Katrhin Ludwig,Debora De Bartolo,Angela Salerno et al.
Katrhin Ludwig et al.
Congenital anomalies of the tubular gastrointestinal tract are an important cause of morbidity not only in infants, but also in children and adults. The gastrointestinal (GI) tract, composed of all three primitive germ ...
Gastrointestinal pathology in infantile and pediatric patients: the evidence of a pattern-based histological approach and of a multidisciplinary integration [0.03%]
基于模式的病理形态学方法在婴幼儿及儿童胃肠道疾病诊断中的应用以及多学科整合的证据支持
Paola Parente,Matteo Fassan,Rita Alaggio
Paola Parente
Editorial
Pathologica. 2022 Feb;114(1):1-2. DOI:10.32074/1591-951X-552 2022
Carlo Patriarca,Giorgio Sirugo,Mattia Barbareschi
Carlo Patriarca
The persecutions of the Jews that began with legislation introduced by Italy's fascist government in the year 1938 ("Leggi Razziali" i.e. "Racial Laws") also affected the sphere of anatomic pathology, coming to bear on Italian physicians be...
Severe rectal prolapse and solitary rectal ulcer in a young anorectic woman with myxoid degeneration of visceral adipose tissue [0.03%]
黏液样变性内脏脂肪组织年轻厌食症女性的重度直肠脱垂和孤立性直肠溃疡
Mariavittoria Vescovo,Ludovica Pesci,Lucia Lapenna et al.
Mariavittoria Vescovo et al.
Rectal prolapse is a disorder in which the rectum protrudes from the anal canal. Solitary rectal ulcer may coexist. Both conditions have been associated with chronic constipation and excessive straining during defecation. Rectal prolapse ha...
Case Reports
Pathologica. 2021 Dec;113(6):475-480. DOI:10.32074/1591-951X-253 2021
Sinonasal teratocarcinosarcoma treated with surgery and proton beam therapy: clinical, histological aspects and differential diagnosis of a new case [0.03%]
手术和质子束治疗鼻窦恶性肿瘤的临床、病理特征及一例新病例的鉴别诊断
Alessia Belotti,Laura Carpenito,Antonio Mario Bulfamante et al.
Alessia Belotti et al.
Sinonasal teratocarcinosarcoma is a rare aggressive malignant tumor with a primary setting involving the nasal cavity followed by the ethmoid sinus and maxillary sinus. It accounts for approximately 3% of all head and neck cancers and less ...
Case Reports
Pathologica. 2021 Dec;113(6):469-474. DOI:10.32074/1591-951X-215 2021
An encapsulated oncoytic neoplasm of follicular origin of thyroid, expressing neuroendocrine markers. A case report and literature review [0.03%]
甲状腺滤泡来源的类上皮细胞肿瘤并表达神经内分泌标志物一例报告及文献复习
Marcello Filotico,Francesca Plutino
Marcello Filotico
A case is reported of an oncocytic tumor of the thyroid expressing simultaneously follicular and neuroendocrine markers, but not calcitonin. The data reported in the literature and the possible relationships of these lesions with the calcin...
A case of retroperitoneal tumor displaying epithelial differentiation, prominent myxoid stroma and loss of INI1/SMARCB1 [0.03%]
一例显示上皮分化、黏液样间质和INI1/SMARCB1缺失的腹膜后肿瘤病理报告
Bharat Rekhi,Ann Thomas
Bharat Rekhi
The clinicopathological spectrum of INI1 deficient tumors is expanding. Epithelioid sarcoma (ES) is a rare sarcoma of uncertain differentiation, more often occurring in the extremities and uncommonly in the deep soft tissues. Histopathologi...
Case Reports
Pathologica. 2021 Dec;113(6):456-462. DOI:10.32074/1591-951X-250 2021
Marco Ungari,Giulia Tanzi,Elena Varotti et al.
Marco Ungari et al.
Trichogerminoma, first described by Sau et al. in 1992, is a rare cutaneous adnexal neoplasm of the hair germ cell and usually associated with benign clinical course and favorable outcome. About 30 cases have been reported, all with similar...
Case Reports
Pathologica. 2021 Dec;113(6):449-455. DOI:10.32074/1591-951X-137 2021
Phosphoglyceride crystal deposition disease involving adnexa uteri: a case report with histogenetic consideration [0.03%]
关于伴有副性腺受累的磷脂晶体沉积病的一个病例报告及组织发生学考虑
Toshitsugu Nakamura,Masayuki Fujiwara,Kikue Hara et al.
Toshitsugu Nakamura et al.
We present a rare case of phosphoglyceride crystal deposition disease (PCDD), as a gynecologic disease, with reference to histogenesis of crystal deposition. An 84-year-old woman, who had undergone simple hysterectomy for uterine leiomyoma ...
Case Reports
Pathologica. 2021 Dec;113(6):442-448. DOI:10.32074/1591-951X-193 2021
Recurrent primary endobronchial fetal rhabdomyoma: a case report and literature review [0.03%]
复发性支气管胚胎横纹肌肉瘤的病例报告及文献回顾
Stefano Marletta,Anna Caliò,Adele Fioravanzo et al.
Stefano Marletta et al.
Fetal rhabdomyoma is an extremely rare benign rhabdomyoblastic tumor with myotube-like differentiation, mainly arising on mucosal surfaces of the head and neck region of both children and young patients, almost invariably definitively treat...