Meconium Periorchitis [0.03%]
胎粪污染所致附睾炎
Anusha Kulkarni,Kiruthiga Kala Gnanasekaran,Heena Shah et al.
Anusha Kulkarni et al.
Meconium periorchitis (MPO) is an unusual entity that presents as a scrotal mass in the early neonatal period and is seen in 1 in 30,000 live births. MPO is associated with meconium peritonitis, that leads to leakage of sterile meconium thr...
Spondylocostal Dysostosis-1 Associated With Pancreatic Heterotopia: Coincidence or True Association? [0.03%]
脊椎肋骨发育不全1型伴胰腺异位：偶然或真正关联？
Sihem Darouich,Samia Darouich,Ahmed Khemiri et al.
Sihem Darouich et al.
Spondylocostal dysostosis type 1 is caused by mutations in the DLL3 gene, which encodes a Notch1 ligand. These mutations lead to defective somitogenesis, resulting in a consistent pattern of abnormal vertebral segmentation. Disruptions in t...
Recurrent Diffuse Chorioamniotic Hemosiderosis of the Placenta in a Mother With Congenital Heart Disease [0.03%]
患有先天性心脏病的母亲的胎盘反复出现弥散性绒毛羊膜含铁血黄素沉着症
Charlotte F Kim,Heather L Keir
Charlotte F Kim
A woman in her mid-20s with repaired congenital heart disease (CHD) delivered a 33-week neonate in 2024 following preterm labor and a 24-week neonate in 2025 for non-reassuring fetal heart tones. Placental examination in both cases revealed...
Clinical, Endoscopic, and Upper Gastrointestinal Histological Manifestations in Pediatric Inflammatory Bowel Disease: Insights from a Large Cohort [0.03%]
儿童炎症性肠病的临床、内镜和上消化道病理表现：一项大型队列研究的新见解
Allen Choi,Eyas Alzayadneh,Patrick Breheny et al.
Allen Choi et al.
Background: Upper GI involvement is common in pediatric IBD, but the relative frequencies of specific endoscopic and histologic abnormalities at diagnosis remain poorly defined. ...
Angiosarcoma Arising in 1 of 2 Adolescent Twins With Cryptogenic Cirrhosis and MAF Gene Mutation [0.03%]
隐源性肝硬化伴MAF基因突变的孪生青少年中发生血管肉瘤病例报告
Michael P Duggan,Rajasekharan Warrier,Adrienne Burgin et al.
Michael P Duggan et al.
Primary hepatic angiosarcoma (HAS) is an exceedingly rare tumor that is often idiopathic and usually fatal. It typically occurs in a bimodal age distribution, in older adults or very young children. We describe a unique case of HAS arising ...
B cell Chronic Intervillositis and Maternal Floor Infarction in a Placenta of a Stillbirth [0.03%]
死产胎盘的B细胞 intervillitis和母体螺旋动脉浸润性疾病
Henning Feist,Nora Schaumann
Henning Feist
Chronic histiocytic intervillositis with recurrence risk and perinatal adverse outcome is defined by the detection of maternal CD68-positive macrophages. Intervillous accumulation of B lymphocytes is a rare finding in miscarriage specimens ...
Stage 2 Basal Plate Myometrial Fibers in Delivered Placentas: Frequent Placenta Retention but Rarely Indicative of Clinical Placenta Accreta Spectrum [0.03%]
二期胎盘底蜕膜肌纤维化在产后胎盘中的作用：频繁引起胎盘滞留但极少提示临床胎盘粘连谱系病变
Jonathan L Hecht,Sophia Bellegarde,Anna M Modest et al.
Jonathan L Hecht et al.
Objectives: We describe the clinical characteristics of patients with Stage 2 Basal plate myometrial fibers (BPMF), a histologic lesion resembling Placenta accreta spectrum (PAS). ...
Iron Deficiency Associated Thrombocytosis May Reach Very High Levels in Children and Usually Shows Inverse Correlation with Hemoglobin and MCV: Report of a Pediatric Case and a Brief Literature Review [0.03%]
儿童缺铁性血小板增多症可达到很高水平，通常与血红蛋白和MCV呈负相关：一例儿科病例报告及简要文献复习
Roopa Kodimyala,Basil Kahwash,Kathleen Nicol et al.
Roopa Kodimyala et al.
In this report, we describe the case of a child with iron deficiency anemia associated with markedly elevated platelet count. We provide detailed sequential data showing platelet count correction towards normal levels as anemia improved wit...
Pediatric Bullous Pemphigoid Induced by Rivaroxaban: A Rare Case Report With Underlying Hereditary Hypercoagulability [0.03%]
利伐沙班诱导的儿童大疱性天疱疮1例——伴有遗传性高凝状态的罕见病例报告
Yen Hoang Phan,Phi Duong Nguyen,Khanh Ngoc Minh Nguyen et al.
Yen Hoang Phan et al.
Bullous pemphigoid (BP) is a rare autoimmune blistering disorder in pediatric patients. Although various medications have been implicated as potential triggers, hypersensitivity reactions associated with Rivaroxaban, a direct Factor Xa inhi...
An Atypical Presentation of a Large Congenital Umbilical Cord Hernia Antenatally Diagnosed as an Omphalocele With the Sole Left Lobe of the Liver: A Case Report [0.03%]
巨大脐带疝的非典型病例报告：产前被诊断为脐膨出并仅有单侧左半肝的罕见案例报告
Zlatan Zvizdic,Edin Medjedovic,Asmir Jonuzi et al.
Zlatan Zvizdic et al.
We report an infrequent case of a full-term male neonate presenting with a large congenital hernia of the umbilical cord (6 cm × 6 cm) containing only the entire left lobe of the liver. Prenatal ultrasonography suggested an omphalocele; ho...