Current issue
Archive
Manuscripts accepted
About the journal
Editorial board
Abstracting and indexing
Contact
Instructions for authors
Ethical standards and procedures
Editorial System
Submit your Manuscript
|
4/2024
vol. 99 abstract:
Case report
Harlequin syndrome associated with mediastinal ganglioneuroma: a case report
Aleksandra Czapla
1
,
Szymon Ejzak
1
,
Katarzyna Pawelec
2
,
Jadwiga Małdyk
3
,
Mariusz Cieślak
2
Pediatr Pol 2024; 99 (4): 374-377
Online publish date: 2024/12/30
View
full text
Get citation
ENW EndNote
BIB JabRef, Mendeley
RIS Papers, Reference Manager, RefWorks, Zotero
AMA
APA
Chicago
Harvard
MLA
Vancouver
Harlequin syndrome (HS) is a rare disorder of the autonomic nervous system, caused by unilateral damage to sympathetic fibers innervating the face. The symptoms appear in response to physical activity or heat exposure and present with hemifacial flushing and asymmetric sweating. HS can be idiopathic or associated with an underlying disease. One of the causes of HS in the pediatric population might be a differentiated benign neuroblastic neoplasm-ganglioneuroma. It is often detected in older children and adults, with the most typical location within the posterior mediastinum. In this paper, we present the case of a 3-year-old patient with face discoloration and a massive mediastinal tumor (ganglioneuroma). This study highlights the importance of identifying the cause of HS and the possibility of ganglioneuroma occurring in younger children.
keywords:
Harlequin syndrome, ganglioneuroma, mediastinal tumor |