Primary immature teratoma in the liver with growing teratoma syndrome and gliomatosis peritonei: a rare case report
Primary liver immature teratoma is extremely rare and only 4 cases have been reported, let alone with growing teratoma syndrome (GTS) and/or gliomatosis peritonei (GP). (Source: Diagnostic Pathology)
Source: Diagnostic Pathology - October 29, 2022 Category: Pathology Authors: RenMing Liu, JianNing Chen, ChunKui Shao and Na Cheng Tags: Case Report Source Type: research
Tubulovillous adenoma with high-grade dysplasia of the vulva harboring high tumor mutational burden and cancer-associated mutations: a case report
Vulvar cancer is a rare disease, accounting for approximately 5% of gynecological malignancies. Primary adenocarcinoma of intestinal-type of the vulva or its precancerous lesion is extremely rare, and details ... (Source: Diagnostic Pathology)
Source: Diagnostic Pathology - October 28, 2022 Category: Pathology Authors: Hanako Sato, Kosuke Murakami, Tomoyuki Otani and Noriomi Matsumura Tags: Case Report Source Type: research
Correction: Mu heavy chain disease with MYD88 L265P mutation: An unusual manifestation of lymphoplasmacytic lymphoma
(Source: Diagnostic Pathology)
Source: Diagnostic Pathology - October 20, 2022 Category: Pathology Authors: Vandana Baloda, Sarah E. Wheeler, David L. Murray, Mindy C. Kohlhagen, Jeffrey A. Vos, Svetlana A. Yatsenko, Mounzer E. Agha, Miroslav Djokic, Steven H. Swerdlow and Nathanael G. Bailey Tags: Correction Source Type: research
A case of death of patient with ovarian fibroma combined with Meigs Syndrome and literature review
Ovarian fibroma is the most common benign pure stromal tumor. It has no specific clinical manifestation, most of which are pelvic or adnexal masses. 10-15% of cases with hydrothorax or ascites, after tumor res... (Source: Diagnostic Pathology)
Source: Diagnostic Pathology - October 17, 2022 Category: Pathology Authors: Na Tan, Kai-yuan Jin, Xiao-rong Yang, Cheng-fang Li, Jin Yao and Hong Zheng Tags: Case Report Source Type: research
Multiple orthokeratinized odontogenic cysts: clinical, pathological, and genetic characteristics
Orthokeratinized odontogenic cyst (OOC) is a rare developmental odontogenic cyst of the jaw. It was originally believed to be a variant of odontogenic keratocyst (OKC) but is now considered to be a distinct en... (Source: Diagnostic Pathology)
Source: Diagnostic Pathology - October 14, 2022 Category: Pathology Authors: Sawako Ono, Katsutoshi Hirose, Shintaro Sukegawa, Satoko Nakamura, Daisuke Motooka, Yuri Iwamoto, Yumiko Hori, Kaori Oya, Yasuo Fukuda and Satoru Toyosawa Tags: Brief Report Source Type: research
Two cases of spindle cell tumors with S100 and CD34 co-expression showing novel RAF1 fusions
Recently, a novel group of CD34 and S100 co-expression spindle cell tumors with distinctive stromal and perivascular hyalinization harboring recurrent gene fusions involving RET, RAF1, BRAF, and NTRK1/2 gene has ... (Source: Diagnostic Pathology)
Source: Diagnostic Pathology - October 13, 2022 Category: Pathology Authors: Li-Hua Gong, Wei-Feng Liu, Xiao-Hui Niu and Yi Ding Tags: Case Report Source Type: research
Pulmonary papillary adenoma with malignant potential: a case report and literature review
We report a 66-year-old female patient with a tumor in the lower lobe of the right lung and present the clinicopathological feat... (Source: Diagnostic Pathology)
Source: Diagnostic Pathology - October 13, 2022 Category: Pathology Authors: Ping Liu, Junjian Feng, Min Yang, Jingqiu Chen, Luyao Fu and Junxu Lu Tags: Case Report Source Type: research
Uterine choriocarcinoma arising from serous carcinoma in a postmenopausal woman: an analysis of next-generation sequencing and PD-L1 immunochemistry
Uterine somatic choriocarcinoma is a rare, clinically aggressive malignant tumor. They frequently concur with other cancer. However, the molecular pathogenesis between somatic choriocarcinoma and the concurren... (Source: Diagnostic Pathology)
Source: Diagnostic Pathology - October 13, 2022 Category: Pathology Authors: Meiping Li, Lei Bao, Bo Lu, Wenshun Ge and Lifang Ren Tags: Case Report Source Type: research
Thymofibrolipoma: a case report and review of the literature
Thymofibrolipoma has been described as a variant of thymolipoma. To date, 3 cases have been reported, and the lesion have been described to consist of extensive areas of collagenous tissue interspersed with is... (Source: Diagnostic Pathology)
Source: Diagnostic Pathology - October 12, 2022 Category: Pathology Authors: Ryu Jokoji and Emiko Tomita Tags: Case Report Source Type: research
Accuracy of next-generation sequencing for molecular profiling of small specimen of lung cancer: a prospective pilot study of side-by-side comparison
Successful practice of precision medicine in advanced lung cancers relies on therapeutic regimens tailored to individual molecular characteristics. The aim of this study was to investigate the accuracy of smal... (Source: Diagnostic Pathology)
Source: Diagnostic Pathology - October 12, 2022 Category: Pathology Authors: Xiaosong Ben, Dan Tian, Weitao Zhuang, Rixin Chen, Sichao Wang, Zihao Zhou, Cheng Deng, Ruiqing Shi, Songlin Liu, Dongkun Zhang, Jiming Tang, Liang Xie, Haiyu Zhou, Zhou Zhang, Min Li, Xuanye Zhang & hellip; Tags: Research Source Type: research
Diagnostic challenge in mixed phenotype acute leukemia with T/megakaryocyte or T/myeloid lineages accompanied by t(3;3)
The diagnosis of mixed phenotype acute leukemia (MPAL) with T/megakaryocyte or T/myeloid lineages accompanied by t(3;3) is always a challenge. Therefore, multiple experimental methods are usually required to a... (Source: Diagnostic Pathology)
Source: Diagnostic Pathology - October 5, 2022 Category: Pathology Authors: Yannan Jia, Dong Lin, Zhe Wang, Chengwen Li, Huijun Wang, Jianxiang Wang and Yingchang Mi Tags: Case Report Source Type: research
Primary small intestinal extranodal NK/T cell lymphoma, nasal type with kidney involvement: a rare case report and literature review
Extranodal NK/T cell lymphoma, nasal type (EN-NK/T-NT) is a rare and aggressive type of non-Hodgkin ’s lymphoma. EN-NK/T-NT seldom occurs in the gastrointestinal tract, and renal involvement is relatively rare. (Source: Diagnostic Pathology)
Source: Diagnostic Pathology - October 5, 2022 Category: Pathology Authors: Shuyan Mao, Changying Diao and Lei Cao Tags: Case Report Source Type: research
Cutaneous metastasis of carcinomatous component of ovarian carcinosarcoma: A case report and review of the literature
We report an unusual case of ovarian carcinosarcoma with cutaneous metastasis of carcinomatous component that displayed distinct clinical manifestation. A 4... (Source: Diagnostic Pathology)
Source: Diagnostic Pathology - October 5, 2022 Category: Pathology Authors: Jinhang Li, Chen Cao, Peng Liu, Zhifeng Yan, Deyin Xing and Aijun Liu Tags: Case Report Source Type: research
A two-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family: clinical presentations, pathological characteristics and genetic analysis: a case report
Hyperparathyroidism-Jaw Tumor (HPT-JT) is caused by inactivating germline mutations of CDC73. This hereditary disease can present with a range of symptoms. Jaw ossifying fibroma (OF) is one of the most importa... (Source: Diagnostic Pathology)
Source: Diagnostic Pathology - September 24, 2022 Category: Pathology Authors: Dun Yang, Jiaoyun Zheng, Fei Tang, Qiongzhi He, Hui Huang and Peng Zhou Tags: Case Report Source Type: research
DICER1-associated central nervous system sarcoma with neural lineage differentiation: a case report
DICER1-associated central nervous system sarcoma (DCS) without evidence of other cancer-related syndromes is rare. Though the morphology of DCS was highly variable, the immunophenotype was predominant myogenic ph... (Source: Diagnostic Pathology)
Source: Diagnostic Pathology - September 24, 2022 Category: Pathology Authors: Kun Yao, Zejun Duan, Jing Feng, Changxiang Yan and Xueling Qi Tags: Case Report Source Type: research
