Gopi Praveen, Potty Vasudevan Sambu, Kaurav Rustam Singh, Govindan Krishna
Department of Urology, Government Medical College, Thiruvananthapuram, Kerala, India.
Department of Pathology, Government Medical College, Thiruvananthapuram, Kerala, India.
Int J Appl Basic Med Res. 2018 Oct-Dec;8(4):259-262. doi: 10.4103/ijabmr.IJABMR_256_17.
Castleman's disease (CD) is a rare disorder characterized by proliferation of the lymphoid tissue. Clinically, it presents in two forms either a unicentric (UC) or multicentric. Mediastinum is the most common location. UC retroperitoneal presentation is rare. We report a case of 29-year-old female who presented with left loin pain, and on abdominal imaging, evaluation identified a retroperitoneal mass in the left hypochondrium in the pararenal space. Mass was surgically excised entirely. Histopathological examination demonstrated hyaline vascular type of CD. CD should be considered in differential diagnosis of retroperitoneal mass, especially in equivocal cases. We also reviewed literature of 134 cases of retroperitoneal CD to analyze the presentation, management, and outcome.
卡斯特曼病(CD)是一种以淋巴组织增生为特征的罕见疾病。临床上,它表现为两种形式,即单中心型(UC)或多中心型。纵隔是最常见的发病部位。UC型腹膜后表现罕见。我们报告一例29岁女性,她因左腰部疼痛就诊,腹部影像学检查发现肾旁间隙左季肋部有一个腹膜后肿块。肿块被完整手术切除。组织病理学检查显示为透明血管型CD。在腹膜后肿块的鉴别诊断中应考虑CD,尤其是在不明确的病例中。我们还回顾了134例腹膜后CD的文献,以分析其表现、治疗和预后。