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Ganglioneuroma in a child with hereditary spherocytosis

机译:小儿遗传性球细胞增多症的神经节神经瘤

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摘要

Hereditary spherocytosis (HS) is the most frequent cause of congenital hemolytic anemia. Extramedullary hematopoiesis (EMH) mimicking a mass may develop in the lymph nodes, kidneys, pleura, mediastinum, adrenal gland, and in particular the spleen and liver. Other than EMH, B-cell lymphoma, acute lymphoblastic leukemia, and pancreatic schwannoma cases were reported in patients with HS. We present a 13-year-old female patient with HS and ganglioneuroma in the adrenal gland. This association is probably coincidental; however, with increasing cancer cases in HS and the genetic studies being made, this association will be clarified.
机译:遗传性球囊细胞增多症(HS)是先天性溶血性贫血的最常见原因。模仿肿块的髓外造血(EMH)可能在淋巴结,肾脏,胸膜,纵隔,肾上腺,特别是脾脏和肝脏中发展。除EMH外,HS患者还报告了B细胞淋巴瘤,急性淋巴细胞白血病和胰腺神经鞘瘤病例。我们介绍了一名13岁的女性肾上腺HS和神经节神经瘤的女性患者。这种联系可能是偶然的。然而,随着HS中癌症病例的增加以及进行遗传学研究,这种关联将得到澄清。

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