Uda Chihiro, Ohta Ryuichi, Senaha Yoko, Sano Chiaki
Family Medicine, Fuchu Hospital, Osaka, JPN.
Community Care, Unnan City Hospital, Unnan, JPN.
Cureus. 2024 Nov 1;16(11):e72844. doi: 10.7759/cureus.72844. eCollection 2024 Nov.
Castleman disease (CD) is a rare lymphoproliferative disorder that can present with nonspecific symptoms, making diagnosis challenging, particularly in elderly patients. This case report describes a 93-year-old woman who presented with intermittent abdominal pain, which was unresponsive to standard treatments and showed no systemic signs of infection or malignancy. Initial imaging revealed scattered lymphadenopathy, raising concern for a lymphoproliferative disorder. A laparoscopic lymph node biopsy was performed, leading to a diagnosis of unicentric CD (UCD). The patient was treated with corticosteroids, which resulted in a marked improvement in her symptoms, including the complete resolution of her abdominal pain. This case emphasizes the importance of considering CD in the differential diagnosis of unexplained abdominal pain in elderly patients, as early diagnosis and treatment can prevent complications and significantly improve outcomes. The successful use of corticosteroids in this patient highlights a nonsurgical treatment option for UCD in cases where surgical excision is not feasible.
卡斯特曼病(CD)是一种罕见的淋巴增生性疾病,可表现为非特异性症状,这使得诊断具有挑战性,尤其是在老年患者中。本病例报告描述了一名93岁女性,她出现间歇性腹痛,对标准治疗无反应,且未表现出感染或恶性肿瘤的全身症状。初始影像学检查发现散在淋巴结肿大,这引起了对淋巴增生性疾病的关注。进行了腹腔镜淋巴结活检,结果诊断为单中心卡斯特曼病(UCD)。患者接受了皮质类固醇治疗,其症状得到显著改善,包括腹痛完全缓解。该病例强调了在老年患者不明原因腹痛的鉴别诊断中考虑卡斯特曼病的重要性,因为早期诊断和治疗可以预防并发症并显著改善预后。在该患者中成功使用皮质类固醇突出了在手术切除不可行的情况下UCD的一种非手术治疗选择。