High-Risk Histological Subtypes of Papillary Thyroid Carcinoma Predict More Aggressive Disease in Pediatric Patients [0.03%]
高风险乳头状甲状腺癌的组织亚型可预测儿科患者的侵袭性病变
Lauren N Parsons,Amanda May Hopp,Jason A Jarzembowski
Lauren N Parsons
Introduction: Papillary thyroid carcinoma (PTC) is uncommon in children compared with adults. Studies have examined the significance of histologic subtype on outcomes in adults; less is known about its importance in pedia...
Clinical Significance of Renal Tissue in Neonatal Sacrococcygeal Teratoma: A Case Report With Review of Literature [0.03%]
骶尾部畸胎瘤肾组织的临床意义——1例报道及文献复习
Alessio Conte,Silvia Rebella,Gabriele Gaggero et al.
Alessio Conte et al.
Congenital sacrococcygeal teratomas (SCTs) are rare tumors with highly variable prognosis, influenced by associated abnormalities and marked histological heterogeneity. SCTs may exhibit somatic renal differentiation, encompassing a wide spe...
Novel Pediatric Presentation of Pseudomyogenic Hemangioendothelioma: Diagnostic Pitfalls and Considerations of an Atypical Case [0.03%]
假肌性血管内皮瘤的新型儿科病例表现：罕见病例诊断陷阱及注意事项
Lydia Du,Saad Ranginwala,Ian Gelarden
Lydia Du
Pseudomyogenic hemangioendothelioma (PMH) is a rare, often multicentric neoplasm occurring primarily in soft tissue. Fewer than 50 cases of isolated bone lesions are described, with nearly all restricted to bone(s) of 1 region of the body. ...
Comparative Analysis of Molecular Profiles of Sporadic Odontogenic Keratocyst and Bilateral Odontogenic Keratocyst: A Next Generation Sequencing Study [0.03%]
基于下一代测序的成釉细胞瘤样囊肿和牙源性丛状型成釉细胞瘤基因组特征分析
Krishna Verma,Deepak Pandiar,Reshma Poothakulath Krishnan
Krishna Verma
Aim: To comparatively analyse and interpret the molecular profiles of sporadic odontogenic keratocysts (OKC) with bilateral non-syndromic odontogenic keratocysts employing next-generation sequencing (NGS). ...
A Case Report of I-Cell Disease (Mucolipidosis Type II) With a Novel Placental-Focused Diagnostic Approach [0.03%]
以新型胎盘聚焦诊断方法发现一例I细胞病(Ⅱ型黏脂贮积病)病例报告
Nicolas LaScala,Laura Rose,Jennifer Sanchez et al.
Nicolas LaScala et al.
Inclusion cell disease (I-cell disease/Mucolipiodsis Type II) is an autosomal recessive lysosomal storage disorder that results in accumulation of substrates (cholesterol, phospholipids, and glycosaminoglycans) in various tissues. The clini...
Pathology of Progressive Familial Intrahepatic Cholestasis: An update [0.03%]
进行性家族性肝内胆汁淤积症的病理学：最新研究进展
Suvradeep Mitra,Mukul Vij,Jagadeesh Menon et al.
Suvradeep Mitra et al.
Progressive familial intrahepatic cholestasis (PFIC) comprises a heterogeneous group of rare, autosomal recessive liver disorders characterised by defective bile formation and secretion, leading to progressive cholestasis, pruritus, growth ...
Jutamas Wongphoom,Panachai Nimitpanya,Nawaluk Atiroj et al.
Jutamas Wongphoom et al.
Introduction: CD15 expression has been used as a marker of endothelial immaturity in the placenta and is linked to the setting of antenatal hypoxia. If so, expression should be increased in fetal anemia, especially when s...
Retropharyngeal Ectopic Thyroid Found Histologically in Late-Term Fetuses: A Case Report With an Embryological Study [0.03%]
胎盘晚期末期胎儿咽后异位甲状腺的组织学发现：附有胚胎学研究的病例报告
Yun-Feng Liu,Zhe-Wu Jin,Feng Han et al.
Yun-Feng Liu et al.
Objective: To identify a pathogenesis of retropharyngeal ectopic thyroid (ET) independent of the thyroglossal duct-derived usual ET. Methods: ...
Liver Biopsy-Associated Diagnosis of Glycogen Storage Disease Type IV (Andersen Disease) [0.03%]
肝活检在糖原累积病Ⅳ型( Andersen病)诊断中的应用
Ryou Ishikawa,Takeo Kondo,Sonoko Kondo et al.
Ryou Ishikawa et al.
Glycogen storage disease type IV (Andersen disease) is caused by a deficiency of the glycogen branching enzyme. We report a case in which liver biopsy played a key role in establishing the diagnosis. A 2-year-old girl presented to our hospi...
Pediatric SMARCB1/INI1-Deficient Undifferentiated Pancreatic Carcinoma: Presentation of an Additional Case of a Rare Tumor [0.03%]
SMARCB1/INI1缺陷型儿童胰腺癌一例报告
Di Ding,Dongmei Ding,Feng Tian et al.
Di Ding et al.
Objective: To investigate the clinical and pathological features of pediatric SMARCB1/INI-1 deficient undifferentiated pancreatic carcinoma. Methods: ...