Recurrent paratesticular aggressive angiomyxoma in an elderly patient: a rare case report [0.03%]
老年患者复发性附睾旁侵袭性血管黏液瘤一例报告
Ahmed Chaabouni,Wafa Elleuch,Mahmoud Ghozzia et al.
Ahmed Chaabouni et al.
Aggressive angiomyxoma is a rare benign mesenchymal tumor with local infiltrative potential and a high risk of local recurrence. Its occurrence in the paratesticular region is exceptional. We report the case of an 86-year-old male patient, ...
Multiple ventral hernias in a 30-year-old female with Down syndrome: a case report and review of the literature [0.03%]
唐氏综合征30岁女性多发性腹壁疝的病例报告及文献综述
Seyed Abbas Fatemiyoun,Saina Sadeghipour,Farzad Rafiei et al.
Seyed Abbas Fatemiyoun et al.
Background: Ventral hernias are common abdominal wall defects, usually occurring as isolated entities related to prior surgery, trauma, or increased intra-abdominal pressure. The occurrence of multiple synchronous ventral...
Dina Sadeghi,Seyedeh Rojina Mortazavi,Tara Khoeini
Dina Sadeghi
Background: Brain death is defined as the irreversible cessation of all cerebral and brainstem functions, confirmed through clinical examination and, when necessary, ancillary testing. While the diagnostic criteria are we...
Oncocytic lipoadenoma of the parotid presenting as an unusual neck mass: a case report [0.03%]
一例罕见的腮腺肿瘤病例报告：腮腺黏液表皮样癌伴有上皮肌纹状脂肪组织及乳头囊性瘤成分
Somayeh Sheidaei,Mahdi Naeimaei Aali,Saman Rezaei
Somayeh Sheidaei
Background: Oncocytic lipoadenoma is an extremely rare benign tumor of the salivary glands, with fewer than 50 cases reported in the literature. Most cases occur in the parotid gland, with atypical locations presenting di...
A presentation of spinal epidural abscess in a seven-year-old VACTERL patient: a case report [0.03%]
VACTERL患儿并发脊髓硬膜外脓肿一例报告
Sarah Kebbeh,Sana Masoud,Mary Alakkash et al.
Sarah Kebbeh et al.
Background: Spinal epidural abscess is a rare but potentially life-threatening infection of the central nervous system. VACTERL association is a rare congenital condition characterized by vertebral, anal, cardiac, tracheo...
Toripalimab-induced isolated ACTH deficiency associated with gastroparesis: a case report [0.03%]
特瑞普利单抗诱导的孤立性ACTH缺乏症合并胃轻瘫病例报告
Chicheng Lu,Weijie Li,Qiyong Li
Chicheng Lu
Immune checkpoint inhibitors can cause isolated ACTH deficiency, a rare condition often misdiagnosed due to nonspecific symptoms. We report a cholangiocarcinoma patient on toripalimab and lenvatinib who experienced recurrent gastrointestina...
Osimertinib-induced acute decompensated heart failure: a case report and review of the literature [0.03%]
奥希替尼诱导的急性心力衰竭病例报告及文献回顾
Hou-Chen Lee,Meng-Heng Hsieh,Horng-Chyuan Lin
Hou-Chen Lee
Background: Non-small cell lung cancer (NSCLC), which is one of the most common cancer types, has caused lots of deaths to patients worldwide. Aside from the surgical treatment or chemotherapy, the third-generation epider...
Late presentation of an anomalous left coronary artery originating from the pulmonary artery (ALCAPA) in a 70-year-old male: a case report [0.03%]
左冠状动脉起源于肺动脉（ALCAPA）的病例报告：70岁男性患者的迟发表现
Seyedeh Zeinab Seyedi,Ali Abedi,Bita Mollashahi et al.
Seyedeh Zeinab Seyedi et al.
Background: Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA), also known as Bland-White-Garland syndrome, is a rare congenital anomaly with an estimated incidence of approximately 1 in 300,0...
NTRK fusion in metastatic castration-resistant prostate cancer treated with entrectinib: a case report [0.03%]
恩曲替尼治疗转移性去势抵抗性前列腺癌合并NTRK融合的病例报告
Shuichi Tatarano,Akihiko Mitsuke,Yoichi Osako et al.
Shuichi Tatarano et al.
Background: The tropomyosin receptor kinase (TRK) inhibitors have demonstrated substantial efficacy in solid tumors harboring neurotrophic tyrosine receptor kinase (NTRK) gene fusions. Although NTRK fusions have been spor...
Spinal muscular atrophy type 2 with severe kyphoscoliosis: a case report [0.03%]
脊髓肌肉萎缩症二期并发重度脊柱畸形一例报告
Weifan Ren,Bo Jin,Yungen Hu et al.
Weifan Ren et al.
Background: Spinal muscular atrophy (SMA) is a rare autosomal recessive neuromuscular disorder caused by homozygous deletion or mutation of the SMN1 gene. Scoliosis is a common complication in patients with SMA type 2, of...