Department of Pathology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.
Department of Radiodiagnosis, Jawaharlal Nehru Medical College & Hospital, Aligarh Muslim University, Aligarh, India.
Rev Esp Patol. 2024 Oct-Dec;57(4):300-304. doi: 10.1016/j.patol.2024.06.001. Epub 2024 Jul 23.
Castleman disease, a rare lymphoproliferative disorder characterized by non-neoplastic lymph node enlargement, typically presents as nodal involvement, while extranodal manifestations are uncommon. We present a unique case of unicentric Castleman disease localized to the gluteal region in a 27-year-old female. Initially mistaken for a neurogenic or vascular tumour, fine needle aspiration cytology (FNAC) revealed a polymorphous population of lymphoid cells with numerous traversing capillaries suggestive of reactive hyperplasia, possibly Castleman disease, which was later confirmed by histopathology. This case highlights the diagnostic challenges posed by rare extranodal presentations of Castleman disease and underscores the importance of interdisciplinary collaboration in accurate diagnosis and management.
血管滤泡性淋巴结增生症,一种罕见的淋巴组织增生性疾病,其特征为非肿瘤性淋巴结肿大,通常表现为淋巴结受累,而结外表现则较为罕见。我们报告了一例独特的血管滤泡性淋巴结增生症病例,该患者为 27 岁女性,病变局限于臀部。最初误诊为神经源性或血管性肿瘤,细针穿刺细胞学检查(FNAC)显示多形性淋巴细胞群,伴有许多贯穿的毛细血管,提示反应性增生,可能为血管滤泡性淋巴结增生症,随后通过组织病理学证实。本病例强调了罕见的结外血管滤泡性淋巴结增生症表现所带来的诊断挑战,并突出了跨学科合作在准确诊断和管理中的重要性。