A Rare Case of Castleman's Syndrome Presentıng wıth a Mass ın the Bıfurcatıon of the Celıac Trunk.
Autor: | Arslan A; Department of Radiology, University Of Health Sciences Ümraniye Training and Research Hospital, Selimiye, Tıbbiye Cd No: 38, 34668 Üsküdar/İstanbul, Turkey., Fidancı Ö; Department of Radiology, University Of Health Sciences Ümraniye Training and Research Hospital, Selimiye, Tıbbiye Cd No: 38, 34668 Üsküdar/İstanbul, Turkey., İhvan A; Department of Pathology, University Of Health Sciences Ümraniye Training and Research Hospital, Selimiye, Tıbbiye Cd No: 38, 34668 Üsküdar/İstanbul, Turkey., Yıldırak MK; Department of General Surgery, University Of Health Sciences Ümraniye Training and Research Hospital, Selimiye, Tıbbiye Cd No: 38, 34668 Üsküdar/İstanbul, Turkey., Özkan ÖF; Department of General Surgery, University Of Health Sciences Ümraniye Training and Research Hospital, Selimiye, Tıbbiye Cd No: 38, 34668 Üsküdar/İstanbul, Turkey. |
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Jazyk: | angličtina |
Zdroj: | Current medical imaging [Curr Med Imaging] 2023 Oct 20. Date of Electronic Publication: 2023 Oct 20. |
DOI: | 10.2174/0115734056253347231017073858 |
Abstrakt: | Introduction: Castleman's disease is an extremely rare disease in the abdomen region characterized by benign lymphoepithelial proliferation. Case Presentation: We report a case of a 63-year-old female who presented with abdominal pain. Abdominal CT Angio and dynamic contrast-enhanced abdominal MRI revealed a mass lesion showing markedly contrast enhancement, no vascular invasion sign, and diffusion restriction lesion in the truncus coelicus bifurcation region. The mass was surgically resected completely. Pathological evaluation showed a hyaline-vascular type of Castleman's disease. Conclusion: Castleman's disease should be kept in mind in the differential diagnosis of an isolated intra-abdominal mass. (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.) |
Databáze: | MEDLINE |
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