Challenging diagnosis of a large maxillary lesion: the multi-disciplinary approach [0.03%]
大型上颌区病变的诊断及多学科协作治疗
Eloise Turner,Laura Wade,Panayotis E Dais et al.
Eloise Turner et al.
We report the case of a fit and well pregnant patient in her 20s who presented with a progressively expansile swelling of the left maxilla. Despite extraction of the presumed causative tooth, the lesion continued to enlarge, extending to th...
Case Reports
BMJ case reports. 2026 Jul 27;19(7):e271808. DOI:10.1136/bcr-2025-271808 2026
Ophthalmic features of WAGR syndrome: strategies for timely diagnosis, surveillance and improved quality of life [0.03%]
WAGR综合征的眼科特征：及时诊断、监测及提高生活质量的策略
Sohini Mandal,Srikanta Kumar Padhy
Sohini Mandal
A toddler presented with photophobia and difficulty in focusing on objects since the age of 2 months. Further examination revealed complete aniridia, horizontal jerk nystagmus and a history of genitourinary anomalies. The suspicion of WAGR ...
Case Reports
BMJ case reports. 2026 Jul 27;19(7):e265300. DOI:10.1136/bcr-2025-265300 2026
Mahdhir Amat Tugiman,Pankhuri Punj,Shavershree Govender
Mahdhir Amat Tugiman
Congenital uterine anomalies occur as a result of a failure of the fusion and resorption of the Müllerian ducts in utero. Although Müllerian anomalies are relatively uncommon, they can complicate reproductive health and even cause death.W...
Case Reports
BMJ case reports. 2026 Jul 27;19(7):e271003. DOI:10.1136/bcr-2025-271003 2026
Duc Truong Nguyen,Trieu Dat Vo,Trong-Vien Cai
Duc Truong Nguyen
Torsion of a pedunculated uterine leiomyoma is a rare gynaecological emergency. Its nonspecific symptoms can mimic other common conditions, posing significant diagnostic challenges. We present a case that highlights these diagnostic difficu...
Case Reports
BMJ case reports. 2026 Jul 27;19(7):e272895. DOI:10.1136/bcr-2026-272895 2026
Early-onset non-oliguric hyperkalaemia in a moderate preterm infant following maternal magnesium sulfate therapy [0.03%]
早发性非少尿型高钾血症一例：足月小婴儿继母硫酸镁治疗后发生
Pasupathi Raj Balamurugan,Roma Debbarma,Santhosh Shimpiger et al.
Pasupathi Raj Balamurugan et al.
Early neonatal hyperkalaemia is uncommon but may cause life-threatening arrhythmias if untreated. While most cases occur in extremely low-birth-weight infants after 24 hours of life, hyperkalaemia within the first few hours after birth is u...
Case Reports
BMJ case reports. 2026 Jul 24;19(7):e274813. DOI:10.1136/bcr-2026-274813 2026
Patient-specific approach to the correction of a post-traumatic zygomatic deformity [0.03%]
个性化治疗方案在处理颌骨畸形中的应用
Camilla Pagnacco,Sachin M Salvi,Samantha Houlton et al.
Camilla Pagnacco et al.
Fractures of the zygomaticomaxillary complex (ZMC) represent one of the most frequent midfacial injuries and, if untreated, can result in significant functional and aesthetic sequelae. While open reduction and internal fixation is the stand...
Case Reports
BMJ case reports. 2026 Jul 24;19(7):e271620. DOI:10.1136/bcr-2025-271620 2026
Fenfluramine in refractory SCN1A-related 'genetic epilepsy with febrile seizures plus' [0.03%]
氯卡色林治疗难治性SCN1A相关性遗传性发热惊厥加癫痫患者疗效观察
Tatsuya Takahashi,Yuichi Abe,Itaru Hayakawa
Tatsuya Takahashi
A child with SCN1A-related 'genetic epilepsy with febrile seizures plus' (GEFS+) presented in infancy with recurrent febrile and afebrile seizures, frequently progressing to generalised tonic-clonic status epilepticus. Despite a severe seiz...
Case Reports
BMJ case reports. 2026 Jul 24;19(7):e273440. DOI:10.1136/bcr-2026-273440 2026
Michael Gregory Snow,Jiaxin Yuan,Hiba Qari et al.
Michael Gregory Snow et al.
Lipomas are commonly occurring benign adipocytic tumours of mesenchymal origin and can be found anywhere there is native fatty tissue. In the head and neck region, they typically arise in the cervical fibrofatty tissue of the neck and rarel...
Case Reports
BMJ case reports. 2026 Jul 24;19(7):e274192. DOI:10.1136/bcr-2026-274192 2026
Co-occurrence of hypodontia, taurodontism and talon cusp in the primary dentition [0.03%]
乳牙期小牙症、牛牙症和牙尖切迹的并存现象
Dhruvi Raj Solanki,Punit Ratnakar Fulzele,Ishani Rahate et al.
Dhruvi Raj Solanki et al.
Brucellosis-associated haemophagocytic lymphohistiocytosis in a child [0.03%]
儿童布鲁氏菌病相关性噬血细胞性淋巴组织细胞增生症
Ahmad Zaher Kour,Hamda Al Abri
Ahmad Zaher Kour
Haemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory syndrome that may be triggered by infections, including brucellosis. Brucellosis-associated HLH is uncommon in children and may mimic malignancy or severe vir...
Case Reports
BMJ case reports. 2026 Jul 24;19(7):e272220. DOI:10.1136/bcr-2026-272220 2026