Results 51 to 60 of about 5,947 (182)

Obstructive Pyelonephritis Secondary to Ureteral Compression by an Intra‐Abdominal Desmoid Tumor in Familial Adenomatous Polyposis: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT In patients with familial adenomatous polyposis, intra‐abdominal desmoid tumors should be recognized as a rare but important cause of ureteral obstruction and obstructive pyelonephritis. Prompt cross‐sectional imaging, early recognition, and multidisciplinary management are essential for preserving renal function, treating infection, and ...
Alireza Mehrban   +5 more
wiley   +1 more source

Spindle Cell Fibromatosis of the Breast: A Lesson in Malignancy Mimicry

open access: yesClinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Spindle cell fibromatosis of the breast (SCFB) is a rare benign tumor that closely mimics malignancy on imaging and clinical examination. Accurate diagnosis relies on histopathology and immunohistochemistry, particularly β‐catenin staining, to guide appropriate management and avoid overtreatment while addressing its locally aggressive behavior
Valerie Fiore   +5 more
wiley   +1 more source

Targeting Stem Cell Behavior in Desmoid Tumors (Aggressive Fibromatosis) by Inhibiting Hedgehog Signaling

open access: yesNeoplasia: An International Journal for Oncology Research, 2013
Desmoid tumor (also called aggressive fibromatosis) is a lesion of mesenchymal origin that can occur as a sporadic tumor or a manifestation of the preneoplastic syndrome, familial adenomatous polyposis caused by a mutation in adenomatous polyposis coli ...
Ronak Ghanbari-Azarnier   +4 more
doaj   +1 more source

Locally Aggressive Desmoid Tumor With L4–L5 Vertebral Invasion and Progressive Neurological Deficit: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Desmoid‐type fibromatosis is a rare, non‐metastatic fibroblastic neoplasm that may cause major morbidity through locally infiltrative growth. Spinal involvement with vertebral destruction and neurological deficit is particularly uncommon and may mimic malignant spindle‐cell or primary osseous tumors.
Ghada A. AlAnsari   +4 more
wiley   +1 more source

Intestinal transplantation in Australia: progress, challenges and future directions

open access: yesInternal Medicine Journal, Volume 56, Issue 7, Page 1182-1189, July 2026.
Abstract Background Intestinal transplant is a rare procedure reserved for patients with intestinal failure who cannot be sustained on total parenteral nutrition due to severe, life‐threatening complications. This study aims to describe the activity and outcomes of intestinal transplantation undertaken in Australia.
Brooke Chapman   +5 more
wiley   +1 more source

11‐year‐old girl presenting with blurred vision and progressive right arm weakness

open access: yes
Brain Pathology, Volume 36, Issue 6, November 2026.
Trung Toan Tran   +6 more
wiley   +1 more source

Concomitant Medication Effects on Immunotherapy Outcomes in Sarcoma: A Pooled Post Hoc Analysis of Seven Phase II Trials

open access: yesCancer Medicine, Volume 15, Issue 6, June 2026.
ABSTRACT Background Concomitant medications (CMs) influence outcomes in patients receiving immune checkpoint inhibitors (ICIs), but their impact in sarcoma remains undefined. We assessed the association between CM use and ICI outcomes in patients with advanced or metastatic sarcoma. Methods This pooled analysis included patients from seven investigator‐
Adel Shahnam   +16 more
wiley   +1 more source

Intraabdominal desmoid tumor.

open access: yesJBR-BTR : organe de la Societe royale belge de radiologie (SRBR) = orgaan van de Koninklijke Belgische Vereniging voor Radiologie (KBVR), 2000
info:eu-repo/semantics ...
Sy, Marieme N'Dye   +2 more
openaire   +2 more sources

Incidental Rectus Abdominis Leiomyoma Discovered During Emergency Cesarean Section: A Rare Case Report From Northern Tanzania

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Uterine fibroids, also referred to as leiomyomas, are benign uterine tumors with a lifetime prevalence of approximately 75% depending on race, age, and a variety of genetic and environmental factors. Extra‐uterine leiomyomas are uncommon, and their occurrence within the rectus abdominis muscle is exceptionally rare.
Ibrahim Salum   +9 more
wiley   +1 more source

Abdominal Wall Desmoid Tumor Misdiagnosed as Schwannoma: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT We present the case of a 35‐year‐old woman with an abdominal wall mass initially diagnosed radiologically as a schwannoma. Histopathology revealed desmoid fibromatosis through β‐catenin positivity, despite no trauma or surgical history. Complete excision with negative margins was curative, highlighting immunohistochemistry's diagnostic value ...
Faten Limaiem, Mohamed Hajri
wiley   +1 more source

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