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期刊名:International journal of surgical pathology

缩写:INT J SURG PATHOL

ISSN:1066-8969

e-ISSN:1940-2465

IF/分区:1.0/Q3

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共收录本刊相关文章索引2845
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Recep Bedir,Anil Can Yalçin Recep Bedir
The presence of ectopic breast tissue within axillary lymph nodes is a benign condition that must be distinguished from primary or metastatic carcinoma. Here, we present a patient who was previously diagnosed with invasive breast cancer in ...
Jie Zhang,Rui Wang,Zhixing Cao et al. Jie Zhang et al.
Renal cell carcinoma (RCC) with hemangioblastoma-like features, which was not included in the 2022 edition of the World Health Organization Classification of Tumors of the Urinary System and Male Genital Organs, is an extremely rare RCC rep...
Athanase Billis,Ana P C Queiroz,Ana Yoshie et al. Athanase Billis et al.
We report the clinicopathological findings of the first series of 4 patients from Brazil with eosinophilic solid and cystic renal cell carcinoma (ESC RCC). In our study, there were 3 female patients and 1 male patient. The youngest female p...
Amal Youssef,David J Supeck,Richard E Sharpe Jr et al. Amal Youssef et al.
Pleomorphic adenoma of the breast is a rare tumor, with fewer than 100 patients described in the English literature, mainly as case reports and small case series. Histologically, breast pleomorphic adenoma resembles its more common salivary...
Kristin J Rybski,Bin Zhang,Jinbo Fan et al. Kristin J Rybski et al.
Secondary angiosarcoma of the breast is a rare and aggressive malignancy, with characteristic MYC amplification. It typically arises in the field of prior radiation for breast cancer treatment, or rarely, in patients with a history of radic...
Kaito Nakama,Masayuki Ota,Takanori Aihara et al. Kaito Nakama et al.
Mesonephric-like adenocarcinoma (MLA) is a rare tumor that is typically found in the ovary or uterus, characterized by immunohistochemical positivity for TTF1 (NKX2-1), PAX8, and GATA3, and negativity for estrogen receptor. Although known f...
Richard Koleják,Jan Mraček,Ivan Šubrt et al. Richard Koleják et al.
Primary intracranial sarcoma, DICER1-mutant, is a rare central nervous system tumor that predominantly affects children, only occasionally described in adults. We report on a 30-year-old man with a primary high-grade tumor initially diagnos...
Shinsuke Sugenoya,Takeshi Uehara,Mai Iwaya et al. Shinsuke Sugenoya et al.
Hepatocellular carcinoma (HCC) is a leading cause of cancer-related deaths. The role of leucine-rich repeat-containing G protein-coupled receptor 5 (LGR5), a cancer stem cell marker, in HCC remains unclear. This study evaluated LGR5 express...
Ergin Erginöz,Gökçe Hande Çavuş,Tülin Öztürk et al. Ergin Erginöz et al.
IntroductionInvasive ductal carcinoma (IDC) with neuroendocrine differentiation (NED) is a rare subgroup of breast cancer that is treated the same way as invasive ductal carcinoma-no special type (IDC-NST). In this study, we aimed to study ...
Hema A Venkatappa,Suma Mysore Narayana,Prakruthi Kaushik et al. Hema A Venkatappa et al.
The survivors of childhood neuroblastoma face a 2.8 to 10.4 times higher risk of developing a second malignancy compared to the general population. Here, a 10-month-old boy presented with an abdominal mass, urine dribbling, and fever. Exami...