Results 11 to 20 of about 331,017 (218)

Characteristic of Endometrial Stromal Sarcoma by Algorithm of Potential Biomarkers for Uterine Mesenchymal Tumor

Current Issues in Molecular Biology, 2023
The benign tumor uterine leiomyoma (UL) develops from the smooth muscle tissue that constitutes the uterus, whereas malignant tumor uterine sarcoma develops from either the smooth muscle tissue or stroma and is different from UL and endometrial cancer ...
Takuma Hayashi, Kenji Sano, Nobuo Yaegashi, Kaoru Abiko, Ikuo Konishi   +4 more
doaj   +1 more source

Form follows function: Morphological and immunohistological insights into epithelial–mesenchymal transition characteristics of tumor buds

Tumor Biology, 2017
In cancer biology, the architectural concept “form follows function” is reflected by cell morphology, migration, and epithelial–mesenchymal transition protein pattern. In vivo, features of epithelial–mesenchymal transition have been associated with tumor
Kathrin Enderle-Ammour, Moritz Bader, Theresa Dorothee Ahrens, Kai Franke, Sylvia Timme, Agnes Csanadi, Jens Hoeppner, Birte Kulemann, Jochen Maurer, Philip Reiss, Oliver Schilling, Tobias Keck, Thomas Brabletz, Elmar Stickeler, Martin Werner, Ulrich Friedrich Wellner, Peter Bronsert   +16 more
doaj   +1 more source

Endoscopic submucosal excavation for gastric plexiform fibromyxoma: A case report and systematic review of literature

Frontiers in Oncology, 2023
Plexiform fibromyxoma (PF) is a rare mesenchymal tumor of which the pathogenesis and molecular changes are still unclear. Histologically, it is characterized by a cluster of bland spindle or ovoid cells growing in the mucoid or fibromyxoid stroma rich in
Ziqin Xia, Zhidai Zhou, Wei Guo, Hongling Wang, Fan Wang, Feng Zhou   +5 more
doaj   +1 more source

Aggressive angiomyxoma of the vulva: An uncommon entity

Indian Dermatology Online Journal, 2012
Aggressive angiomyxoma is a rare, locally invasive mesenchymal tumor occurring usually in women of reproductive age, which carries a high risk for local relapse; hence the need to differentiate it from the other mesenchymal tumors occurring in this ...
Mahendra M Kura, Saurabh R Jindal, Usha N Khemani   +2 more
doaj   +1 more source

Solitary Fibrous Tumor of the Supraclavicular Region

Turkish Archives of Otorhinolaryngology, 2014
Solitary fibrous tumors of the head and neck are extremely rare, slow-growing, and generally asymptomatic benign neoplasms. To the best of our knowledge, only 153 cases of solitary fibrous tumors in the head and neck have been previously reported in the ...
Çağatay Han Ülkü, Yasin Kürşad Varsak, Osman Yılmaz   +2 more
doaj   +1 more source

Tumor-induced osteomalacia – a mystery illness beyond aches, pains, and depression

Endocrine Regulations, 2021
Objective. Tumor-induced osteomalacia (TIO) is a rare paraneoplastic syndrome characterized by chronic hypophosphatemia and osteomalacia. We present case of a patient with a protracted clinical course of TIO.
Ni Huajing (Jing), Clifton-Bligh Roderick, Brzozowska Malgorzata Monika   +2 more
doaj   +1 more source

Odontogenic myxoma of posterior maxilla – A rare case report

Journal of Family Medicine and Primary Care, 2020
Odontogenic myxoma is a benign, rare neoplasm of mesenchymal origin comprising of 3%–6% of all odontogenic tumors. Odontogenic myxoma occurs more commonly in the second and third decade and is more commonly seen in mandible compared with maxilla but ...
Soundarya Ramesh, Poornima Govindraju, Balaji Pachipalusu   +2 more
doaj   +1 more source

Leiomyosarcoma, a rare smooth muscle cancer in the pancreas: An adjuvant radiotherapy treatment approach

Cancer Reports, 2023
Background Leiomyosarcoma of visceral organs is uncommon, and pancreatic primary occurrence is even rarer. In terms of curative treatment, patients are generally managed with surgery alone, without significant data on the role or efficacy of adjuvant ...
Ali Taghizadeh Kermani, Alireza Khooei, Mohsen Aliakbarian, Soudeh Arastouei   +3 more
doaj   +1 more source

Ovarian Sex Cord Stromal Tumors in Children and Adolescents—The European Standard Clinical Practice Recommendations

Pediatric Blood &Cancer, EarlyView.
ABSTRACT As part of the European Cooperative Study Group for Paediatric Rare Tumours initiative, we developed standard clinical practice guidelines for ovarian sex cord stromal tumors, based on comprehensive national and international cohort analyses, literature review, and a final expert consensus conference.
Dominik T. Schneider, Kris‐Ann Schultz, Nora Schnitzler, Michael Abele, Tal Ben‐Ami, Ewa Bien, Gianni Bisogno, Ines B. Brecht, Maja Cesen, Andrea Ferrari, Michaela Kuhlen, Malgorzata A. Krawczyk, Ricardo Lopez‐Almaraz, Yves Reguerre, Calogero Virgone, Daniel Orbach   +15 more
wiley   +1 more source

Case Report: Acral MYH10::ALK fusion superficial mesenchymal neoplasm: first proof of metastatic potential

Frontiers in Oncology
BackgroundSuperficial ALK-rearranged soft tissue tumors are rare mesenchymal neoplasms showing heterogenous morphology and clinical behavior. They usually present as slowly enlarging nodules in young adults and can mimic other spindle cell tumors.
Masih Kameh Khosh, Masih Kameh Khosh, Sascha Wellenbrock, Sascha Wellenbrock, Daniel Kameh Khosh, Tobias Hirsch, Tobias Hirsch, Abbas Agaimy, Dan Mon O'Dey   +8 more
doaj   +1 more source