A rare early-onset bilateral renal cysts, focal seizures in a 1-year-old male with tuberous sclerosis and No mutation identified [0.03%]
一名一岁男性患者，双肾囊肿、局灶性癫痫与结节性硬化症但未检测到突变
Dana Salahat,Ramzi Mujahed,Mohanad Jaber et al.
Dana Salahat et al.
Tuberous Sclerosis Complex (TSC) is a rare genetic disorder characterized by the development of benign tumors in multiple organs. This report presents an unusual case of early-onset renal cystic disease in a 1-year-old male with TSC, despit...
Successful heart transplantation in a patient with glycogen storage disease [0.03%]
糖原累积病患者成功行心脏移植手术
Hannaneh Yousefi-Koma,Babak Sharif-Kashani,Zargham-Hossein Ahmadi et al.
Hannaneh Yousefi-Koma et al.
Background: Polyglucosan body myopathy is a type of glycogen storage disease characterized by abnormal glycogen structure formation. Progressive heart failure is the primary cause of mortality in affected patients. ...
Dimitrios Karponis,Zoe C Venables
Dimitrios Karponis
Mixed Adenoneuroendocrine carcinoma of uterine cervix: a case series and review of literature [0.03%]
子宫颈混合性腺神经内分泌癌的病例系列及文献回顾
Sara Salehiazar,Komeil Mirzaei Baboli,Elliott Lebby et al.
Sara Salehiazar et al.
Klippel-trenaunay syndrome in a child with coexisting lymphangioma, vascular insufficiency, and multiple soft tissue swellings: a case report [0.03%]
儿童 Klippel-Trenaunay 综合征伴生淋巴管瘤、血管功能不全和多发软组织肿胀1例报告
Muhammad Abrar Amir,Muhammad Aniq Amir,Syed Ali Arsal et al.
Muhammad Abrar Amir et al.
Introduction: Klippel-Trenaunay syndrome (KTS) is a complex and extremely rare congenital vascular syndrome. The disorder presents with a vascular malformation syndrome involving cutaneous capillaries and venous (hemangio...
Unmasking Hirata: a mysterious case of Hypoglycemia triggered by immunologic storm [0.03%]
剥开ヒラタ氏病例的面纱——免疫风暴触发的低血糖症神秘病例分析
Mohammed AbuBaha,Hossam Salameh,Bara AbuBaha et al.
Mohammed AbuBaha et al.
We report a rare case of Insulin Autoimmune Syndrome in a 35-year-old woman with prior autoimmune features who developed hypoglycemia after an allergic reaction. Diagnosis was confirmed by insulin autoantibodies. Immunosuppressive therapy y...
Asymptomatic central venous occlusion secondary to central venous catheter-use complicating pacemaker implantation: a leadless solution [0.03%]
中心静脉导管使用导致的无症状中央静脉闭塞继发于起搏器植入术的治疗：一种无引线解决方案
James Baudry,Christopher Cassidy,Kanarath Balachandran
James Baudry
Abnormal central venous anatomy can obstruct cardiac-device implantation. We report a 54-year-old patient found to be in complete heart-block after identification of profound bradycardia, requiring cardiac-pacing. Echocardiography revealed ...
A case of transformation of Waldenström's Macroglobulinemia to diffuse large B cell lymphoma [0.03%]
一例华氏巨球蛋白血病转化弥漫大B细胞淋巴瘤的病例报告
Meher B Ali,Kathryn Kline
Meher B Ali
Waldenström's Macroglobulinemia (WM) is a lymphoplasmacytic lymphoma which can rarely transform into diffuse large B cell lymphoma (DLBCL). Usually, the diagnosis of WM precedes DLBCL. A 79-year-old male presented to the hospital for worse...
Metachronous Pheochromocytoma and Cholangiocarcinoma in a patient with Neurofibromatosis type 1: a case report [0.03%]
1型神经纤维瘤病患者的异时性嗜铬细胞瘤和胆管癌病例报告
Yousra Al Harrak,Sihame Lkhoyaali,Oumaima Lamsyah et al.
Yousra Al Harrak et al.
Neurofibromatosis type 1 (NF1) is an autosomal dominant tumor predisposition syndrome caused by mutations in the NF1 gene encoding neurofibromin, leading to an increased risk of benign and malignant tumors, including pheochromocytomas and r...
Percutaneous device closure of iatrogenic right ventricular perforation during attempted ventricular septal defect closure: a case report [0.03%]
经皮封堵器封堵试图闭合室间隔缺损时意外造成右心室穿孔的临床应用：个例报告
Muhammad Raza Sarfraz,Saqlain Anwar,Nadeem Sadiq et al.
Muhammad Raza Sarfraz et al.
Cardiac perforation is a rare but life-threatening complication of transcatheter cardiac procedures, particularly in children where tissue fragility increases risk. We present a rare case of iatrogenic right ventricular perforation during t...