Popliteal Artery Entrapment Syndrome in Children: Experience With Four Cases of Acute Ischaemia and Review of the Literature.

Autor: Settembre N; Department of Vascular Surgery, Nancy University Hospital, University of Lorraine, Nancy, France. Electronic address: nicla.settembre@yahoo.com., Bouziane Z; Department of Vascular Surgery, Nancy University Hospital, University of Lorraine, Nancy, France., Bartoli MA; Department of Vascular Surgery, Marseille University Hospital, Marseille, France., Nabokov V; Department of Vascular Surgery, Saint Petersburg University Hospital, Saint Petersburg, Russia., Venermo M; Department of Vascular Surgery, Helsinki University Hospital, University of Helsinki, Helsinki, Finland., Feugier P; Department of Vascular Surgery, Lyon University Hospital, Lyon, France., Malikov S; Department of Vascular Surgery, Nancy University Hospital, University of Lorraine, Nancy, France.
Jazyk: angličtina
Zdroj: European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery [Eur J Vasc Endovasc Surg] 2017 Apr; Vol. 53 (4), pp. 576-582. Date of Electronic Publication: 2017 Feb 17.
DOI: 10.1016/j.ejvs.2016.12.032
Abstrakt: Objective: Popliteal artery entrapment syndrome (PAES) is an uncommon anatomical anomaly, frequently described in adults. The most common symptom is claudication. Acute limb ischaemia (ALI) in children is rare, but it may evolve and lead to limb loss or lifelong complications. Clinical and surgical experience of PAES in children is reported. Data from the literature are analysed in order to assess the severity of this disease and to identify the factors characterising the diagnosis and the outcome of treatment in paediatric patients.
Methods: Four children (aged 7-16 years) were referred with ALI due to PAES. Among the 439 articles reporting cases of PAES, 55 patients under 18 years of age were the focus. The PAES cases were classified according to the Love and Whelan classification modified by Rich.
Results: Data from 79 children (106 limbs, 27 bilateral PAES) were collected and analysed. Type I PAES was present in 41 (39%), Type II in 23 (22%), Type III in 24 (23%), Type IV in 12 (11%), and Type V in two (2%) limbs. A functional PAES was present in one patient bilaterally. In two cases, the type of PAES was not reported. Claudication occurred in 68 cases (64%), and ALI in 19 (18%). In 60 cases (57%), revascularisation with or without myotomy was required; myotomy alone was performed in 41 cases (39%).
Conclusions: Symptomatic PAES in children should be considered a severe condition requiring urgent investigation in order to avoid any delays in the treatment. Early diagnosis and treatment are essential to prevent serious complications. The long-term outcomes of surgical treatment with the correction of the anatomical anomaly and vascular reconstruction are satisfactory with a low complication rate.
(Copyright © 2017 European Society for Vascular Surgery. Published by Elsevier Ltd. All rights reserved.)
Databáze: MEDLINE
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