特发性多中心卡斯特曼病。

Vipul Chaudhari, Simran Jatin Thakkar, Namita Padwal, Niteen Karnik
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引用次数: 0

摘要

摘要:一名老年男子因发热和寒战就诊六个月,伴有食欲不振和体重减轻、双侧水肿和无触痛的腹股沟淋巴结病。左侧睾丸肿大、坚实、无触痛。检查结果显示贫血、白细胞减少、红细胞沉降率升高和高丙种球蛋白血症。腹部超声波检查显示,主动脉周围、主动脉前、腹腔前和双侧盆腔区域有多个肿大坏死的淋巴结。腹股沟淋巴结的细针穿刺细胞学(FNAC)检查未发现耐酸杆菌(AFB)。然而,切除活检显示淋巴组织结构被弥漫增生的成熟浆细胞侵蚀,提示为多中心卡斯特曼病的浆细胞变异型。由于怀疑是肿瘤性睾丸肿大,患者接受了双侧睾丸切除术,组织病理学检查显示睾丸有血肿和萎缩,睾丸实质继发受累于浆细胞变异型卡斯特曼病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Idiopathic multicentric Castleman disease.

Abstract: An elderly man presented with fever and chills for six months, associated with loss of appetite and weight loss, bilateral edema, and non-tender inguinal lymphadenopathy. The left-sided testicle was bulky, firm, and non-tender. Investigations revealed anemia, leukopenia, elevated erythrocyte sedimentation rate, and hypergammaglobulinemia. Ultrasound of the abdomen revealed multiple enlarged necrotic lymph nodes in the periaortic, preaortic, precaval, and bilateral pelvic regions. Fine-needle aspiration cytology (FNAC) of the inguinal nodes showed no acid-fast bacilli (AFB). However, excision biopsy revealed lymphoid tissue with effacement of architecture by diffuse proliferation of mature plasma cells, suggestive of the plasma cell variant of multicentric Castleman disease. Due to suspicion of neoplastic testicular enlargement, the patient underwent bilateral orchidectomy, and histopathology showed hematocele with atrophy of the testis and secondary involvement of the testicular parenchyma by plasma cell variant of Castleman disease.

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