卡斯尔曼氏病是儿童背痛的罕见病因

Awadelkarim Moahmed, A. Dsouza, A. Qazi, A. Alduaiji, M. Ba'ath
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引用次数: 0

摘要

理由:Castleman病(CD)是一种不常见的淋巴增生性疾病,其特征是存在外来的淋巴组织大量生长。它分为两种类型:单中心(局部)和多中心(系统)亚型。切除术是治疗局部疾病的理想选择。病人关心:病人有慢性背痛,影响了他的日常活动。诊断:在为背痛进行的腰椎磁共振成像中偶然发现了CD的诊断,并显示腹膜后腔静脉旁淋巴结病,随后切除,组织病理学证实了CD。结果:手术切除使他的背痛完全缓解。经验教训:CD有不特定的临床表现,背痛在我们的病例中是不寻常的表现。此外,我们的患者患有努南综合征,提示可能与CD有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Castleman's disease as an unusual cause of back pain in childhood
Rationale: Castleman's disease (CD) is an uncommon lymphoproliferative disorder that is distinguished by the presence of exotic heavy growth of lymphoid tissue. It is divided into two types: unicentric (localised) and multicentric (systemic) subtypes. Excision is the ideal therapeutic option for localised disease. Patient concern: Patient had a chronic back pain which affecting his daily activity. Diagnosis: The diagnosis of CD was incidentally detected on a magnetic resonance imaging of the lumbar spine performed for back pain and revealed retroperitoneal paracaval lymphadenopathy, which was then excised, and the histopathology confirmed CD. Outcome: Surgical excision resulted in complete resolution of his back pain. Lessons: CD has unspecific clinical presentation and back pain is unusual presentation in our case. In addition, our patient had Noonan's syndrome suggesting a possible association with CD.
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