Unicentric Castleman disease masquerading as a gluteal mass: A diagnostic challenge

Q4 Medicine
Sana Ahuja , Adil Aziz Khan , Saifullah Khalid , Sufian Zaheer
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引用次数: 0

Abstract

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.
伪装成臀部肿块的单中心 Castleman 病:诊断难题
卡斯特曼病是一种罕见的淋巴细胞增生性疾病,以非肿瘤性淋巴结肿大为特征,通常表现为结节受累,而结节外表现并不常见。我们报告了一例独特的单中心卡斯特曼病病例,患者为一名 27 岁女性,病变部位位于臀部。起初被误认为是神经源性或血管性肿瘤,细针穿刺细胞学检查(FNAC)发现了多形性淋巴细胞群,其中有大量横行毛细血管,提示为反应性增生,可能是卡斯特曼病,后经组织病理学证实。该病例凸显了罕见的卡斯特曼病结外表现所带来的诊断挑战,并强调了跨学科合作在准确诊断和管理中的重要性。
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来源期刊
Revista Espanola de Patologia
Revista Espanola de Patologia Medicine-Pathology and Forensic Medicine
CiteScore
0.90
自引率
0.00%
发文量
53
审稿时长
34 days
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