Background and Purpose Intracranial hemorrhage (ICH) is a common finding in patients
presenting to the emergency department with acute neurological symptoms. Noncontrast head …