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一名幼儿腘窝囊肿破裂后发生幼年特发性关节炎的罕见病例。

A Rare Case of Juvenile Idiopathic Arthritis following a Ruptured Baker's Cyst in a Toddler.

作者信息

Üstüner Deniz, Asaid Fatma, Pervaiz Muhammad, Oligbu Godwin

机构信息

Department of Paediatrics, Dr Gray's Hospital, NHS Grampian, Aberdeen, UK.

出版信息

Case Rep Pediatr. 2020 Apr 6;2020:1601348. doi: 10.1155/2020/1601348. eCollection 2020.

Abstract

A Baker's cyst is usually an incidental finding in adults being investigated for a joint arthropathy, and its rupture preceding the diagnosis of juvenile idiopathic arthritis (JIA) is rare in children. Here, we describe a case of a 4-year-old girl who presented to the Emergency Department with right calf pain, swelling, and no preceding history of trauma. MRI confirmed a ruptured Baker's cyst with inflammatory arthropathy alongside an extensive synovial proliferation throughout the knee joint with large joint effusions and associated soft tissue oedema tracking superiorly and inferiorly along the medial head of gastrocnemius and anteriorly along the tibia. Further investigations revealed bilateral uveitis consistent with a diagnosis of juvenile idiopathic arthritis.

摘要

贝克囊肿通常是在因关节病接受检查的成年人中偶然发现的,而在儿童中,其在幼年特发性关节炎(JIA)诊断之前破裂的情况很少见。在此,我们描述一例4岁女孩,她因右小腿疼痛、肿胀就诊于急诊科,且无前驱创伤史。磁共振成像(MRI)证实为破裂的贝克囊肿合并炎性关节病,同时整个膝关节存在广泛的滑膜增生,伴有大量关节积液以及相关的软组织水肿,沿腓肠肌内侧头上下延伸,并沿胫骨前方延伸。进一步检查发现双侧葡萄膜炎,符合幼年特发性关节炎的诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32e4/7165340/52f1b00aef6a/CRIPE2020-1601348.001.jpg

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