Intagliata Eva, Vecchio Rosario, Vizzini Clarissa, Villari Loredana, Cacciola Rossella Rosaria, Cacciola Emma, Vecchio Veronica
Department of General Surgery and Medical Surgical Specialties, University of Catania, Policlinico "G. Rodolico-San Marco", Via S. Sofia 78, 95123 Catania, Italy.
Pathological Anatomy Unit, University of Catania, Italy Policlinico "G. Rodolico-San Marco", Via S. Sofia 78, 95123 Catania, Italy.
J Surg Case Rep. 2024 Feb 16;2024(2):rjae073. doi: 10.1093/jscr/rjae073. eCollection 2024 Feb.
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.
卡斯特尔曼病是一种罕见的良性疾病,其特征为淋巴结肿大和血管滤泡性淋巴组织增生。我们报告一例57岁男性患者,因腹部隐痛伴后背放射痛行影像学检查时偶然发现最大直径约4厘米的腹膜后结节状肿块而入住我院外科。该患者接受了腹腔镜下肿块切除术,术中及术后均未出现并发症。病理诊断证实为卡斯特尔曼病的透明血管型。文献中仅发现两例报告十二指肠旁单中心卡斯特尔曼病的定位与我们的病例相似。尽管罕见,但在所有淋巴结疾病的鉴别诊断中都必须考虑卡斯特尔曼病,以避免不恰当的治疗。