Report of two primary renal tumors with myxoid features. Differential diagnosis between benign and malignant entities [0.03%]
具有黏液样特征的两种原发性肾肿瘤的报告。良性与恶性病变的鉴别诊断
Adele Fioravanzo,Guido Martignoni,Matteo Brunelli et al.
Adele Fioravanzo et al.
Renal mesenchymal neoplasms are rare entities which can have a benign or a malignant behavior. Herein we describe two renal mesenchymal tumors with myxoid stroma, investigating the wide spectrum of differential diagnosis. With our first cas...
Case Reports
Pathologica. 2021 Dec;113(6):427-435. DOI:10.32074/1591-951X-180 2021
NeuN, a DNA-binding neuron-specific protein expressed by Merkel cell carcinoma: analysis of 15 cases [0.03%]
神经元特异性DNA结合蛋白NeuN阳性梅克尔细胞癌15例分析
Marco Ungari,Laura Manotti,Giulia Tanzi et al.
Marco Ungari et al.
Aim: Merkel cell carcinoma (MCC) is an aggressive cutaneous neuroendocrine carcinoma, with an increasing worldwide incidence. It presents as a painless red to purple nodule on sun-exposed skin. MCC is presumed to arise fr...
Survey on postmortem screening and management of COVID-19 related deaths [0.03%]
关于与COVID-19相关死亡的死后筛查和管理的调查研究
Sameera A Gunawardena,Cristina Cordeiro,Giancarlo Di Vella et al.
Sameera A Gunawardena et al.
The COVID-19 pandemic is associated with a high case fatality rate in some countries even thought the majority of cases are asymptomatic. Scientific studies on this novel virus is limited and there is uncertainty regarding the best practice...
Fibrinous and hemorrhagic pericarditis with cardiac tamponade due to acute myeloid leukemia [0.03%]
急性髓系白血病所致心包 fibrin 血形成及心脏压塞综合征
Magda Zanelli,Maurizio Zizzo,Francesca Sanguedolce et al.
Magda Zanelli et al.
Pediatric autoimmune disorders with gastrointestinal expressions: from bench to bedside [0.03%]
具有胃肠表现的儿科自身免疫疾病：从基础到临床研究
Paola Francalanci,Barbara Cafferata,Rita Alaggio et al.
Paola Francalanci et al.
The gastrointestinal (GI) tract may be involved in systemic autoimmune diseases or may be the target of organ-specific autoimmunity. Autoimmune enteropathy (AIE) is a rare disorder characterized by severe and protracted diarrhea, weight los...
Histopathology of intestinal villi in neonatal and paediatric age: main features with clinical correlation - Part II [0.03%]
新生儿和儿童期肠绒毛的组织病理学：主要特征及其临床相关性 - 第二部分
Chiara Rossi,Gloria Simoncelli,Giovanni Arpa et al.
Chiara Rossi et al.
In this paper, we will continue the description of histological findings of infantile and paediatric small bowel alterations with the main clinical pictures and differential diagnosis. We emphasise once again the need to evaluate the biopsi...
Histopathology of intestinal villi in neonatal and paediatric age: main features with clinical correlation - Part I [0.03%]
新生儿和小儿年龄肠道绒毛的组织病理学：主要特征及临床相关性 - 第一部分
Chiara Rossi,Gloria Simoncelli,Giovanni Arpa et al.
Chiara Rossi et al.
The neonatal and paediatric spectrum of small bowel disorders encompass a wide variety of conditions, ranging from food allergies to life-threatening surgical emergencies or life-long medical conditions and, as such, it comes with a whole s...
Very Early Onset-IBD: evidence for the need of a multidisciplinary approach [0.03%]
极早期发作的炎症性肠病：需要多学科治疗的证据
Paola Parente,Maria Pastore,Federica Grillo et al.
Paola Parente et al.
Very early onset inflammatory bowel disease (VEO-IBD) represents approximately 25% of cases of IBD-like colitis occurring during childhood and, by definition, it is characterized by an onset prior to 6 years of age. This subgroup of patient...
The contribution of Juan Rosai to the pathology of soft tissue tumors [0.03%]
Juan Rosai对软组织肿瘤病理学的贡献
Marta Sbaraglia,Elena Bellan,Thomas Mentzel et al.
Marta Sbaraglia et al.
The conceptual evolution in the field of soft tissue tumor pathology has been mostly driven by a relatively small group of individuals that includes giants of the past and the present such as James Ewing, Raffaele Lattes, Arthur Purdy Stout...
Rosai-Dorfman disease. A legacy of Professor Rosai that is still not exploited completely [0.03%]
Rosai-Dorfman病。仍未能被完全开发的Professor Rosai的遗产
Claudio Doglioni
Claudio Doglioni
Rosai-Dorfman disease (RDD) is a rare form of non-Langerhans cell histiocytosis described by Rosai and Dorfman in 1969. It is a fascinating disease characterized by accumulation of large, pale histiocytes, frequently showing the emperipoles...