更深的诅咒:一名巨结肠患者的评估揭示了先天性中枢性低通气综合征和神经母细胞瘤的罕见关联。

Pub Date : 2022-11-29 eCollection Date: 2022-01-01 DOI:10.1055/s-0042-1758826
Shimon Eric Jacobs, Laura Tiusaba, Elizaveta Bokova, Tamador Al-Shamaileh, Teresa Lynn Russell, Emily C Rutan, Harutyun Haroyan, Yong Wang, Christina Feng, Andrea Badillo, Marc A Levitt
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引用次数: 0

摘要

我们报告一例罕见的2岁男性患者,因便秘的初步评估和最终治疗先天性巨结肠疾病(HSCR),其术前检查偶然发现后路棘旁肿块。肿块活检后,患者表现为低通气和缺氧,需要延迟拔管,引起对先天性中枢性低通气综合征(CCHS)的怀疑。我们关注HSCR和CCHS之间已知的关联历史,以及最近发现的连接HSCR、CCHS和神经母细胞瘤的配对样同源盒2B基因突变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A Deeper Curse: A Hirschsprung Patient's Evaluation Unmasks a Rare Association with Congenital Central Hypoventilation Syndrome and Neuroblastoma.

We present a rare case of a 2-year-old male patient referred for primary evaluation of constipation and ultimately treatment of Hirschsprung disease (HSCR) whose preoperative workup incidentally revealed a posterior paraspinal mass. Following the biopsy of the mass, the patient exhibited hypoventilation and hypoxia requiring a delayed extubation, raising suspicion for congenital central hypoventilation syndrome (CCHS). We focus on the known history of associations between HSCR and CCHS, in addition to recently found genetic mutations in paired-like homeobox 2B that link HSCR, CCHS, and neuroblastoma.

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