Retroperitoneal paraduodenal unicentric Castleman disease: case report and review of the literature

Author:

Intagliata Eva1ORCID,Vecchio Rosario1,Vizzini Clarissa1,Villari Loredana2,Cacciola Rossella Rosaria34,Cacciola Emma56,Vecchio Veronica34

Affiliation:

1. Department of General Surgery and Medical Surgical Specialties, University of Catania, Policlinico “G. Rodolico—San Marco” , Via S. Sofia 78, 95123 Catania , Italy

2. Pathological Anatomy Unit, University of Catania, Italy Policlinico “G. Rodolico—San Marco” , Via S. Sofia 78, 95123 Catania , Italy

3. Department of Biomedical Science , Hematologic Unit, , Via S. Sofia 78, 95123 Catania , Italy

4. University of Catania, Policlinico “G. Rodolico—San Marco” , Hematologic Unit, , Via S. Sofia 78, 95123 Catania , Italy

5. Department of Medical Sciences , Surgical Sciences and Advanced Technologies, Hemostasis Unit, , Via S. Sofia 78, 95123 Catania , Italy

6. University of Catania, Italy, Policlinico “G. Rodolico—San Marco” , Surgical Sciences and Advanced Technologies, Hemostasis Unit, , Via S. Sofia 78, 95123 Catania , Italy

Abstract

Abstract Castleman disease is a rare and benign disorder, characterized by enlarged lymph nodes and angiofollicular lymphoid hyperplasia. We report a case of a 57-year-old male, who was admitted to our surgical department because of a retroperitoneal nodular mass measuring about 4 cm in maximum diameter, incidentally discovered on a radiologic exam performed for the onset of vague abdominal pain with posterior irradiation. The patient was subdue to laparoscopic removal of the mass and no intra- and post-operative complications were recorded. Histologic diagnosis of hyaline-vascular variant of the Castleman disease was confirmed. Only two cases have been found in the literature reporting the paraduodenal unicentric Castleman disease localization like our case. Although rare, the Castleman disease must be considered in the differential diagnosis among all the lymph nodes diseases, for avoiding improper therapies.

Publisher

Oxford University Press (OUP)

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