Year: 2025
Type: article
Study design: Case Report
Abstract: Castleman disease (CD) is a rare lymphoproliferative disorder of uncertain etiology, most commonly affecting the chest and neck, with retroperitoneal involvement being exceptionally rare. It can present as either unicentric or multicentric disease, with the unicentric form typically affecting younger individuals. Due to its rarity and overlapping features with conditions like non-Hodgkin lymphoma and paraganglioma. CD is often misdiagnosed, making immunohistochemical analysis crucial for accurate diagnosis. We report a rare case of retroperitoneal CD in a 23-year-old female referred to our hospital after a CT scan revealed a retroperitoneal tumor anterior to the lower pole of her left kidney at the L3-L4 vertebral level. An initial core biopsy suggested paraganglioma; however, following laparoscopic tumorectomy, histopathological analysis confirmed Castleman disease of the hyaline vascular and plasma cell type.
Source: Journal of Surgical Case Reports
DOI: 10.1093/jscr/rjaf086
Authors: Ajit Khadga, Mahesh Bahadur Adhikari, Bipin Maharjan, Ravi Kiran Gautam, Prashant Mishra, Birodh Basnet, Deepak Kumar Yadav, Shoshan Acharya
Institution: Nepal Mediciti Hospital
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $1,000
OpenAlex ID: W4407913766
