The spiked helmet sign in severe sepsis: an unusual electrocardiographic finding in a critically ill patient [0.03%]
严重脓毒症的「带刺盔状征」：危重患者中一种不常见的心电图表现
Hashim Manea,Ahmed Qasim Mohammed Alhatemi,Mohammedbaqer Ali Al-Ghuraibawi et al.
Hashim Manea et al.
Background: The 'spiked helmet' sign is a rare electrocardiographic (ECG) phenomenon characterized by transient ST-segment elevations mimicking an acute coronary syndrome, typically seen in critically ill patients. While ...
Post-traumatic distal radioulnar synostosis in a child: a rare case report and literature review [0.03%]
儿童桡尺远端关节炎后骨化性滑膜炎的罕见病例报告及文献回顾
Mouna Lazrak,Hidaya Zitan,Sarah Hosni et al.
Mouna Lazrak et al.
Radioulnar synostosis is a rare but severe complication of pediatric forearm trauma that results in the loss of forearm rotation and functional impairment. We report the case of a 7-year-old boy who developed post-traumatic distal radioulna...
An incidental situs Inversus Totalis in a Pediatric case of granulomatous Panuveitis. A case report [0.03%]
一名儿童肉芽肿性全葡萄膜炎偶然发现内脏反位的一例报告
Carlos Eduardo Solórzano Flores,Daniel Aguilar,Fabiola Langner-Salinas et al.
Carlos Eduardo Solórzano Flores et al.
Situs inversus totalis (SIT) is a rare congenital abnormality characterized by a mirror-image transposition of thoracic and abdominal organs. Although SIT is a recognized congenital anomaly, it is often unfamiliar to physicians because it i...
Jan V Stevens,Ehsan Aliniagerdroudbari,Osaevbie Woghiren et al.
Jan V Stevens et al.
A 49-year-old woman presented with a chronic, painful umbilical mass refractory to antibiotics and incision and drainage, ultimately diagnosed as well-differentiated squamous cell carcinoma (SCC) with positive margins. Imaging revealed an a...
Late diagnosis of Kartagener syndrome in a 38-year-old female presenting with palpitations in a resource-limited emergency department [0.03%]
一名38岁女性患者因心悸在资源有限的急诊科就诊时被诊断出患有卡塔格内综合征
Ömer Atlı
Ömer Atlı
Kartagener syndrome, a subset of primary ciliary dyskinesia, is typically diagnosed in childhood due to its classic triad of situs inversus, chronic sinusitis, and bronchiectasis. We report a compelling case of a 38-year-old woman from a re...
Unmasking Oligosecretory multiple myeloma: a case report highlighting diagnostic pitfalls [0.03%]
揭秘寡分泌型多发性骨髓瘤一例并探讨其诊断难点
Carlos Solórzano Flores,Adolfo Izaguirre,Evangie Bravo Monroig et al.
Carlos Solórzano Flores et al.
Oligosecretory multiple myeloma (OSMM) is a rare subtype of plasma cell dyscrasia that poses significant diagnostic challenges due to the absence of a clear monoclonal (M) spike on serum protein electrophoresis. We report the case of a 64-y...
Unusual presentation of primary cutaneous mucinosis with Blaschkoid Hemibody distribution: case report [0.03%]
以Blaschko线分布为特点的原发性皮肤黏蛋白病1例
Maryam Ghaleb,Kaoutar Benchekroun,Fatima Zahra El Ali et al.
Maryam Ghaleb et al.
Primary cutaneous mucinosis (PCM) is a rare condition characterized by dermal mucin deposition without systemic disease, thyroid dysfunction, or paraproteinemia. The following report details the case of a 25-year-old female patient who exhi...
COVID-19 vaccine-induced parkinsonism due to LGI1 antibody encephalitis: case report and brief literature review [0.03%]
新冠疫苗诱导的LGI1抗体脑炎性帕金森综合征：病例报告和文献简述
Abdalla Khabazeh,Jetish Kumar,Volney Sheen
Abdalla Khabazeh
Anti-LGI1 encephalitis is an autoimmune disorder of the brain, characterized by subacute cognitive impairment, faciobrachial dystonic seizures, and hyponatremia. Although rare, recent reports suggest that LGI1 encephalitis may be triggered ...
Abdullah Dukhan,Haya Hamsho,Fatima Kader Agha et al.
Abdullah Dukhan et al.
Dermatitis neglecta, is a localized inflammatory skin condition often resulting from inadequate hygiene, or psychological factors. It is usually treated with cleansing by alcohol. In our paper we report two cases of patients who developed d...
Case report: post-delivery thrombotic thrombocytopenic purpura complicated by malignant catatonia [0.03%]
个例报道：产后溶血性尿毒症综合征合并恶性类木僵状态
Ameer Ahmed Alajali,Ahmed Abdulhussain Shahatta,Sajjad Ghanim Al-Badri et al.
Ameer Ahmed Alajali et al.
Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening thrombotic microangiopathy characterized by thrombocytopenia, microangiopathic hemolytic anemia (MAHA), renal dysfunction, fever, and neurological symptoms. Postpartum TT...