




Anastomosing hemangioma is histologically characterized by anastomosing, sinusoidal-like vascular channels lined by endothelial cells, distinguishing it from conventional cavernous hemangiomas which contain larger dilated vascular spaces.
The progressive centripetal fill-in enhancement pattern observed on multiphasic imaging resembles that of a typical hepatic hemangioma and is a key distinguishing feature that should raise suspicion for AH.
AH has an indolent clinical course and favorable prognosis, with reported lesions showing slow growth or stability during imaging surveillance over several years, with no documented local recurrences or metastases.
Imaging alone may not reliably distinguish AH from aggressive neoplasms, particularly when the lesion is large, heterogeneous, or in an unusual location, making tissue diagnosis important for definitive diagnosis.
When imaging features are sufficiently reassuring and the diagnosis is supported by clinical context or pathology, observation may be appropriate; surgical resection is often performed when malignancy cannot be excluded or when diagnostic uncertainty warrants tissue diagnosis.
AH is a recently recognized entity in the 2020 WHO classification and most commonly arises in the genitourinary tract, with additional reported cases in liver, gastrointestinal tract, retroperitoneum, and soft tissues.
Describe a slowly growing, well-circumscribed hypervascular renal or retroperitoneal mass with peripheral nodular enhancement and progressive centripetal fill-in on multiphasic imaging as consistent with anastomosing hemangioma, emphasizing the benign enhancement pattern that resembles hepatic hemangioma and distinguishes it from aggressive malignancies.