{"database":"JPOST Repository","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Tabular":["https://storage.jpostdb.org/JPST004032/files/C23005_Re.pg_matrix.tsv","https://storage.jpostdb.org/JPST004032/files/C23005_Re.tsv","https://storage.jpostdb.org/JPST004032/files/C23005_Re.pr_matrix.tsv"],"Mzml":["https://storage.jpostdb.org/JPST004032/files/T_Cjo228_031.mzML","https://storage.jpostdb.org/JPST004032/files/N_Cjo228_032.mzML"],"Raw":["https://storage.jpostdb.org/JPST004032/files/N_Cjo228_032.raw","https://storage.jpostdb.org/JPST004032/files/T_Cjo228_031.raw"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Proteomics"],"submitter":["Yuki Yoshimatsu"],"species":["Homo Sapiens (human)"],"full_dataset_link":["https://repository.jpostdb.org/entry/JPST004032"],"submitter_affiliation":["Kazusa DNA Research Institute."],"sample_protocol":[""],"repository":["jPOST"],"data_protocol":[""],"pubmed_abstract":["<h4>Introduction</h4>Endometriosis-associated intestinal tumors (EAITs) are rare malignancies that arise from ectopic endometrial tissue, and their clinical and molecular characteristics remain poorly defined.<h4>Case presentation</h4>We report a 53-year-old woman who presented with rectal bleeding. Imaging revealed a rectal mass invading the uterus. An initial endoscopic biopsy was inconclusive; however, a subsequent CT-guided biopsy confirmed adenocarcinoma. Immunohistochemical analysis suggested a gynecological origin. The patient underwent posterior total pelvic exenteration with bilateral lymphadenectomy. Histopathological evaluation confirmed endometriosis-associated endometrioid adenocarcinoma with ovarian metastasis. Postoperative chemotherapy was administered, and the patient has remained disease-free for 3.5 years.<h4>Conclusions</h4>This case highlights the diagnostic challenges and clinical complexity of EAITs. Tumor proteomic profiling provided additional biological insights and may serve as a reference for future comparative and translational research."],"pubmed_title":["Endometriosis-Associated Intestinal Tumor: A Case Report and Literature Review with Comprehensive Proteomic Data."],"pubmed_authors":["Toyota Naoyuki N, Yoshimatsu Yuki Y, Kamozawa Chihiro C, Nakanishi Ryo R, Fujita Shin S, Abe Makoto M, Konno Ryo R, Kawashima Yusuke Y, Kondo Tadashi T"],"additional_accession":[]},"is_claimable":false,"name":"Endometriosis-associated intestinal tumor: A Case Report and Review of Literature with Comprehensive Proteomic Analysis","description":"This study reports a rare case of endometriosis-associated intestinal tumor (EAIT) in a 53-year-old woman who presented with rectal bleeding. Imaging and histopathology confirmed endometrioid adenocarcinoma arising from rectal endometriosis with ovarian metastasis. The patient underwent posterior total pelvic exenteration followed by adjuvant chemotherapy and has remained disease-free for 3.5 years. Comprehensive proteomic profiling of the tumor identified 9,294 proteins, with data deposited in the jPOST repository. This case highlights the diagnostic challenges, clinical management strategies, and biological insights of EAIT, providing a valuable reference for future comparative and translational research.","dates":{"publication":"Tue Jun 30 00:00:00 BST 2026"},"accession":"PXD067723","cross_references":{"TAXONOMY":["9606"],"pubmed":["41853299"]}}