The Association of Fetal Cyanotic Versus Non-Cyanotic Cardiac Malformations and Placental Vascular Malperfusion [0.03%]
胎儿发绀型与非发绀型先天性心脏病与胎盘血管灌注不良关联性分析
Esra Karakus,Merve Emin,Merve Ozturk Agaoglu et al.
Esra Karakus et al.
Objective: Placental abnormalities are frequently observed in congenital heart disease (CHD) pregnancies, yet detailed histopathological evaluations are limited. This study investigated placental vascular lesions in CHD c...
Congenital Eruption Cyst: A Case Report Listing Histopathological Features With Literature Review and Differential Diagnoses [0.03%]
先天性导萌囊肿：文献回顾、鉴别诊断及组织病理特征的一个病例报告
Maxemilian Nascimento,Paramjeet Kaur Sagoo,Neetha Santosh
Maxemilian Nascimento
Congenital eruption cysts manifest in neonates when the dental follicle separates from the crown of an erupting tooth coronal to the alveolar ridge. Clinical diagnosis can be challenging as it can present clinically similar to congenital ep...
Atypical Teratoid Rhabdoid Tumor With TTF-1 Expression: A Case Report and Possible Insight Into Its Embryologic Origin [0.03%]
具有TTF-1表达的非典型畸胎样横纹肌样瘤一例及其可能的胚胎起源探讨
Sumit Das,Harris Wang,Jake Mandziuk
Sumit Das
Atypical teratoid rhabdoid tumor (AT/RT) of the brain is a highly malignant (CNS WHO grade 4) embryonal neoplasm. Majority of AT/RTs occur in the posterior fossa although supratentorial examples may also be observed. Pathologically, the tum...
BK Polyomavirus-Associated Kidney and Bladder Carcinomas Following Heart and Lung Transplantation in Childhood [0.03%]
儿童心脏和肺移植后 BK 多瘤病毒相关的肾脏和膀胱癌
Joseph Kimball,Jasmine Steele,Sara O Vargas et al.
Joseph Kimball et al.
BK polyomavirus-associated carcinoma of the kidney or bladder following cardiac or pulmonary transplantation has been reported in only 7 individuals, all but 1 being adults. We now report 2 additional pediatric patients, the first having re...
A Rare Cause of Genetic Liver Disease in Children: Transaldolase Deficiency with a Novel Pathogenic Variant in Two Siblings [0.03%]
儿童罕见遗传性肝病的原因：两名兄弟姐妹中发现新型致病突变的转醛糖酶缺乏症
Ozlem Sumer Cosar,Gulsum Kayhan,Gulen Akyol et al.
Ozlem Sumer Cosar et al.
Transaldolase deficiency is a rare autosomal recessive disease caused by biallelic mutations in the TALDO1 gene. This disorder is characterized by multisystem involvement, including liver disease. Here, we present 2 siblings with transaldol...
Histiocytic Sarcoma Arising From Pediatric Rosai Dorfman Disease: Two Novel Cases and Literature Review [0.03%]
儿科Rosai-Dorfman病发生郎格汉斯细胞组织细胞增生症二例及文献复习
Sam Sirotnikov,Rajeswari Jayakumar,Sunita Park et al.
Sam Sirotnikov et al.
Rosai-Dorfman Disease (RDD) is an uncommon histiocytic disorder that can affect lymph nodes and/or extranodal sites. It is marked by the accumulation of abnormal histiocytes that demonstrate emperipolesis-the active, non-destructive engulfm...
Patricia Okiro,Marc Hendricks,Komala Pillay
Patricia Okiro
Sex cord-stromal tumours (SCSTs) in children are rare gonadal neoplasms exhibiting differentiation towards sex cord stromal elements. This case series explores paediatric SCSTs, presenting clinical, gross, histologic, and immunohistochemica...
EWSR1 Fusion Driven Pediatric B-Acute Lymphoblastic Leukemia: Diagnosis and Review of Literature [0.03%]
EWSR1基因重排驱动的儿童B细胞急性淋巴细胞白血病：诊断及文献回顾
Molly Talman,Ashwani K Yenamandra,Yassmine Akkari et al.
Molly Talman et al.
B-lymphoblastic leukemia/lymphoma (B-ALL) is the most prevalent childhood malignancy, with improved survival rates attributed to advances in diagnosis and treatment. Herein, we present a case of B-ALL in a 6-year-old female who presented wi...
Chitayat Syndrome: A Rare Case of Respiratory Distress in a Preterm Infant [0.03%]
迟亚特综合征：早产儿呼吸困难的罕见病例报告
Gabriela Živković,Alen Švigir,Ivan Pavić et al.
Gabriela Živković et al.
Childhood interstitial lung diseases (chILDs) are rare respiratory conditions with significant mortality rates in neonates. They can be misdiagnosed as the symptoms overlap with other, more common neonatal diseases. Since chILD can be a man...