Results 41 to 50 of about 34,984 (234)

A rare case of primary renal leiomyosarcoma with peritoneal sarcomatosis – A case report

Journal of Dr. NTR University of Health Sciences, 2022
Primary renal leiomyosarcoma is an extremely rare renal malignancy. This case report presents clinicopathological and immunophenotypic features of a case of primary renal leiomyosarcoma with peritoneal sarcomatosis.
Maruthi D. Karri, Kaumudi Konkay, Vijaya S. Mandava, Geetha V. Panchakarla, Padmavathi D. Chaganti   +4 more
doaj   +1 more source

Interventional oncology in children: Where are we now?

Journal of Medical Imaging and Radiation Oncology, EarlyView.
Abstract Paediatric Interventional Oncology (IO) lags behind adult IO due to a scarcity of specific outcome data. The suboptimal way to evolve this field is relying heavily on adult experiences. The distinct tumour types prevalent in children, such as extracranial germ cell tumours, sarcomas, and neuroblastoma, differ strongly from those found in ...
Premal Amrishkumar Patel, Fernando Gómez Muñoz   +1 more
wiley   +1 more source

Case Report of Maxillary Alveolar Rhabdomyosarcoma Misdiagnosed as Periapical Lesion: Clinicopathological Alerts and Life‐Saving Lessons for Dentists

Australian Endodontic Journal, EarlyView.
ABSTRACT This report describes a rare case of alveolar rhabdomyosarcoma initially presenting with clinical features resembling an endodontic lesion. A 15‐year‐old male presented with progressive right maxillary swelling initially treated as a dental abscess.
Saliha Akçay Köprücü, Erdal Rahman Köprücü, Aysun Atasoy Sındıraç, Ümit Çobanoğlu   +3 more
wiley   +1 more source

Resecting Beyond the Central Pelvic Compartment in Pelvic Exenterations for Gynaecological Malignancies: Outcomes From a Tertiary Unit

Australian and New Zealand Journal of Obstetrics and Gynaecology, EarlyView.
ABSTRACT Background Pelvic exenterations (PE) in solid organ gynaecological malignancies have historically been confined to the central pelvic compartment but an expansion of resection extent to include the lateral compartment is now technically feasible. There remains uncertainty about its influence on outcomes.
Chia Yew Kong, Norman J. Galbraith, Aiste McCormick, Amy Haddock, Michael Ratcliffe, John Telfer, Steven Lo, Neil Fairbairn, Michael Palmer, Seamus Teahan, Simon Morton, Rhona Lindsay, Kevin Burton, Nadeem Siddiqui, Campbell S. Roxburgh, Peter S. Chong, Colin W. Steele, Martha Quinn   +17 more
wiley   +1 more source

Mesenteric Lymph Node Recurrence of a Primary Colorectal Leiomyosarcoma

Case Reports in Surgery, 2020
Primary colorectal leiomyosarcoma is an excessively rare entity. It is associated with an aggressive behavior and typically favor hematogenous spread. The current standard of care is surgical resection.
Amélie Beauchamp, Roy Hajjar, Sharmila Khullar, Mathieu Latour, Frank Schwenter, Herawaty Sebajang   +5 more
doaj   +1 more source

CASE REPORT HIGHLIGHTING PULMONARY ARTERY PSEUDOANEURYSMS SECONDARY TO METASTATIC UTERINE LEIOMYOSARCOMA [PDF]

, 2023
Nicole C Noff, Usman Ilyas, Asma Hosna, KEVIN GEORGE, Alli El-ijla, Vincent Rizzo   +5 more
openalex   +1 more source

Precision Oncology for Pediatric Solid Tumors Using In‐Hospital Pediatric/AYA Malignancy‐Specific Panel Sequencing

Cancer Science, EarlyView.
Our findings indicate that a pediatric/AYA‐specific targeted panel deployed in a hospital can deliver rapid, clinically actionable molecular insights with high diagnostic and prognostic yield. This complements larger sequencing platforms by offering speed, focused content, and easier interpretation.
Masato Kojima, Sho Kurihara, Isamu Saeki, Ryo Touge, Keigo Nakashima, Shuhei Karakawa, Fumiyuki Yamasaki, Satoshi Okada, Eiso Hiyama   +8 more
wiley   +1 more source

Acral Mesenchymal Spindle Cell Neoplasm With a Novel HMGA2::NCOA2 Fusion

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Molecular profiling has revolutionized the field of soft tissue pathology, enhancing diagnostic precision and treatment strategies. The integration of molecular analysis and immunohistochemistry has been crucial for classifying diagnostically challenging acral mesenchymal neoplasms.
Grace Z. Armstrong, Carina A. Dehner, Eitan Halper‐Stromberg, Esther Baranov, Anna C. Eden, Rachel P. Kowal   +5 more
wiley   +1 more source

Atypical Fibroxanthoma/Pleomorphic Dermal Sarcoma With Osseous Metaplasia: A Series of Three Cases

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Atypical fibroxanthoma (AFX) and pleomorphic dermal sarcoma (PDS) are rare mesenchymal tumors typically arising on sun‐damaged skin of the head and neck in elderly patients. PDS is a more aggressive tumor but with similar demographics, cellular morphology, immunohistochemical features, and genetic findings.
Taylor Novice, Yitong Xu, Thomas Brenn, Scott C. Bresler   +3 more
wiley   +1 more source

Primary Leiomyosarcoma of the Adrenal Gland: A Case Report with Immunohistochemical Study and Literature Review

Case Reports in Urology, 2014
Primary adrenal leiomyosarcoma is extremely rare tumor. We report a case with adrenal leiomyosarcoma. Our case was a 48-year-old man who presented with lower urinary tract symptoms.
Murat Tolga Gulpinar, Asif Yildirim, Berrin Gucluer, Ramazan Gokhan Atis, Cengiz Canakci, Cenk Gurbuz, Turhan Caskurlu   +6 more
doaj   +1 more source