Digital Clubbing and Hodgkin Disease in Children: A Case Report and Review of Literature

IF 0.3 Q4 PEDIATRICS Journal of Pediatrics Review Pub Date : 2021-07-01 DOI:10.32598/JPR.9.3.786.1
H. Karami, Amir Mohammad Beyzaee, F. Masiha, M. Ghasemi, A. Nosrati, S. Mousavi, Mohammad Naderisorki, S. Behzadnia
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引用次数: 0

Abstract

Introduction: Digital clubbing (hypertrophic osteoarthropathy) as the initial presentation of lymphoma is rarely reported, particularly in children. In this study, we report a patient with intrathoracic Hodgkin Disease (HD) and digital clubbing as the first presentation, and we will review the literature regarding the same condition. Case Presentation: A 10-year-old boy presented with a 2-month history of cough, mild dyspnea, and night sweats, with prominent digital clubbing. A chest x-ray and a computed tomography scan of the chest showed multiple mediastinal masses. A mediastinal lymph node biopsy was done. Pathologic examination was indicative of nodular sclerosis HD. Conclusions: In patients with digital clubbing, intrathoracic malignancies should be considered a differential diagnosis and must be ruled out by precise examination and paraclinical help.
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儿童指突和霍奇金病病例报告及文献复习
引言:指棒病(肥大性骨关节病)作为淋巴瘤的最初表现很少报道,尤其是在儿童中。在这项研究中,我们报告了一名以胸内霍奇金病(HD)和指棒炎为首发症状的患者,我们将回顾有关相同情况的文献。病例介绍:一名10岁男孩有2个月的咳嗽、轻度呼吸困难和盗汗病史,并伴有明显的指节。胸部x光片和胸部计算机断层扫描显示多个纵隔肿块。纵隔淋巴结活检。病理检查提示结节性硬化HD。结论:对于指棒炎患者,胸腔内恶性肿瘤应被视为鉴别诊断,必须通过精确的检查和临床辅助来排除。
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20
审稿时长
8 weeks
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